Original source

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

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

Chromosome 15:63057028 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3502949, COSM3502948, COSM3502947, COSM3502946, COSM3502945 ; HGMD-PUBLIC CM010475 ; PhenCode FHC0616 (T/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 44 HGVS names - Show

About this variant

This variant overlaps 28 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays