Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.22 (G)
Location

Chromosome 5:74689390 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3683901

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Hide

5:g.74689390A>G
ENST00000511181.5:c.-314A>G
ENST00000261416.11:c.362A>G
ENSP00000261416.7:p.Lys121Arg
ENST00000515528.1:n.417A>G
ENST00000513079.5:n.427A>G

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3985 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays