Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)

Chromosome 5:1279324 (forward strand) | View in location tab


with COSMIC COSM3723835 (G/A), COSM3723836 (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NM_198253.2:c.2097C>T

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 6 transcripts, has 2595 sample genotypes and is associated with 1 phenotype.

Variant displays