Variant #0000889150 (NC_000010.10:g.50732331T>C, NM_000124.2:c.1145A>G (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.50732331T>C
DNA change (hg38) -
Published as ERCC6(NM_001346440.1):c.1145A>G (p.E382G)
ISCN -
DB-ID ERCC6_000140
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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/. - c.1145A>G r.(?) p.(Glu382Gly)
PGBD3 NM_170753.2 ?/. - c.-260A>G r.(?) p.(=)


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