NM_004817.4(TJP2):c.239+19T>C
|
rs2498417
|
0.90366
|
NM_004817.4(TJP2):c.1446C>A (p.Asp482Glu)
|
rs2309428
|
0.77489
|
NM_004817.4(TJP2):c.2992-19G>A
|
rs2282335
|
0.39706
|
NM_004817.4(TJP2):c.2715C>T (p.Thr905=)
|
rs2282336
|
0.22650
|
NM_004817.4(TJP2):c.2727G>A (p.Ala909=)
|
rs2095876
|
0.22643
|
NM_004817.4(TJP2):c.382C>A (p.Gln128Lys)
|
rs41305539
|
0.10827
|
NM_004817.4(TJP2):c.1672-20C>G
|
rs80014470
|
0.09453
|
NM_004817.4(TJP2):c.1137A>G (p.Leu379=)
|
rs17062695
|
0.08425
|
NM_004817.4(TJP2):c.3029C>T (p.Ser1010Phe)
|
rs41277907
|
0.05575
|
NM_004817.4(TJP2):c.2004G>A (p.Met668Ile)
|
rs34774441
|
0.04571
|
NM_004817.4(TJP2):c.2275+16T>G
|
rs73450890
|
0.04139
|
NM_004817.4(TJP2):c.2131T>C (p.Ser711Pro)
|
rs35797487
|
0.02532
|
NM_004817.4(TJP2):c.1350C>T (p.Ser450=)
|
rs17062723
|
0.02463
|
NM_004817.4(TJP2):c.342+12G>T
|
rs7027812
|
0.01934
|
NM_004817.4(TJP2):c.1917C>T (p.Asp639=)
|
rs12340440
|
0.01348
|
NM_004817.4(TJP2):c.2646G>A (p.Ala882=)
|
rs11788754
|
0.01323
|
NM_004817.4(TJP2):c.2778C>T (p.Asp926=)
|
rs140442228
|
0.01321
|
NM_004817.4(TJP2):c.2367A>G (p.Ala789=)
|
rs75668442
|
0.01213
|
NM_004817.4(TJP2):c.297G>A (p.Ser99=)
|
rs72709079
|
0.00975
|
NM_004817.4(TJP2):c.3495G>A (p.Glu1165=)
|
rs111595785
|
0.00843
|
NM_004817.4(TJP2):c.2810T>C (p.Leu937Pro)
|
rs28556975
|
0.00841
|
NM_004817.4(TJP2):c.2137A>G (p.Ser713Gly)
|
rs116545275
|
0.00763
|
NM_004817.4(TJP2):c.1063G>C (p.Gly355Arg)
|
rs78681604
|
0.00381
|
NM_004817.4(TJP2):c.2040G>A (p.Gly680=)
|
rs111723895
|
0.00330
|
NM_004817.4(TJP2):c.-16G>T
|
rs199557806
|
0.00310
|
NM_004817.4(TJP2):c.1057-17A>G
|
rs41277895
|
0.00093
|
NM_004817.4(TJP2):c.918C>T (p.Ile306=)
|
rs374523970
|
0.00041
|
NM_004817.4(TJP2):c.2852G>A (p.Arg951His)
|
rs368776552
|
0.00018
|
NM_004817.4(TJP2):c.3392C>T (p.Thr1131Met)
|
rs139636763
|
0.00015
|
NM_004817.4(TJP2):c.2909G>A (p.Arg970Gln)
|
rs150494393
|
0.00011
|
NM_004817.4(TJP2):c.2859G>T (p.Ser953=)
|
rs369972534
|
0.00009
|
NM_004817.4(TJP2):c.61-7293C>G
|
rs566121116
|
0.00006
|
NM_004817.4(TJP2):c.1210G>A (p.Asp404Asn)
|
rs1060499649
|
0.00001
|
NM_004817.4(TJP2):c.3372G>A (p.Thr1124=)
|
rs745427593
|
0.00001
|
NM_004817.4(TJP2):c.1202A>G (p.Glu401Gly)
|
rs1057515614
|
|
NM_004817.4(TJP2):c.1628C>T (p.Ser543Leu)
|
|
|
NM_004817.4(TJP2):c.239+14del
|
rs764370644
|
|
NM_004817.4(TJP2):c.3238G>A (p.Gly1080Ser)
|
|
|