Variant #0000617696 (NC_000019.9:g.45912070A>G, NM_012099.1:c.844A>G (CD3EAP))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45912070A>G
DNA change (hg38) g.45408812A>G
Published as ERCC1(NM_001983.4):c.*863T>C
ISCN -
DB-ID CD3EAP_000012
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) 0.00531 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*863T>C r.(=) p.(=)
PPP1R13L NM_006663.3 -/. - c.-3835T>C r.(?) p.(=)
FOSB NM_006732.2 -/. - c.-59775A>G r.(?) p.(=)
CD3EAP NM_012099.1 -/. - c.844A>G r.(?) p.(Thr282Ala)


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