Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.21 (G)
Location

Chromosome 3:122284922 (forward strand) | View in location tab

Co-located

with COSMIC COSM3767201 (A/G) ; HGMD-PUBLIC CM044584 ; PhenCode CASRdb_c.2968A>G (A/G)

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 5 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2683 sample genotypes and is mentioned in 19 citations.

Variant displays