Original source

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

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

Chromosome 10:73490271 (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 5 HGVS names - click the plus to show

10:g.73490271A>G
ENST00000398786.2:c.-6+7214T>C
ENST00000224721.6:c.3640A>G
ENSP00000224721.6:p.Thr1214Ala
ENST00000398792.3:n.317A>G

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

Variation displays