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 10:101770378 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1345400 ; HGMD-PUBLIC CM082674

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 9234

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays