Variant #0000326617 (NC_000019.9:g.45922388C>T, NM_012099.1:c.*9629C>T (CD3EAP))

Chromosome 19
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.45922388C>T
DNA change (hg38) g.45419130C>T
Published as ERCC1(NM_001166049.1):c.493G>A (p.(Ala165Thr))
ISCN -
DB-ID ERCC1_000006
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 -?/. - c.493G>A r.(?) p.(Ala165Thr)
FOSB NM_006732.2 -?/. - c.-49457C>T r.(?) p.(=)
CD3EAP NM_012099.1 -?/. - c.*9629C>T r.(=) p.(=)


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