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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF10_chr8_1818926_1963641 | 1832506 | G | GCAGAGA | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
a0001a0002a0003others(7): Show | a0001c0002a0001c0003a0001c0004others(41): Show | a0001c0002t0026a0001c0003t0001a0001c0003t0009others(50): Show | a0001c0002t0026g0267 a0001c0003t0001g0284 a0001c0003t0009g0282 others(54): Show |
57 | 362 | 0.1575 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832999 | G | GAGAGAT | intron_variant | MODIFIER | NA18939.hp1 NA18982.hp2 NA19002.hp2 |
a0001 | a0001c0002a0001c0010a0001c0067 | a0001c0002t0001a0001c0010t0001a0001c0067t0001 | a0001c0002t0001g0046 a0001c0010t0001g0047 a0001c0067t0001g0045 |
3 | 362 | 0.0083 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833035 | G | GACAGAC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(59): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0019others(82): Show | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0002g0069 others(114): Show |
117 | 190 | 0.6158 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAAAA | intron_variant | MODIFIER | HG00438.hp1 HG00673.hp1 HG02895.hp1 others(11): Show |
a0001a0002a0025 | a0001c0046a0001c0047a0001c0063others(10): Show | a0001c0046t0001a0001c0047t0011a0001c0063t0002others(10): Show | a0001c0046t0001g0333 a0001c0046t0001g0334 a0001c0047t0011g0335 others(11): Show |
14 | 171 | 0.0819 | 6 | c.679 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTGTG | intron_variant | MODIFIER | HG00323.hp1 HG00673.hp2 HG00735.hp1 others(20): Show |
a0001a0004a0007 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0006others(17): Show | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0003g0019 others(20): Show |
23 | 61 | 0.3770 | 6 | c.118 others(25): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | C | CTGTGTG | intron_variant | MODIFIER | HG00140.hp2 HG02717.hp2 HG03540.hp1 |
a0001a0002a0012 | a0001c0020a0002c0017a0012c0084 | a0001c0020t0016a0002c0017t0002a0012c0084t0008 | a0001c0020t0016g0308 a0002c0017t0002g0043 a0012c0084t0008g0352 |
3 | 46 | 0.0652 | 6 | c.214 others(25): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936493 | A | AATATAT | intron_variant | MODIFIER | HG02015.hp2 HG02258.hp1 HG02698.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0272 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | 336 | 0.0179 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATAT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(24): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0032others(2): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0276 others(23): Show |
27 | 247 | 0.1093 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAATAT | intron_variant | MODIFIER | HG00642.hp2 HG02451.hp1 HG02735.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0008 | a0001c0001t0001a0002c0002t0002a0002c0008t0002 | a0001c0001t0001g0312 a0002c0002t0002g0035 a0002c0002t0002g0051 others(5): Show |
8 | 85 | 0.0941 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AATATAT | intron_variant | MODIFIER | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(25): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0012others(1): Show | a0001c0001t0001g0284 a0001c0001t0001g0301 a0001c0001t0001g0309 others(25): Show |
28 | 105 | 0.2667 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156943065 | C | CTTTTTT | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0008a0002c0004t0009others(2): Show | a0002c0004t0005g0061 a0002c0004t0005g0114 a0002c0004t0005g0116 others(14): Show |
18 | 228 | 0.0789 | 6 | c.323 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157008406 | G | GCACACA | intron_variant | MODIFIER | HG00558.hp1 HG02630.hp2 NA18943.hp2 others(6): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0002t0012a0002c0002t0017others(1): Show | a0002c0002t0002g0038 a0002c0002t0002g0056 a0002c0002t0002g0070 others(6): Show |
9 | 17 | 0.5294 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACA | intron_variant | MODIFIER | HG01074.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0010a0001c0005t0001 | a0001c0001t0001g0270 a0001c0001t0001g0289 a0001c0001t0001g0290 others(16): Show |
19 | 159 | 0.1195 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013263 | T | TCACACA | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0002t0024a0002c0002t0029others(1): Show | a0002c0002t0002g0003 a0002c0002t0002g0036 a0002c0002t0002g0044 others(7): Show |
11 | 43 | 0.2558 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACC | intron_variant | MODIFIER | HG00408.hp1 HG03654.hp2 HG03831.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0071 a0002c0002t0002g0097 a0002c0002t0002g0100 |
3 | 313 | 0.0096 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157029261 | T | TTTGTTG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0011a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(163): Show |
170 | 183 | 0.9290 | 6 | c.32+ others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157046231 | G | GCCGCCA | upstream_gene_variant | MODIFIER | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(8): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0005a0003c0003t0006 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(8): Show |
11 | 360 | 0.0306 | 6 | c.-19 others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 490 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120334861 | G | GTATATA | upstream_gene_variant | MODIFIER | HG01243.hp1 HG03225.hp2 HG04115.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0023a0001c0001t0026 | a0001c0001t0001g0184 a0001c0001t0023g0178 a0001c0001t0026g0230 |
