Variant #0000000098 (NC_000021.8:g.27264121G>A, APP(NM_000484.3):c.2124C>T)

Individual ID 00000098
Chromosome 21
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27264121G>A
Reference BalbĂ­n M1, Abrahamson M, Gustafson L, Nilsson K, Brun A, Grubb A.(1992)
DB-ID APP_000007
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00187 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     
APP NM_000484.3 ./. 17 c.2124C>T r.(=) p.(=) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000098 ? ? APP 1 Y Yang