Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.29 (T)
Location

Chromosome 10:122454932 (forward strand) | View in location tab

Co-located

with COSMIC COSM3751582 (G/T) ; HGMD-PUBLIC CM066533

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

10:g.122454932G>T
ENST00000528446.1:c.205G>T
ENSP00000436682.1:p.Ala69Ser

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2869 individual genotypes, is associated with 16 phenotypes and is mentioned in 213 citations.

Variation displays