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 1:201333494 (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 30 HGVS names - click the plus to show

1:g.201333494G>A
ENST00000491504.1:n.1630C>T
ENST00000367318.5:c.391C>T
ENSP00000356287.5:p.Arg131Trp
ENST00000503459.1:n.260C>T
ENST00000458432.2:c.427C>T
ENSP00000387874.2:p.Arg143Trp
ENST00000367317.4:c.391C>T
ENSP00000356286.4:p.Arg131Trp
ENST00000360372.4:c.376C>T
ENSP00000353535.4:p.Arg126Trp
ENST00000367315.2:c.391C>T
ENSP00000356284.2:p.Arg131Trp
ENST00000509001.1:c.391C>T
ENSP00000422031.1:p.Arg131Trp
ENST00000421663.2:c.397C>T
ENSP00000404134.2:p.Arg133Trp
ENST00000367322.1:c.391C>T
ENSP00000356291.1:p.Arg131Trp
ENST00000438742.1:c.376C>T
ENSP00000414036.1:p.Arg126Trp
ENST00000455702.1:c.421C>T
ENSP00000402238.1:p.Arg141Trp
ENST00000367320.2:c.301C>T
ENSP00000356289.2:p.Arg101Trp
ENST00000515042.1:n.317C>T
ENST00000236918.7:c.406C>T
ENSP00000236918.7:p.Arg136Trp
ENST00000479297.1:n.46C>T
ENST00000466570.1:n.647C>T

Variation displays