Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Effect: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Exon: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.
DNA change (cDNA): Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.
RNA change: Description of variant at RNA level (following HGVS recommendations).
- r.123c>u
- r.? = unknown
- r.(?) = RNA not analysed but probably transcribed copy of DNA variant
- r.spl? = RNA not analysed but variant probably affects splicing
- r.(spl?) = RNA not analysed but variant may affect splicing
- r.0? = change expected to abolish transcription
Protein: Description of variant at protein level (following HGVS recommendations).
- p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
- p.Arg345Pro = change derived from RNA analysis
- p.? = unknown effect
- p.0? = probably no protein produced
Variant/VariO/DNA: VariO of DNA
Variant/VariO/protein: VariO of protein
Allele: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
DNA change (genomic) (hg19): Description of variant at DNA level, based on the genomic DNA reference sequence (following HGVS recommendations).
- g.12345678C>T
- g.12345678_12345890del
- g.12345678_12345890dup
Reference: Reference to publication describing the variant, including links to OMIM (when available), PubMed or or other source, e.g. "den Dunnen ASHG2003 P2346".
DB-ID: Database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro.
Frequency: Frequency in which the variant was found; e.g 5/760 chromosomes (in 5 of 760 chromosomes tested), 1/33 patients (in 1 of 33 patients analysed in study), 0.05 controls (in 5% of control cases tested).
![](gfx/trans.png)
![](gfx/order_arrow.png) Effect
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![](gfx/trans.png)
![](gfx/order_arrow.png) Exon
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![](gfx/trans.png)
![Ascending Ascending](gfx/order_arrow_asc.png) DNA change (cDNA)
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![](gfx/trans.png)
![](gfx/order_arrow.png) RNA change
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![](gfx/trans.png)
![](gfx/order_arrow.png) Protein
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![](gfx/trans.png)
![](gfx/order_arrow.png) Variant/VariO/DNA
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![](gfx/trans.png)
![](gfx/order_arrow.png) Variant/VariO/protein
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![](gfx/trans.png)
![](gfx/order_arrow.png) DNA change (genomic) (hg19)
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![](gfx/trans.png)
![](gfx/order_arrow.png) Reference
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![](gfx/trans.png)
![](gfx/order_arrow.png) DB-ID
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![](gfx/trans.png)
![](gfx/order_arrow.png) Frequency
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![](gfx/trans.png)
![](gfx/order_arrow.png) Owner
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./. |
5UTR |
c.-194_-185dup |
r.(=) |
p.(=) |
VariO:0142 DNA insertion |
- |
g.68522107_68522116dup |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000001 |
- |
Y Yang |
./. |
1 |
c.7delG |
r.(?) |
p.(Ala3Argfs*30) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68521916delC |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542 |
CLN6_000002 |
- |
Y Yang |
./. |
1 |
c.13C>T |
r.(?) |
p.(Arg5Trp) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68521910G>A |
C. Freehauf, pers comm |
CLN6_000003 |
- |
Y Yang |
./. |
1 |
c.34G>A |
r.(?) |
p.(Ala12Thr) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68521889C>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000047 |
- |
Y Yang |
./. |
1 |
c.49G>A |
r.(?) |
p.(Gly17Ser) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68521874C>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000048 |
