Variant #0000567740 (NC_000019.9:g.45912917T>C, NM_012099.1:c.*158T>C (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.45912917T>C
DNA change (hg38) g.45409659T>C
Published as ERCC1(NM_001983.3):c.*16A>G
ISCN -
DB-ID CD3EAP_000005
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_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 -?/. - c.*16A>G r.(=) p.(=)
PPP1R13L NM_006663.3 -?/. - c.-4682A>G r.(?) p.(=)
FOSB NM_006732.2 -?/. - c.-58928T>C r.(?) p.(=)
CD3EAP NM_012099.1 -?/. - c.*158T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.