Variant #0000276248 (NC_000019.9:g.45860760C>T, NM_000400.3:c.1349G>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.45860760C>T
DNA change (hg38) g.45357502C>T
Published as ERCC2(NM_000400.3):c.1349G>A (p.R450H, p.(Arg450His))
ISCN -
DB-ID ERCC2_000022 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) 0.00019 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/. - c.1349G>A r.(?) p.(Arg450His)
KLC3 NM_177417.2 ?/. - c.*6145C>T r.(=) p.(=)


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