Variant #0000267874 (NC_000013.10:g.103498666del, NC_000013.10(NM_001204425.1):c.1451-5802del (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.103498666del
DNA change (hg38) g.102846316del
Published as ERCC5(NM_000123.4):c.50delT (p.V17Afs*19)
ISCN -
DB-ID ERCC5_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ERCC5 NM_000123.2 +/. - c.50del r.(?) p.(Val17AlafsTer19)
BIVM NM_001159596.1 +/. - c.*6451del r.(?) p.(=)
BIVM-ERCC5 NM_001204425.1 +/. - c.1451-5802del r.(=) p.(=)
KDELC1 NM_024089.2 +/. - c.-47646del r.(?) p.(=)


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