Variant #0000276365 (NC_000010.10:g.50732668del, NM_000124.2:c.809del (ERCC6))

Chromosome 10
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.50732668del
DNA change (hg38) g.49524622del
Published as ERCC6(NM_000124.2):c.809delG (p.G270Afs*59)
ISCN -
DB-ID ERCC6_000083
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 2020-06-26 14:44:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 +/. - c.809del r.(?) p.(Gly270AlafsTer59)
PGBD3 NM_170753.2 +/. - c.-596del r.(?) p.(=)


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