regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGG others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03098.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0014a0001c0001t0022 | a0001c0001t0004g0111a0001c0001t0014g0041a0001c0001t0022g0081 | 3 | 198 | 0.0152 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0060 | 1 | 198 | 0.0051 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0025 | a0001c0001t0025g0103 | 1 | 198 | 0.0051 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA19083.hp2 | a0001 | a0001c0009 | a0001c0009t0003 | a0001c0009t0003g0014 | 1 | 198 | 0.0051 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0111 | 1 | 198 | 0.0051 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0087 | 1 | 198 | 0.0051 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02647.hp1 HG03710.hp1 NA18957.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(1): Show | a0001c0001t0001g0018a0001c0001t0003g0174a0001c0001t0010g0080others(1): Show | 4 | 198 | 0.0202 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0123 | 1 | 198 | 0.0051 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG02523.hp2 NA18995.hp2 NA19043.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0022a0001c0003t0002a0001c0003t0003 | a0001c0001t0022g0081a0001c0003t0002g0129a0001c0003t0003g0168 | 3 | 198 | 0.0152 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(23): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0002c0010others(6): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(10): Show | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0203others(50): Show | 57 | 347 | 0.1643 | 30 | c.174 others(49): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0010 | a0001c0010t0003 | a0001c0010t0003g0114 | 1 | 248 | 0.0040 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(23): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0119 | 1 | 248 | 0.0040 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(23): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0125 | 1 | 248 | 0.0040 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841156 | T | TCTCACTG others(23): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0011 | 1 | 248 | 0.0040 | 30 | c.543 others(47): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(23): Show |
upstream_gene_variant | MODIFIER | HG00639.hp1 HG02055.hp1 HG02129.hp1 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0006a0001c0001t0011a0001c0001t0017others(15): Show | a0001c0001t0006g0025a0001c0001t0011g0301a0001c0001t0017g0175others(21): Show | 24 | 310 | 0.0774 | 30 | c.-12 others(41): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(23): Show |
intron_variant | MODIFIER | NA18962.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0169 | 1 | 310 | 0.0032 | 30 | c.100 others(49): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119321279 | C | CTATATAT others(23): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0002t0001others(7): Show | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | 310 | 0.0677 | 30 | c.100 others(49): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(23): Show |
intron_variant | MODIFIER | HG03239.hp2 HG04228.hp1 NA18971.hp2 others(4): Show |
a0001a0015 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0008a0001c0001t0018a0001c0001t0020others(4): Show | a0001c0001t0008g0170a0001c0001t0018g0208a0001c0001t0020g0064others(4): Show | 7 | 310 | 0.0226 | 30 | c.683 others(47): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG01258.hp2 HG02129.hp2 NA18943.hp2 others(2): Show |
a0001a0013 | a0001c0001a0013c0031 | a0001c0001t0002a0001c0001t0004a0013c0031t0004 | a0001c0001t0002g0117a0001c0001t0004g0154a0001c0001t0004g0175others(2): Show | 5 | 398 | 0.0126 | 30 | c.226 others(49): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144556598 | A | AGGCAAAG others(23): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(6): Show |
a0001a0004 | a0001c0003a0001c0005a0001c0010others(1): Show | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(3): Show | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(6): Show | 9 | 246 | 0.0366 | 30 | c.513 others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144617425 | A | ACAAACCA others(23): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0003 | a0003c0011 | a0003c0011t0001 | a0003c0011t0001g0072 | 1 | 246 | 0.0041 | 30 | c.-81 others(49): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751277 | G | GTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0006 | a0002c0006t0008 | a0002c0006t0008g0240 | 1 | 286 | 0.0035 | 30 | c.155 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(23): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02056.hp1 HG02896.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0169a0001c0001t0002g0096others(3): Show | 6 | 286 | 0.0210 | 30 | c.313 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCAC others(23): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0030 | 1 | 286 | 0.0035 | 30 | c.385 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(23): Show |
intron_variant | MODIFIER | HG02129.hp2 HG03834.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066a0001c0001t0001g0127 | 2 | 286 | 0.0070 | 30 | c.245 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(23): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 230 | 0.0044 | 30 | c.53+ others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12843089 | G | GGTTTGGG others(23): Show |
intron_variant | MODIFIER | NA18982.hp2 NA19054.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | 230 | 0.0087 | 30 | c.54- others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(23): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(14): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0212others(14): Show | 17 | 230 | 0.0739 | 30 | c.862 others(45): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11174616 | C | CTTTCTTT others(23): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0011 | 1 | 144 | 0.0069 | 30 | c.162 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11453194 | C | CTATATAT others(23): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | 30 | c.589 others(51): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAAAGAAA others(23): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0138 | 1 | 144 | 0.0069 | 30 | c.588 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285909 | C | CCCAACCC others(23): Show |
downstream_gene_variant | MODIFIER | HG01109.hp2 HG02976.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005 | a0001c0001t0003g0047a0001c0001t0005g0002 | 2 | 442 | 0.0045 | 30 | c.*30 others(41): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2900 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285966 | T | TCCCAACC others(23): Show |
downstream_gene_variant | MODIFIER | HG02257.hp1 HG03130.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 | 2 | 442 | 0.0045 | 30 | c.*31 others(41): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2957 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17690410 | G | GTCTCAAG others(23): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0018 | a0002c0018t0002 | a0002c0018t0002g0155 | 1 | 168 | 0.0060 | 30 | c.318 others(49): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1823999 | C | CGCGGGGG others(23): Show |
5_prime_UTR_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0003 | a0001c0003t0063 | a0001c0003t0063g0089 | 1 | 363 | 0.0028 | 30 | c.-15 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19393 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ARHGEF10_chr8_1818926_1963641 | 1888175 | G | GAGTGGAG others(23): Show |
intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0306 | 1 | 363 | 0.0028 | 30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888183 | T | TGAGGGTT others(23): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
a0001a0006a0013others(2): Show | a0001c0001a0001c0003a0001c0004others(37): Show | a0001c0001t0002a0001c0003t0001a0001c0003t0003others(51): Show | a0001c0001t0002g0053a0001c0003t0001g0057a0001c0003t0001g0059others(73): Show | 76 | 363 | 0.2094 | 30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888730 | A | AGAGTTAT others(23): Show |
intron_variant | MODIFIER | NA18944.hp2 NA18982.hp2 NA19066.hp1 |
a0001 | a0001c0011a0001c0066a0001c0067 | a0001c0011t0054a0001c0066t0022a0001c0067t0001 | a0001c0011t0054g0228a0001c0066t0022g0227a0001c0067t0001g0063 | 3 | 363 | 0.0083 | 30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889492 | G | GGTATTGA others(23): Show |
intron_variant | MODIFIER | HG02015.hp1 NA18944.hp1 NA18983.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0002a0001c0002t0001a0001c0008t0002others(2): Show | a0001c0001t0002g0239a0001c0002t0001g0064a0001c0008t0002g0152others(3): Show | 6 | 363 | 0.0165 | 30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889845 | A | AGGTTTGT others(23): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0346 | 1 | 363 | 0.0028 | 30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTTTCT others(23): Show |
downstream_gene_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(35): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(2): Show | a0002c0002t0002g0028a0002c0002t0002g0031a0002c0002t0002g0032others(35): Show | 38 | 362 | 0.1050 | 30 | c.*59 others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTTTTT others(23): Show |
downstream_gene_variant | MODIFIER | HG02896.hp2 NA19030.hp1 |
a0002 | a0002c0004 | a0002c0004t0022 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | 362 | 0.0055 | 30 | c.*59 others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936493 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0287 | 1 | 362 | 0.0028 | 30 | c.463 others(47): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0002 | a0002c0004 | a0002c0004t0008 | a0002c0004t0008g0199 | 1 | 362 | 0.0028 | 30 | c.463 others(47): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAAAAAA others(23): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0105 | 1 | 362 | 0.0028 | 30 | c.463 others(47): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0002 | a0002c0004 | a0002c0004t0008 | a0002c0004t0008g0196 | 1 | 362 | 0.0028 | 30 | c.463 others(47): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(23): Show |
intron_variant | MODIFIER | NA18906.hp2 NA19011.hp1 NA19056.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0004a0002c0002t0016a0003c0003t0003 | a0001c0001t0004g0172a0002c0002t0016g0236a0003c0003t0003g0237others(2): Show | 5 | 362 | 0.0138 | 30 | c.33- others(47): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120494296 | G | GGAATGGT others(23): Show |
downstream_gene_variant | MODIFIER | NA19005.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0080 | 1 | 308 | 0.0033 | 30 | c.*92 others(41): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4360 | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362132 | A | AGGAGGAG others(23): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0005 | a0005c0009 | a0005c0009t0009 | a0005c0009t0009g0068 | 1 | 298 | 0.0034 | 30 | c.-11 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | A | AGTGTGTG others(23): Show |
downstream_gene_variant | MODIFIER | HG01891.hp1 HG03209.hp1 |
a0002 | a0002c0006 | a0002c0006t0007 | a0002c0006t0007g0270a0002c0006t0007g0276 | 2 | 298 | 0.0067 | 30 | c.*44 others(41): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar |