Variant #0001050783 (NC_000002.11:g.128046975G>A, NM_000122.1:c.760C>T (ERCC3))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.128046975G>A
DNA change (hg38) -
Published as ERCC3(NM_000122.2):c.760C>T (p.(Gln254*)), ERCC3(NM_001303418.1):c.568C>T (p.Q190*)
ISCN -
DB-ID ERCC3_000025 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC3 NM_000122.1 +/. - c.760C>T r.(?) p.(Gln254Ter)


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