Original source

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

C/A/T|Ancestral: C|Ambiguity code: H

Chromosome 5:151851406 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM940872, CM086829, CM940871

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2264, 2265, NM_000171.3:c.896G>A, NM_000171.3:c.896G>T

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 4 phenotypes.

Variant displays