Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 10:93777551 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082912

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12773

This variation has 6 HGVS names - click the plus to show

10:g.93777551T>A
ENST00000371413.3:c.365T>A
ENSP00000360467.3:p.Ile122Lys
ENST00000485458.1:n.280T>A
ENST00000371418.6:c.365T>A
ENSP00000360472.4:p.Ile122Lys

Variation displays