Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 15:38351113 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM093925

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16211

HGVS names

This variant has 3 HGVS names - Hide

15:g.38351113A>T
ENST00000299084.8:c.784A>T
ENSP00000299084.4:p.Arg262Ter

About this variant

This variant overlaps 1 transcript and is associated with 2 phenotypes.

Variant displays