Variant #0001071861 (NC_000005.9:g.224632_224633delinsTG, NM_004168.2:c.308_309delinsTG (SDHA))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.224632_224633delinsTG
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHA_000228
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jean-Pierre Bayley
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Jean-Pierre Bayley
Date created 2026-04-02 15:34:37 +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     
SDHA NM_004168.2 +?/+? - c.308_309delinsTG r.(?) p.(Ala103Val)


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