Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 1:55075501 (forward strand) | View in location tab

Co-located

with COSMIC COSM3747027 (A/G), COSM3747026 (A/G)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

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

1:g.55075501A>G
ENST00000294383.6:c.7403T>C
ENSP00000294383.5:p.Val2468Ala

This variation has assays on 10 chips - click the plus to show

Variation displays