Variant #0000692836 (NC_000019.9:g.45860791C>T, NM_000400.3:c.1318G>A (ERCC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45860791C>T
DNA change (hg38) -
Published as ERCC2(NM_000400.3):c.1318G>A (p.A440T)
ISCN -
DB-ID ERCC2_000102
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/. - c.1318G>A r.(?) p.(Ala440Thr)
KLC3 NM_177417.2 ?/. - c.*6176C>T r.(=) p.(=)


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