Original source

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

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

Chromosome 1:55541174 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

1:g.55541174A>G
ENST00000407756.1:c.6923T>C
ENSP00000385700.1:p.Val2308Ala
ENST00000294383.6:c.7403T>C
ENSP00000294383.5:p.Val2468Ala

This variation has assays on 8 chips - click the plus to show

Variation displays