Genomic variant #0000116386

Individual ID 00073096
Chromosome 5
Allele Paternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.226106T>G
DNA change (hg38) g.225991T>G
Published as -
ISCN -
DB-ID SDHA_000020
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Herma Renkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHA NM_004168.2 +/? 5 c.565T>G - r.565u>g p.(Cys189Gly) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000073253 DNA;RNA DSCA;RT-PCR;SEQ - - SDHA 2 Herma Renkema