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 | 12187752 | TG | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(73): 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 | 12191770 | AT | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(71): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(91): Show |
94 | 176 | 0.5341 | -1 | c.159 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12193470 | CA | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(8): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0048a0001c0001t0061a0001c0002t0024others(5): Show | a0001c0001t0048g0052 a0001c0001t0061g0173 a0001c0002t0024g0128 others(8): Show |
11 | 176 | 0.0625 | -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 | 12194622 | GT | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(79): Show | a0001c0001t0001g0112 a0001c0001t0001g0164 a0001c0001t0002g0020 others(93): Show |
96 | 176 | 0.5455 | -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 | 12195985 | CT | C | intron_variant | MODIFIER | HG01993.hp2 HG02976.hp2 HG03491.hp1 others(2): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0041a0001c0002t0019a0001c0002t0109others(2): Show | a0001c0001t0041g0046 a0001c0002t0019g0174 a0001c0002t0109g0036 others(2): Show |
5 | 176 | 0.0284 | -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 | 12197720 | TC | T | intron_variant | MODIFIER | NA18522.hp1 NA20129.hp1 |
a0001 | a0001c0004a0001c0022 | a0001c0004t0021a0001c0022t0049 | a0001c0004t0021g0080 a0001c0022t0049g0061 |
2 | 176 | 0.0114 | -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 | 12200487 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(76): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(101): Show |
104 | 176 | 0.5909 | -1 | c.167 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12205587 | CT | C | intron_variant | MODIFIER | HG02615.hp2 NA18522.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0067a0001c0003t0016 | a0001c0002t0067g0059 a0001c0003t0016g0029 |
2 | 176 | 0.0114 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12206384 | CA | C | intron_variant | MODIFIER | HG00438.hp2 HG02040.hp2 HG02109.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(13): Show | a0001c0001t0002g0020 a0001c0001t0002g0169 a0001c0001t0006g0064 others(14): Show |
17 | 176 | 0.0966 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12208843 | TA | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(90): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(117): Show |
120 | 176 | 0.6818 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12210325 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(53): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(71): Show |
74 | 176 | 0.4205 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12215313 | GA | G | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(43): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(51): Show |
54 | 176 | 0.3068 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12219258 | CT | C | intron_variant | MODIFIER | HG01175.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0017a0001c0002t0018a0001c0002t0019others(8): Show | a0001c0001t0017g0025 a0001c0002t0018g0037 a0001c0002t0019g0174 others(8): Show |
11 | 176 | 0.0625 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12221115 | TC | T | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(8): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(8): Show |
11 | 176 | 0.0625 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12225801 | TA | T | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(11): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(11): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(11): Show |
14 | 176 | 0.0796 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12227899 | TA | T | intron_variant | MODIFIER | HG00323.hp2 HG00741.hp1 HG01071.hp1 others(25): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(24): Show | a0001c0001t0001g0141 a0001c0001t0002g0065 a0001c0001t0002g0081 others(25): Show |
28 | 176 | 0.1591 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12228488 | AC | A | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(10): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(10): Show |
13 | 176 | 0.0739 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12237697 | AG | A | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG00673.hp1 others(21): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(19): Show | a0001c0001t0006g0031 a0001c0001t0014g0118 a0001c0001t0015g0085 others(21): Show |
24 | 176 | 0.1364 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12238303 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(76): Show | a0001c0001t0001g0112 a0001c0001t0001g0163 a0001c0001t0002g0020 others(89): Show |
92 | 176 | 0.5227 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12239639 | CA | C | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | a0001c0001t0001g0108 a0001c0001t0002g0020 a0001c0001t0002g0065 others(38): Show |
41 | 176 | 0.2330 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12239819 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(61): Show | a0001c0001t0001g0112 a0001c0001t0001g0163 a0001c0001t0002g0169 others(75): Show |
78 | 176 | 0.4432 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12242367 | AT | A | intron_variant | MODIFIER | HG00639.hp2 HG01069.hp2 HG01257.hp2 others(6): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0002t0022a0001c0003t0001others(6): Show | a0001c0001t0006g0064 a0001c0002t0022g0007 a0001c0003t0001g0103 others(6): Show |
9 | 176 | 0.0511 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12245483 | AT | A | intron_variant | MODIFIER | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0015others(16): Show | a0001c0001t0006g0031 a0001c0001t0008g0137 a0001c0001t0015g0085 others(18): Show |
21 | 176 | 0.1193 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12250832 | AC | A | intron_variant | MODIFIER | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(17): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(17): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(17): Show |
20 | 176 | 0.1136 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12257690 | AT | A | intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(39): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(35): Show | a0001c0001t0002g0020 a0001c0001t0002g0169 a0001c0001t0006g0031 others(39): Show |
42 | 176 | 0.2386 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12260490 | GA | G | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG03225.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(4): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(4): Show |
7 | 176 | 0.0398 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12260644 | AG | A | intron_variant | MODIFIER | HG02486.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
a0001a0006 | a0001c0002a0001c0006a0006c0017 | a0001c0002t0019a0001c0006t0021a0001c0006t0078others(1): Show | a0001c0002t0019g0174 a0001c0006t0021g0073 a0001c0006t0078g0027 others(1): Show |
4 | 176 | 0.0227 | -1 | c.167 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12270679 | TG | T | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG03225.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(4): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(4): Show |
7 | 176 | 0.0398 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12273342 | GT | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(84): Show | a0001c0001t0001g0112 a0001c0001t0001g0163 a0001c0001t0002g0065 others(101): Show |
104 | 176 | 0.5909 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12274540 | CT | C | intron_variant | MODIFIER | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0017a0001c0001t0027a0001c0002t0069others(7): Show | a0001c0001t0017g0025 a0001c0001t0027g0082 a0001c0002t0069g0017 others(7): Show |
10 | 176 | 0.0568 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12275692 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(123): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(159): Show |
162 | 176 | 0.9205 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12275881 | GT | G | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp2 HG01099.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0026a0001c0001t0048a0001c0001t0102others(11): Show | a0001c0001t0026g0062 a0001c0001t0048g0052 a0001c0001t0102g0001 others(12): Show |
15 | 176 | 0.0852 | -1 | c.167 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12282083 | CA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0002t0067others(4): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0009g0090 others(6): Show |
9 | 176 | 0.0511 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12282108 | AT | A | intron_variant | MODIFIER | HG00673.hp1 HG01081.hp1 HG01109.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0015others(13): Show | a0001c0001t0006g0031 a0001c0001t0008g0137 a0001c0001t0015g0085 others(14): Show |
17 | 176 | 0.0966 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12286344 | AT | A | intron_variant | MODIFIER | HG01109.hp1 HG01167.hp1 HG01496.hp1 others(16): Show |
a0001a0006a0007 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0009a0001c0001t0035a0001c0002t0069others(16): Show | a0001c0001t0009g0111 a0001c0001t0035g0087 a0001c0002t0069g0017 others(16): Show |
19 | 176 | 0.1080 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12288607 | GC | G | intron_variant | MODIFIER | HG02257.hp2 HG02559.hp1 |
a0001 | a0001c0012a0001c0013 | a0001c0012t0002a0001c0013t0094 | a0001c0012t0002g0028 a0001c0013t0094g0126 |
2 | 176 | 0.0114 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12298996 | TA | T | intron_variant | MODIFIER | HG00280.hp1 HG01167.hp1 HG01261.hp1 others(7): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0009a0001c0002t0003a0001c0002t0073others(7): Show | a0001c0001t0009g0111 a0001c0002t0003g0134 a0001c0002t0073g0096 others(7): Show |
10 | 176 | 0.0568 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12299779 | AT | A | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(82): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(66): Show | a0001c0001t0001g0141 a0001c0001t0002g0020 a0001c0001t0002g0065 others(82): Show |
85 | 176 | 0.4830 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12299988 | AG | A | intron_variant | MODIFIER | HG01109.hp1 HG01496.hp1 HG02015.hp2 others(4): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0035a0001c0002t0069a0001c0002t0075others(4): Show | a0001c0001t0035g0087 a0001c0002t0069g0017 a0001c0002t0075g0129 others(4): Show |
7 | 176 | 0.0398 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12303191 | GT | G | intron_variant | MODIFIER | HG01109.hp1 HG01496.hp1 HG02015.hp2 others(7): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0035a0001c0002t0067a0001c0002t0069others(7): Show | a0001c0001t0035g0087 a0001c0002t0067g0059 a0001c0002t0069g0017 others(7): Show |
10 | 176 | 0.0568 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12303352 | AT | A | intron_variant | MODIFIER | HG01109.hp1 HG01496.hp1 HG02015.hp2 others(4): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0035a0001c0002t0069a0001c0002t0075others(4): Show | a0001c0001t0035g0087 a0001c0002t0069g0017 a0001c0002t0075g0129 others(4): Show |
7 | 176 | 0.0398 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12308891 | GA | G | intron_variant | MODIFIER | HG02451.hp2 HG03579.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0036a0001c0004t0080 | a0001c0001t0036g0030 a0001c0004t0080g0054 |
2 | 176 | 0.0114 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12312694 | GA | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(130): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(172): Show |
175 | 176 | 0.9943 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12323517 | TA | T | intron_variant | MODIFIER | HG01069.hp2 HG01358.hp1 HG01884.hp1 others(18): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0108 a0001c0001t0002g0169 a0001c0001t0006g0064 others(18): Show |
21 | 176 | 0.1193 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12329639 | AC | A | intron_variant | MODIFIER | HG00558.hp2 HG00673.hp2 HG02523.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0034a0001c0002t0081a0001c0002t0089others(1): Show | a0001c0001t0034g0063 a0001c0002t0081g0021 a0001c0002t0089g0072 others(1): Show |
4 | 176 | 0.0227 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12332483 | GC | G | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG03225.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(2): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(2): Show |
5 | 176 | 0.0284 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12339370 | CA | C | intron_variant | MODIFIER | HG01358.hp1 HG02258.hp2 HG02486.hp1 others(14): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0004a0001c0006others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(14): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0012g0009 others(14): Show |
17 | 176 | 0.0966 | -1 | c.178 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12348194 | TC | T | intron_variant | MODIFIER | HG01261.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0002t0019a0001c0002t0024others(2): Show | a0001c0001t0002g0081 a0001c0002t0019g0174 a0001c0002t0024g0050 others(2): Show |
5 | 176 | 0.0284 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12348911 | AG | A | intron_variant | MODIFIER | HG01261.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0013a0001c0001t0028others(11): Show | a0001c0001t0002g0081 a0001c0001t0013g0150 a0001c0001t0028g0122 others(11): Show |
14 | 176 | 0.0796 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12351383 | TC | T | intron_variant | MODIFIER | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(23): Show |
a0001a0003a0008 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0013a0001c0001t0017others(23): Show | a0001c0001t0002g0081 a0001c0001t0013g0150 a0001c0001t0017g0101 others(23): Show |
26 | 176 | 0.1477 | -1 | c.178 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | chr16 | TogoVar |