Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.21 (G)
Location

Chromosome 5:74689390 (forward strand) | View in location tab

Co-located

with COSMIC COSM149850 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

5:g.74689390A>G
ENST00000511181.3:c.-314A>G
ENST00000261416.9:c.362A>G
ENSP00000261416.7:p.Lys121Arg
ENST00000515528.1:n.417A>G
ENST00000513079.3:n.427A>G

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

Variation displays