This variant has been flagged

Variation has more than 3 different alleles

Original source

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

T/A/C/G | Ancestral: T | Ambiguity code: N

Chromosome 12:25227342 (forward strand) | View in location tab


with COSMIC COSM1158660 (T/C), COSM552 (T/C), COSM551 (T/G), COSM1140131 (T/A), COSM553 (T/A), COSM3688142 (T/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 2 phenotypes.

Variant displays