Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome 16:172929 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


LSDB HbVar.3

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and is mentioned in 2 citations.

Variant displays