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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP8_chr22_44747575_44867784 | 44833076 | T | TTTTTC | intron_variant | MODIFIER | HG00280.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
a0001a0013 | a0001c0007a0001c0008a0013c0038others(1): Show | a0001c0007t0001a0001c0008t0001a0013c0038t0005others(1): Show | a0001c0007t0001g0058 a0001c0007t0001g0140 a0001c0008t0001g0380 others(2): Show |
5 | 321 | 0.0156 | 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 | 44858369 | G | GTTTTC | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(22): Show |
a0002a0004a0006others(3): Show | a0002c0011a0002c0013a0002c0019others(9): Show | a0002c0011t0005a0002c0013t0005a0002c0019t0008others(9): Show | a0002c0011t0005g0016 a0002c0011t0005g0086 a0002c0011t0005g0284 others(22): Show |
25 | 143 | 0.1748 | 5 | c.878 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTTTT | intron_variant | MODIFIER | HG01099.hp1 HG01346.hp1 HG01516.hp2 others(29): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0003a0002c0006others(11): Show | a0001c0001t0003a0002c0003t0004a0002c0006t0004others(12): Show | a0001c0001t0003g0006 a0002c0003t0004g0011 a0002c0003t0004g0180 others(29): Show |
32 | 68 | 0.4706 | 5 | c.878 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44860550 | C | CAACTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0004a0001c0007others(60): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(69): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(327): Show |
330 | 388 | 0.8505 | 5 | c.981 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 275640 | C | CGCGGG | upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(10): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(22): Show |
43 | 440 | 0.0977 | 5 | c.-50 others(16): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4950 | chr16 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1888287 | G | GGCACT | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01243.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0001others(15): Show | a0001c0001t0002g0249 a0001c0001t0003g0102 a0001c0002t0001g0248 others(17): Show |
20 | 358 | 0.0559 | 5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888375 | T | TGAGGA | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0050a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0050g0174 a0002c0028t0001g0201 a0002c0033t0002g0012 others(4): Show |
7 | 362 | 0.0193 | 5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | ATATAT | intron_variant | MODIFIER | HG00323.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0001g0271 a0001c0001t0001g0303 a0001c0001t0001g0307 others(9): Show |
12 | 232 | 0.0517 | 5 | c.463 others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATAT | intron_variant | MODIFIER | HG01243.hp2 HG02818.hp2 HG03486.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0002a0002c0002t0017 | a0001c0001t0004g0167 a0002c0002t0002g0001 a0002c0002t0002g0040 others(3): Show |
6 | 83 | 0.0723 | 5 | c.463 others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | C | CAAAAA | intron_variant | MODIFIER | HG00741.hp2 HG01433.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0004t0005others(1): Show | a0001c0001t0001g0341 a0002c0002t0002g0053 a0002c0002t0002g0074 others(6): Show |
9 | 164 | 0.0549 | 5 | c.33- others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120393258 | A | ATAATT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(140): Show |
144 | 306 | 0.4706 | 5 | c.33- others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAA | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0003 | a0001c0001t0002a0001c0001t0006a0001c0006t0002others(1): Show | a0001c0001t0002g0100 a0001c0001t0002g0106 a0001c0001t0002g0108 others(9): Show |
12 | 83 | 0.1446 | 5 | c.33- others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120411581 | C | CTTTTT | intron_variant | MODIFIER | HG00597.hp2 HG02602.hp2 HG02698.hp2 others(9): Show |
a0001 | a0001c0004 | a0001c0004t0005a0001c0004t0012 | a0001c0004t0005g0046 a0001c0004t0005g0047 a0001c0004t0005g0048 others(9): Show |
12 | 115 | 0.1043 | 5 | c.199 others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120428030 | T | TTTCCC | 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.407 others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120436983 | T | TAAATA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0009a0001c0001t0029a0001c0002t0002others(8): Show | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0005 others(56): Show |
60 | 306 | 0.1961 | 5 | c.925 others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120477177 | T | TTGTTG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(24): Show | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(140): Show |
144 | 305 | 0.4721 | 5 | c.336 others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120480722 | A | AAGTCT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0016 | a0001c0002t0003g0001 a0001c0002t0003g0015 a0001c0002t0003g0024 others(24): Show |
28 | 306 | 0.0915 | 5 | c.423 others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7352832 | C | CTTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0013others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(30): Show | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0001g0108 others(91): Show |
94 | 108 | 0.8704 | 5 | c.-11 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367870 | T | TATATA | intron_variant | MODIFIER | HG02622.hp2 HG02886.hp1 NA18943.hp2 |
a0002a0003 | a0002c0005a0003c0003 | a0002c0005t0001a0003c0003t0026 | a0002c0005t0001g0258 a0002c0005t0001g0259 a0003c0003t0026g0085 |
3 | 247 | 0.0121 | 5 | c.16- others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7373463 | G | GTTTGT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
a0001a0002a0005others(18): Show | a0001c0001a0001c0019a0001c0021others(30): Show | a0001c0001t0002a0001c0001t0004a0001c0019t0006others(40): Show | a0001c0001t0002g0055 a0001c0001t0004g0003 a0001c0001t0004g0006 others(94): Show |
97 | 285 | 0.3404 | 5 | c.275 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7395531 | C | CAGGAG | intron_variant | MODIFIER | HG02165.hp2 NA18967.hp1 NA18990.hp2 others(3): Show |
a0005a0007 | a0005c0008a0007c0010 | a0005c0008t0002a0007c0010t0001a0007c0010t0033 | a0005c0008t0002g0288 a0007c0010t0001g0285 a0007c0010t0001g0287 others(3): Show |
6 | 296 | 0.0203 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7410809 | C | CAAAAA | intron_variant | MODIFIER | HG00438.hp1 HG02165.hp2 HG02647.hp2 others(3): Show |
a0002a0006a0007 | a0002c0005a0006c0039a0007c0010 | a0002c0005t0013a0006c0039t0001a0007c0010t0001others(1): Show | a0002c0005t0013g0036 a0006c0039t0001g0241 a0007c0010t0001g0287 others(3): Show |
6 | 55 | 0.1091 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7411285 | T | TCCCTC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0013others(25): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | a0001c0001t0001g0193 a0001c0001t0002g0028 a0001c0001t0002g0033 others(143): Show |
146 | 288 | 0.5069 | 5 | c.967 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7416578 | T | TGTGTG | intron_variant | MODIFIER | HG00738.hp2 NA19066.hp1 NA20752.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0090 a0001c0002t0003g0166 a0001c0002t0003g0182 |
3 | 292 | 0.0103 | 5 | c.968 others(24): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7431510 | C | CAAAAA | intron_variant | MODIFIER | HG01099.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
a0001a0002a0024 | a0001c0013a0002c0004a0002c0007others(1): Show | a0001c0013t0001a0002c0004t0004a0002c0007t0001others(1): Show | a0001c0013t0001g0291 a0002c0004t0004g0235 a0002c0007t0001g0009 others(4): Show |
7 | 113 | 0.0619 | 5 | c.968 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7459212 | A | ATTTTG | intron_variant | MODIFIER | HG03139.hp2 NA18942.hp1 NA20300.hp1 |
a0001a0002 | a0001c0001a0001c0019a0002c0004 | a0001c0001t0002a0001c0019t0006a0002c0004t0002 | a0001c0001t0002g0055 a0001c0019t0006g0139 a0002c0004t0002g0049 |
3 | 296 | 0.0101 | 5 | c.236 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466381 | C | CAAAAA | intron_variant | MODIFIER | HG01109.hp1 HG01952.hp2 HG02818.hp2 others(5): Show |
a0001a0002a0006others(1): Show | a0001c0002a0002c0006a0006c0009others(1): Show | a0001c0002t0003a0002c0006t0007a0006c0009t0009others(1): Show | a0001c0002t0003g0168 a0001c0002t0003g0181 a0002c0006t0007g0272 others(5): Show |
8 | 47 | 0.1702 | 5 | c.290 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7466804 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
a0001a0002a0028 | a0001c0002a0002c0005a0002c0006others(1): Show | a0001c0002t0003a0002c0005t0001a0002c0006t0007others(1): Show | a0001c0002t0003g0280 a0002c0005t0001g0221 a0002c0006t0007g0270 others(6): Show |
9 | 130 | 0.0692 | 5 | c.290 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16213711 | A | AATTTT | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(5): Show |
a0003a0008 | a0003c0003a0008c0015 | a0003c0003t0001a0008c0015t0001 | a0003c0003t0001g0012 a0003c0003t0001g0032 a0003c0003t0001g0033 others(1): Show |
8 | 358 | 0.0223 | 5 | c.-12 others(16): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1060 | chr1 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41880441 | A | AGGAAG | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00741.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(18): Show |
22 | 232 | 0.0948 | 5 | c.-28 others(16): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2742 | chr19 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154186886 | C | CTTTTT | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp1 HG02071.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0001c0001t0007a0002c0003t0010 | a0001c0001t0002g0214 a0001c0001t0002g0225 a0001c0001t0002g0235 others(5): Show |
8 | 30 | 0.2667 | 5 | c.148 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73643814 | C | CAAAAA | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
a0001a0003a0005others(4): Show | a0001c0021a0003c0058a0005c0061others(4): Show | a0001c0021t0008a0003c0058t0001a0005c0061t0002others(6): Show | a0001c0021t0008g0102 a0003c0058t0001g0139 a0005c0061t0002g0001 others(6): Show |
9 | 93 | 0.0968 | 5 | c.-12 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73690065 | A | ATTATT | 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 | 5 | c.33+ others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73731011 | T | TAAAAA | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(13): Show |
a0003a0004a0005others(9): Show | a0003c0005a0003c0048a0004c0004others(12): Show | a0003c0005t0001a0003c0048t0006a0004c0004t0001others(13): Show | a0003c0005t0001g0043 a0003c0048t0006g0176 a0004c0004t0001g0170 others(13): Show |
