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 14:104780214 (forward strand)|View in location tab

Co-located variants

COSMIC COSM33765 ; dbSNP rs34409589 (C/-)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and is associated with 7 phenotypes.

Variant displays