Variant #0001061493 (NC_000010.10:g.104591274A>G, NM_000102.3:c.1234T>C (CYP17A1))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.104591274A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr10_006529
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2493235395
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-12-16 10:58:03 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP17A1 NM_000102.3 +/. - c.1234T>C r.(?) p.(Phe412Leu) -


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