Variant #0000000026 (NC_000002.11:g.128017009C>T, ERCC3(NM_000122.1):c.2080G>A)

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.128017009C>T
Reference -
DB-ID ERCC3_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00078 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC3 NM_000122.1 ?/? 14 c.2080G>A r.(?) p.(Ala694Thr)