Variant #0000525868 (NC_000005.9:g.60214178_60214179del, NM_000082.3:c.313_314del (ERCC8))

Chromosome 5
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.60214178_60214179del
DNA change (hg38) g.60918351_60918352del
Published as ERCC8(NM_001007233.3):c.139_140delGT (p.V47Tfs*6)
ISCN -
DB-ID ERCC8_000025
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC8 NM_000082.3 +/. - c.313_314del r.(?) p.(Val105ThrfsTer6)


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