Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 15:66436837 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1517232, COSM1374186 ; HGMD-PUBLIC CM080433

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB 4945

HGVS names

This variant has 7 HGVS names - Hide

15:g.66436837G>T
ENST00000307102.9:c.383G>T
ENSP00000302486.4:p.Gly128Val
ENST00000425818.2:n.894G>T
LRG_725:g.54965G>T
LRG_725t1:c.383G>T
LRG_725p1:p.Gly128Val

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays