Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 10:119672373 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4502915 ; HGMD-PUBLIC CM090724

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and is associated with 6 phenotypes.

Variant displays