regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACTN2_chr1_236681499_236769631 | 236730271 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 168 | 344 | 0.4884 | 1 | c.616 others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236731905 | C | CT | intron_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0012a0001c0003t0001others(7): Show | a0001c0001t0001g0110a0001c0001t0012g0019a0001c0001t0012g0109others(19): Show | 22 | 344 | 0.0640 | 1 | c.697 others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236732615 | G | GT | intron_variant | MODIFIER | HG02109.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0005a0001c0001t0011a0001c0004t0002others(1): Show | a0001c0001t0005g0055a0001c0001t0011g0067a0001c0001t0011g0090others(3): Show | 6 | 344 | 0.0174 | 1 | c.697 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236737548 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(125): Show | 128 | 344 | 0.3721 | 1 | c.876 others(8): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236742535 | T | TA | intron_variant | MODIFIER | HG01361.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(5): Show | a0001c0001t0004g0037a0001c0001t0004g0071a0001c0001t0004g0074others(10): Show | 13 | 344 | 0.0378 | 1 | c.110 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236743569 | C | CT | intron_variant | MODIFIER | HG02145.hp1 HG02572.hp2 HG02723.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(2): Show | a0001c0001t0003g0238a0001c0001t0004g0075a0001c0001t0004g0178others(4): Show | 7 | 344 | 0.0204 | 1 | c.125 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236746165 | C | CA | intron_variant | MODIFIER | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
a0001a0003 | a0001c0001a0001c0007a0001c0010others(2): Show | a0001c0001t0004a0001c0007t0004a0001c0010t0002others(2): Show | a0001c0001t0004g0028a0001c0007t0004g0070a0001c0007t0004g0083others(5): Show | 8 | 344 | 0.0233 | 1 | c.140 others(10): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236751089 | C | CA | intron_variant | MODIFIER | HG01099.hp1 HG01109.hp1 HG01981.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0013a0001c0016others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(5): Show | a0001c0001t0004g0071a0001c0001t0004g0074a0001c0001t0004g0078others(10): Show | 13 | 344 | 0.0378 | 1 | c.165 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236751221 | A | AT | intron_variant | MODIFIER | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(10): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(5): Show | a0001c0001t0003g0238a0001c0001t0004g0069a0001c0001t0011g0036others(10): Show | 13 | 344 | 0.0378 | 1 | c.165 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236758325 | C | CG | intron_variant | MODIFIER | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(18): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0012a0001c0003t0020a0001c0004t0002others(2): Show | a0001c0001t0012g0019a0001c0001t0012g0109a0001c0001t0012g0337others(18): Show | 21 | 344 | 0.0611 | 1 | c.230 others(18): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236758452 | A | AT | intron_variant | MODIFIER | HG01192.hp1 HG01978.hp2 HG02015.hp1 others(16): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0018others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0017others(6): Show | a0001c0001t0001g0242a0001c0001t0003g0234a0001c0001t0017g0097others(16): Show | 19 | 344 | 0.0552 | 1 | c.230 others(9): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236765120 | C | CA | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0275others(60): Show | 63 | 344 | 0.1831 | 1 | c.*25 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 490 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236765375 | G | GA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0011a0001c0001t0018others(13): Show | a0001c0001t0002g0156a0001c0001t0011g0067a0001c0001t0011g0090others(82): Show | 85 | 344 | 0.2471 | 1 | c.*27 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 745 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236765665 | C | CA | downstream_gene_variant | MODIFIER | HG01109.hp2 HG01123.hp1 HG01168.hp2 others(63): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0004others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | a0001c0001t0001g0312a0001c0001t0003g0238a0001c0001t0004g0102others(63): Show | 66 | 344 | 0.1919 | 1 | c.*30 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1035 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236767381 | C | CA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0032a0001c0001t0002g0156a0001c0001t0003g0104others(86): Show | 89 | 344 | 0.2587 | 1 | c.*47 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 2751 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236768415 | G | GT | downstream_gene_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG01123.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0291others(22): Show | 25 | 344 | 0.0727 | 1 | c.*57 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 3785 | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236769433 | C | CT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0032a0001c0001t0001g0260a0001c0001t0002g0156others(86): Show | 89 | 344 | 0.2587 | 1 | c.*68 others(12): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 4803 | chr1 | TogoVar | ||||||
