Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)

Chromosome 3:165773492 (forward strand) | View in location tab


with COSMIC COSM3759860 (C/T) ; HGMD-PUBLIC CM920127

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 8 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 2591 sample genotypes, is associated with 5 phenotypes and is mentioned in 15 citations.

Variant displays