Variant #0000862524 (NC_000011.9:g.34910348del, NM_003477.2:c.-27855del (PDHX))

Chromosome 11
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.34910348del
DNA change (hg38) -
Published as APIP(NM_015957.4):c.283delA (p.S95Afs*8)
ISCN -
DB-ID APIP_000022
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 2022-05-09 15:51:19 +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     
PDHX NM_003477.2 ?/. - c.-27855del r.(?) p.(=)
APIP NM_015957.2 ?/. - c.283del r.(?) p.(Ser95Alafs*8)


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