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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF18_chr19_7343937_7477478 | 7385915 | C | CCTCT | intron_variant | MODIFIER | HG02922.hp2 HG03098.hp2 HG03139.hp2 |
a0002a0006 | a0002c0004a0006c0010 | a0002c0004t0002a0002c0004t0004a0006c0010t0009 | a0002c0004t0002g0050 a0002c0004t0004g0002 a0006c0010t0009g0067 |
3 | 298 | 0.0101 | 4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7403529 | T | TTTTC | intron_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(25): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0002c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(8): Show | a0001c0001t0001g0056 a0001c0001t0002g0159 a0001c0002t0002g0129 others(25): Show |
28 | 298 | 0.0940 | 4 | c.967 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7410809 | C | CAAAA | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0002a0001c0018others(13): Show | a0001c0001t0002a0001c0002t0003a0001c0018t0001others(14): Show | a0001c0001t0002g0042 a0001c0001t0002g0055 a0001c0001t0002g0070 others(36): Show |
39 | 298 | 0.1309 | 4 | c.967 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7416530 | C | CGTGT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(39): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(14): Show | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0173 others(39): Show |
42 | 298 | 0.1409 | 4 | c.968 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7416605 | G | GTTTT | intron_variant | MODIFIER | HG00423.hp1 HG01255.hp1 HG01255.hp2 others(10): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0016others(7): Show | a0001c0001t0002a0001c0002t0003a0001c0016t0014others(7): Show | a0001c0001t0002g0175 a0001c0002t0003g0085 a0001c0002t0003g0154 others(10): Show |
13 | 298 | 0.0436 | 4 | c.968 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7422866 | A | ACACC | intron_variant | MODIFIER | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0029a0001c0002t0003 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(7): Show |
10 | 298 | 0.0336 | 4 | c.968 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7442124 | C | CCCTT | intron_variant | MODIFIER | HG01243.hp2 HG02015.hp1 HG02055.hp1 others(5): Show |
a0003a0007a0009others(1): Show | a0003c0003a0007c0009a0009c0012others(1): Show | a0003c0003t0001a0003c0003t0027a0007c0009t0001others(3): Show | a0003c0003t0001g0200 a0003c0003t0001g0211 a0003c0003t0001g0212 others(5): Show |
8 | 298 | 0.0269 | 4 | c.136 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7442225 | C | CTCTT | intron_variant | MODIFIER | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
a0001a0002a0016others(1): Show | a0001c0001a0001c0016a0001c0052others(3): Show | a0001c0001t0030a0001c0016t0014a0001c0052t0001others(3): Show | a0001c0001t0030g0008 a0001c0016t0014g0096 a0001c0052t0001g0266 others(3): Show |
6 | 298 | 0.0201 | 4 | c.136 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7452453 | A | AATTT | intron_variant | MODIFIER | HG01106.hp2 HG02071.hp1 HG03704.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0019a0001c0021others(3): Show | a0001c0001t0002a0001c0019t0006a0001c0021t0006others(3): Show | a0001c0001t0002g0043 a0001c0019t0006g0057 a0001c0019t0006g0063 others(6): Show |
9 | 298 | 0.0302 | 4 | c.185 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466381 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
a0001a0002a0004others(4): Show | a0001c0002a0001c0044a0001c0045others(7): Show | a0001c0002t0002a0001c0002t0003a0001c0002t0036others(11): Show | a0001c0002t0002g0038 a0001c0002t0002g0129 a0001c0002t0003g0039 others(50): Show |
53 | 298 | 0.1779 | 4 | c.290 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466804 | C | CAAAA | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(28): Show |
a0001a0002a0009others(5): Show | a0001c0001a0001c0002a0001c0016others(9): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(12): Show | a0001c0001t0001g0109 a0001c0002t0002g0038 a0001c0002t0003g0040 others(28): Show |
31 | 298 | 0.1040 | 4 | c.290 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466836 | A | AAAGG | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01169.hp2 others(14): Show |
a0001a0002a0018others(4): Show | a0001c0013a0001c0052a0002c0007others(5): Show | a0001c0013t0001a0001c0052t0001a0002c0007t0001others(5): Show | a0001c0013t0001g0010 a0001c0013t0001g0195 a0001c0013t0001g0204 others(14): Show |
17 | 298 | 0.0571 | 4 | c.290 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | A | AGTGT | downstream_gene_variant | MODIFIER | HG00609.hp2 HG01074.hp2 HG01169.hp2 others(5): Show |
a0001a0003a0010others(2): Show | a0001c0001a0001c0013a0003c0003others(3): Show | a0001c0001t0030a0001c0013t0001a0003c0003t0001others(3): Show | a0001c0001t0030g0008 a0001c0013t0001g0195 a0001c0013t0001g0204 others(5): Show |
8 | 298 | 0.0269 | 4 | c.*44 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7475525 | A | AACAC | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(41): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0002a0001c0013others(14): Show | a0001c0001t0001a0001c0001t0035a0001c0002t0003others(16): Show | a0001c0001t0001g0053 a0001c0001t0001g0216 a0001c0001t0035g0149 others(41): Show |
44 | 298 | 0.1477 | 4 | c.*52 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3048 | chr19 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16194835 | G | GGGAA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0006a0002c0002others(15): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
286 | 362 | 0.7901 | 4 | c.*37 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 3018 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16213728 | T | TTTTA | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(38): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
41 | 362 | 0.1133 | 4 | c.-12 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1077 | chr1 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16215419 | G | GTATT | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(24): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(7): Show |
27 | 362 | 0.0746 | 4 | c.-29 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 2768 | chr1 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41880451 | G | GGGAA | upstream_gene_variant | MODIFIER | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(31): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0011 | a0001c0001t0001a0001c0002t0001a0009c0011t0001 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
34 | 234 | 0.1453 | 4 | c.-28 others(15): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2732 | chr19 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41885454 | T | TTTTA | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(76): Show |
a0001a0004a0005others(6): Show | a0001c0001a0001c0002a0001c0009others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(9): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
79 | 234 | 0.3376 | 4 | c.-20 others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41894135 | A | AGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
a0001a0003a0005others(5): Show | a0001c0001a0001c0002a0001c0009others(9): Show | a0001c0001t0001a0001c0002t0001a0001c0009t0001others(9): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(59): Show |
89 | 234 | 0.3803 | 4 | c.645 others(17): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41907905 | C | CACAA | downstream_gene_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(11): Show | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(74): Show |
89 | 234 | 0.3803 | 4 | c.*81 others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 454 | chr19 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154124372 | C | CTTTT | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
a0002a0005a0009others(1): Show | a0002c0002a0002c0003a0002c0015others(4): Show | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(24): Show | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0038 others(89): Show |
93 | 283 | 0.3286 | 4 | c.108 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154164456 | T | TTATC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0006a0001c0008others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(263): Show |
270 | 283 | 0.9541 | 4 | c.148 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154186136 | G | GACAC | intron_variant | MODIFIER | HG02109.hp1 HG02257.hp1 HG02523.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0014a0001c0001t0036others(2): Show | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0014g0277 others(3): Show |
6 | 283 | 0.0212 | 4 | c.148 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154186886 | C | CTTTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0004 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(5): Show | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0191 others(24): Show |
28 | 283 | 0.0989 | 4 | c.148 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154202798 | C | CTGTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0006a0001c0008others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(67): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(265): Show |
272 | 283 | 0.9611 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154211867 | A | ATGTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(24): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(99): Show |
103 | 283 | 0.3640 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154213201 | T | TAGAG | intron_variant | MODIFIER | HG01433.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | 283 | 0.0283 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154213216 | A | AGAGT | intron_variant | MODIFIER | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(2): Show | a0001c0001t0004a0001c0001t0023a0001c0008t0023others(7): Show | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0023g0131 others(12): Show |
15 | 283 | 0.0530 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154213239 | G | GTATA | intron_variant | MODIFIER | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
a0002 | a0002c0003 | a0002c0003t0018a0002c0003t0045a0002c0003t0046 | a0002c0003t0018g0092 a0002c0003t0045g0095 a0002c0003t0046g0093 |
3 | 283 | 0.0106 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | T | TACAC | intron_variant | MODIFIER | HG00323.hp1 HG00741.hp2 HG01081.hp2 others(9): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0010a0001c0001t0011a0001c0001t0015others(6): Show | a0001c0001t0010g0138 a0001c0001t0010g0140 a0001c0001t0011g0141 others(9): Show |
12 | 283 | 0.0424 | 4 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154237538 | T | TCACA | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG01071.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0020others(8): Show | a0001c0001t0002g0240 a0001c0001t0004g0139 a0001c0001t0004g0219 others(11): Show |
15 | 283 | 0.0530 | 4 | c.209 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239289 | A | AGTGT | intron_variant | MODIFIER | HG02155.hp1 NA18947.hp1 NA18960.hp1 others(1): Show |
a0001a0002a0011 | a0001c0001a0002c0002a0011c0012 | a0001c0001t0007a0002c0002t0003a0011c0012t0003 | a0001c0001t0007g0172 a0002c0002t0003g0045 a0002c0002t0003g0083 others(1): Show |
4 | 283 | 0.0141 | 4 | c.209 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154256886 | T | TTATC | 3_prime_UTR_variant | MODIFIER | HG03195.hp2 NA19043.hp1 |
a0003 | a0003c0004 | a0003c0004t0031a0003c0004t0032 | a0003c0004t0031g0010 a0003c0004t0032g0008 |
2 | 283 | 0.0071 | 4 | c.*14 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1419 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73639228 | C | CATAT | intron_variant | MODIFIER | HG00733.hp2 HG01069.hp1 HG01167.hp2 others(9): Show |
a0001a0002a0006others(6): Show | a0001c0025a0002c0002a0002c0003others(8): Show | a0001c0025t0005a0002c0002t0001a0002c0003t0001others(8): Show | a0001c0025t0005g0131 a0002c0002t0001g0130 a0002c0002t0001g0132 others(9): Show |
12 | 188 | 0.0638 | 4 | c.-12 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73658962 | T | TACAC | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(16): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0028a0002c0002others(11): Show | a0001c0001t0002a0001c0028t0001a0002c0002t0002others(14): Show | a0001c0001t0002g0008 a0001c0028t0001g0181 a0002c0002t0002g0086 others(16): Show |
19 | 188 | 0.1011 | 4 | c.-11 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73687393 | C | CTCTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
a0001a0002a0003others(34): Show | a0001c0001a0001c0021a0001c0023others(60): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(89): Show | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(131): Show |
134 | 188 | 0.7128 | 4 | c.33+ others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73691296 | T | TACAC | intron_variant | MODIFIER | HG00323.hp2 HG01891.hp1 HG02451.hp2 others(4): Show |
a0002a0003a0004others(3): Show | a0002c0002a0003c0007a0004c0004others(3): Show | a0002c0002t0003a0003c0007t0011a0004c0004t0005others(4): Show | a0002c0002t0003g0124 a0003c0007t0011g0148 a0004c0004t0005g0183 others(4): Show |
7 | 188 | 0.0372 | 4 | c.33+ others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73703647 | T | TTGTG | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(14): Show |
a0003a0004a0005others(10): Show | a0003c0005a0003c0048a0004c0004others(13): Show | a0003c0005t0001a0003c0048t0006a0004c0004t0001others(14): Show | a0003c0005t0001g0043 a0003c0048t0006g0176 a0004c0004t0001g0170 others(14): Show |
17 | 188 | 0.0904 | 4 | c.33+ others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73722211 | G | GGAGA | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
a0001a0002a0003others(16): Show | a0001c0021a0002c0002a0002c0003others(26): Show | a0001c0021t0008a0002c0002t0001a0002c0002t0002others(37): Show | a0001c0021t0008g0102 a0002c0002t0001g0003 a0002c0002t0001g0130 others(50): Show |
53 | 188 | 0.2819 | 4 | c.34- others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73731011 | T | TAAAA | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG01167.hp2 others(14): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0003a0003c0007others(11): Show | a0002c0002t0001a0002c0002t0005a0002c0003t0001others(14): Show | a0002c0002t0001g0132 a0002c0002t0005g0022 a0002c0003t0001g0129 others(14): Show |
17 | 188 | 0.0904 | 4 | c.34- others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73738482 | C | CGTGT | intron_variant | MODIFIER | HG00741.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
a0003a0005a0007others(3): Show | a0003c0007a0005c0008a0007c0009others(3): Show | a0003c0007t0001a0003c0007t0011a0005c0008t0001others(5): Show | a0003c0007t0001g0045 a0003c0007t0001g0140 a0003c0007t0011g0148 others(6): Show |
9 | 188 | 0.0479 | 4 | c.34- others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73739828 | A | AAAAT | intron_variant | MODIFIER | HG00733.hp2 HG01891.hp1 HG02145.hp2 others(16): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0003others(11): Show | a0001c0001t0002a0002c0002t0005a0002c0003t0001others(16): Show | a0001c0001t0002g0050 a0002c0002t0005g0022 a0002c0003t0001g0129 others(16): Show |
19 | 188 | 0.1011 | 4 | c.34- others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73783345 | A | AGTGT | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(33): Show |
a0001a0003a0004others(10): Show | a0001c0001a0001c0023a0003c0005others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0001others(21): Show | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0038 others(33): Show |
36 | 188 | 0.1915 | 4 | c.910 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73802870 | C | CTCTG | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(26): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0006a0003c0005others(14): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0001others(20): Show | a0002c0002t0001g0132 a0002c0002t0001g0182 a0002c0002t0002g0158 others(26): Show |
29 | 188 | 0.1543 | 4 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73804082 | C | CAAAA | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
a0003a0006a0007 | a0003c0058a0006c0047a0007c0013 | a0003c0058t0001a0006c0047t0008a0007c0013t0001others(2): Show | a0003c0058t0001g0139 a0006c0047t0008g0136 a0007c0013t0001g0137 others(2): Show |
5 | 188 | 0.0266 | 4 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806341 | A | AGTAT | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
a0003a0004a0026others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140 a0004c0004t0001g0155 a0004c0004t0001g0167 others(4): Show |
7 | 188 | 0.0372 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73806356 | T | TATAC | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
a0003a0004a0026others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140 a0004c0004t0001g0155 a0004c0004t0001g0167 others(4): Show |
7 | 188 | 0.0372 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73807487 | C | CTTTT | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
a0003a0004a0010others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140 a0004c0004t0001g0155 a0004c0004t0001g0167 others(4): Show |
7 | 188 | 0.0372 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73815190 | G | GTGTA | intron_variant | MODIFIER | HG02809.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
a0002a0003a0006others(2): Show | a0002c0002a0003c0007a0006c0010others(2): Show | a0002c0002t0001a0003c0007t0005a0006c0010t0001others(2): Show | a0002c0002t0001g0182 a0003c0007t0005g0151 a0006c0010t0001g0185 others(2): Show |
5 | 188 | 0.0266 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |