view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100733825 | G | GAAA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(59): Show |
62 | 136 | 0.4559 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100735002 | A | AAAC | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0003t0014g0234 others(7): Show |
10 | 280 | 0.0357 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100735023 | C | CAAA | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0001a0002c0002t0002a0002c0004t0007 | a0002c0002t0001g0013 a0002c0002t0001g0015 a0002c0002t0001g0016 others(3): Show |
6 | 284 | 0.0211 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | C | CTTT | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0004others(3): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0066 others(9): Show |
12 | 164 | 0.0732 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100764005 | C | CTCT | intron_variant | MODIFIER | HG02055.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0018a0002c0002t0039a0002c0011t0017 | a0002c0002t0018g0205 a0002c0002t0018g0206 a0002c0002t0039g0200 others(1): Show |
4 | 227 | 0.0176 | 3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAA | intron_variant | MODIFIER | HG00738.hp2 HG01358.hp2 HG02897.hp2 others(4): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0002c0004others(2): Show | a0001c0001t0001a0002c0002t0020a0002c0004t0007others(2): Show | a0001c0001t0001g0095 a0001c0001t0001g0186 a0001c0001t0001g0202 others(4): Show |
7 | 20 | 0.3500 | 3 | c.251 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837662 | C | CATT | intron_variant | MODIFIER | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0031a0001c0003t0006others(6): Show | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0066 others(17): Show |
20 | 284 | 0.0704 | 3 | c.313 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875761 | C | CGGG | intron_variant | MODIFIER | HG00544.hp2 HG01928.hp2 HG02056.hp2 others(33): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0030a0001c0003t0006others(5): Show | a0001c0001t0001g0022 a0001c0001t0001g0091 a0001c0001t0001g0103 others(33): Show |
36 | 162 | 0.2222 | 3 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100876005 | T | TTAA | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(6): Show | a0001c0001t0001g0139 a0001c0001t0001g0259 a0001c0001t0001g0279 others(34): Show |
37 | 284 | 0.1303 | 3 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100895493 | C | CTTT | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(18): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0005 | a0001c0003t0001a0001c0003t0006a0001c0003t0014others(4): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0172 others(18): Show |
21 | 237 | 0.0886 | 3 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100899669 | C | CTTT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(30): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0172 others(30): Show |
33 | 277 | 0.1191 | 3 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100904247 | C | CTCT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(29): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0003g0107 others(29): Show |
32 | 277 | 0.1155 | 3 | c.385 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100914509 | G | GAAC | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(34): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(5): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0172 others(34): Show |
37 | 62 | 0.5968 | 3 | c.486 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980550 | T | TTTC | intron_variant | MODIFIER | HG00408.hp2 HG02630.hp1 HG03130.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002a0002c0002t0035 | a0001c0001t0002g0020 a0002c0002t0002g0141 a0002c0002t0002g0222 others(1): Show |
4 | 284 | 0.0141 | 3 | c.245 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100996996 | C | CTTT | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01496.hp2 NA18959.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0041a0001c0003t0001 | a0001c0001t0001g0193 a0001c0001t0001g0215 a0001c0001t0041g0127 others(1): Show |
4 | 130 | 0.0308 | 3 | c.*81 others(14): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3056 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12804971 | T | TCTG | intron_variant | MODIFIER | HG02622.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | 228 | 0.0219 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12814235 | G | GTTT | intron_variant | MODIFIER | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0004t0010a0001c0005t0001others(2): Show | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0004t0010g0034 others(4): Show |
7 | 162 | 0.0432 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12818335 | G | GAAA | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG00738.hp2 others(39): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
42 | 127 | 0.3307 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12828628 | T | TTTC | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0003 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | 228 | 0.0219 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12828636 | C | CTTT | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(3): Show | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0181 others(5): Show |
8 | 101 | 0.0792 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12842148 | T | TAAA | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0003 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | 134 | 0.0373 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12845506 | C | CAAA | intron_variant | MODIFIER | HG02559.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0010 | a0001c0001t0001g0033 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | 219 | 0.0228 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12846098 | G | GAAA | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01243.hp1 others(17): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(5): Show | a0001c0001t0001g0192 a0001c0001t0001g0200 a0001c0001t0001g0204 others(17): Show |
20 | 129 | 0.1550 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12847510 | C | CTTT | intron_variant | MODIFIER | HG02258.hp1 HG02622.hp2 NA18906.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0009a0001c0005t0007 | a0001c0001t0001g0026 a0001c0001t0009g0151 a0001c0005t0007g0039 |
3 | 160 | 0.0188 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849568 | C | CTTT | intron_variant | MODIFIER | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(4): Show | a0001c0001t0001g0139 a0001c0001t0001g0174 a0001c0001t0001g0224 others(7): Show |
10 | 192 | 0.0521 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849594 | T | TTTG | intron_variant | MODIFIER | HG00423.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0019others(1): Show | a0001c0001t0001g0204 a0001c0001t0001g0214 a0001c0001t0008g0040 others(5): Show |
8 | 121 | 0.0661 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12852277 | C | CTTT | intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG02145.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0002g0016 others(6): Show |
9 | 116 | 0.0776 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12863148 | T | TAAG | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0001g0174 a0001c0001t0001g0187 a0001c0001t0003g0028 others(8): Show |
11 | 228 | 0.0482 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868572 | A | ATGC | intron_variant | MODIFIER | HG02622.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(1): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
8 | 226 | 0.0354 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12870048 | C | CTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(112): Show |
115 | 175 | 0.6571 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12897710 | C | CTTT | intron_variant | MODIFIER | HG01517.hp2 HG01891.hp2 HG01981.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0009 a0001c0001t0001g0174 a0001c0001t0002g0008 others(10): Show |
13 | 123 | 0.1057 | 3 | c.198 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903121 | A | AGAG | intron_variant | MODIFIER | HG00733.hp1 HG01928.hp2 HG02071.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0002g0114 others(16): Show |
19 | 221 | 0.0860 | 3 | c.199 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12910446 | C | CTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(136): Show |
139 | 156 | 0.8910 | 3 | c.275 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12912318 | C | CAGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(189): Show |
192 | 228 | 0.8421 | 3 | c.275 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12913968 | C | CAAA | intron_variant | MODIFIER | HG02074.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0005t0001others(4): Show | a0001c0001t0001g0147 a0001c0001t0004g0106 a0001c0005t0001g0173 others(6): Show |
9 | 49 | 0.1837 | 3 | c.276 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12919387 | C | CTTT | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp2 HG02922.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(3): Show | a0001c0001t0001g0030 a0001c0001t0003g0060 a0001c0001t0003g0078 others(5): Show |
8 | 35 | 0.2286 | 3 | c.388 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12920375 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(99): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(99): Show |
102 | 129 | 0.7907 | 3 | c.464 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12938582 | T | TTAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(15): Show |
a0001 | a0001c0001a0001c0005a0001c0012 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(7): Show | a0001c0001t0002g0008 a0001c0001t0003g0047 a0001c0001t0003g0048 others(15): Show |
18 | 149 | 0.1208 | 3 | c.583 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12946478 | T | TAAA | intron_variant | MODIFIER | HG03942.hp1 NA18942.hp2 NA18963.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0019 a0001c0001t0003g0083 a0001c0001t0004g0002 others(6): Show |
9 | 74 | 0.1216 | 3 | c.861 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12946799 | T | TAAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(144): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
147 | 210 | 0.7000 | 3 | c.862 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | C | CAAA | intron_variant | MODIFIER | HG01192.hp1 HG01517.hp1 HG01891.hp2 others(5): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0003a0001c0001t0025a0001c0001t0027others(5): Show | a0001c0001t0003g0072 a0001c0001t0025g0038 a0001c0001t0027g0222 others(5): Show |
8 | 103 | 0.0777 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12966155 | C | CAAA | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp1 HG01243.hp2 others(26): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0148 others(26): Show |
29 | 134 | 0.2164 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12970378 | A | AAAG | intron_variant | MODIFIER | HG00673.hp2 HG01109.hp2 HG01192.hp1 others(30): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0148 others(30): Show |
33 | 173 | 0.1908 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12976612 | C | CAAA | intron_variant | MODIFIER | HG00673.hp2 HG01074.hp2 HG01106.hp2 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(42): Show |
45 | 130 | 0.3462 | 3 | c.176 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG00741.hp2 HG01884.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0158 others(8): Show |
11 | 77 | 0.1429 | 3 | c.231 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12992148 | T | TTGA | downstream_gene_variant | MODIFIER | HG02572.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0187 a0001c0001t0003g0090 |
2 | 228 | 0.0088 | 3 | c.*19 others(14): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 506 | chr17 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1075236 | C | CTTT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
a0001a0002a0004others(6): Show | a0001c0002a0001c0004a0001c0017others(21): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0013others(40): Show | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0013 others(121): Show |
206 | 313 | 0.6581 | 3 | c.118 others(20): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1090460 | A | ATTT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0004a0002c0001others(16): Show | a0001c0002t0001a0001c0004t0001a0001c0004t0005others(25): Show | a0001c0002t0001g0002 a0001c0004t0001g0202 a0001c0004t0005g0015 others(45): Show |
71 | 279 | 0.2545 | 3 | c.*44 others(14): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3833 | chr19 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32086574 | T | TATA | intron_variant | MODIFIER | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
a0001 | a0001c0002a0001c0018 | a0001c0002t0005a0001c0018t0023 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | 184 | 0.0326 | 3 | c.-16 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32143202 | A | AGTT | intron_variant | MODIFIER | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(77): Show |
a0001a0002a0006others(3): Show | a0001c0001a0002c0004a0006c0016others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(76): Show |
80 | 138 | 0.5797 | 3 | c.386 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |