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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAA | C | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0037others(7): Show | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0129others(18): Show | 21 | 286 | 0.0734 | -4 | c.251 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100800759 | TAAAG | T | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0015others(2): Show | 5 | 286 | 0.0175 | -4 | c.312 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | GTTTA | G | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0012others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(32): Show | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0066others(131): Show | 134 | 286 | 0.4685 | -4 | c.312 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100820948 | TTTTG | T | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(51): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(14): Show | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0026others(51): Show | 54 | 286 | 0.1888 | -4 | c.312 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100850873 | CTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(17): Show |
a0001a0002a0005 | a0001c0003a0001c0010a0002c0002others(3): Show | a0001c0003t0014a0001c0010t0001a0002c0002t0002others(10): Show | a0001c0003t0014g0234a0001c0003t0014g0235a0001c0010t0001g0238others(17): Show | 20 | 286 | 0.0699 | -4 | c.313 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | GGTGT | G | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(44): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(13): Show | a0001c0001t0001g0047a0001c0001t0001g0135a0001c0001t0001g0136others(44): Show | 47 | 286 | 0.1643 | -4 | c.313 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100863059 | AACAC | A | intron_variant | MODIFIER | HG02622.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0001t0031a0001c0008t0001others(3): Show | a0001c0001t0001g0047a0001c0001t0031g0251a0001c0008t0001g0004others(4): Show | 7 | 286 | 0.0245 | -4 | c.384 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | GTCTC | G | intron_variant | MODIFIER | HG02145.hp1 HG03098.hp2 HG03139.hp2 |
a0002 | a0002c0002a0002c0005 | a0002c0002t0004a0002c0005t0016 | a0002c0002t0004g0040a0002c0005t0016g0031a0002c0005t0016g0032 | 3 | 286 | 0.0105 | -4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTG | C | intron_variant | MODIFIER | HG01106.hp2 HG01884.hp1 HG02165.hp2 others(1): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0007others(1): Show | a0001c0001t0002a0002c0002t0023a0003c0007t0005others(1): Show | a0001c0001t0002g0022a0002c0002t0023g0191a0003c0007t0005g0059others(1): Show | 4 | 286 | 0.0140 | -4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100881829 | TTTTG | T | intron_variant | MODIFIER | HG00544.hp2 HG01123.hp1 HG01433.hp1 others(47): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0030a0001c0003t0022others(9): Show | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0126others(47): Show | 50 | 286 | 0.1748 | -4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100893937 | TTAAG | T | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(30): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(30): Show | 33 | 286 | 0.1154 | -4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100895220 | ATCAT | A | intron_variant | MODIFIER | HG01884.hp1 HG02630.hp1 HG03540.hp2 |
a0002a0004 | a0002c0002a0004c0013 | a0002c0002t0002a0004c0013t0038 | a0002c0002t0002g0139a0002c0002t0002g0222a0004c0013t0038g0236 | 3 | 286 | 0.0105 | -4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100899671 | TTTTG | T | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0008a0001c0010others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(121): Show | 124 | 286 | 0.4336 | -4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100899730 | TTTTG | T | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(32): Show |
a0001a0002 | a0001c0003a0002c0005 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(5): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(32): Show | 35 | 286 | 0.1224 | -4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATAT | A | intron_variant | MODIFIER | HG01433.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
