Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 6:121447932 (forward strand)|View in location tab

Co-located variants

COSMIC COSM295804 ; HGMD-PUBLIC CM014191

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 3 HGVS names - Hide

6:g.121447932G>A
ENST00000282561.3:c.1085G>A
ENSP00000282561.3:p.Arg362Gln

About this variant

This variant overlaps 1 transcript, has 2526 sample genotypes and is associated with 5 phenotypes.

Variant displays