Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.03 (G)
Location

Chromosome 10:71730514 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021540

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

10:g.71730514A>G
ENST00000616684.1:c.3760A>G
ENSP00000482036.1:p.Thr1254Ala
ENST00000398786.2:c.-6+7214T>C
ENST00000398809.5:c.3622A>G
ENSP00000381789.5:p.Thr1208Ala
ENST00000622827.1:c.3625A>G
ENSP00000483211.1:p.Thr1209Ala
ENST00000224721.7:c.3775A>G
ENSP00000224721.7:p.Thr1259Ala
ENST00000398792.3:n.317A>G

This variation has assays on 4 chips - click the plus to show

Variation displays