a0001a0002 | a0001c0008a0002c0002 | a0001c0008t0010a0002c0002t0002a0002c0002t0015others(1): Show | a0001c0008t0010g0253a0002c0002t0002g0006a0002c0002t0002g0045others(2): Show | 5 | 286 | 0.0175 | -4 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100914336 | CATCT | C | intron_variant | MODIFIER | HG01070.hp2 HG01975.hp1 HG02559.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004a0002c0011 | a0002c0002t0017a0002c0002t0018a0002c0004t0007others(1): Show | a0002c0002t0017g0046a0002c0002t0018g0193a0002c0002t0018g0194others(3): Show | 6 | 286 | 0.0210 | -4 | c.486 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | TTGTG | T | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(10): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0006a0001c0003t0026 | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(10): Show | 13 | 286 | 0.0455 | -4 | c.486 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100950356 | GTATT | G | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016a0002c0004t0007g0060a0002c0004t0007g0074others(5): Show | 8 | 286 | 0.0280 | -4 | c.116 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100966759 | CAGAG | C | intron_variant | MODIFIER | HG01081.hp1 HG02257.hp2 HG02818.hp1 others(2): Show |
a0002 | a0002c0002a0002c0006 | a0002c0002t0008a0002c0006t0008 | a0002c0002t0008g0028a0002c0002t0008g0029a0002c0002t0008g0230others(2): Show | 5 | 286 | 0.0175 | -4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | AAAAT | A | intron_variant | MODIFIER | HG00733.hp1 HG01070.hp2 HG01515.hp2 others(6): Show |
a0001a0002 | a0001c0003a0001c0015a0002c0002others(2): Show | a0001c0003t0006a0001c0015t0001a0002c0002t0002others(4): Show | a0001c0003t0006g0112a0001c0015t0001g0277a0002c0002t0002g0139others(6): Show | 9 | 286 | 0.0315 | -4 | c.253 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100996998 | TTTTC | T | downstream_gene_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016a0002c0004t0007g0060a0002c0004t0007g0074others(5): Show | 8 | 286 | 0.0280 | -4 | c.*81 others(15): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3058 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100998855 | CAAAG | C | downstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(57): Show |
a0001 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0034others(6): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(57): Show | 60 | 286 | 0.2098 | -4 | c.*10 others(17): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4915 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12796136 | ATATC | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(221): Show | 224 | 230 | 0.9739 | -4 | c.53+ others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATA | T | intron_variant | MODIFIER | HG01109.hp1 HG02027.hp1 NA18968.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0018a0001c0003t0001 | a0001c0001t0001g0180a0001c0001t0018g0103a0001c0003t0001g0128 | 3 | 230 | 0.0130 | -4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12842430 | AAAAG | A | intron_variant | MODIFIER | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(4): Show | a0001c0001t0001g0033a0001c0001t0001g0202a0001c0001t0001g0225others(7): Show | 10 | 230 | 0.0435 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12845805 | AACAC | A | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0080a0001c0001t0005g0081 | 2 | 230 | 0.0087 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849922 | AGTTT | A | intron_variant | MODIFIER | HG00423.hp2 HG01891.hp2 HG02027.hp2 others(12): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0016others(12): Show | 15 | 230 | 0.0652 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTAT | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(85): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(85): Show | 88 | 230 | 0.3826 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTA | T | intron_variant | MODIFIER | HG01106.hp1 HG02698.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(2): Show | a0001c0001t0001g0189a0001c0001t0003g0064a0001c0001t0016g0141others(2): Show | 5 | 230 | 0.0217 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12874165 | TAGAA | T | intron_variant | MODIFIER | HG01978.hp1 HG02273.hp2 HG02559.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0027a0001c0001t0001g0114a0001c0001t0001g0140others(1): Show | 4 | 230 | 0.0174 | -4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12886971 | TTTTG | T | intron_variant | MODIFIER | HG01074.hp2 HG01884.hp2 HG01934.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0030a0001c0001t0003g0164a0001c0001t0004g0002others(10): Show | 13 | 230 | 0.0565 | -4 | c.54- others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894227 | TGAGA | T | intron_variant | MODIFIER | HG01192.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009a0001c0001t0025 | a0001c0001t0003g0028a0001c0001t0003g0075a0001c0001t0009g0191others(1): Show | 4 | 230 | 0.0174 | -4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894771 | GTTTT | G | intron_variant | MODIFIER | HG01192.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009a0001c0001t0025 | a0001c0001t0003g0028a0001c0001t0003g0075a0001c0001t0009g0191others(1): Show | 4 | 230 | 0.0174 | -4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12898956 | GATTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
a0001a0004a0006 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(126): Show | 129 | 230 | 0.5609 | -4 | c.198 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12900933 | TTTTA | T | intron_variant | MODIFIER | HG00423.hp2 HG02602.hp2 HG02698.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0014a0003c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0214a0001c0001t0002g0015a0001c0001t0003g0172others(4): Show | 7 | 230 | 0.0304 | -4 | c.198 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | TGAGA | T | intron_variant | MODIFIER | HG02965.hp2 HG03225.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0012a0001c0004t0010 | a0001c0001t0012g0095a0001c0004t0010g0031 | 2 | 230 | 0.0087 | -4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | AGTGT | A | intron_variant | MODIFIER | HG01192.hp1 HG01258.hp2 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0025 | a0001c0001t0001g0193a0001c0001t0003g0028a0001c0001t0025g0036 | 3 | 230 | 0.0130 | -4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12915035 | TTTTG | T | intron_variant | MODIFIER | HG02071.hp1 HG03831.hp2 HG03942.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0013a0001c0001t0002g0019a0001c0001t0003g0088others(4): Show | 7 | 230 | 0.0304 | -4 | c.276 others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12926475 | AATAT | A | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG01884.hp2 others(46): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0114others(46): Show | 49 | 230 | 0.2130 | -4 | c.465 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | TACAC | T | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(52): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0017a0001c0001t0001g0094a0001c0001t0001g0111others(52): Show | 55 | 230 | 0.2391 | -4 | c.582 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12942132 | TTTAA | T | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG02027.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0144others(6): Show | 9 | 230 | 0.0391 | -4 | c.651 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTT | C | intron_variant | MODIFIER | HG01192.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0214a0001c0001t0003g0074others(4): Show | 7 | 230 | 0.0304 | -4 | c.113 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12967249 | CTTTT | C | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp2 HG01934.hp1 others(11): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(6): Show | a0001c0001t0001g0007a0001c0001t0001g0147a0001c0001t0001g0189others(11): Show | 14 | 230 | 0.0609 | -4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12969282 | CTCTT | C | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG01981.hp2 others(10): Show |
a0001a0005 | a0001c0001a0005c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0132others(10): Show | 13 | 230 | 0.0565 | -4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12971683 | GTGTT | G | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG01981.hp2 others(10): Show |
a0001a0005 | a0001c0001a0005c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0132others(10): Show | 13 | 230 | 0.0565 | -4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12991869 | TTTAC | T | downstream_gene_variant | MODIFIER | HG00673.hp2 HG01884.hp1 HG02027.hp2 others(14): Show |
a0001a0006 | a0001c0001a0001c0004a0006c0015 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(3): Show | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0010others(14): Show | 17 | 230 | 0.0739 | -4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 227 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12992127 | TTTGA | T | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(16): Show |
a0001a0005 | a0001c0001a0001c0003a0005c0013 | a0001c0001t0001a0001c0001t0003a0001c0001t0022others(3): Show | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0041others(16): Show | 19 | 230 | 0.0826 | -4 | c.*19 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 485 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1072058 | CTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
a0002a0004a0005others(2): Show | a0002c0001a0002c0015a0002c0021others(9): Show | a0002c0001t0003a0002c0001t0005a0002c0001t0007others(15): Show | a0002c0001t0003g0003a0002c0001t0003g0013a0002c0001t0003g0028others(51): Show | 75 | 418 | 0.1794 | -4 | c.422 others(21): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTT | C | intron_variant | MODIFIER | HG00738.hp1 HG01261.hp2 HG01433.hp2 others(8): Show |
a0002a0004 | a0002c0001a0002c0021a0004c0005 | a0002c0001t0003a0002c0001t0004a0002c0001t0007others(3): Show | a0002c0001t0003g0030a0002c0001t0003g0097a0002c0001t0003g0117others(7): Show | 11 | 418 | 0.0263 | -4 | c.118 others(23): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1084346 | GGTGA | G | splice_region_variant others(1): Show |
LOW | NA18970.hp2 NA18971.hp1 NA19091.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0208a0001c0002t0001g0243a0001c0002t0001g0262 | 3 | 418 | 0.0072 | -4 | c.306 others(17): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |