Variant #0000567742 (NC_000019.9:g.45916903C>T, NM_012099.1:c.*4144C>T (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.45916903C>T
DNA change (hg38) g.45413645C>T
Published as ERCC1(NM_202001.2):c.875G>A (p.W292*)
ISCN -
DB-ID ERCC1_000001
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) 0.00194 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 -/. - c.843+32G>A r.(=) p.(=)
FOSB NM_006732.2 -/. - c.-54942C>T r.(?) p.(=)
CD3EAP NM_012099.1 -/. - c.*4144C>T r.(=) p.(=)


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