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 15:63044072 (forward strand) | View in location tab

Co-located

with COSMIC COSM3969204 (G/A), COSM3969206 (G/A), COSM3969205 (G/A) ; HGMD-PUBLIC CM014116

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 25 HGVS names - click the plus to show

Variation displays