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 | 7466381 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
a0001a0002a0004others(3): Show | a0001c0002a0001c0042a0001c0043others(6): Show | a0001c0002t0002a0001c0002t0003a0001c0002t0036others(10): Show | a0001c0002t0002g0038 a0001c0002t0002g0158 a0001c0002t0003g0039 others(50): Show |
53 | 92 | 0.5761 | 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 | a0001c0001t0001g0108 a0001c0002t0002g0038 a0001c0002t0003g0041 others(28): Show |
31 | 152 | 0.2039 | 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 |
a0001a0002a0020others(3): Show | a0001c0013a0001c0048a0002c0007others(4): Show | a0001c0013t0001a0001c0048t0001a0002c0007t0001others(4): Show | a0001c0013t0001g0008 a0001c0013t0001g0064 a0001c0013t0001g0077 others(14): Show |
17 | 230 | 0.0739 | 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 | a0001c0001t0030g0010 a0001c0013t0001g0064 a0001c0013t0001g0077 others(5): Show |
8 | 164 | 0.0488 | 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(4): Show | a0001c0001a0001c0002a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0035a0001c0002t0003others(14): Show | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0035g0123 others(41): Show |
44 | 245 | 0.1796 | 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(282): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0006a0002c0002others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
285 | 360 | 0.7917 | 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 |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
41 | 266 | 0.1541 | 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 | 273 | 0.0989 | 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 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
34 | 132 | 0.2576 | 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(75): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(4): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(54): Show |
78 | 232 | 0.3362 | 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(85): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
88 | 103 | 0.8544 | 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 |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(71): Show |
89 | 232 | 0.3836 | 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 |
a0002a0005a0009 | a0002c0002a0002c0003a0002c0014others(3): Show | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(19): Show | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0038 others(89): Show |
93 | 255 | 0.3647 | 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(266): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0006a0001c0008others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(55): Show | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | 282 | 0.9539 | 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 | a0001c0001t0001a0001c0001t0012a0001c0001t0030others(2): Show | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0012g0276 others(3): Show |
6 | 26 | 0.2308 | 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(24): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0004 | a0001c0001t0002a0001c0001t0009a0001c0001t0018others(3): Show | a0001c0001t0002g0190 a0001c0001t0002g0202 a0001c0001t0002g0215 others(23): Show |
27 | 49 | 0.5510 | 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(268): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0006a0001c0008others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(57): Show | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | 282 | 0.9610 | 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(19): Show | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(97): Show |
103 | 114 | 0.9035 | 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(1): Show | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(5): Show |
8 | 91 | 0.0879 | 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 | a0001c0001t0004a0001c0001t0019a0001c0008t0019others(6): Show | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0019g0132 others(12): Show |
15 | 272 | 0.0551 | 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 | a0002c0003t0016a0002c0003t0035a0002c0003t0036 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
3 | 280 | 0.0107 | 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 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(5): Show | a0001c0001t0002g0146 a0001c0001t0009g0139 a0001c0001t0009g0145 others(9): Show |
12 | 22 | 0.5455 | 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 | a0001c0001t0002a0001c0001t0004a0001c0001t0018others(7): Show | a0001c0001t0002g0238 a0001c0001t0004g0140 a0001c0001t0004g0218 others(11): Show |
15 | 35 | 0.4286 | 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 |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0007a0002c0002t0003a0002c0003t0003 | a0001c0001t0007g0171 a0002c0002t0003g0045 a0002c0002t0003g0084 others(1): Show |
4 | 225 | 0.0178 | 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 | a0003c0004t0026a0003c0004t0027 | a0003c0004t0026g0011 a0003c0004t0027g0009 |
2 | 282 | 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 | a0001c0025t0005g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(9): Show |
12 | 170 | 0.0706 | 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 | 85 | 0.2235 | 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(130): Show |
a0001a0002a0003others(34): Show | a0001c0001a0001c0021a0001c0023others(59): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(88): Show | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0028 others(130): Show |
133 | 186 | 0.7151 | 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 | 73 | 0.0959 | 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 | 143 | 0.1189 | 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 a0002c0002t0001g0006 a0002c0002t0001g0131 others(50): Show |
53 | 186 | 0.2849 | 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 a0002c0003t0001g0128 others(14): Show |
17 | 124 | 0.1371 | 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 | 71 | 0.1268 | 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 a0002c0003t0001g0128 others(16): Show |
19 | 116 | 0.1638 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0038 others(33): Show |
36 | 115 | 0.3130 | 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 | 89 | 0.3258 | 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 a0006c0047t0008g0137 a0007c0013t0001g0136 others(2): Show |
5 | 85 | 0.0588 | 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 a0004c0004t0001g0154 a0004c0004t0001g0167 others(4): Show |
7 | 186 | 0.0376 | 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 a0004c0004t0001g0154 a0004c0004t0001g0167 others(4): Show |
7 | 186 | 0.0376 | 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 a0004c0004t0001g0154 a0004c0004t0001g0167 others(4): Show |
7 | 175 | 0.0400 | 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 | 89 | 0.0562 | 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 | 73815251 | A | AGCTC | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(21): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0003a0003c0049others(11): Show | a0002c0002t0001a0002c0002t0002a0002c0003t0001others(15): Show | a0002c0002t0001g0096 a0002c0002t0001g0131 a0002c0002t0001g0132 others(21): Show |
24 | 186 | 0.1290 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73837710 | T | TCTTC | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG04199.hp1 |
a0005a0007 | a0005c0024a0007c0009 | a0005c0024t0002a0007c0009t0001a0007c0009t0002 | a0005c0024t0002g0064 a0007c0009t0001g0121 a0007c0009t0002g0040 |
3 | 170 | 0.0176 | 4 | c.114 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73857564 | T | TACAC | intron_variant | MODIFIER | HG00733.hp1 NA18988.hp1 NA19065.hp2 |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0002a0005c0008t0002 | a0001c0001t0002g0058 a0001c0001t0002g0099 a0005c0008t0002g0083 |
3 | 131 | 0.0229 | 4 | c.179 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73858425 | C | CCTCA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
a0001a0002a0003others(31): Show | a0001c0021a0001c0023a0001c0025others(53): Show | a0001c0021t0008a0001c0023t0001a0001c0025t0001others(81): Show | a0001c0021t0008g0102 a0001c0023t0001g0034 a0001c0025t0001g0156 others(114): Show |
117 | 186 | 0.6290 | 4 | c.204 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73869222 | T | TGGGG | intron_variant | MODIFIER | HG01106.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0025a0002c0002a0003c0058others(5): Show | a0001c0025t0001a0002c0002t0001a0002c0002t0005others(6): Show | a0001c0025t0001g0156 a0002c0002t0001g0182 a0002c0002t0005g0022 others(6): Show |
9 | 65 | 0.1385 | 4 | c.242 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73894845 | G | GGGAA | intron_variant | MODIFIER | HG02258.hp2 HG02965.hp2 HG03139.hp1 |
a0002a0012 | a0002c0002a0012c0073 | a0002c0002t0001a0002c0002t0003a0012c0073t0001 | a0002c0002t0001g0131 a0002c0002t0003g0124 a0012c0073t0001g0143 |
3 | 186 | 0.0161 | 4 | c.384 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73910381 | C | CAAAA | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0025a0001c0071others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(35): Show | a0001c0001t0001g0003 a0001c0001t0001g0063 a0001c0001t0002g0094 others(49): Show |
52 | 110 | 0.4727 | 4 | c.464 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73913347 | A | ATGTT | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
a0001a0002a0003others(29): Show | a0001c0001a0001c0021a0001c0023others(59): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(93): Show | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0063 others(129): Show |
132 | 186 | 0.7097 | 4 | c.494 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73938160 | C | CCACA | intron_variant | MODIFIER | HG00140.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0028a0002c0002others(6): Show | a0001c0001t0002a0001c0028t0001a0002c0002t0001others(6): Show | a0001c0001t0002g0032 a0001c0028t0001g0146 a0002c0002t0001g0182 others(6): Show |
9 | 23 | 0.3913 | 4 | c.494 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |