Original source

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

T/A | Ancestral: T | Ambiguity code: W

Chromosome 17:7673766 (forward strand) | View in location tab


with COSMIC COSM45649 (T/C), COSM44227 (T/A), COSM43614 (T/G), COSM131474 (T/A), COSM131484 (T/C), COSM3958796 (T/A), COSM1744596 (T/A) ; HGMD-PUBLIC CM083790 ; PhenCode TP53_g.13834A>C (T/G), TP53_g.13834A>T (T/A), TP53_g.13834A>G (T/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 5934

HGVS names

This variant has 71 HGVS names - Show

About this variant

This variant overlaps 42 transcripts and is associated with 3 phenotypes.

Variant displays