Variant #0000723429 (NC_000011.9:g.34938284C>T, NM_003477.2:c.82C>T (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.34938284C>T
DNA change (hg38) -
Published as PDHX(NM_003477.3):c.82C>T (p.L28=)
ISCN -
DB-ID APIP_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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDHX NM_003477.2 ?/. - c.82C>T r.(?) p.(Leu28=)
APIP NM_015957.2 ?/. - c.-453G>A r.(?) p.(=)


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