Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.09 (G)
Location

Chromosome 2:47790942 (forward strand) | View in location tab

Co-located

with COSMIC COSM4133863 (A/G) ; PhenCode MMR_c.276A>G (A/G)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 8 synonyms - click the plus to show

This variant has 17 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 15 transcripts, has 4336 sample genotypes, is associated with 3 phenotypes and is mentioned in 9 citations.

Variant displays