ACTN3_chr11_66541903_66568334 | 66549732 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
a0001a0002a0003others(11): Show | a0001c0001a0002c0002a0002c0008others(18): Show | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(21): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 303 | 400 | 0.7575 | 1 | c.148 others(9): Show |
ACTN3 | ENSG00000248746.6 | transcript | ENST00000513398.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACTN3_chr11_66541903_66568334 | 66553853 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(84): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0025others(44): Show | 87 | 400 | 0.2175 | 1 | c.383 others(8): Show |
ACTN3 | ENSG00000248746.6 | transcript | ENST00000513398.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACTN3_chr11_66541903_66568334 | 66554289 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0008others(4): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0003others(5): Show | a0001c0001t0001g0100a0001c0001t0001g0103a0002c0002t0001g0019others(14): Show | 24 | 400 | 0.0600 | 1 | c.469 others(16): Show |
ACTN3 | ENSG00000248746.6 | transcript | ENST00000513398.2 | protein_coding | 4/20 | chr11 | TogoVar | ||||||
ACTN3_chr11_66541903_66568334 | 66554456 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
a0001a0002a0003others(11): Show | a0001c0001a0002c0002a0002c0008others(12): Show | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 175 | 400 | 0.4375 | 1 | c.470 others(7): Show |
ACTN3 | ENSG00000248746.6 | transcript | ENST00000513398.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ACTN3_chr11_66541903_66568334 | 66566727 | C | CT | downstream_gene_variant | MODIFIER | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(4): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0012 | a0001c0001t0001a0002c0002t0001a0009c0012t0001 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | 400 | 0.0175 | 1 | c.*35 others(12): Show |
ACTN3 | ENSG00000248746.6 | transcript | ENST00000513398.2 | protein_coding | 3394 | chr11 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38644817 | T | TA | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(59): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(14): Show | a0001c0001t0002g0154a0001c0001t0004g0221a0001c0001t0004g0255others(59): Show | 62 | 314 | 0.1975 | 1 | c.-29 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 2831 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38649186 | C | CG | intron_variant | MODIFIER | HG00423.hp1 HG00741.hp1 HG01978.hp1 others(22): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(11): Show | a0001c0001t0001g0205a0001c0001t0002g0081a0001c0001t0002g0206others(22): Show | 25 | 314 | 0.0796 | 1 | c.162 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38653085 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0010others(3): Show | a0001c0001t0002a0001c0001t0011a0001c0001t0016others(16): Show | a0001c0001t0002g0091a0001c0001t0002g0093a0001c0001t0011g0281others(58): Show | 62 | 314 | 0.1975 | 1 | c.162 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38654561 | C | CA | intron_variant | MODIFIER | HG00323.hp1 HG00642.hp1 HG01891.hp2 others(43): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(13): Show | a0001c0001t0002g0097a0001c0001t0002g0099a0001c0001t0004g0221others(42): Show | 46 | 314 | 0.1465 | 1 | c.162 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38659921 | C | CT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(43): Show | a0001c0001t0001g0170a0001c0001t0002g0099a0001c0001t0002g0163others(118): Show | 123 | 314 | 0.3917 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38662909 | G | GT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(34): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0049others(12): Show | a0001c0001t0002g0093a0001c0001t0006g0249a0001c0001t0049g0076others(33): Show | 37 | 314 | 0.1178 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38666223 | T | TC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(43): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0019 | a0001c0001t0030a0001c0002t0001a0001c0002t0005others(5): Show | a0001c0001t0030g0294a0001c0002t0001g0025a0001c0002t0001g0026others(43): Show | 46 | 314 | 0.1465 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38667706 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(103): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(17): Show | a0001c0001t0002g0101a0001c0001t0002g0104a0001c0001t0002g0105others(102): Show | 106 | 314 | 0.3376 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38670921 | T | TA | intron_variant | MODIFIER | HG00438.hp2 HG01106.hp2 HG02738.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(2): Show | a0001c0001t0002g0112a0001c0001t0006g0298a0001c0002t0001g0009others(6): Show | 9 | 314 | 0.0287 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38670932 | A | AC | intron_variant | MODIFIER | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
a0001a0005 | a0001c0002a0001c0007a0005c0018 | a0001c0002t0040a0001c0007t0001a0005c0018t0001 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | 314 | 0.0159 | 1 | c.162 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38671694 | A | AT | intron_variant | MODIFIER | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
a0001a0005 | a0001c0002a0001c0007a0005c0018 | a0001c0002t0040a0001c0007t0001a0005c0018t0001 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | 314 | 0.0159 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38672238 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(46): Show | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0002g0210others(182): Show | 187 | 314 | 0.5955 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38672943 | C | CT | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0002a0001c0001t0021a0001c0001t0032others(16): Show | a0001c0001t0002g0099a0001c0001t0002g0163a0001c0001t0002g0166others(66): Show | 70 | 314 | 0.2229 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38673665 | T | TC | intron_variant | MODIFIER | HG02896.hp2 HG03139.hp1 HG03209.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0021a0001c0001t0043a0001c0001t0049others(1): Show | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0043g0295others(3): Show | 6 | 314 | 0.0191 | 1 | c.162 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38673681 | T | TA | intron_variant | MODIFIER | HG00642.hp2 HG01891.hp1 HG02897.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | 314 | 0.0159 | 1 | c.162 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38673690 | A | AT | intron_variant | MODIFIER | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0021a0001c0001t0049 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | 314 | 0.0096 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38673701 | T | TA | intron_variant | MODIFIER | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0021a0001c0001t0049 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | 314 | 0.0096 | 1 | c.162 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38673784 | A | AT | intron_variant | MODIFIER | HG01261.hp2 HG01952.hp2 HG02145.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0020a0001c0001t0022others(5): Show | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0105others(9): Show | 12 | 314 | 0.0382 | 1 | c.162 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38674166 | G | GT | intron_variant | MODIFIER | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
a0002 | a0002c0008 | a0002c0008t0011 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | 314 | 0.0096 | 1 | c.162 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | TogoVar | ||||||
ACTN4_chr19_38642649_38736589 | 38676139 | C | CG | intron_variant | MODIFIER | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
a0001 | a0001c0002a0001c0004a0001c0006others(1): Show | a0001c0002t0001a0001c0004t0005a0001c0004t0013others(5): Show | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | 314 | 0.0828 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38679859 | G | GA | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
a0001 | a0001c0002a0001c0003a0001c0010others(4): Show | a0001c0002t0012a0001c0002t0033a0001c0002t0045others(8): Show | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(28): Show | 32 | 314 | 0.1019 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38680212 | G | GT | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00642.hp1 others(31): Show |
a0001a0003 | a0001c0001a0003c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0086a0001c0001t0001g0205a0001c0001t0002g0081others(31): Show | 34 | 314 | 0.1083 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38681129 | G | GA | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(62): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0010others(15): Show | a0001c0001t0002g0079a0001c0001t0002g0081a0001c0001t0002g0126others(62): Show | 65 | 314 | 0.2070 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38686965 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0020others(1): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0005others(9): Show | a0001c0001t0019g0299a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 87 | 314 | 0.2771 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38688390 | C | CA | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(60): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | a0001c0001t0001g0205a0001c0001t0002g0080a0001c0001t0002g0102others(59): Show | 63 | 314 | 0.2006 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38688732 | C | CA | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(18): Show | a0001c0001t0002g0166a0001c0001t0004g0221a0001c0001t0004g0255others(61): Show | 65 | 314 | 0.2070 | 1 | c.163 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38691401 | C | CA | intron_variant | MODIFIER | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0022a0001c0002t0001a0001c0002t0007others(6): Show | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0002t0001g0218others(26): Show | 29 | 314 | 0.0924 | 1 | c.163 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACTN4_chr19_38642649_38736589 | 38694264 | C | CT | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
a0001 | a0001c0002a0001c0003a0001c0010others(4): Show | a0001c0002t0001a0001c0002t0012a0001c0002t0033others(9): Show | a0001c0002t0001g0283a0001c0002t0012g0003a0001c0002t0012g0301others(28): Show | 32 | 314 | 0.1019 | 1 | c.163 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |