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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(83): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(21): Show | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0098 others(83): Show |
86 | 95 | 0.9053 | -5 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100798692 | ATATTT | A | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0008a0002c0002t0009others(1): Show | a0002c0002t0002g0141 a0002c0002t0008g0028 a0002c0002t0008g0029 others(3): Show |
6 | 284 | 0.0211 | -5 | c.312 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100816521 | AGATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0005a0002c0002t0006 | a0002c0002t0005g0047 a0002c0002t0005g0048 a0002c0002t0005g0055 others(1): Show |
4 | 284 | 0.0141 | -5 | c.312 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(1): Show | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0001t0002g0020 others(19): Show |
22 | 55 | 0.4000 | -5 | c.313 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100863074 | ACACAC | A | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(21): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0010others(5): Show | a0001c0001t0037a0001c0003t0014a0001c0010t0001others(10): Show | a0001c0001t0037g0041 a0001c0003t0014g0234 a0001c0003t0014g0235 others(21): Show |
24 | 284 | 0.0845 | -5 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100903710 | ATATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(11): Show |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(2): Show | a0002c0002t0002g0141 a0002c0002t0004g0174 a0002c0002t0005g0047 others(11): Show |
14 | 266 | 0.0526 | -5 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100950288 | ATATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(21): Show |
a0002a0003a0005 | a0002c0002a0003c0007a0005c0016 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(5): Show | a0002c0002t0002g0252 a0002c0002t0004g0113 a0002c0002t0005g0047 others(21): Show |
24 | 284 | 0.0845 | -5 | c.116 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100956595 | AAATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(260): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(49): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(260): Show |
263 | 284 | 0.9261 | -5 | c.116 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTT | C | intron_variant | MODIFIER | HG00733.hp2 HG01109.hp2 HG01978.hp2 others(4): Show |
a0002 | a0002c0002a0002c0006 | a0002c0002t0002a0002c0002t0011a0002c0006t0011 | a0002c0002t0002g0149 a0002c0002t0011g0038 a0002c0002t0011g0224 others(4): Show |
7 | 30 | 0.2333 | -5 | c.245 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802964 | TATATA | T | intron_variant | MODIFIER | HG02129.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0213 a0001c0001t0002g0107 |
2 | 228 | 0.0088 | -5 | c.53+ others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12868584 | ATGCAT | A | intron_variant | MODIFIER | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | 223 | 0.0135 | -5 | c.54- others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12886970 | TTTTTG | T | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(48): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0001g0139 others(48): Show |
51 | 228 | 0.2237 | -5 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12900932 | TTTTTA | T | intron_variant | MODIFIER | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0127 others(51): Show |
54 | 228 | 0.2368 | -5 | c.198 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGA | G | intron_variant | MODIFIER | HG02074.hp2 HG02129.hp2 NA19074.hp2 |
a0001a0006 | a0001c0004a0006c0016 | a0001c0004t0005a0006c0016t0002 | a0001c0004t0005g0067 a0001c0004t0005g0068 a0006c0016t0002g0169 |
3 | 186 | 0.0161 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903114 | GAGAGA | G | intron_variant | MODIFIER | HG01070.hp2 HG01258.hp1 HG01517.hp2 others(4): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0028others(1): Show | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0197 others(4): Show |
7 | 212 | 0.0330 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903116 | GAGAGA | G | intron_variant | MODIFIER | HG01891.hp2 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009 a0001c0001t0003g0072 |
2 | 224 | 0.0089 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12913172 | CAGAAG | C | intron_variant | MODIFIER | HG02071.hp1 HG03831.hp2 HG03942.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0012 a0001c0001t0002g0019 a0001c0001t0003g0083 others(4): Show |
7 | 228 | 0.0307 | -5 | c.276 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1068957 | CTTTAT | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
a0001a0002a0005others(5): Show | a0001c0002a0001c0004a0001c0017others(19): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0013others(33): Show | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0013 others(126): Show |
193 | 416 | 0.4639 | -5 | c.421 others(20): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1070505 | TCTTTC | T | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01891.hp1 others(54): Show |
a0002a0004a0005others(8): Show | a0002c0001a0002c0015a0002c0019others(19): Show | a0002c0001t0004a0002c0015t0001a0002c0019t0009others(19): Show | a0002c0001t0004g0006 a0002c0001t0004g0008 a0002c0001t0004g0022 others(38): Show |
57 | 416 | 0.1370 | -5 | c.421 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | chr19 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
a0002a0004a0005others(1): Show | a0002c0001a0002c0015a0002c0021others(7): Show | a0002c0001t0003a0002c0001t0005a0002c0001t0007others(11): Show | a0002c0001t0003g0003 a0002c0001t0003g0019 a0002c0001t0003g0020 others(33): Show |
62 | 184 | 0.3370 | -5 | c.118 others(24): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1077650 | TGCTGG | T | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01978.hp1 others(10): Show |
a0002a0003 | a0002c0001a0002c0015a0002c0031others(2): Show | a0002c0001t0004a0002c0015t0001a0002c0031t0004others(2): Show | a0002c0001t0004g0008 a0002c0001t0004g0134 a0002c0001t0004g0138 others(6): Show |
13 | 416 | 0.0313 | -5 | c.118 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32114258 | CTCTTT | C | intron_variant | MODIFIER | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
a0003 | a0003c0003 | a0003c0003t0001a0003c0003t0019 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | 184 | 0.0163 | -5 | c.371 others(24): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32131278 | CTTTAT | C | intron_variant | MODIFIER | HG00609.hp2 HG02809.hp1 |
a0004a0010 | a0004c0014a0010c0017 | a0004c0014t0015a0010c0017t0016 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | 184 | 0.0109 | -5 | c.386 others(26): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAA | C | intron_variant | MODIFIER | HG01257.hp2 HG01975.hp1 HG02257.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0115 a0001c0001t0002g0039 a0001c0001t0002g0103 others(3): Show |
6 | 28 | 0.2143 | -5 | c.418 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174617 | TCTTTC | T | intron_variant | MODIFIER | HG00609.hp1 NA18965.hp1 NA19007.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0016a0002c0002t0009 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0064 others(4): Show |
7 | 144 | 0.0486 | -5 | c.162 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11196135 | AAAAAC | A | intron_variant | MODIFIER | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(2): Show | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0043 others(5): Show |
8 | 108 | 0.0741 | -5 | c.820 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11649982 | CTTTCT | C | intron_variant | MODIFIER | HG03209.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0046 a0001c0004t0005g0047 |
2 | 144 | 0.0139 | -5 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11661056 | GAAGAA | G | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0124 a0001c0003t0001g0125 |
2 | 144 | 0.0139 | -5 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44749156 | CAAAAA | C | upstream_gene_variant | MODIFIER | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(54): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0007others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(28): Show | a0001c0001t0001g0371 a0001c0001t0003g0081 a0001c0001t0003g0137 others(54): Show |
57 | 243 | 0.2346 | -5 | c.-35 others(16): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3418 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44787321 | CTTTGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(61): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(23): Show | a0001c0001t0001g0101 a0001c0001t0003g0006 a0001c0001t0003g0063 others(61): Show |
64 | 199 | 0.3216 | -5 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44790365 | TTTAAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0004a0001c0007others(56): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(66): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(171): Show |
174 | 388 | 0.4485 | -5 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44790676 | CAAAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG01256.hp1 others(36): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(20): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0003g0074 others(36): Show |
39 | 206 | 0.1893 | -5 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44824607 | GTCTTT | G | intron_variant | MODIFIER | HG02280.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0352 a0005c0015t0001g0353 a0005c0015t0001g0354 others(1): Show |
4 | 388 | 0.0103 | -5 | c.486 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44828425 | ATTTTT | A | intron_variant | MODIFIER | HG01256.hp2 HG02735.hp2 HG02738.hp2 others(8): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0003a0002c0006others(3): Show | a0001c0001t0003a0002c0003t0004a0002c0006t0004others(3): Show | a0001c0001t0003g0089 a0002c0003t0004g0055 a0002c0003t0004g0234 others(8): Show |
11 | 88 | 0.1250 | -5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44830523 | ATTTTC | A | intron_variant | MODIFIER | HG02615.hp2 HG03516.hp2 NA21309.hp2 |
a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0058 a0001c0007t0001g0070 a0001c0007t0001g0382 |
