Variant #0000998312 (NC_000010.10:g.50736565G>A, NM_000124.2:c.550C>T (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.50736565G>A
DNA change (hg38) -
Published as ERCC6(NM_000124.3):c.550C>T (p.(Gln184*))
ISCN -
DB-ID ERCC6_000154
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.550C>T r.(?) p.(Gln184*)
PGBD3 NM_170753.2 +/. - c.-4494C>T r.(?) p.(=)


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