Variant #0000268927 (NC_000005.9:g.60194149T>C, NM_000082.3:c.797A>G (ERCC8))

Chromosome 5
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.60194149T>C
DNA change (hg38) g.60898322T>C
Published as ERCC8(NM_000082.3):c.797A>G (p.D266G), ERCC8(NM_000082.4):c.797A>G (p.(Asp266Gly)), ERCC8(NM_001007233.3):c.623A>G (p.D208G)
ISCN -
DB-ID ERCC8_000015 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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC8 NM_000082.3 +/. - c.797A>G r.(?) p.(Asp266Gly)


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