3 | 388 | 0.0077 | -5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44859222 | GTTGAA | G | intron_variant | MODIFIER | HG02965.hp1 HG03041.hp2 HG03654.hp2 |
a0001a0008 | a0001c0004a0001c0007a0008c0030 | a0001c0004t0001a0001c0007t0001a0008c0030t0001 | a0001c0004t0001g0029 a0001c0007t0001g0107 a0008c0030t0001g0105 |
3 | 388 | 0.0077 | -5 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP9_chr12_57467269_57484866 | 57473418 | TAAATA | T | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
a0001a0011 | a0001c0001a0001c0008a0011c0017 | a0001c0001t0001a0001c0008t0001a0011c0017t0001 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0070 others(3): Show |
11 | 404 | 0.0272 | -5 | c.202 others(22): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 17/17 | chr12 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17537038 | TTTTTA | T | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0006a0001c0011others(43): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(48): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(146): Show |
149 | 166 | 0.8976 | -5 | c.-29 others(16): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2659 | chr1 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17686101 | TCTTTC | T | intron_variant | MODIFIER | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
a0002a0004 | a0002c0034a0002c0041a0004c0005 | a0002c0034t0002a0002c0041t0008a0004c0005t0002 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | 166 | 0.0482 | -5 | c.301 others(24): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1889602 | GAGTGT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(13): Show |
a0001a0005a0006 | a0001c0002a0001c0003a0001c0005others(11): Show | a0001c0002t0001a0001c0003t0020a0001c0005t0001others(12): Show | a0001c0002t0001g0273 a0001c0003t0020g0084 a0001c0005t0001g0325 others(13): Show |
16 | 362 | 0.0442 | -5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1917764 | TTTTTC | T | intron_variant | MODIFIER | HG01074.hp2 HG03486.hp2 HG03540.hp1 |
a0001 | a0001c0003a0001c0020 | a0001c0003t0001a0001c0003t0058a0001c0020t0016 | a0001c0003t0001g0198 a0001c0003t0058g0338 a0001c0020t0016g0308 |
3 | 362 | 0.0083 | -5 | c.214 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156930015 | TTTTTC | T | downstream_gene_variant | MODIFIER | HG00099.hp2 HG01074.hp1 HG01106.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0336 |
3 | 360 | 0.0083 | -5 | c.*59 others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4824 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156959927 | CCCCCT | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
a0002a0003 | a0002c0002a0002c0008a0003c0003 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(7): Show | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(80): Show |
86 | 360 | 0.2389 | -5 | c.128 others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | CAAAAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0006a0002c0004t0005a0002c0004t0009others(1): Show | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(16): Show |
20 | 175 | 0.1143 | -5 | c.33- others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157028734 | CAAAGA | C | intron_variant | MODIFIER | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0004a0002c0004t0022 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | 360 | 0.0083 | -5 | c.32+ others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120341901 | TTTGAG | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011a0001c0001t0013 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
15 | 306 | 0.0490 | -5 | c.32+ others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120406550 | TTTTTA | T | intron_variant | MODIFIER | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0005 others(2): Show |
5 | 306 | 0.0163 | -5 | c.56+ others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3485931 | CAAAAA | C | downstream_gene_variant | MODIFIER | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(7): Show |
a0002a0005a0010 | a0002c0003a0002c0012a0005c0013others(1): Show | a0002c0003t0002a0002c0012t0002a0005c0013t0005others(1): Show | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(4): Show |
10 | 12 | 0.8333 | -5 | c.*53 others(16): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4819 | chr1 | TogoVar | |||||||
ARHGEF17_chr11_73303276_73374388 | 73329356 | TATATA | T | intron_variant | MODIFIER | HG02055.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
a0002 | a0002c0002a0002c0003a0002c0030 | a0002c0002t0001a0002c0003t0002a0002c0030t0014 | a0002c0002t0001g0043 a0002c0003t0002g0054 a0002c0003t0002g0057 others(2): Show |
5 | 212 | 0.0236 | -5 | c.319 others(26): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7347395 | CAAAAA | C | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(26): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0004a0002c0005others(10): Show | a0001c0001t0002a0001c0001t0011a0002c0004t0002others(13): Show | a0001c0001t0002g0220 a0001c0001t0011g0205 a0001c0001t0011g0206 others(26): Show |
29 | 90 | 0.3222 | -5 | c.-19 others(16): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1541 | chr19 | TogoVar |