Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 10:102832610 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1345509 ; HGMD-PUBLIC CM960476

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_010_CYP17A1_609300_0012, 16224

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variant displays