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 17:39665762 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1610160 ; HGMD-PUBLIC CM000576 ; PhenCode TCAP:c.157C>T (C/T)

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_220_TCAP_604488_0001, 12687

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays