Variant #0000001889 (NC_000008.10:g.75274121C>T, GDAP1(NM_018972.2):c.487C>T)

Individual ID 00001889
Chromosome 8
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.75274121C>T
Reference Cuesta A1, Pedrola L, Sevilla T, García-Planells J, Chumillas MJ, Mayordomo F, LeGuern E, Marín I, Vílchez JJ, Palau F.(2002)
DB-ID GDAP1_000004 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
GDAP1 NM_018972.2 ./. 4 c.487C>T r.(?) p.(Gln163*) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001889 ? ? GDAP1 1 Y Yang