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

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

Chromosome 7:55181314 (forward strand) | View in location tab


with COSMIC COSM13425 (G/A), COSM6242 (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 36 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and is associated with 1 phenotype.

Variant displays