Original source

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

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

Chromosome 17:7674221 (forward strand) | View in location tab


with COSMIC COSM11564 (G/C), COSM45116 (G/-), COSM10656 (G/A), COSM44920 (G/T), COSM120007 (G/A), COSM1189381 (G/C), COSM120005 (G/A), COSM1189382 (G/C), COSM3388183 (G/A), COSM1640831 (G/A), COSM120006 (G/A), COSM1189383 (G/C) ; HGMD-PUBLIC CM900211, CM010465 ; PhenCode TP53_g.13379C>G (G/C), TP53_g.13379C>T (G/A), TP53_g.13379C>A (G/T), TP53_g.13379del (G/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 74 HGVS names - Show

About this variant

This variant overlaps 42 transcripts and is associated with 4 phenotypes.

Variant displays