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 6:121447932 (forward strand) | View in location tab

Co-located

with COSMIC COSM295804 (G/A) ; HGMD-PUBLIC CM014191

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

6:g.121447932G>A
ENST00000282561.3:c.1085G>A
ENSP00000282561.3:p.Arg362Gln

Variation displays