Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R

Chromosome 16:50711058 (forward strand) | View in location tab


with COSMIC COSM3888617 (G/A) ; HGMD-PUBLIC CM051409

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays