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

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

Chromosome 3:41224607 (forward strand) | View in location tab


with COSMIC COSM5681 (A/G), COSM5691 (A/T), COSM5690 (A/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 8 synonyms - Show

HGVS names

This variant has 60 HGVS names - Show

About this variant

This variant overlaps 33 transcripts and is associated with 3 phenotypes.

Variant displays