NM_000310.4(PPT1):c.401T>C (p.Ile134Thr)
|
rs1800205
|
0.04289
|
NM_000310.4(PPT1):c.837G>C (p.Gln279His)
|
rs72937434
|
0.02506
|
NM_000310.4(PPT1):c.*3C>A
|
rs150454815
|
0.00889
|
NM_000310.4(PPT1):c.363-4G>A
|
rs117284255
|
0.00318
|
NM_000310.4(PPT1):c.904A>G (p.Ile302Val)
|
rs146902902
|
0.00091
|
NM_000310.4(PPT1):c.364A>T (p.Arg122Trp)
|
rs137852695
|
0.00061
|
NM_000310.4(PPT1):c.451C>T (p.Arg151Ter)
|
rs137852700
|
0.00038
|
NM_000310.4(PPT1):c.329A>G (p.Asn110Ser)
|
rs142894102
|
0.00010
|
NM_000310.4(PPT1):c.513G>A (p.Ala171=)
|
rs150924738
|
0.00010
|
NM_000310.4(PPT1):c.363-5C>T
|
rs112553480
|
0.00009
|
NM_000310.4(PPT1):c.802C>T (p.Arg268Cys)
|
rs200813294
|
0.00008
|
NM_000310.4(PPT1):c.17G>A (p.Cys6Tyr)
|
rs202241486
|
0.00006
|
NM_000310.4(PPT1):c.223A>C (p.Thr75Pro)
|
rs137852696
|
0.00006
|
NM_000310.4(PPT1):c.541G>A (p.Val181Met)
|
rs148412181
|
0.00006
|
NM_000310.4(PPT1):c.29T>A (p.Leu10Ter)
|
rs137852699
|
0.00004
|
NM_000310.4(PPT1):c.535C>T (p.Arg179Cys)
|
rs560471003
|
0.00004
|
NM_000310.4(PPT1):c.543G>A (p.Val181=)
|
rs374121503
|
0.00004
|
NM_000310.4(PPT1):c.310A>G (p.Lys104Glu)
|
rs386833641
|
0.00003
|
NM_000310.4(PPT1):c.587G>A (p.Arg196His)
|
rs939858453
|
0.00003
|
NM_000310.4(PPT1):c.803G>A (p.Arg268His)
|
rs763536047
|
0.00003
|
NM_000310.4(PPT1):c.14G>C (p.Gly5Ala)
|
rs757580857
|
0.00002
|
NM_000310.4(PPT1):c.416T>C (p.Val139Ala)
|
rs766961054
|
0.00002
|
NM_000310.4(PPT1):c.353G>A (p.Gly118Asp)
|
rs143657539
|
0.00001
|
NM_000310.4(PPT1):c.3G>A (p.Met1Ile)
|
rs386833645
|
0.00001
|
NM_000310.4(PPT1):c.433G>C (p.Gly145Arg)
|
rs369186379
|
0.00001
|
NM_000310.4(PPT1):c.550G>A (p.Glu184Lys)
|
rs386833655
|
0.00001
|
NM_000310.4(PPT1):c.900C>T (p.His300=)
|
rs747432731
|
0.00001
|
NM_000310.4(PPT1):c.118G>A (p.Gly40Arg)
|
rs1649899406
|
|
NM_000310.4(PPT1):c.17G>T (p.Cys6Phe)
|
rs202241486
|
|
NM_000310.4(PPT1):c.189T>C (p.Pro63=)
|
|
|
NM_000310.4(PPT1):c.195T>A (p.Ile65=)
|
|
|
NM_000310.4(PPT1):c.26T>C (p.Leu9Pro)
|
|
|
NM_000310.4(PPT1):c.404A>G (p.Asn135Ser)
|
rs1342695798
|
|
NM_000310.4(PPT1):c.474C>A (p.His158Gln)
|
|
|
NM_000310.4(PPT1):c.627+4A>G
|
rs572153728
|
|
NM_000310.4(PPT1):c.629G>T (p.Gly210Val)
|
|
|
NM_000310.4(PPT1):c.635A>G (p.Asn212Ser)
|
|
|
NM_000310.4(PPT1):c.67G>A (p.Ala23Thr)
|
|
|
NM_000310.4(PPT1):c.802C>A (p.Arg268Ser)
|
|
|
NM_000310.4(PPT1):c.824A>T (p.Asp275Val)
|
rs775402028
|
|