Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with COSMIC COSM33765 (C/T) ; dbSNP rs34409589 (C/-)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 21 HGVS names - click the plus to show

About this variant

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

Variant displays