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 15:45109895 (forward strand) | View in location tab

Co-located

with COSMIC COSM3420336 (G/A) ; HGMD-PUBLIC CM053838

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14080

This variation has 6 HGVS names - click the plus to show

15:g.45109895G>A
ENST00000389039.8:c.1126C>T
ENSP00000373691.6:p.Arg376Trp
ENST00000558383.1:n.1457C>T
ENST00000603300.1:c.1126C>T
ENSP00000475084.1:p.Arg376Trp

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays