Original source

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

G/A|Ancestral: G|Ambiguity code: R

Chromosome 14:20474555 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM870015 ; PhenCode NPbase_D0064:g.6146G>A (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2010_April_001_033_NP_164050_0001, 4317

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variant displays