Variant #0000658611 (NC_000019.9:g.45920156C>T, NM_012099.1:c.*7397C>T (CD3EAP))

Chromosome 19
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.45920156C>T
DNA change (hg38) g.45416898C>T
Published as ERCC1(NM_001983.3):c.526-1G>A
ISCN -
DB-ID CD3EAP_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-16 09:50:36 +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.526-1G>A r.spl? p.?
FOSB NM_006732.2 +/. - c.-51689C>T r.(?) p.(=)
CD3EAP NM_012099.1 +/. - c.*7397C>T r.(=) p.(=)


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