- |
Y Yang |
./. |
2_3 |
c.83_297del |
r.spl? |
p.? |
VariO:0141 DNA deletion |
- |
g.68506628_68521840del |
Al-Muhaizea et al 2009 Pediatr Neruol 41: 74-76 |
CLN6_000004 |
- |
Y Yang |
./. |
2 |
c.184C>T |
r.(?) |
p.(Arg62Cys) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68510888G>A |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000005 |
- |
Y Yang |
./. |
2 |
c.185G>A |
r.(?) |
p.(Arg62His) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68510887C>T |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000006 |
- |
Y Yang |
./. |
2i |
c.198+2dup |
r.spl? |
p.? |
VariO:0142 DNA insertion |
- |
g.68510872dup |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000007 |
- |
Y Yang |
./. |
2i |
c.198+104T>C |
r.(=) |
p.(=) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
- |
g.68510770A>G |
GOS, UK |
CLN6_000008 |
- |
Y Yang |
./. |
3 |
c.209C>T |
r.(?) |
p.(Pro70Leu) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68506716G>A |
C Armour pers comm |
CLN6_000009 |
- |
Y Yang |
./. |
3 |
c.214G>C |
r.(?) |
p.(Glu72Gln) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68506711C>G |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000011 |
- |
Y Yang |
./. |
3 |
c.214G>T |
r.(?) |
p.(Glu72*) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0015 protein truncation |
g.68506711C>A |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542;Gao et al. 2002. Am J Hum Genet 70: 324-335 |
CLN6_000010 |
- |
Y Yang |
./. |
3 |
c.247G>C |
r.(?) |
p.(Asp83His) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68506678C>G |
C. Freehauf, pers comm |
CLN6_000012 |
- |
Y Yang |
./. |
3 |
c.248A>T |
r.(?) |
p.(Asp83Val) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68506677T>A |
B. Garavaglia pers comm |
CLN6_000013 |
- |
Y Yang |
./. |
3 |
c.251delA |
r.(?) |
p.(Tyr84Serfs*32) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68506674delT |
R. Niezen-de Boer pers comm |
CLN6_000014 |
- |
Y Yang |
./. |
3 |
c.251delA |
r.(?) |
p.(Tyr84Serfs*32) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68506674delT |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000014 |
- |
Y Yang |
./. |
3 |
c.268_271dup |
r.(?) |
p.(Val91Glufs*42) |
VariO:0142 DNA insertion |
VariO:0023 amphigoric amino acid indel |
g.68506654_68506657dup |
Teixeira et al. 2003 Hum Mut 21: 502-508;Moore et al 2008 Clin Genet. 74:213-22 |
CLN6_000015 |
- |
Y Yang |
./. |
3 |
c.270C>A |
r.(?) |
p.(Asn90Lys) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68506655G>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000049 |
- |
Y Yang |
./. |
4 |
c.307C>T |
r.(?) |
p.(Arg103Trp) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504192G>A |
Cismondi et al 2008 Hum Genet 124: 324;C. Armour pers comm |
CLN6_000016 |
- |
Y Yang |
./. |
4 |
c.311C>T |
r.(?) |
p.(Ser104Phe) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504188G>A |
M. Elleder pers comm |
CLN6_000017 |
- |
Y Yang |
./. |
4 |
c.311C>T |
r.(?) |
p.(Ser104Phe) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504188G>A |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000017 |
- |
Y Yang |
./. |
4 |
c.316dup |
r.(?) |
p.(Arg106Profs*26) |
VariO:0142 DNA insertion |
VariO:0023 amphigoric amino acid indel |
g.68504183dup |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542 |
CLN6_000018 |
- |
Y Yang |
./. |
4 |
c.316_317insC |
r.(?) |
p.(Arg106Profs*26) |
VariO:0142 DNA insertion |
VariO:0023 amphigoric amino acid indel |
g.68504182_68504183insG |
Guerreiro R1, Bras JT, Vieira M, Warrier V, Agrawal S, Stewart H, Anderson G, Mole SE.(2013) |
CLN6_000056 |
- |
Y Yang |
./. |
4 |
c.348C>A |
r.(?) |
p.(Ser116Arg) |
- |
- |
g.68504151G>T |
Sato R et al. (2016) |
CLN6_000059 |
- |
XY Liu |
./. |
4 |
c.368G>A |
r.(?) |
p.(Gly123Asp) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68504131C>T |
