Variant #0000326613 (NC_000019.9:g.45900039G>A, NM_012099.1:c.-9916G>A (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.45900039G>A
DNA change (hg38) g.45396781G>A
Published as PPP1R13L(NM_001142502.1):c.476C>T (p.(Pro159Leu))
ISCN -
DB-ID PPP1R13L_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
PPP1R13L NM_006663.3 ?/. - c.476C>T r.(?) p.(Pro159Leu)
CD3EAP NM_012099.1 ?/. - c.-9916G>A r.(?) p.(=)


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