Variant #0000808941 (NC_000019.9:g.45900279A>C, NM_012099.1:c.-9676A>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.45900279A>C
DNA change (hg38) -
Published as PPP1R13L(NM_001142502.1):c.236T>G (p.F79C), PPP1R13L(NM_006663.4):c.236T>G (p.F79C)
ISCN -
DB-ID CD3EAP_000027 See all 2 reported entries
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) 0.00208 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP1R13L NM_006663.3 ?/. - c.236T>G r.(?) p.(Phe79Cys)
CD3EAP NM_012099.1 ?/. - c.-9676A>C r.(?) p.(=)


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