Variant #0000276311 (NC_000010.10:g.50732330C>T, NM_000124.2:c.1146G>A (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.50732330C>T
DNA change (hg38) g.49524284C>T
Published as ERCC6(NM_000124.2):c.1146G>A (p.E382=), ERCC6(NM_001346440.1):c.1146G>A (p.E382=)
ISCN -
DB-ID ERCC6_000079 See all 2 reported entries
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) 0.0019 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 -?/. - c.1146G>A r.(?) p.(Glu382=)
PGBD3 NM_170753.2 -?/. - c.-259G>A r.(?) p.(=)


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