Original source

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

C/A/T | Ancestral: C | Ambiguity code: H

Chromosome 17:7675088 (forward strand) | View in location tab


with COSMIC COSM10718 (C/A), COSM10648 (C/T), COSM45416 (C/G), COSM99914 (C/T), COSM1679508 (C/A), COSM99022 (C/T), COSM1679510 (C/A), COSM99023 (C/T), COSM1679512 (C/A), COSM3355994 (C/T), COSM1640851 (C/T), COSM1679509 (C/A), COSM99024 (C/T), COSM1679511 (C/A) ; HGMD-PUBLIC CM062017, CM951224 ; PhenCode TP53_g.12512G>T (C/A), TP53_g.12512G>C (C/G), TP53_g.12512G>A (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 152 HGVS names - Show

About this variant

This variant overlaps 84 transcripts, is associated with 4 phenotypes and is mentioned in 4 citations.

Somatic mutation displays