Variant #0000000868 (NC_000005.9:g.60240799C>A, ERCC8(NM_000082.3):c.37G>T)

Individual ID 00000868
Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.60240799C>A
Reference Cao H1, Williams C, Carter M, Hegele RA.(2004)
DB-ID ERCC8_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
ERCC8 NM_000082.3 ./. 1 c.37G>T r.(?) p.(Glu13*) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000868 ? ? ERCC8 1 Y Yang