Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 13:103520549 (forward strand) | View in location tab

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

13:g.103520549G>A
ENST00000602836.1:c.3896G>A
ENSP00000473384.1:p.Ala1300Thr
ENST00000355739.4:c.2620G>A
ENSP00000347978.4:p.Ala874Thr
ENST00000481099.1:n.740G>A
ENST00000375954.1:c.319G>A
ENSP00000365121.1:p.Ala107Thr
LRG_464:g.27376G>A
LRG_464t1.1:c.2620G>A
LRG_464p1.1:p.Ala874Thr

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays