Variant #0000804440 (NC_000010.10:g.50724720T>C, NC_000010.10(NM_000124.2):c.1397+7359A>G (ERCC6))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50724720T>C
DNA change (hg38) -
Published as ERCC6(NM_001277058.1):c.1845A>G (p.E615=)
ISCN -
DB-ID ERCC6_000130
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) 3.0E-5 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 2021-09-17 14:40:49 +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+7359A>G r.(=) p.(=)
PGBD3 NM_170753.2 -?/. - c.441A>G r.(?) p.(Glu147=)


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