Variant #0000866186 (NC_000019.9:g.45912243G>C, NM_012099.1:c.1017G>C (CD3EAP))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45912243G>C
DNA change (hg38) -
Published as CD3EAP(NM_001297590.1):c.1023G>C (p.M341I)
ISCN -
DB-ID CD3EAP_000034
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 ?/. - c.*690C>G r.(=) p.(=)
PPP1R13L NM_006663.3 ?/. - c.-4008C>G r.(?) p.(=)
FOSB NM_006732.2 ?/. - c.-59602G>C r.(?) p.(=)
CD3EAP NM_012099.1 ?/. - c.1017G>C r.(?) p.(Met339Ile)


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