Original source

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

G/C/T|Ancestral: G|Ambiguity code: B|MAF: 0.46 (G)

Chromosome 17:7676154 (forward strand)|View in location tab

Co-located variants

COSMIC COSM45985, COSM250061 ; HGMD-PUBLIC CM961374 ; PhenCode TP53_g.11446del (G/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 11 synonyms - Show

HGVS names

This variant has 114 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 86 transcripts, has 3227 sample genotypes, is associated with 8 phenotypes and is mentioned in 242 citations.

Variant displays