Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 12:40298488 (forward strand) | View in location tab


with COSMIC COSM693216 (A/T) ; HGMD-PUBLIC CS053469

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NM_198578.3:c.3342A>G

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts, has 1 sample genotype, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays