Variant #0000556616 (NC_000016.9:g.14041848C>T, NM_005236.2:c.2395C>T (ERCC4))

Chromosome 16
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.14041848C>T
DNA change (hg38) g.13947991C>T
Published as ERCC4(NM_005236.2):c.2395C>T (p.R799W, p.(Arg799Trp)), ERCC4(NM_005236.3):c.2395C>T (p.R799W)
ISCN -
DB-ID ERCC4_000006 See all 17 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) 0.00049 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 2019-07-18 18:22:55 +02:00 (CEST)
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     

Haplotype     
ERCC4 NM_005236.2 ?/. - c.2395C>T r.(?) p.(Arg799Trp) -


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