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 22:36293787 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1416045

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000022.9:g.35019779G>A

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2504 sample genotypes.

Variant displays