Original source

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

T/A/G | Ancestral: T | Ambiguity code: D

Chromosome 12:21178955 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NC_000012.10:g.21223156T>A

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 1 phenotype.

Variant displays