Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.27 (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

Variation displays