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 17:81512000 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM032825

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 28 HGVS names - click the plus to show

17:g.81512000G>A
ENST00000575994.2:c.266C>T
ENSP00000460464.1:p.Thr89Ile
ENST00000576214.2:n.287C>T
ENST00000576209.2:n.151C>T
ENST00000576917.2:n.319C>T
ENST00000572105.3:c.266C>T
ENSP00000462823.1:p.Thr89Ile
ENST00000575842.2:c.266C>T
ENSP00000458162.1:p.Thr89Ile
ENST00000615544.1:c.266C>T
ENSP00000477968.1:p.Thr89Ile
ENST00000571691.2:c.239C>T
ENSP00000461407.1:p.Thr80Ile
ENST00000573283.2:c.266C>T
ENSP00000458435.1:p.Thr89Ile
ENST00000571721.2:c.266C>T
ENSP00000460660.1:p.Thr89Ile
ENST00000331925.3:c.266C>T
ENSP00000331514.2:p.Thr89Ile
ENST00000575087.2:c.266C>T
ENSP00000459124.1:p.Thr89Ile
ENST00000576544.2:c.266C>T
ENSP00000461672.1:p.Thr89Ile
ENST00000575659.2:c.266C>T
ENSP00000459119.1:p.Thr89Ile
ENST00000570382.1:c.266C>T
ENSP00000466346.1:p.Thr89Ile

Variation displays