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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CUL5_chr11_108003898_108112761 | 108006626 | C | CATACT | upstream_gene_variant | MODIFIER | HG02451.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0004a0001c0002t0011 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(5): Show | 8 | 312 | 0.0256 | 5 | c.-27 others(16): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2271 | chr11 | TogoVar | ||||||
CUL5_chr11_108003898_108112761 | 108016232 | T | TTTCTC | intron_variant | MODIFIER | HG01192.hp2 NA18964.hp2 NA18989.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | 312 | 0.0096 | 5 | c.24+ others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108040611 | C | CAAAAA | intron_variant | MODIFIER | HG01261.hp1 HG01517.hp1 HG02055.hp2 others(4): Show |
a0001 | a0001c0002a0001c0005 | a0001c0002t0003a0001c0002t0035a0001c0005t0018 | a0001c0002t0003g0036a0001c0002t0003g0037a0001c0002t0003g0043others(4): Show | 7 | 312 | 0.0224 | 5 | c.135 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108048648 | C | CTTTTT | intron_variant | MODIFIER | HG01081.hp2 HG02280.hp1 HG02602.hp2 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0013 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0002g0087others(4): Show | 7 | 312 | 0.0224 | 5 | c.235 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108063661 | A | AAAAAT | intron_variant | MODIFIER | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(43): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(4): Show | a0001c0002t0002g0080a0001c0002t0002g0087a0001c0002t0002g0088others(42): Show | 46 | 312 | 0.1474 | 5 | c.781 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL5_chr11_108003898_108112761 | 108068314 | T | TTTTTG | intron_variant | MODIFIER | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0071a0001c0002t0006g0072a0001c0002t0006g0073others(4): Show | 7 | 312 | 0.0224 | 5 | c.781 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CUL9_chr6_43177196_43229587 | 43227829 | T | TCTGTA | downstream_gene_variant | MODIFIER | NA18747.hp1 NA18747.hp2 NA18989.hp2 others(1): Show |
a0001a0005 | a0001c0002a0005c0018 | a0001c0002t0001a0005c0018t0001 | a0001c0002t0001g0002a0001c0002t0001g0056a0001c0002t0001g0059others(1): Show | 4 | 276 | 0.0145 | 5 | c.*33 others(16): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3243 | chr6 | TogoVar | ||||||
CUTC_chr10_99727234_99761134 | 99738389 | G | GTGTGT | intron_variant | MODIFIER | HG04204.hp2 NA18987.hp1 NA19072.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0069a0001c0001t0001g0129a0001c0002t0001g0131 | 3 | 410 | 0.0073 | 5 | c.134 others(22): Show |
CUTC | ENSG00000119929.13 | transcript | ENST00000370476.10 | protein_coding | 2/8 | chr10 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 101827244 | C | CCTTCT | intron_variant | MODIFIER | HG00621.hp2 HG00735.hp2 HG01192.hp2 others(20): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0006others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0042others(20): Show | 23 | 132 | 0.1742 | 5 | c.63+ others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101999217 | C | CTTTTT | intron_variant | MODIFIER | HG00621.hp2 HG01099.hp1 HG01169.hp1 others(19): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(5): Show | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0049others(19): Show | 22 | 132 | 0.1667 | 5 | c.175 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102034145 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0013others(7): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(14): Show | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | 132 | 0.4924 | 5 | c.222 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102073165 | C | CTTTTT | intron_variant | MODIFIER | HG02723.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
a0001 | a0001c0001a0001c0013 | a0001c0001t0001a0001c0013t0004 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | 132 | 0.0303 | 5 | c.301 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102102247 | C | CCTCTT | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(92): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0013others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(20): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(92): Show | 95 | 132 | 0.7197 | 5 | c.440 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102117397 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(11): Show | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 47 | 132 | 0.3561 | 5 | c.707 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102132328 | C | CGCACG | intron_variant | MODIFIER | HG01981.hp1 HG03209.hp2 HG03471.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0090a0001c0002t0001g0035a0002c0003t0001g0003 | 3 | 132 | 0.0227 | 5 | c.707 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 8/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102180919 | G | GTATTT | intron_variant | MODIFIER | HG01255.hp2 HG01515.hp2 HG02818.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0023 | 3 | 132 | 0.0227 | 5 | c.105 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102201025 | T | TAAAAA | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(3): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0004t0001 | a0001c0002t0001g0095a0002c0003t0001g0004a0002c0003t0001g0080others(3): Show | 6 | 132 | 0.0455 | 5 | c.125 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102239739 | T | TTTTTC | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(11): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(2): Show | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0057others(11): Show | 14 | 132 | 0.1061 | 5 | c.125 others(26): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101827244 | C | CCTTCT | intron_variant | MODIFIER | HG00621.hp2 HG00735.hp2 HG01123.hp1 others(22): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0011a0001c0001t0023a0001c0001t0048others(15): Show | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0023g0117others(22): Show | 25 | 136 | 0.1838 | 5 | c.30+ others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101999217 | C | CTTTTT | intron_variant | MODIFIER | HG00621.hp2 HG01099.hp1 HG01169.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0023others(12): Show | a0001c0001t0006g0009a0001c0001t0006g0029a0001c0001t0010g0085others(18): Show | 21 | 136 | 0.1544 | 5 | c.142 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102034145 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(42): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0047others(62): Show | 65 | 136 | 0.4779 | 5 | c.189 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102102247 | C | CCTCTT | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(96): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(59): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0024others(96): Show | 99 | 136 | 0.7279 | 5 | c.407 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102117397 | C | CAAAAA | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(32): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0006g0029others(47): Show | 50 | 136 | 0.3677 | 5 | c.674 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102132328 | C | CGCACG | intron_variant | MODIFIER | HG01981.hp1 HG03209.hp2 HG03471.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0011a0001c0001t0023a0001c0004t0031 | a0001c0001t0011g0003a0001c0001t0023g0117a0001c0004t0031g0059 | 3 | 136 | 0.0221 | 5 | c.674 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 8/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102180919 | G | GTATTT | intron_variant | MODIFIER | HG01255.hp2 HG01515.hp2 HG02818.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0063 | a0001c0002t0001g0093a0001c0002t0001g0095a0001c0002t0001g0115others(1): Show | 4 | 136 | 0.0294 | 5 | c.101 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102201025 | T | TAAAAA | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0017a0001c0001t0041others(2): Show | a0001c0001t0011g0004a0001c0001t0011g0048a0001c0001t0017g0037others(3): Show | 6 | 136 | 0.0441 | 5 | c.206 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102239739 | T | TTTTTC | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(11): Show |
a0001 | a0001c0001a0001c0004a0001c0009 | a0001c0001t0003a0001c0001t0045a0001c0001t0048others(9): Show | a0001c0001t0003g0047a0001c0001t0045g0041a0001c0001t0048g0056others(11): Show | 14 | 136 | 0.1029 | 5 | c.388 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102247496 | C | CGGGAT | intron_variant | MODIFIER | HG02630.hp2 HG03471.hp2 NA20129.hp2 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0009a0001c0006t0005a0001c0006t0009 | a0001c0003t0009g0028a0001c0006t0005g0077a0001c0006t0009g0070 | 3 | 136 | 0.0221 | 5 | c.388 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111035613 | C | CTTTTT | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0002g0012others(14): Show | 17 | 100 | 0.1700 | 5 | c.63+ others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111080675 | A | AAAAAT | intron_variant | MODIFIER | HG01081.hp1 HG02486.hp1 HG03540.hp1 |
a0001 | a0001c0004a0001c0005a0001c0014 | a0001c0004t0004a0001c0005t0001a0001c0014t0001 | a0001c0004t0004g0041a0001c0005t0001g0019a0001c0014t0001g0042 | 3 | 100 | 0.0300 | 5 | c.63+ others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111156985 | C | CAAAAA | intron_variant | MODIFIER | HG01069.hp2 HG01169.hp1 HG01884.hp2 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | a0001c0001t0001g0091a0001c0001t0003g0081a0001c0002t0001g0048others(14): Show | 17 | 100 | 0.1700 | 5 | c.64- others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111193945 | A | ACTCTC | intron_variant | MODIFIER | HG00597.hp2 HG01069.hp2 HG01081.hp1 others(70): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(70): Show | 73 | 100 | 0.7300 | 5 | c.64- others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | chr12 | TogoVar | ||||||
CUX2_chr12_111029165_111355554 | 111263625 | A | AAAAAC | intron_variant | MODIFIER | HG02257.hp1 HG02886.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0013a0001c0003t0001g0017 | 2 | 100 | 0.0200 | 5 | c.223 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111265309 | T | TTTTTA | intron_variant | MODIFIER | HG01069.hp1 HG01169.hp1 HG01169.hp2 others(13): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0001g0091others(13): Show | 16 | 100 | 0.1600 | 5 | c.301 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111276643 | G | GTTTGT | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
