Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 10:13283695 (forward strand) | View in location tab

Co-located

with COSMIC COSM427259 (G/T) ; HGMD-PUBLIC CM971176 ; ESP rs28939671 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

10:g.13283695G>A
ENST00000396913.4:c.523C>T
ENSP00000380121.2:p.Arg175Trp
ENST00000453759.4:c.523C>T
ENSP00000412525.2:p.Arg175Trp
ENST00000396920.5:c.772C>T
ENSP00000380126.3:p.Arg258Trp
ENST00000263038.6:c.823C>T
ENSP00000263038.4:p.Arg275Trp

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays