This variant 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: 0.13 (A)

Chromosome 2:85625544 (forward strand) | View in location tab


with COSMIC COSM148888 (G/A)

Most severe consequence
Synonymous variant
Evidence status


This variant has 39 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 48 transcripts and has 4264 sample genotypes.

Variant displays