a0001a0005a0006 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0091a0001c0001t0002g0012a0001c0001t0002g0030others(24): Show | 27 | 100 | 0.2700 | 5 | c.301 others(24): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111301038 | C | CAAAAA | intron_variant | MODIFIER | HG01169.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0003t0001 | a0001c0001t0002g0030a0001c0001t0002g0079a0001c0001t0002g0083others(8): Show | 11 | 100 | 0.1100 | 5 | c.753 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111319730 | T | TCAAAA | intron_variant | MODIFIER | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0007others(1): Show | a0001c0001t0002a0001c0003t0001a0001c0007t0001others(1): Show | a0001c0001t0002g0016a0001c0001t0002g0062a0001c0003t0001g0046others(3): Show | 6 | 100 | 0.0600 | 5 | c.200 others(22): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111351709 | C | CTTTTT | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0061others(5): Show | 8 | 100 | 0.0800 | 5 | c.*33 others(16): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1156 | chr12 | TogoVar | ||||||
CWC27_chr5_64763930_65023750 | 64880854 | A | ATTTTT | intron_variant | MODIFIER | HG02559.hp2 HG02965.hp1 NA19043.hp1 others(2): Show |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0002a0002c0004t0002g0003a0002c0004t0002g0005others(2): Show | 5 | 260 | 0.0192 | 5 | c.939 others(22): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWF19L1_chr10_100227298_100272638 | 100267910 | T | TCTAAC | upstream_gene_variant | MODIFIER | HG01255.hp2 HG01433.hp2 HG01928.hp1 others(49): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(6): Show | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0089others(44): Show | 52 | 364 | 0.1429 | 5 | c.-31 others(14): Show |
CWF19L1 | ENSG00000095485.18 | transcript | ENST00000354105.10 | protein_coding | 273 | chr10 | TogoVar | ||||||
CWF19L2_chr11_107321360_107462825 | 107380046 | C | CAAAAA | intron_variant | MODIFIER | HG00544.hp1 HG01243.hp2 HG01934.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0186a0001c0001t0001g0195a0001c0001t0001g0198others(7): Show | 10 | 392 | 0.0255 | 5 | c.187 others(26): Show |
CWF19L2 | ENSG00000152404.16 | transcript | ENST00000282251.10 | protein_coding | 12/17 | chr11 | TogoVar | ||||||
CWF19L2_chr11_107321360_107462825 | 107427227 | T | TTTTTC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0011a0001c0015others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(23): Show | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0026others(309): Show | 314 | 392 | 0.8010 | 5 | c.143 others(24): Show |
CWF19L2 | ENSG00000152404.16 | transcript | ENST00000282251.10 | protein_coding | 8/17 | chr11 | TogoVar | ||||||
CWF19L2_chr11_107321360_107462825 | 107439035 | G | GGAAAA | intron_variant | MODIFIER | HG02559.hp2 HG02647.hp2 HG02818.hp1 |
a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0354a0002c0002t0003g0362a0002c0002t0003g0366 | 3 | 392 | 0.0077 | 5 | c.664 others(18): Show |
CWF19L2 | ENSG00000152404.16 | transcript | ENST00000282251.10 | protein_coding | 6/17 | chr11 | TogoVar | ||||||
CWF19L2_chr11_107321360_107462825 | 107449647 | G | GAAAGT | intron_variant | MODIFIER | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(31): Show |
a0004a0006a0010 | a0004c0004a0006c0006a0010c0008 | a0004c0004t0001a0004c0004t0002a0006c0006t0003others(1): Show | a0004c0004t0001g0349a0004c0004t0001g0350a0004c0004t0001g0351others(30): Show | 34 | 392 | 0.0867 | 5 | c.339 others(22): Show |
CWF19L2 | ENSG00000152404.16 | transcript | ENST00000282251.10 | protein_coding | 3/17 | chr11 | TogoVar | ||||||
CXADR_chr21_17508043_17575100 | 17530114 | A | ATTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0113others(101): Show | 106 | 352 | 0.3011 | 5 | c.44- others(22): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
CXCL11_chr4_76028682_76041070 | 76040536 | C | CCCCCA | upstream_gene_variant | MODIFIER | HG01243.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0007 | 5 | 422 | 0.0119 | 5 | c.-45 others(16): Show |
CXCL11 | ENSG00000169248.13 | transcript | ENST00000306621.8 | protein_coding | 4467 | chr4 | TogoVar | ||||||
CXCL12_chr10_44372067_44390097 | 44375484 | T | TGCTGG | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): Show | 365 | 442 | 0.8258 | 5 | c.*31 others(16): Show |
CXCL12 | ENSG00000107562.18 | transcript | ENST00000343575.11 | protein_coding | 1582 | chr10 | TogoVar | ||||||
CXCL12_chr10_44372067_44390097 | 44389720 | T | TGGGGG | upstream_gene_variant | MODIFIER | HG01257.hp1 HG01258.hp2 HG01975.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0002g0017others(2): Show | 6 | 442 | 0.0136 | 5 | c.-47 others(16): Show |
CXCL12 | ENSG00000107562.18 | transcript | ENST00000343575.11 | protein_coding | 4624 | chr10 | TogoVar | ||||||
CXCL12_chr10_44372067_44390097 | 44389722 | T | TGGGGG | upstream_gene_variant | MODIFIER | HG01255.hp2 HG03688.hp1 NA18952.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0001a0001c0001t0002g0004a0001c0001t0002g0017others(5): Show | 14 | 442 | 0.0317 | 5 | c.-47 others(16): Show |
CXCL12 | ENSG00000107562.18 | transcript | ENST00000343575.11 | protein_coding | 4626 | chr10 | TogoVar | ||||||
CXCL12_chr10_44372067_44390097 | 44389724 | T | TGTGGG | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(4): Show | 28 | 442 | 0.0634 | 5 | c.-47 others(16): Show |
CXCL12 | ENSG00000107562.18 | transcript | ENST00000343575.11 | protein_coding | 4628 | chr10 | TogoVar |