Original source

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

C/G/T|Ancestral: C|Ambiguity code: B

Chromosome 16:31191418 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM091090, CM104702, CM091086

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 28 HGVS names - Show

About this variant

This variant overlaps 26 transcripts and is associated with 4 phenotypes.

Variant displays