16 | 123 | 0.1301 | 5 | c.34- others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | C | CTTCTT | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG02622.hp1 others(7): Show |
a0002a0003a0004others(4): Show | a0002c0003a0003c0007a0004c0004others(5): Show | a0002c0003t0001a0003c0007t0001a0004c0004t0001others(5): Show | a0002c0003t0001g0076 a0002c0003t0001g0093 a0003c0007t0001g0186 others(7): Show |
10 | 29 | 0.3448 | 5 | c.34- others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806390 | A | ACAATC | 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 | 5 | c.102 others(26): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73910381 | C | CAAAAA | intron_variant | MODIFIER | HG00621.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0023a0002c0002a0003c0007others(2): Show | a0001c0023t0001a0002c0002t0002a0002c0002t0005others(3): Show | a0001c0023t0001g0034 a0002c0002t0002g0158 a0002c0002t0005g0022 others(3): Show |
6 | 64 | 0.0938 | 5 | c.464 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73929979 | A | ATATAT | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
a0001a0002a0003others(24): Show | a0001c0001a0001c0021a0001c0023others(47): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0008others(70): Show | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0063 others(95): Show |
98 | 186 | 0.5269 | 5 | c.494 others(26): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155949264 | T | TAAATA | intron_variant | MODIFIER | HG01243.hp1 HG01515.hp1 HG03239.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0062 others(5): Show |
10 | 281 | 0.0356 | 5 | c.288 others(24): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | TogoVar | |||||||
ARHGEF2_chr1_155941854_155983547 | 155964159 | A | ATATAT | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 NA18963.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0064 |
3 | 240 | 0.0125 | 5 | c.724 others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | |||||||
ARHGEF2_chr1_155941854_155983547 | 155964161 | A | ATATAT | intron_variant | MODIFIER | HG01168.hp1 HG01168.hp2 NA19067.hp1 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0003c0004t0001 | a0001c0001t0001g0065 a0001c0001t0002g0102 a0003c0004t0001g0066 |
3 | 116 | 0.0259 | 5 | c.724 others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | |||||||
ARHGEF2_chr1_155941854_155983547 | 155964163 | A | ATATAT | intron_variant | MODIFIER | HG01109.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0089 a0001c0003t0001g0028 a0001c0003t0001g0197 |
4 | 80 | 0.0500 | 5 | c.724 others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | |||||||
ARHGEF37_chr5_149576498_149639968 | 149582668 | T | TAAAGA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
a0001a0002a0003others(14): Show | a0001c0002a0001c0030a0002c0001others(21): Show | a0001c0002t0004a0001c0002t0005a0001c0002t0006others(46): Show | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
250 | 392 | 0.6378 | 5 | c.-12 others(22): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149624649 | C | CTGTAA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
a0001a0003a0004others(10): Show | a0001c0002a0001c0005a0001c0030others(19): Show | a0001c0002t0004a0001c0002t0005a0001c0002t0006others(52): Show | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(244): Show |
269 | 391 | 0.6880 | 5 | c.146 others(22): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149636474 | A | ATTTTT | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
a0001a0008 | a0001c0002a0008c0009 | a0001c0002t0020a0008c0009t0003a0008c0009t0026 | a0001c0002t0020g0110 a0008c0009t0003g0310 a0008c0009t0003g0311 others(4): Show |
7 | 391 | 0.0179 | 5 | c.*42 others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1507 | chr5 | TogoVar | |||||||
ARHGEF37_chr5_149576498_149639968 | 149636478 | A | ATTTAT | downstream_gene_variant | MODIFIER | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
a0004 | a0004c0010 | a0004c0010t0014 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 |
3 | 384 | 0.0078 | 5 | c.*42 others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1511 | chr5 | TogoVar | |||||||
ARHGEF37_chr5_149576498_149639968 | 149636495 | A | AAAAAG | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(7): Show |
a0001a0004a0008 | a0001c0002a0004c0010a0008c0009 | a0001c0002t0020a0004c0010t0014a0008c0009t0003others(1): Show | a0001c0002t0020g0110 a0004c0010t0014g0312 a0004c0010t0014g0317 others(7): Show |
10 | 309 | 0.0324 | 5 | c.*43 others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1528 | chr5 | TogoVar | |||||||
ARHGEF38_chr4_105547620_105685914 | 105561400 | T | TAATAG | intron_variant | MODIFIER | HG02559.hp2 HG03540.hp2 |
a0001a0002 | a0001c0002a0002c0012 | a0001c0002t0007a0002c0012t0010 | a0001c0002t0007g0023 a0002c0012t0010g0024 |
2 | 125 | 0.0160 | 5 | c.196 others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561464 | A | AGAATG | intron_variant | MODIFIER | HG01346.hp1 HG02071.hp1 |
a0001 | a0001c0001a0001c0020 | a0001c0001t0001a0001c0020t0004 | a0001c0001t0001g0060 a0001c0020t0004g0061 |
2 | 112 | 0.0179 | 5 | c.196 others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105580110 | T | TTTCTC | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0004others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | 184 | 0.8261 | 5 | c.197 others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |