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 | MAF: 0.01 (A)
Location

Chromosome 12:40363526 (forward strand) | View in location tab

Co-located

with COSMIC COSM431072 (G/A), COSM431073 (G/A) ; HGMD-PUBLIC CM057191

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

12:g.40363526G>A
ENST00000479187.3:n.3834G>A
ENST00000298910.9:c.7153G>A
ENSP00000298910.7:p.Gly2385Arg
ENST00000430804.3:c.*3826G>A

This variation has assays on 5 chips - click the plus to show

Variation displays