Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 2:227289222 (forward strand) | View in location tab

Co-located

with COSMIC COSM1614461 (G/C), COSM1614460 (G/C) ; HGMD-PUBLIC CM022780

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 893, NP_000082.2:p.GLY985VAL

This variation has 12 HGVS names - click the plus to show

Variation displays