Original source

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

T/A/G | Ancestral: T | Ambiguity code: D

Chromosome 12:25227341 (forward strand) | View in location tab


with COSMIC COSM554 (T/G), COSM1135364 (T/G), COSM1146992 (T/A), COSM555 (T/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 2 sample genotypes and is associated with 2 phenotypes.

Variant displays