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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CUX1_chr7_101811007_102288958 | 101827244 | CCTTCT | C | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01168.hp2 others(15): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(5): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0054others(15): Show | 18 | 132 | 0.1364 | -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 | 101834165 | CTTTTT | C | intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0005 | a0001c0001t0004a0002c0003t0001a0002c0003t0013others(1): Show | a0001c0001t0004g0031a0002c0003t0001g0068a0002c0003t0001g0105others(3): Show | 6 | 132 | 0.0455 | -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 | 101957840 | ATTAAT | A | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0005 | a0001c0002t0001g0087a0001c0002t0005g0129 | 2 | 132 | 0.0152 | -5 | c.174 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 101984090 | ATATAT | A | intron_variant | MODIFIER | HG00639.hp1 HG01258.hp1 HG02280.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(3): Show | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0127others(9): Show | 12 | 132 | 0.0909 | -5 | c.175 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102021614 | CTTTTT | C | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(14): Show | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(67): Show | 70 | 132 | 0.5303 | -5 | c.175 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102042925 | GACTAT | G | intron_variant | MODIFIER | HG01884.hp1 HG01978.hp1 HG02056.hp2 others(18): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0001t0011a0001c0002t0001others(5): Show | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0040others(18): Show | 21 | 132 | 0.1591 | -5 | c.222 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102046569 | ATTTTT | A | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(64): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(11): Show | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0049others(64): Show | 67 | 132 | 0.5076 | -5 | c.222 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102052179 | CCACTG | C | intron_variant | MODIFIER | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0004others(2): Show | a0001c0001t0001a0001c0001t0011a0001c0002t0001others(3): Show | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0040others(15): Show | 18 | 132 | 0.1364 | -5 | c.223 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102059631 | CAAAAA | C | intron_variant | MODIFIER | HG01258.hp1 HG01496.hp2 HG02257.hp2 others(4): Show |
a0001a0002a0003 | a0001c0002a0002c0003a0002c0005others(2): Show | a0001c0002t0007a0002c0003t0002a0002c0005t0001others(2): Show | a0001c0002t0007g0118a0002c0003t0002g0052a0002c0003t0002g0076others(4): Show | 7 | 132 | 0.0530 | -5 | c.223 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102070932 | GTTTCT | G | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(113): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(10): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(22): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(113): Show | 116 | 132 | 0.8788 | -5 | c.301 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102092932 | AGAAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(22): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(22): Show | 25 | 132 | 0.1894 | -5 | c.302 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 4/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102098807 | ATTTTT | A | intron_variant | MODIFIER | HG01074.hp1 HG01099.hp2 HG01884.hp2 others(29): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0011a0001c0002t0001others(8): Show | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0025others(29): Show | 32 | 132 | 0.2424 | -5 | c.439 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102180914 | TTATTG | T | intron_variant | MODIFIER | HG01515.hp1 HG01978.hp1 HG02055.hp2 others(7): Show |
a0001a0002a0003 | a0001c0001a0002c0005a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0004a0002c0005t0001others(2): Show | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0057others(7): Show | 10 | 132 | 0.0758 | -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 | 102215229 | CTTTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0008 | a0001c0001t0001a0001c0002t0001a0006c0008t0001 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0102others(4): Show | 7 | 132 | 0.0530 | -5 | c.125 others(26): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102221737 | TAAAAA | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0006others(7): Show | a0001c0001t0001g0029a0001c0002t0001g0008a0001c0002t0001g0020others(48): Show | 51 | 132 | 0.3864 | -5 | c.125 others(26): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101811007_102288958 | 102259757 | AGAAAG | A | intron_variant | MODIFIER | HG00544.hp2 HG02976.hp2 NA18954.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0057a0001c0002t0001g0088a0001c0002t0001g0125others(1): Show | 4 | 132 | 0.0303 | -5 | c.125 others(26): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 101827244 | CCTTCT | C | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01168.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0011others(12): Show | a0001c0001t0006g0029a0001c0001t0006g0082a0001c0001t0010g0111others(15): Show | 18 | 136 | 0.1324 | -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 | 101834165 | CTTTTT | C | intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0041a0001c0003t0021others(2): Show | a0001c0001t0003g0008a0001c0001t0041g0075a0001c0003t0021g0065others(3): Show | 6 | 136 | 0.0441 | -5 | c.30+ others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101957840 | ATTAAT | A | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0048 | a0001c0001t0003g0036a0001c0001t0048g0056 | 2 | 136 | 0.0147 | -5 | c.141 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 101984090 | ATATAT | A | intron_variant | MODIFIER | HG00639.hp1 HG01258.hp1 HG02280.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0006a0001c0001t0017others(6): Show | a0001c0001t0003g0036a0001c0001t0006g0043a0001c0001t0017g0007others(10): Show | 13 | 136 | 0.0956 | -5 | c.142 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102021614 | CTTTTT | C | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(45): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0036others(66): Show | 69 | 136 | 0.5074 | -5 | c.142 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102042925 | GACTAT | G | intron_variant | MODIFIER | HG01884.hp2 HG01978.hp1 HG02056.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(15): Show | a0001c0001t0003g0040a0001c0001t0010g0111a0001c0001t0011g0048others(20): Show | 23 | 136 | 0.1691 | -5 | c.189 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102046569 | ATTTTT | A | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(65): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(39): Show | a0001c0001t0003g0008a0001c0001t0003g0036a0001c0001t0003g0040others(65): Show | 68 | 136 | 0.5000 | -5 | c.189 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102052179 | CCACTG | C | intron_variant | MODIFIER | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0057a0001c0002t0001a0001c0003t0001others(12): Show | a0001c0001t0057g0090a0001c0002t0001g0054a0001c0003t0001g0101others(16): Show | 19 | 136 | 0.1397 | -5 | c.190 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102059631 | CAAAAA | C | intron_variant | MODIFIER | HG01123.hp2 HG01258.hp1 HG01496.hp2 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0001t0006a0001c0004t0002others(3): Show | a0001c0001t0003g0024a0001c0001t0006g0043a0001c0001t0006g0082others(5): Show | 8 | 136 | 0.0588 | -5 | c.190 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102070932 | GTTTCT | G | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(71): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0024others(117): Show | 120 | 136 | 0.8824 | -5 | c.268 others(20): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102092932 | AGAAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00735.hp2 HG01168.hp2 others(22): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(17): Show | a0001c0001t0003g0040a0001c0001t0010g0085a0001c0001t0017g0007others(22): Show | 25 | 136 | 0.1838 | -5 | c.269 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 4/23 | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102098807 | ATTTTT | A | intron_variant | MODIFIER | HG01074.hp1 HG01099.hp2 HG01884.hp1 others(32): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(24): Show | a0001c0001t0003g0008a0001c0001t0003g0040a0001c0001t0010g0045others(32): Show | 35 | 136 | 0.2574 | -5 | c.406 others(22): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102132323 | GCACGC | G | intron_variant | MODIFIER | HG03471.hp2 NA20129.hp2 |
a0001 | a0001c0006 | a0001c0006t0005a0001c0006t0009 | a0001c0006t0005g0077a0001c0006t0009g0070 | 2 | 136 | 0.0147 | -5 | c.674 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102180914 | TTATTG | T | intron_variant | MODIFIER | HG01123.hp2 HG01515.hp1 HG01978.hp1 others(8): Show |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0002a0001c0004t0014others(5): Show | a0001c0003t0001g0023a0001c0004t0002g0052a0001c0004t0002g0061others(8): Show | 11 | 136 | 0.0809 | -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 | 102215229 | CTTTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0048a0001c0002t0001a0001c0003t0004others(3): Show | a0001c0001t0048g0056a0001c0002t0001g0063a0001c0003t0004g0034others(4): Show | 7 | 136 | 0.0515 | -5 | c.313 others(26): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102221737 | TAAAAA | T | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0022others(26): Show | a0001c0001t0002g0105a0001c0001t0006g0009a0001c0001t0006g0029others(50): Show | 53 | 136 | 0.3897 | -5 | c.313 others(24): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CUX1_chr7_101812626_102263233 | 102259757 | AGAAAG | A | downstream_gene_variant | MODIFIER | HG00544.hp2 HG02976.hp2 NA18954.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0012a0001c0002t0070a0001c0004t0014 | a0001c0002t0012g0032a0001c0002t0012g0057a0001c0002t0070g0122others(1): Show | 4 | 136 | 0.0294 | -5 | c.*10 others(18): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 1525 | chr7 | TogoVar | ||||||
CUX2_chr12_111029165_111355554 | 111145854 | TTTTTG | T | intron_variant | MODIFIER | HG01099.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0018others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(7): Show | 10 | 100 | 0.1000 | -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 | 111148525 | TTTATG | T | intron_variant | MODIFIER | HG02109.hp2 HG02818.hp1 HG03579.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0006a0001c0002t0001g0051a0001c0003t0001g0008others(1): Show | 4 | 100 | 0.0400 | -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 | 111165933 | GATTAT | G | intron_variant | MODIFIER | HG02622.hp2 HG02897.hp2 NA19030.hp2 |
