Variant #0001047169 (NC_000011.9:g.61205343T>C, NC_000011.9(NM_017841.2):c.260+23T>C (SDHAF2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61205343T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHAF2_000017 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs112606325
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01712 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-06 14:40:02 +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     

Predict/SIFT     

Predicted     
SDHAF2 NM_017841.2 -/. - c.260+23T>C r.(?) p.(?) - -


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