Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.42 (T)
Location

Chromosome 17:80205094 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

17:g.80205094C>T
ENST00000576824.2:n.289G>A
ENST00000573346.2:n.144+239G>A
ENST00000575500.2:c.*918C>T
ENST00000573882.2:c.2458C>T
ENSP00000458715.1:p.Arg820Trp
ENST00000572730.1:n.617+239G>A
ENST00000344227.3:c.2458C>T
ENSP00000344549.2:p.Arg820Trp

This variation has assays on 11 chips - click the plus to show

Variation displays