a0001 | a0001c0004a0001c0009a0001c0022 | a0001c0004t0005a0001c0009t0001a0001c0022t0005 | a0001c0004t0005g0007a0001c0009t0001g0035a0001c0022t0005g0034 | 3 | 100 | 0.0300 | -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 | 111205141 | CGTCTT | C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0013a0001c0001t0002g0012a0001c0001t0002g0085others(15): Show | 18 | 100 | 0.1800 | -5 | c.64- others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111263625 | AAAAAC | A | intron_variant | MODIFIER | HG01169.hp1 HG02055.hp2 HG03453.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0004t0001 | a0001c0001t0002g0079a0001c0001t0003g0078a0001c0001t0003g0080others(3): Show | 6 | 100 | 0.0600 | -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 | TTTTTA | T | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp1 HG02486.hp1 others(10): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0001others(8): Show | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0003g0045others(10): Show | 13 | 100 | 0.1300 | -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 | 111303221 | GAAAAA | G | intron_variant | MODIFIER | HG00597.hp2 HG02717.hp2 NA19030.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0007others(1): Show | a0001c0001t0004a0001c0003t0001a0001c0007t0001others(1): Show | a0001c0001t0004g0054a0001c0003t0001g0094a0001c0007t0001g0098others(1): Show | 4 | 100 | 0.0400 | -5 | c.754 others(20): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CUX2_chr12_111029165_111355554 | 111325293 | CAAAAG | C | intron_variant | MODIFIER | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
a0001a0006 | a0001c0002a0001c0010a0001c0013others(4): Show | a0001c0002t0001a0001c0002t0007a0001c0010t0001others(5): Show | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0001g0023others(27): Show | 30 | 100 | 0.3000 | -5 | c.292 others(24): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CWC15_chr11_94957620_94978556 | 94959001 | CTTAAT | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 23 | 410 | 0.0561 | -5 | c.*43 others(16): Show |
CWC15 | ENSG00000150316.12 | transcript | ENST00000279839.8 | protein_coding | 3618 | chr11 | TogoVar | ||||||
CWC15_chr11_94957620_94978556 | 94973293 | TAGGCG | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(7): Show | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(66): Show | 193 | 410 | 0.4707 | -5 | c.-9+ others(18): Show |
CWC15 | ENSG00000150316.12 | transcript | ENST00000279839.8 | protein_coding | 1/6 | chr11 | TogoVar | ||||||
CWC22_chr2_179939876_180012297 | 179939957 | CATAGT | C | downstream_gene_variant | MODIFIER | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
a0005 | a0005c0007 | a0005c0007t0002 | a0005c0007t0002g0039a0005c0007t0002g0225 | 3 | 376 | 0.0080 | -5 | c.*51 others(16): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4918 | chr2 | TogoVar | ||||||
CWC27_chr5_64763930_65023750 | 64840361 | TTAAAA | T | intron_variant | MODIFIER | HG02080.hp1 HG02523.hp2 HG03139.hp2 others(2): Show |
a0002 | a0002c0002a0002c0006 | a0002c0002t0002a0002c0006t0002 | a0002c0002t0002g0033a0002c0002t0002g0045a0002c0002t0002g0066others(2): Show | 5 | 260 | 0.0192 | -5 | c.938 others(24): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | chr5 | TogoVar | ||||||
CWC27_chr5_64763930_65023750 | 64870481 | TTAAAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
a0002a0003 | a0002c0002a0002c0004a0002c0006others(2): Show | a0002c0002t0001a0002c0002t0002a0002c0004t0001others(6): Show | a0002c0002t0001g0043a0002c0002t0001g0110a0002c0002t0001g0175others(96): Show | 99 | 260 | 0.3808 | -5 | c.939 others(24): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | chr5 | TogoVar | ||||||
CWC27_chr5_64763930_65023750 | 64874154 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(4): Show | a0001c0001t0003a0002c0002t0001a0002c0002t0002others(8): Show | a0001c0001t0003g0072a0002c0002t0001g0043a0002c0002t0001g0110others(97): Show | 100 | 260 | 0.3846 | -5 | c.939 others(24): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 64940842 | CTTTTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
a0002 | a0002c0004 | a0002c0004t0001a0002c0004t0002 | a0002c0004t0001g0249a0002c0004t0002g0002a0002c0004t0002g0003others(4): Show | 7 | 260 | 0.0269 | -5 | c.104 others(26): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CWC27_chr5_64763930_65023750 | 65023323 | TATTTA | T | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00642.hp1 HG01167.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(5): Show | a0001c0001t0001g0230a0001c0003t0001g0098a0001c0003t0001g0248others(24): Show | 27 | 260 | 0.1039 | -5 | c.*50 others(16): Show |
CWC27 | ENSG00000153015.17 | transcript | ENST00000381070.8 | protein_coding | 4574 | chr5 | TogoVar | ||||||
CWF19L1_chr10_100227298_100272638 | 100266839 | GTTTGT | G | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0002others(8): Show | a0001c0001t0001g0204a0001c0001t0001g0248a0001c0002t0001g0247others(83): Show | 99 | 364 | 0.2720 | -5 | c.23+ others(18): Show |
CWF19L1 | ENSG00000095485.18 | transcript | ENST00000354105.10 | protein_coding | 1/13 | chr10 | TogoVar |