view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNX29_chr16_11971734_12579287 | 12040592 | AG | A | intron_variant | MODIFIER | HG02965.hp1 HG03471.hp2 |
a0001 | a0001c0006a0001c0025 | a0001c0006t0021a0001c0025t0096 | a0001c0006t0021g0073 a0001c0025t0096g0076 |
2 | 176 | 0.0114 | -1 | c.248 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12042815 | TC | T | intron_variant | MODIFIER | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0027a0001c0001t0052a0001c0003t0016others(3): Show | a0001c0001t0027g0082 a0001c0001t0052g0026 a0001c0003t0016g0029 others(3): Show |
6 | 176 | 0.0341 | -1 | c.248 others(7): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 4/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12043355 | AT | A | intron_variant | MODIFIER | HG00323.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0027a0001c0001t0052a0001c0002t0076others(6): Show | a0001c0001t0027g0082 a0001c0001t0052g0026 a0001c0002t0076g0100 others(6): Show |
9 | 176 | 0.0511 | -1 | c.428 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12043747 | TG | T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(45): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(41): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0009g0090 others(45): Show |
48 | 176 | 0.2727 | -1 | c.428 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 5/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12045391 | AC | A | intron_variant | MODIFIER | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0027a0001c0001t0052a0001c0003t0016others(3): Show | a0001c0001t0027g0082 a0001c0001t0052g0026 a0001c0003t0016g0029 others(3): Show |
6 | 176 | 0.0341 | -1 | c.429 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 5/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12049333 | CT | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(38): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0009g0090 others(41): Show |
44 | 176 | 0.2500 | -1 | c.748 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12050878 | AT | A | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG02523.hp2 others(6): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0101others(5): Show | a0001c0001t0002g0020 a0001c0001t0004g0132 a0001c0001t0101g0019 others(6): Show |
9 | 176 | 0.0511 | -1 | c.749 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12051332 | TA | T | intron_variant | MODIFIER | HG00558.hp1 HG00741.hp1 HG03834.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0014a0001c0002t0088others(2): Show | a0001c0001t0001g0153 a0001c0001t0014g0118 a0001c0002t0088g0018 others(2): Show |
5 | 176 | 0.0284 | -1 | c.749 others(8): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12053284 | CA | C | intron_variant | MODIFIER | HG00558.hp1 HG01993.hp2 HG02258.hp2 others(14): Show |
a0001a0004a0007 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0014a0001c0001t0017a0001c0001t0036others(14): Show | a0001c0001t0014g0118 a0001c0001t0017g0025 a0001c0001t0036g0030 others(14): Show |
17 | 176 | 0.0966 | -1 | c.112 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12057823 | TA | T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(77): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0002g0020 others(92): Show |
95 | 176 | 0.5398 | -1 | c.112 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 8/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12057825 | TA | T | intron_variant | MODIFIER | HG00733.hp1 HG01261.hp2 HG02258.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0007a0001c0001t0030a0001c0002t0024others(6): Show | a0001c0001t0007g0008 a0001c0001t0030g0014 a0001c0002t0024g0050 others(6): Show |
9 | 176 | 0.0511 | -1 | c.112 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 8/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12058797 | GT | G | intron_variant | MODIFIER | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(90): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(76): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0002g0020 others(90): Show |
93 | 176 | 0.5284 | -1 | c.112 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12058915 | CT | C | intron_variant | MODIFIER | HG02258.hp2 HG02886.hp2 HG03579.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0017a0001c0001t0036a0001c0007t0064 | a0001c0001t0017g0025 a0001c0001t0036g0030 a0001c0007t0064g0113 |
3 | 176 | 0.0171 | -1 | c.112 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 8/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12068006 | CT | C | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
a0001a0004a0005others(2): Show | a0001c0001a0001c0002a0001c0006others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(52): Show | a0001c0001t0001g0112 a0001c0001t0001g0164 a0001c0001t0002g0065 others(63): Show |
66 | 176 | 0.3750 | -1 | c.124 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12068497 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(32): Show |
a0001a0002 | a0001c0003a0001c0004a0001c0013others(3): Show | a0001c0003t0001a0001c0003t0002a0001c0003t0004others(24): Show | a0001c0003t0001g0089 a0001c0003t0001g0103 a0001c0003t0001g0154 others(32): Show |
35 | 176 | 0.1989 | -1 | c.124 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12076303 | CT | C | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
a0001a0005a0006others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(40): Show | a0001c0001t0002g0065 a0001c0001t0004g0078 a0001c0001t0004g0132 others(44): Show |
47 | 176 | 0.2671 | -1 | c.132 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12077278 | TA | T | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(46): Show |
a0001a0005a0006others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(41): Show | a0001c0001t0002g0065 a0001c0001t0002g0169 a0001c0001t0004g0078 others(46): Show |
49 | 176 | 0.2784 | -1 | c.132 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12078202 | TG | T | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(35): Show |
a0001a0005a0007 | a0001c0001a0001c0002a0001c0015others(2): Show | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(31): Show | a0001c0001t0004g0078 a0001c0001t0004g0132 a0001c0001t0008g0137 others(35): Show |
38 | 176 | 0.2159 | -1 | c.132 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12079513 | TA | T | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
a0001a0005a0006others(1): Show | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(43): Show | a0001c0001t0002g0065 a0001c0001t0002g0169 a0001c0001t0004g0078 others(48): Show |
51 | 176 | 0.2898 | -1 | c.140 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12080692 | CT | C | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
a0001a0004a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(46): Show | a0001c0001t0001g0164 a0001c0001t0002g0065 a0001c0001t0002g0169 others(52): Show |
55 | 176 | 0.3125 | -1 | c.140 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12081636 | GC | G | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
a0001a0005a0006others(1): Show | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(39): Show | a0001c0001t0002g0065 a0001c0001t0002g0169 a0001c0001t0004g0078 others(44): Show |
47 | 176 | 0.2671 | -1 | c.140 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12081674 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(43): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0008a0001c0001t0017a0001c0001t0034others(40): Show | a0001c0001t0008g0104 a0001c0001t0017g0025 a0001c0001t0034g0063 others(43): Show |
46 | 176 | 0.2614 | -1 | c.140 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12086009 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(47): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(57): Show |
60 | 176 | 0.3409 | -1 | c.140 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12091038 | AG | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG01081.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0034a0001c0002t0093others(15): Show | a0001c0001t0001g0163 a0001c0001t0034g0063 a0001c0002t0093g0086 others(16): Show |
19 | 176 | 0.1080 | -1 | c.140 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12091775 | CA | C | intron_variant | MODIFIER | HG00673.hp1 HG00733.hp1 HG01261.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0030a0001c0001t0032others(12): Show | a0001c0001t0002g0065 a0001c0001t0030g0014 a0001c0001t0032g0130 others(13): Show |
16 | 176 | 0.0909 | -1 | c.140 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12101386 | AT | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG02257.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0048a0001c0003t0002a0001c0004t0020others(2): Show | a0001c0001t0048g0052 a0001c0003t0002g0058 a0001c0003t0002g0077 others(5): Show |
8 | 176 | 0.0455 | -1 | c.140 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12107338 | GT | G | intron_variant | MODIFIER | HG02523.hp1 NA18942.hp1 NA18969.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0034a0001c0003t0006a0001c0003t0104others(3): Show | a0001c0001t0034g0063 a0001c0003t0006g0144 a0001c0003t0104g0156 others(3): Show |
6 | 176 | 0.0341 | -1 | c.140 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12125605 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG01069.hp2 HG01081.hp2 others(7): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0024a0001c0002t0093a0001c0003t0001others(7): Show | a0001c0002t0024g0128 a0001c0002t0093g0086 a0001c0003t0001g0133 others(7): Show |
10 | 176 | 0.0568 | -1 | c.140 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12127424 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(19): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(116): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(144): Show |
147 | 176 | 0.8352 | -1 | c.146 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12128818 | TG | T | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(22): Show |
25 | 176 | 0.1421 | -1 | c.146 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12133281 | GT | G | intron_variant | MODIFIER | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0002g0169 others(32): Show |
