Variant #0000539979 (NC_000010.10:g.50736469C>T, NM_000124.2:c.646G>A (ERCC6))

Chromosome 10
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.50736469C>T
DNA change (hg38) g.49528423C>T
Published as ERCC6(NM_000124.2):c.646G>A (p.D216N)
ISCN -
DB-ID ERCC6_000111
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/. - c.646G>A r.(?) p.(Asp216Asn)
PGBD3 NM_170753.2 ?/. - c.-4398G>A r.(?) p.(=)


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