Variant #0000276294 (NC_000013.10:g.103524644del, NM_001204425.1:c.4137del (BIVM-ERCC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103524644del
DNA change (hg38) g.102872294del
Published as ERCC5(NM_000123.3):c.2775delT (p.G926Afs*56)
ISCN -
DB-ID ERCC5_000045 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) Retrieve
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 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 +/. - c.2775del r.(?) p.(Gly926AlafsTer56)
BIVM NM_001159596.1 +/. - c.*32429del r.(?) p.(=)
BIVM-ERCC5 NM_001204425.1 +/. - c.4137del r.(?) p.(Gly1380AlafsTer56)


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