This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.29 (A)

Chromosome 7:55161562 (forward strand) | View in location tab


with COSMIC COSM3721608 (G/A), COSM3721609 (G/A) ; HGMD-PUBLIC CM942312

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 48 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 24 transcripts, has 3857 individual genotypes, is associated with 1 phenotype and is mentioned in 31 citations.

Variation displays