Wheeler et al. 2002Am J Hum Genet 70: 537-542 |
CLN6_000019 |
- |
Y Yang |
./. |
4 |
c.368G>A |
r.(?) |
p.(Gly123Asp) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68504131C>T |
Wheeler et al. 2002Am J Hum Genet 70: 537-542 |
CLN6_000019 |
- |
Y Yang |
./. |
4 |
c.395_396delCT |
r.(?) |
p.(Ser132Cysfs*18) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68504103_68504104delAG |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542;Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7;Al-Muhaizea et al 2009 Pediatr Neurol 41: 74-76 |
CLN6_000020 |
- |
Y Yang |
./. |
4 |
c.406C>T |
r.(?) |
p.(Arg136Cys) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504093G>A |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000021 |
- |
Y Yang |
./. |
4 |
c.426C>G |
r.(?) |
p.(Tyr142*) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0015 protein truncation |
g.68504073G>C |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000022 |
- |
Y Yang |
./. |
4 |
c.445C>T |
r.(?) |
p.(Arg149Cys) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504054G>A |
Ray pers comm |
CLN6_000023 |
- |
Y Yang |
./. |
4 |
c.445C>T |
r.(?) |
p.(Arg149Cys) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504054G>A |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000023 |
- |
Y Yang |
./. |
4 |
c.460_462delATC |
r.(?) |
p.(Ile154del) |
VariO:0141 DNA deletion |
VariO:0016 sequence retaining amino acid deletion |
g.68504037_68504039delGAT |
Wheeler et al. 2002 Am J Hum Genet 70: 537-542;Teixeira et al. 2003 Hum Mut 21: 502-508;Creegan pers comm |
CLN6_000024 |
- |
Y Yang |
./. |
4 |
c.476C>T |
r.(?) |
p.(Pro159Leu) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68504023G>A |
Kousi et al 2009. Brain 132:810-9 |
CLN6_000025 |
- |
Y Yang |
./. |
4 |
c.485T>G |
r.(?) |
p.(Leu162Arg) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68504014A>C |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000026 |
- |
Y Yang |
./. |
4i |
c.486+1G>T |
r.spl? |
p.? |
VariO:0136 DNA substitution; VariO:0316 transversion |
- |
g.68504012C>A |
Teixeira et al. 2003 Hum Mut 21: 502-508 |
CLN6_000027 |
- |
Y Yang |
./. |
4i |
c.486+8C>T |
r.(=) |
p.(=) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
- |
g.68504005G>A |
Cismondi IA, Kohan R, Mole S, Oller AM and Noher de HAc I. pers comm |
CLN6_000028 |
- |
Y Yang |
./. |
4i |
c.486+8C>T |
r.(=) |
p.(=) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
- |
g.68504005G>A |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000028 |
- |
Y Yang |
./. |
5 |
c.506T>C |
r.(?) |
p.(Leu169Pro) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68503637A>G |
- |
CLN6_000029 |
- |
Y Yang |
./. |
5 |
c.506T>C |
r.(?) |
p.(Leu169Pro) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68503637A>G |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000050 |
- |
Y Yang |
./. |
5 |
c.510_512delCTA |
r.(?) |
p.(Tyr172del) |
VariO:0141 DNA deletion |
VariO:0016 sequence retaining amino acid deletion |
g.68503631_68503633delTAG |
Gao et al. 2002. Am J Hum Genet 70: 324-335 |
CLN6_000030 |
- |
Y Yang |
./. |
5 |
c.516T>A |
r.(?) |
p.(Tyr172*) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0015 protein truncation |
g.68503627A>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000051 |
- |
Y Yang |
./. |
5 |
c.519delT |
r.(?) |
p.(Asp173Glufs*33) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68503624delA |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000031 |
- |
Y Yang |
./. |
5 |
c.522dup |
r.(?) |
p.(Tyr175Valfs*27) |
VariO:0142 DNA insertion |
VariO:0023 amphigoric amino acid indel |
g.68503621dup |
Cismondi et al 2008 Hum Genet 124: 323-324 |
CLN6_000032 |
- |
Y Yang |
./. |
5i |
c.542+5G>T |
r.spl? |
p.? |
VariO:0136 DNA substitution; VariO:0316 transversion |
- |
g.68503596C>A |
