Variant #0001056714 (NC_000019.9:g.45867799G>A, NM_000400.3:c.601C>T (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.45867799G>A
DNA change (hg38) -
Published as ERCC2(NM_000400.3):c.601C>T (p.H201Y), ERCC2(NM_000400.4):c.601C>T (p.(His201Tyr), p.H201Y)
ISCN -
DB-ID ERCC2_000074 See all 3 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) 0.00055 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/. - c.601C>T r.(?) p.(His201Tyr)
KLC3 NM_177417.2 ?/. - c.*13184G>A r.(=) p.(=)


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