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

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

Chromosome 3:41224610 (forward strand) | View in location tab


with COSMIC COSM5677 (C/G), COSM5669 (C/T), COSM5673 (C/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 9 synonyms - Show

HGVS names

This variant has 60 HGVS names - Show

About this variant

This variant overlaps 33 transcripts and is associated with 5 phenotypes.

Variant displays