Original source

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

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

Chromosome 1:201365244 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951219, CM068093, CM031383

Most severe consequence
Clinical significance

Synonyms

LSDB 5867

This variation has 27 HGVS names - click the plus to show

1:g.201365244A>T
ENST00000367318.7:c.328T>A
ENSP00000356287.5:p.Phe110Ile
ENST00000503459.1:n.197T>A
ENST00000491504.3:n.1567T>A
ENST00000458432.4:c.151T>A
ENSP00000387874.3:p.Phe51Ile
ENST00000367317.6:c.313T>A
ENSP00000356286.5:p.Phe105Ile
ENST00000367315.4:c.334T>A
ENSP00000356284.3:p.Phe112Ile
ENST00000360372.6:c.291+366T>A
ENST00000367322.3:c.328T>A
ENSP00000356291.1:p.Phe110Ile
ENST00000509001.3:c.328T>A
ENSP00000422031.1:p.Phe110Ile
ENST00000421663.4:c.151T>A
ENSP00000404134.3:p.Phe51Ile
ENST00000438742.3:c.313T>A
ENSP00000414036.1:p.Phe105Ile
ENST00000455702.3:c.358T>A
ENSP00000402238.1:p.Phe120Ile
ENST00000367320.4:c.291+366T>A
ENST00000515042.3:n.254T>A
ENST00000236918.9:c.358T>A
ENSP00000236918.8:p.Phe120Ile
ENST00000466570.3:n.584T>A

Variation displays