Original source

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

G/C/T | Ancestral: G | Ambiguity code: B

Chromosome 16:177019 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature and is mentioned in 1 citation.

Variant displays