Variant #0000543840 (NC_000011.9:g.34937926C>G, NM_003477.2:c.-277C>G (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.34937926C>G
DNA change (hg38) g.34916379C>G
Published as PDHX(NM_001135024.1):c.8C>G (p.S3*)
ISCN -
DB-ID APIP_000003
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) 0.00013 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDHX NM_003477.2 ?/. - c.-277C>G r.(?) p.(=)
APIP NM_015957.2 ?/. - c.-95G>C r.(?) p.(=)


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