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 | 12352513 | TA | T | intron_variant | MODIFIER | HG01261.hp2 HG02451.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0042a0001c0002t0019others(3): Show | a0001c0001t0002g0081 a0001c0001t0042g0015 a0001c0002t0019g0174 others(3): Show |
6 | 176 | 0.0341 | -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 | 12355843 | TA | T | intron_variant | MODIFIER | HG00438.hp2 HG00642.hp2 HG01109.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | a0001c0001t0001g0153 a0001c0001t0002g0020 a0001c0001t0002g0169 others(14): Show |
17 | 176 | 0.0966 | -1 | c.178 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12358198 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(55): Show | a0001c0001t0001g0112 a0001c0001t0001g0163 a0001c0001t0002g0081 others(65): Show |
68 | 176 | 0.3864 | -1 | c.189 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12366035 | CT | C | intron_variant | MODIFIER | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(13): Show |
a0001a0003a0008 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0017a0001c0001t0034others(13): Show | a0001c0001t0002g0081 a0001c0001t0017g0101 a0001c0001t0034g0063 others(13): Show |
16 | 176 | 0.0909 | -1 | c.189 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12366042 | CA | C | intron_variant | MODIFIER | HG01109.hp1 HG01358.hp1 HG02451.hp2 others(9): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0027a0001c0001t0061a0001c0002t0069others(9): Show | a0001c0001t0027g0082 a0001c0001t0061g0173 a0001c0002t0069g0017 others(9): Show |
12 | 176 | 0.0682 | -1 | c.189 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12369140 | CT | C | intron_variant | MODIFIER | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(12): Show |
a0001a0003a0008 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0017a0001c0001t0034others(12): Show | a0001c0001t0002g0081 a0001c0001t0017g0101 a0001c0001t0034g0063 others(12): Show |
15 | 176 | 0.0852 | -1 | c.189 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12374290 | GC | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(56): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(74): Show |
77 | 176 | 0.4375 | -1 | c.189 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12380649 | AC | A | intron_variant | MODIFIER | HG01261.hp2 HG02257.hp2 HG03486.hp2 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0002a0001c0002t0024a0001c0013t0094 | a0001c0001t0002g0169 a0001c0002t0024g0050 a0001c0013t0094g0126 |
3 | 176 | 0.0171 | -1 | c.190 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12381101 | AC | A | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(12): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0061a0001c0003t0001a0001c0003t0002others(11): Show | a0001c0001t0061g0173 a0001c0003t0001g0158 a0001c0003t0002g0119 others(12): Show |
15 | 176 | 0.0852 | -1 | c.190 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12381663 | AC | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(128): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(170): Show |
173 | 176 | 0.9830 | -1 | c.190 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12383772 | CT | C | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp2 HG01109.hp1 others(16): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0017a0001c0001t0026others(16): Show | a0001c0001t0002g0065 a0001c0001t0017g0025 a0001c0001t0026g0062 others(16): Show |
19 | 176 | 0.1080 | -1 | c.190 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12390880 | TA | T | intron_variant | MODIFIER | HG01175.hp1 HG01261.hp2 HG02257.hp2 others(9): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0007a0001c0001t0055a0001c0002t0019others(9): Show | a0001c0001t0007g0008 a0001c0001t0055g0121 a0001c0002t0019g0174 others(9): Show |
12 | 176 | 0.0682 | -1 | c.190 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12395822 | TA | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0036a0001c0001t0055others(22): Show | a0001c0001t0002g0065 a0001c0001t0036g0030 a0001c0001t0055g0121 others(24): Show |
27 | 176 | 0.1534 | -1 | c.190 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12398854 | AG | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(34): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(31): Show | a0001c0001t0002g0065 a0001c0001t0002g0081 a0001c0001t0006g0064 others(34): Show |
37 | 176 | 0.2102 | -1 | c.195 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12399066 | TA | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(28): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(25): Show | a0001c0001t0002g0065 a0001c0001t0002g0081 a0001c0001t0006g0064 others(28): Show |
31 | 176 | 0.1761 | -1 | c.195 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 17/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12401359 | AT | A | intron_variant | MODIFIER | HG01891.hp2 HG02523.hp2 HG02615.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0042a0001c0001t0101a0001c0001t0112others(8): Show | a0001c0001t0042g0015 a0001c0001t0101g0019 a0001c0001t0112g0139 others(8): Show |
11 | 176 | 0.0625 | -1 | c.195 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12407175 | GC | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(58): Show | a0001c0001t0002g0020 a0001c0001t0002g0065 a0001c0001t0004g0078 others(67): Show |
70 | 176 | 0.3977 | -1 | c.203 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12407327 | TG | T | intron_variant | MODIFIER | HG00733.hp2 HG01175.hp1 HG02615.hp1 others(2): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0005others(2): Show | a0001c0001t0007a0001c0002t0091a0002c0005t0039others(2): Show | a0001c0001t0007g0008 a0001c0002t0091g0011 a0002c0005t0039g0013 others(2): Show |
5 | 176 | 0.0284 | -1 | c.203 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12409421 | CT | C | intron_variant | MODIFIER | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0013a0001c0001t0028a0001c0001t0101others(6): Show | a0001c0001t0013g0150 a0001c0001t0028g0122 a0001c0001t0101g0019 others(6): Show |
9 | 176 | 0.0511 | -1 | c.203 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12413887 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(75): Show | a0001c0001t0001g0163 a0001c0001t0002g0020 a0001c0001t0002g0065 others(90): Show |
93 | 176 | 0.5284 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12419562 | GC | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(55): Show | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0141 others(68): Show |
71 | 176 | 0.4034 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12420380 | CT | C | intron_variant | MODIFIER | HG02451.hp1 HG02559.hp1 HG02886.hp2 |
a0001 | a0001c0001a0001c0012 | a0001c0001t0002a0001c0001t0017a0001c0012t0002 | a0001c0001t0002g0081 a0001c0001t0017g0025 a0001c0012t0002g0028 |
3 | 176 | 0.0171 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12425529 | TA | T | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
a0001a0006a0007 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(17): Show | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0006g0064 others(20): Show |
23 | 176 | 0.1307 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12425544 | AT | A | intron_variant | MODIFIER | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(9): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0014a0001c0002t0088others(9): Show | a0001c0001t0002g0169 a0001c0001t0014g0099 a0001c0002t0088g0018 others(9): Show |
12 | 176 | 0.0682 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12426061 | AT | A | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(10): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(10): Show | a0001c0001t0001g0112 a0001c0001t0006g0064 a0001c0001t0013g0150 others(10): Show |
13 | 176 | 0.0739 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12426084 | AT | A | intron_variant | MODIFIER | HG00738.hp2 HG01109.hp1 HG01167.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0009a0001c0001t0052a0001c0002t0024others(3): Show | a0001c0001t0009g0111 a0001c0001t0052g0026 a0001c0002t0024g0128 others(3): Show |
6 | 176 | 0.0341 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12430852 | CT | C | intron_variant | MODIFIER | HG02257.hp1 HG03486.hp2 HG03491.hp2 others(3): Show |
a0001a0008 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0002a0001c0003t0056a0001c0004t0095others(3): Show | a0001c0001t0002g0169 a0001c0003t0056g0033 a0001c0004t0095g0151 others(3): Show |
6 | 176 | 0.0341 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12433650 | AG | A | intron_variant | MODIFIER | HG01175.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0002c0005others(1): Show | a0001c0001t0007a0001c0002t0091a0002c0005t0039others(1): Show | a0001c0001t0007g0008 a0001c0002t0091g0011 a0002c0005t0039g0013 others(1): Show |
4 | 176 | 0.0227 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12436222 | AG | A | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(15): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0014a0001c0001t0063others(13): Show | a0001c0001t0001g0163 a0001c0001t0014g0099 a0001c0001t0063g0039 others(15): Show |
18 | 176 | 0.1023 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12447165 | CA | C | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00673.hp2 others(37): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0014a0001c0001t0015a0001c0001t0017others(36): Show | a0001c0001t0014g0099 a0001c0001t0015g0085 a0001c0001t0017g0101 others(37): Show |
40 | 176 | 0.2273 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12449353 | AG | A | intron_variant | MODIFIER | HG01358.hp1 HG02015.hp1 HG02040.hp2 others(8): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0110a0001c0001t0112a0001c0002t0005others(7): Show | a0001c0001t0110g0162 a0001c0001t0112g0139 a0001c0002t0005g0032 others(8): Show |
11 | 176 | 0.0625 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12460657 | CT | C | intron_variant | MODIFIER | HG00673.hp2 HG01167.hp2 HG01261.hp2 others(33): Show |
a0001a0006a0008 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(30): Show | a0001c0001t0002g0065 a0001c0001t0002g0169 a0001c0001t0007g0008 others(33): Show |
36 | 176 | 0.2046 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12461955 | CA | C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0007a0001c0001t0017a0001c0002t0065others(5): Show | a0001c0001t0007g0008 a0001c0001t0017g0025 a0001c0002t0065g0136 others(6): Show |
9 | 176 | 0.0511 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12461979 | AT | A | intron_variant | MODIFIER | HG01891.hp2 HG02040.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0090a0001c0003t0062 | a0001c0002t0090g0170 a0001c0003t0062g0075 |
2 | 176 | 0.0114 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12461981 | AT | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01496.hp1 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0002 | a0001c0003t0001g0158 a0001c0003t0002g0077 a0001c0003t0002g0097 |
3 | 176 | 0.0171 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12465838 | GT | G | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(52): Show | a0001c0001t0001g0163 a0001c0001t0002g0020 a0001c0001t0002g0065 others(56): Show |
59 | 176 | 0.3352 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12467654 | TC | T | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG02622.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0006a0001c0007others(1): Show | a0001c0001t0012a0001c0001t0040a0001c0001t0055others(3): Show | a0001c0001t0012g0009 a0001c0001t0040g0124 a0001c0001t0055g0121 others(3): Show |
6 | 176 | 0.0341 | -1 | c.203 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12472529 | CA | C | intron_variant | MODIFIER | HG02258.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0055a0001c0001t0102others(5): Show | a0001c0001t0002g0065 a0001c0001t0055g0121 a0001c0001t0102g0001 others(5): Show |
8 | 176 | 0.0455 | -1 | c.203 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12476351 | CA | C | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG01346.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(4): Show | a0001c0001t0001g0141 a0001c0001t0004g0132 a0001c0001t0008g0104 others(5): Show |
8 | 176 | 0.0455 | -1 | c.203 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12483319 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(31): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0127 others(31): Show |
34 | 176 | 0.1932 | -1 | c.217 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12489285 | GA | G | intron_variant | MODIFIER | HG02015.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0028a0001c0002t0024a0001c0002t0087others(5): Show | a0001c0001t0028g0122 a0001c0002t0024g0128 a0001c0002t0087g0147 others(5): Show |
8 | 176 | 0.0455 | -1 | c.217 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12496507 | CT | C | intron_variant | MODIFIER | HG01167.hp2 HG02015.hp2 HG02523.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0007a0001c0001t0012a0001c0001t0040others(8): Show | a0001c0001t0007g0175 a0001c0001t0012g0009 a0001c0001t0040g0124 others(8): Show |
11 | 176 | 0.0625 | -1 | c.217 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12498211 | GC | G | intron_variant | MODIFIER | HG01167.hp2 HG02622.hp1 NA19240.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0012a0001c0001t0040a0001c0006t0068 | a0001c0001t0012g0009 a0001c0001t0040g0124 a0001c0006t0068g0003 |
3 | 176 | 0.0171 | -1 | c.217 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12501724 | CA | C | intron_variant | MODIFIER | HG00673.hp2 HG01175.hp1 HG01261.hp2 others(20): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0013a0001c0001t0017others(20): Show | a0001c0001t0001g0163 a0001c0001t0013g0150 a0001c0001t0017g0025 others(20): Show |
23 | 176 | 0.1307 | -1 | c.217 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12511410 | AG | A | intron_variant | MODIFIER | HG02015.hp2 HG02523.hp1 NA19009.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0007a0001c0001t0047a0001c0003t0103others(2): Show | a0001c0001t0007g0175 a0001c0001t0047g0155 a0001c0003t0103g0079 others(2): Show |
5 | 176 | 0.0284 | -1 | c.217 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12516481 | GA | G | intron_variant | MODIFIER | HG00733.hp2 HG02015.hp1 HG03225.hp2 others(10): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0006a0001c0001t0110a0001c0002t0003others(9): Show | a0001c0001t0006g0064 a0001c0001t0110g0162 a0001c0002t0003g0152 others(10): Show |
13 | 176 | 0.0739 | -1 | c.217 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12520773 | TA | T | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(147): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(116): Show | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0153 others(147): Show |
150 | 176 | 0.8523 | -1 | c.217 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12525329 | TA | T | intron_variant | MODIFIER | HG00323.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(17): Show | a0001c0001t0002g0169 a0001c0001t0006g0031 a0001c0001t0007g0008 others(18): Show |
21 | 176 | 0.1193 | -1 | c.231 others(9): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12531408 | AT | A | intron_variant | MODIFIER | HG03098.hp2 HG03130.hp1 HG03491.hp1 others(3): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0055a0001c0002t0018others(3): Show | a0001c0001t0006g0031 a0001c0001t0055g0121 a0001c0002t0018g0034 others(3): Show |
6 | 176 | 0.0341 | -1 | c.231 others(10): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12537479 | AT | A | intron_variant | MODIFIER | HG00140.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0052others(6): Show | a0001c0001t0001g0127 a0001c0001t0004g0078 a0001c0001t0004g0132 others(8): Show |
11 | 176 | 0.0625 | -1 | c.231 others(11): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |