This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.30 (A)

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


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

Most severe consequence
Evidence status

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 2454 individual genotypes and is mentioned in 27 citations.

Variation displays