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 17:81511078 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033588

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

17:g.81511078G>A
ENST00000584254.1:n.32C>T
ENST00000576209.3:n.718C>T
ENST00000572105.4:c.*277C>T
ENST00000576917.3:n.965C>T
ENST00000575842.3:c.833C>T
ENSP00000458162.1:p.Thr278Ile
ENST00000615544.2:c.833C>T
ENSP00000477968.1:p.Thr278Ile
ENST00000573283.3:c.833C>T
ENSP00000458435.1:p.Thr278Ile
ENST00000574671.3:n.692C>T
ENST00000331925.4:c.833C>T
ENSP00000331514.2:p.Thr278Ile
ENST00000575087.3:c.833C>T
ENSP00000459124.1:p.Thr278Ile
ENST00000576544.3:c.833C>T
ENSP00000461672.1:p.Thr278Ile

Variation displays