Variant #0000855625 (NC_000019.9:g.45882962T>A, NM_012099.1:c.-26993T>A (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.45882962T>A
DNA change (hg38) -
Published as PPP1R13L(NM_006663.4):c.*486A>T
ISCN -
DB-ID CD3EAP_000029
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) 0.17723 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 2022-05-09 15:47:41 +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     
PPP1R13L NM_006663.3 -/. - c.*486A>T r.(=) p.(=)
CD3EAP NM_012099.1 -/. - c.-26993T>A r.(?) p.(=)


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