Siintola et al 2005 Clin Genet 68:167-173 |
CLN6_000033 |
- |
Y Yang |
./. |
6 |
c.557T>C |
r.(?) |
p.(Phe186Ser) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68502083A>G |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000052 |
- |
Y Yang |
./. |
6 |
c.662A>C |
r.(?) |
p.(Tyr221Ser) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68501978T>G |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000034 |
- |
Y Yang |
./. |
6 |
c.662A>G |
r.(?) |
p.(Tyr221Cys) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68501978T>C |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000035 |
- |
Y Yang |
./. |
6 |
c.663C>G |
r.(?) |
p.(Tyr221*) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0015 protein truncation |
g.68501977G>C |
Siintola et al 2005 Clin Genet 68:167-173 |
CLN6_000036 |
- |
Y Yang |
./. |
7 |
c.700T>C |
r.(?) |
p.(Phe234Leu) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68500714A>G |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000053 |
- |
Y Yang |
./. |
7 |
c.715_718delTTCG |
r.(?) |
p.(Phe239Profs*29) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68500696_68500699delCGAA |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000037 |
- |
Y Yang |
./. |
7 |
c.722T>C |
r.(?) |
p.(Met241Thr) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition |
VariO:0021 amino acid substitution |
g.68500692A>G |
Sharp et al 2003 Hum Mut 22: 35-42 |
CLN6_000038 |
- |
Y Yang |
./. |
7 |
c.727delG |
r.(?) |
p.(Ala243Profs*26) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68500687delC |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000054 |
- |
Y Yang |
./. |
7 |
c.755G>A |
r.(?) |
p.(Arg252His) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68500659C>T |
Cismondi IA, Kohan R, Mole S, Oller AM and Noher de HAc I. pers comm |
CLN6_000039 |
- |
Y Yang |
./. |
7 |
c.755G>A |
r.(?) |
p.(Arg252His) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68500659C>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000039 |
- |
Y Yang |
./. |
7 |
c.775G>A |
r.(?) |
p.(Gly259Ser) |
VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition |
VariO:0021 amino acid substitution |
g.68500639C>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000055 |
- |
Y Yang |
./. |
7 |
c.776G>T |
r.(?) |
p.(Gly259Val) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68500638C>A |
Cannelli et al. 2009. Biochem Biophys Res Comm 379:892-7 |
CLN6_000040 |
- |
Y Yang |
./. |
7 |
c.794_796delCCT |
r.(?) |
p.(Ser265del) |
VariO:0141 DNA deletion |
VariO:0016 sequence retaining amino acid deletion |
g.68500618_68500620delAGG |
Sharp et al 2003 Hum Mut 22: 35-42;Santorelli pers comm.;Kousi et al 2009. Brain 132:810-9;Al-Muhaizea et al 2009 Pediatr Neruol 41: 74-76 |
CLN6_000041 |
- |
Y Yang |
./. |
7 |
c.809T>C |
r.(?) |
p.(Leu270Pro) |
- |
- |
g.68500605A>G |
Jain P et al. (2016) |
CLN6_000057 |
- |
XY Liu |
./. |
7 |
c.829_837delinsCCTG |
r.(?) |
p.(Val277Profs*5) |
VariO:0143 DNA indel |
VariO:0023 amphigoric amino acid indel |
g.68500577_68500585delinsCAGG |
Sharp et al 2003 Hum Mut 22: 35-42;Teixeira et al. 2003 Hum Mut 21: 502-508 |
CLN6_000042 |
- |
Y Yang |
./. |
7 |
c.889C>A |
r.(?) |
p.(Pro297Thr) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68500525G>T |
K. Chandler pers comm |
CLN6_000043 |
- |
Y Yang |
./. |
7 |
c.889C>A |
r.(?) |
p.(Pro297Thr) |
VariO:0136 DNA substitution; VariO:0316 transversion |
VariO:0021 amino acid substitution |
g.68500525G>T |
Kousi M1, Lehesjoki AE, Mole SE.(2012) |
CLN6_000043 |
- |
Y Yang |
./. |
7 |
c.890delC |
r.(?) |
p.(Pro297Leufs*53) |
VariO:0141 DNA deletion |
VariO:0023 amphigoric amino acid indel |
g.68500524delG |
K. Sims pers comm |
CLN6_000044 |
- |
Y Yang |
./. |
7 |
c.917_918dup |
r.(?) |
p.(Val307Thrfs*44) |
- |
- |
g.68500496_68500497dup |
Sato R et al. (2016) |
CLN6_000058 |
- |
XY Liu |