35 | 176 | 0.1989 | -1 | c.159 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12138184 | GA | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(111): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(140): Show |
143 | 176 | 0.8125 | -1 | c.159 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12143417 | GT | G | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(35): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(41): Show |
44 | 176 | 0.2500 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12145201 | TA | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0017a0001c0001t0048others(19): Show | a0001c0001t0001g0163 a0001c0001t0017g0101 a0001c0001t0048g0052 others(23): Show |
26 | 176 | 0.1477 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12148454 | GT | G | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | a0001c0001t0001g0163 a0001c0001t0002g0065 a0001c0001t0004g0078 others(27): Show |
30 | 176 | 0.1705 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12152034 | TG | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(57): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(72): Show |
75 | 176 | 0.4261 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12152827 | CT | C | intron_variant | MODIFIER | HG02559.hp1 HG03209.hp1 |
a0001 | a0001c0004a0001c0012 | a0001c0004t0092a0001c0012t0002 | a0001c0004t0092g0102 a0001c0012t0002g0028 |
2 | 176 | 0.0114 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12153461 | CA | C | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(23): Show | a0001c0001t0001g0163 a0001c0001t0002g0065 a0001c0001t0002g0169 others(29): Show |
32 | 176 | 0.1818 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12153640 | AT | A | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(18): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0048others(15): Show | a0001c0001t0001g0163 a0001c0001t0004g0078 a0001c0001t0048g0052 others(18): Show |
21 | 176 | 0.1193 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12154346 | AC | A | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(23): Show | a0001c0001t0001g0163 a0001c0001t0002g0065 a0001c0001t0002g0169 others(29): Show |
32 | 176 | 0.1818 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12160694 | TA | T | intron_variant | MODIFIER | HG00558.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(23): Show | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0008g0137 others(29): Show |
32 | 176 | 0.1818 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12164680 | CT | C | intron_variant | MODIFIER | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0014a0001c0001t0017a0001c0001t0040others(9): Show | a0001c0001t0014g0118 a0001c0001t0017g0025 a0001c0001t0040g0124 others(9): Show |
12 | 176 | 0.0682 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12176936 | GT | G | intron_variant | MODIFIER | HG01175.hp1 HG01884.hp2 HG02486.hp1 others(4): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0017a0001c0002t0018a0001c0002t0019others(4): Show | a0001c0001t0017g0025 a0001c0002t0018g0037 a0001c0002t0019g0174 others(4): Show |
7 | 176 | 0.0398 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12180515 | GC | G | intron_variant | MODIFIER | HG01069.hp2 HG01257.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0022a0001c0004t0097 | a0001c0002t0022g0007 a0001c0004t0097g0146 |
2 | 176 | 0.0114 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12181710 | AG | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(114): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(146): Show |
149 | 176 | 0.8466 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12181883 | CT | C | intron_variant | MODIFIER | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0026a0001c0001t0041others(6): Show | a0001c0001t0004g0078 a0001c0001t0026g0062 a0001c0001t0041g0046 others(7): Show |
10 | 176 | 0.0568 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12182189 | GT | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(72): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(93): Show |
96 | 176 | 0.5455 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12182933 | CA | C | intron_variant | MODIFIER | HG01069.hp2 HG01167.hp2 HG02559.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0007a0001c0001t0040others(2): Show | a0001c0001t0002g0065 a0001c0001t0007g0008 a0001c0001t0040g0124 others(2): Show |
5 | 176 | 0.0284 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12187546 | TA | T | intron_variant | MODIFIER | HG01167.hp2 HG01257.hp2 HG03704.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0007a0001c0001t0040others(2): Show | a0001c0001t0001g0163 a0001c0001t0007g0175 a0001c0001t0040g0124 others(2): Show |
5 | 176 | 0.0284 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12187670 | TC | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(9): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0048a0001c0001t0061a0001c0002t0024others(6): Show | a0001c0001t0048g0052 a0001c0001t0061g0173 a0001c0002t0024g0128 others(9): Show |
12 | 176 | 0.0682 | -1 | c.159 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |