Variant #0000567719 (NC_000019.9:g.45864887G>A, NM_000400.3:c.1132C>T (ERCC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45864887G>A
DNA change (hg38) g.45361629G>A
Published as ERCC2(NM_000400.4):c.1132C>T (p.R378C)
ISCN -
DB-ID ERCC2_000066
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 +?/. - c.1132C>T r.(?) p.(Arg378Cys)
KLC3 NM_177417.2 +?/. - c.*10272G>A r.(=) p.(=)


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