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 10:43105018 (forward strand) | View in location tab

Co-located

with COSMIC COSM3686739 (G/A), COSM3686738 (G/A) ; HGMD-PUBLIC CM951123

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variation displays