Variant #0000979052 (NC_000010.10:g.50724538A>C, NC_000010.10(NM_000124.2):c.1397+7541T>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.50724538A>C
DNA change (hg38) -
Published as ERCC6(NM_001277058.2):c.2027T>G (p.(Val676Gly))
ISCN -
DB-ID ERCC6_000150
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) 0.00053 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/. - c.1397+7541T>G r.(=) p.(=)
PGBD3 NM_170753.2 ?/. - c.623T>G r.(?) p.(Val208Gly)


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