Variant #0000983533 (NC_000019.9:g.45895276_45895290del, NM_012099.1:c.-14679_-14665del (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.45895276_45895290del
DNA change (hg38) -
Published as PPP1R13L(NM_006663.4):c.1671_1685del (p.(Gly558_Pro562del)), PPP1R13L(NM_006663.4):c.1671_1685delAGGGCCCGGGGGGCC (p.G558_P562del)
ISCN -
DB-ID CD3EAP_000024 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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP1R13L NM_006663.3 ?/. - c.1671_1685del r.(?) p.(Gly558_Pro562del)
CD3EAP NM_012099.1 ?/. - c.-14679_-14665del r.(?) p.(=)


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