3 | 273 | 0.0110 | 6 | c.-23 others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1551 | chr11 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAA | intron_variant | MODIFIER | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0032a0001c0002t0002others(1): Show | a0001c0001t0002g0019 a0001c0001t0002g0088 a0001c0001t0002g0103 others(6): Show |
9 | 80 | 0.1125 | 6 | c.33- others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120442412 | T | TTATATA | intron_variant | MODIFIER | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0009 | a0001c0001t0007g0135 a0001c0001t0007g0136 a0001c0001t0009g0003 others(3): Show |
6 | 296 | 0.0203 | 6 | c.130 others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120446198 | A | AAATAAT | intron_variant | MODIFIER | HG01099.hp1 HG02559.hp1 HG02723.hp1 |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0029a0001c0002t0034a0001c0008t0020 | a0001c0001t0029g0190 a0001c0002t0034g0013 a0001c0008t0020g0009 |
3 | 74 | 0.0405 | 6 | c.134 others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | A | AACACAC | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00741.hp1 HG01515.hp2 others(26): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0012others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0004t0002others(8): Show | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(17): Show |
29 | 46 | 0.6304 | 6 | c.-27 others(15): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3479714 | T | TGCCCCG | intron_variant | MODIFIER | HG00280.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | 332 | 0.0211 | 6 | c.188 others(21): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | C | CGTGTGT | intron_variant | MODIFIER | HG01106.hp1 HG01255.hp2 HG01346.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0017a0002c0002t0001others(1): Show | a0001c0001t0001g0153 a0001c0001t0001g0157 a0001c0001t0001g0172 others(4): Show |
7 | 68 | 0.1029 | 6 | c.319 others(27): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | C | CGTGTGT | upstream_gene_variant | MODIFIER | HG00408.hp2 HG01070.hp1 HG01099.hp2 others(27): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0002a0001c0016others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0108 a0001c0001t0001g0121 a0001c0001t0001g0245 others(27): Show |
30 | 188 | 0.1596 | 6 | c.-28 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7352832 | C | CTTTTTT | intron_variant | MODIFIER | HG00621.hp1 HG01099.hp2 HG01346.hp1 others(39): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0004others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0193 others(39): Show |
42 | 56 | 0.7500 | 6 | c.-11 others(25): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362020 | A | AAGAAGG | intron_variant | MODIFIER | HG00423.hp2 HG03834.hp2 NA19080.hp1 |
a0001a0002 | a0001c0001a0002c0005a0002c0006 | a0001c0001t0011a0002c0005t0001a0002c0006t0001 | a0001c0001t0011g0207 a0002c0005t0001g0221 a0002c0006t0001g0178 |
3 | 282 | 0.0106 | 6 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362327 | T | TGGAGGA | intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02145.hp2 others(11): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0013a0001c0047others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(7): Show | a0001c0001t0002g0012 a0001c0001t0002g0055 a0001c0001t0004g0003 others(11): Show |
14 | 276 | 0.0507 | 6 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362353 | G | GAGGAGA | intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02145.hp2 others(15): Show |
a0001a0002a0009others(3): Show | a0001c0001a0001c0002a0001c0013others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(11): Show | a0001c0001t0002g0012 a0001c0001t0002g0055 a0001c0001t0004g0003 others(15): Show |
18 | 273 | 0.0659 | 6 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367977 | A | AAGAGAG | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
a0001a0002a0024 | a0001c0001a0002c0007a0024c0037 | a0001c0001t0017a0002c0007t0001a0024c0037t0001 | a0001c0001t0017g0014 a0002c0007t0001g0017 a0002c0007t0001g0018 others(4): Show |
7 | 70 | 0.1000 | 6 | c.16- others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367998 | A | AGAGAGG | intron_variant | MODIFIER | HG00621.hp2 NA18939.hp1 NA18977.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0018 | a0001c0001t0002a0001c0001t0011a0001c0001t0035others(2): Show | a0001c0001t0002g0033 a0001c0001t0002g0035 a0001c0001t0002g0135 others(6): Show |
9 | 280 | 0.0321 | 6 | c.16- others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385443 | C | CATTATT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(18): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0018others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(8): Show | a0001c0001t0001g0053 a0001c0001t0001g0243 a0001c0001t0002g0034 others(18): Show |
21 | 154 | 0.1364 | 6 | 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 | 7385833 | A | ATCTCTC | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(2): Show |
a0001a0005 | a0001c0002a0001c0018a0005c0008 | a0001c0002t0003a0001c0018t0001a0005c0008t0002others(1): Show | a0001c0002t0003g0171 a0001c0018t0001g0197 a0005c0008t0002g0282 others(2): Show |
5 | 103 | 0.0485 | 6 | 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 | 7385835 | C | CTCTCTA | intron_variant | MODIFIER | HG02922.hp2 HG03139.hp2 HG03225.hp2 |
a0002 | a0002c0004 | a0002c0004t0002a0002c0004t0004 | a0002c0004t0002g0049 a0002c0004t0002g0251 a0002c0004t0004g0001 |
3 | 296 | 0.0101 | 6 | 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 | CGTGTGT | intron_variant | MODIFIER | HG00673.hp1 HG00735.hp1 HG01074.hp2 others(23): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(10): Show | a0001c0001t0001g0121 a0001c0001t0001g0193 a0001c0001t0002g0052 others(23): Show |
26 | 85 | 0.3059 | 6 | c.968 others(25): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7431510 | C | CAAAAAA | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
a0002a0003a0008others(1): Show | a0002c0004a0002c0007a0003c0003others(2): Show | a0002c0004t0004a0002c0007t0001a0003c0003t0001others(2): Show | a0002c0004t0004g0234 a0002c0007t0001g0019 a0002c0007t0001g0024 others(6): Show |
9 | 115 | 0.0783 | 6 | 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 | 7437322 | G | GGAGGCT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
a0001a0002a0004others(19): Show | a0001c0001a0001c0013a0001c0016others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | a0001c0001t0001g0193 a0001c0001t0002g0012 a0001c0001t0002g0028 others(131): Show |
134 | 296 | 0.4527 | 6 | 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 | 7450794 | C | CTTTCCG | intron_variant | MODIFIER | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0002a0002c0006a0003c0003others(3): Show | a0001c0002t0002a0001c0002t0003a0002c0006t0003others(5): Show | a0001c0002t0002g0158 a0001c0002t0003g0040 a0001c0002t0003g0088 others(21): Show |
24 | 296 | 0.0811 | 6 | c.173 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7475525 | A | AACACAC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(36): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | a0001c0001t0001g0110 a0001c0001t0001g0120 a0001c0001t0001g0121 others(36): Show |
39 | 240 | 0.1625 | 6 | c.*52 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3048 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7475527 | C | CACACAT | downstream_gene_variant | MODIFIER | HG01106.hp1 HG02970.hp2 NA19043.hp1 others(1): Show |
a0001a0020a0031 | a0001c0001a0001c0016a0020c0057others(1): Show | a0001c0001t0002a0001c0016t0014a0020c0057t0001others(1): Show | a0001c0001t0002g0252 a0001c0016t0014g0133 a0020c0057t0001g0269 others(1): Show |
4 | 296 | 0.0135 | 6 | c.*52 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3050 | chr19 | TogoVar | |||||||
ARHGEF19_chr1_16192854_16217652 | 16213054 | C | CATCCCT | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(6): Show |
a0003a0008 | a0003c0003a0008c0015 | a0003c0003t0001a0008c0015t0001 | a0003c0003t0001g0012 a0003c0003t0001g0032 a0003c0003t0001g0033 others(1): Show |
9 | 360 | 0.0250 | 6 | c.-58 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 403 | chr1 | TogoVar | |||||||
ARHGEF1_chr19_41878184_41912452 | 41894135 | A | AGTGTGT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(41): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0004c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(3): Show | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(31): Show |
44 | 59 | 0.7458 | 6 | c.645 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154186136 | G | GACACAC | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0006a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0194 a0001c0001t0001g0249 a0001c0001t0002g0202 others(65): Show |
68 | 88 | 0.7727 | 6 | 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 | 154211867 | A | ATGTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): Show |
a0001a0002a0010 | a0001c0001a0001c0015a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0203 a0001c0001t0002g0005 a0001c0001t0002g0153 others(44): Show |
49 | 60 | 0.8167 | 6 | c.184 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | T | TACACAC | intron_variant | MODIFIER | HG00140.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0018others(1): Show | a0001c0001t0001g0203 a0001c0001t0002g0224 a0001c0001t0002g0228 others(2): Show |
6 | 16 | 0.3750 | 6 | 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 | 154237538 | T | TCACACA | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(32): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0008a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | a0001c0001t0001g0180 a0001c0001t0001g0184 a0001c0001t0001g0200 others(31): Show |
35 | 55 | 0.6364 | 6 | c.209 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239291 | A | AGTGTGT | intron_variant | MODIFIER | NA18978.hp2 NA18999.hp2 NA19060.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0008 | a0002c0002t0003g0050 a0002c0002t0003g0072 a0002c0002t0003g0076 others(1): Show |
4 | 238 | 0.0168 | 6 | c.209 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73658962 | T | TACACAC | intron_variant | MODIFIER | HG01106.hp1 HG02602.hp2 HG03017.hp1 others(4): Show |
a0001a0002a0003others(4): Show | a0001c0028a0002c0003a0003c0005others(4): Show | a0001c0028t0001a0002c0003t0002a0003c0005t0002others(4): Show | a0001c0028t0001g0146 a0002c0003t0002g0004 a0003c0005t0002g0002 others(4): Show |
7 | 73 | 0.0959 | 6 | c.-11 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73658987 | A | ACACACG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0023a0002c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0001others(20): Show | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0038 others(28): Show |
31 | 186 | 0.1667 | 6 | c.-11 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73691296 | T | TACACAC | intron_variant | MODIFIER | HG01243.hp2 HG03139.hp1 |
a0012 | a0012c0072a0012c0073 | a0012c0072t0005a0012c0073t0001 | a0012c0072t0005g0144 a0012c0073t0001g0143 |
2 | 68 | 0.0294 | 6 | c.33+ others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |