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 5:74721131 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970723

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14257

This variation has 13 HGVS names - click the plus to show

5:g.74721131G>A
ENST00000511181.3:c.952G>A
ENSP00000426285.1:p.Ala318Thr
ENST00000509579.1:c.64G>A
ENSP00000424939.1:p.Ala22Thr
ENST00000505859.1:c.137-187G>A
ENST00000503312.3:c.490-187G>A
ENST00000261416.9:c.1627G>A
ENSP00000261416.7:p.Ala543Thr
ENST00000513867.1:n.75G>A
ENST00000513336.3:c.563G>A
ENSP00000423713.1:p.Ala189Thr
ENST00000513539.1:n.346G>A

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays