Variant #0000680256 (NC_000015.9:g.64448228del, NM_000942.4:c.646del (PPIB))

Chromosome 15
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.64448228del
DNA change (hg38) -
Published as PPIB(NM_000942.4):c.646delG (p.E216Sfs*58)
ISCN -
DB-ID PPIB_000018
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-05-12 10:22:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPIB NM_000942.4 ?/. - c.646del r.(?) p.(Glu216SerfsTer58)
SNX22 NM_024798.2 ?/. - c.*1521del r.(?) p.(=)


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