Original source

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

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

Chromosome 16:47696408 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CP973613

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB 28660_1, NM_000293.2:c.2923T>C

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays