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 | 100756501 | GATAAGAA | G | intron_variant | MODIFIER | HG02486.hp2 HG03098.hp1 HG03130.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0034a0002c0002t0002g0248a0002c0002t0002g0250 | 3 | 286 | 0.0105 | -7 | c.155 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0136a0001c0001t0001g0266a0001c0001t0001g0271others(19): Show | 22 | 286 | 0.0769 | -7 | c.251 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100836177 | GTTAGTTA | G | intron_variant | MODIFIER | HG01243.hp1 HG02559.hp2 HG02922.hp1 others(5): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0002a0002c0002t0018a0002c0011t0017 | a0002c0002t0002g0034a0002c0002t0002g0222a0002c0002t0002g0245others(5): Show | 8 | 286 | 0.0280 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837663 | ATCCTTTT | A | intron_variant | MODIFIER | HG01346.hp1 HG02145.hp2 HG02723.hp1 others(6): Show |
a0001a0002 | a0001c0008a0002c0002a0002c0004others(1): Show | a0001c0008t0001a0002c0002t0002a0002c0002t0011others(4): Show | a0001c0008t0001g0004a0002c0002t0002g0010a0002c0002t0002g0254others(6): Show | 9 | 286 | 0.0315 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0001c0003t0006others(3): Show | a0001c0001t0001g0135a0001c0003t0001g0158a0001c0003t0001g0170others(8): Show | 11 | 286 | 0.0385 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100849220 | TATCACTC | T | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0037a0001c0003t0014a0001c0008t0001others(13): Show | a0001c0001t0037g0041a0001c0003t0014g0234a0001c0003t0014g0235others(26): Show | 29 | 286 | 0.1014 | -7 | c.313 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903710 | ATATATAT | A | intron_variant | MODIFIER | HG01106.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
a0001a0002a0003 | a0001c0008a0002c0002a0003c0007 | a0001c0008t0001a0002c0002t0002a0002c0002t0009others(1): Show | a0001c0008t0001g0004a0002c0002t0002g0252a0002c0002t0009g0035others(4): Show | 7 | 286 | 0.0245 | -7 | c.385 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802753 | CTTTTTTT | C | intron_variant | MODIFIER | HG01109.hp1 HG01517.hp1 HG02109.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0018others(4): Show | a0001c0001t0001g0212a0001c0001t0009g0151a0001c0001t0009g0191others(5): Show | 8 | 230 | 0.0348 | -7 | c.53+ others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802962 | TATATATA | T | intron_variant | MODIFIER | HG01074.hp1 HG02074.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0198a0001c0001t0004g0109 | 2 | 230 | 0.0087 | -7 | c.53+ others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTATTTA | G | intron_variant | MODIFIER | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(11): Show | a0001c0001t0001g0189a0001c0001t0003g0078a0001c0001t0003g0079others(17): Show | 20 | 230 | 0.0870 | -7 | c.54- others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868584 | ATGCATTT | A | intron_variant | MODIFIER | HG02622.hp1 HG03041.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0008a0001c0006t0001 | a0001c0001t0008g0223a0001c0006t0001g0184 | 2 | 230 | 0.0087 | -7 | c.54- others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGAGA | G | intron_variant | MODIFIER | HG01934.hp2 HG02300.hp2 HG02559.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | 230 | 0.0696 | -7 | c.199 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903114 | GAGAGAGA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0112a0001c0001t0003g0056a0001c0001t0004g0217others(6): Show | 9 | 230 | 0.0391 | -7 | c.199 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | CAAAAAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(30): Show |
a0001a0005 | a0001c0001a0005c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(30): Show | 33 | 230 | 0.1435 | -7 | c.152 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | CAAAAAAA | C | intron_variant | MODIFIER | HG02559.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | -7 | c.176 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978678 | CTTTTCTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(37): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0143others(37): Show | 40 | 230 | 0.1739 | -7 | c.176 others(26): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12992357 | TAGCAGCA | T | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(130): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 133 | 230 | 0.5783 | -7 | c.*21 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 715 | chr17 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174616 | CTCTTTCT | C | intron_variant | MODIFIER | NA18944.hp1 NA19005.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025a0001c0001t0001g0037 | 2 | 144 | 0.0139 | -7 | c.162 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174632 | TTTCTTTC | T | intron_variant | MODIFIER | NA19007.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0059 | 1 | 144 | 0.0069 | -7 | c.162 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11266207 | AATCCTCT | A | intron_variant | MODIFIER | NA19056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 144 | 0.0069 | -7 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11287074 | AATTATGT | A | intron_variant | MODIFIER | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0046others(3): Show | 6 | 144 | 0.0417 | -7 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11323866 | CAAAAAAA | C | intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 144 | 0.0069 | -7 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358478 | TTTCTTTC | T | intron_variant | MODIFIER | NA18994.hp1 NA19062.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0022 | a0001c0001t0001g0064a0001c0001t0022g0144 | 2 | 144 | 0.0139 | -7 | c.589 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11454110 | ATTTTTTT | A | intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0049 | 1 | 144 | 0.0069 | -7 | c.589 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11518462 | CTTTTTTT | C | intron_variant | MODIFIER | HG02451.hp1 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | 144 | 0.0139 | -7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11518774 | TCCCTCCC | T | intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0050 | 1 | 144 | 0.0069 | -7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11535878 | AACTATAT | A | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11538841 | TGTGTGTG | T | intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 144 | 0.0069 | -7 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590841 | GAAAAGAA | G | intron_variant | MODIFIER | NA18986.hp1 NA19000.hp1 NA19004.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0007g0076 | 3 | 144 | 0.0208 | -7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590846 | GAAAAGAA | G | intron_variant | MODIFIER | HG02015.hp1 HG02129.hp1 HG03490.hp1 others(2): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0001 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0067others(2): Show | 5 | 144 | 0.0347 | -7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590851 | GAAAAGAA | G | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 144 | 0.0069 | -7 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA | C | intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 144 | 0.0069 | -7 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44782145 | GCCAATGT | G | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
a0001a0002a0006others(1): Show | a0001c0007a0002c0011a0006c0027others(2): Show | a0001c0007t0001a0002c0011t0005a0006c0027t0001others(2): Show | a0001c0007t0001g0058a0001c0007t0001g0202a0002c0011t0005g0061others(4): Show | 7 | 390 | 0.0180 | -7 | c.-71 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44817318 | CCAAAGAG | C | intron_variant | MODIFIER | HG01243.hp1 HG02630.hp1 HG02809.hp1 others(10): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0003a0002c0011others(7): Show | a0001c0001t0001a0002c0003t0004a0002c0011t0005others(7): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0002c0003t0004g0253others(10): Show | 13 | 390 | 0.0333 | -7 | c.386 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44821205 | GCGGATCA | G | intron_variant | MODIFIER | HG01168.hp1 HG01517.hp1 HG02602.hp2 others(1): Show |
a0001a0002 | a0001c0004a0002c0003 | a0001c0004t0001a0001c0004t0003a0002c0003t0004 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0003g0037others(1): Show | 4 | 390 | 0.0103 | -7 | c.387 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT | C | intron_variant | MODIFIER | HG00438.hp2 HG01071.hp2 HG01261.hp1 others(3): Show |
a0001a0003 | a0001c0009a0001c0021a0003c0002 | a0001c0009t0001a0001c0021t0001a0003c0002t0002 | a0001c0009t0001g0077a0001c0009t0001g0205a0001c0021t0001g0014others(3): Show | 6 | 390 | 0.0154 | -7 | c.878 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858450 | CTCTGTCT | C | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(23): Show |
a0002a0004a0008others(3): Show | a0002c0003a0002c0006a0002c0011others(9): Show | a0002c0003t0001a0002c0006t0001a0002c0011t0005others(9): Show | a0002c0003t0001g0106a0002c0003t0001g0387a0002c0006t0001g0059others(23): Show | 26 | 390 | 0.0667 | -7 | c.878 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIA_chr17_81862721_81876337 | 81876006 | CAAAAAAA | C | upstream_gene_variant | MODIFIER | HG01261.hp2 HG02055.hp2 HG02559.hp1 others(9): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0004a0001c0006t0012 | a0001c0001t0001g0005a0001c0001t0004g0013a0001c0001t0004g0042others(1): Show | 12 | 384 | 0.0313 | -7 | c.-47 others(18): Show |
ARHGDIA | ENSG00000141522.12 | transcript | ENST00000269321.12 | protein_coding | 4670 | chr17 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17538282 | CCTGTCTG | C | upstream_gene_variant | MODIFIER | HG01106.hp2 HG01884.hp2 HG02622.hp2 |
a0001 | a0001c0001a0001c0044 | a0001c0001t0001a0001c0001t0005a0001c0044t0004 | a0001c0001t0001g0163a0001c0001t0005g0162a0001c0044t0004g0161 | 3 | 168 | 0.0179 | -7 | c.-17 others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1415 | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1870233 | ATTTTTTT | A | intron_variant | MODIFIER | HG00642.hp1 HG01346.hp1 HG01884.hp1 others(13): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0005others(9): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(11): Show | a0001c0001t0002g0066a0001c0001t0019g0278a0001c0002t0001g0037others(13): Show | 16 | 363 | 0.0441 | -7 | c.679 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120351448 | TATATATA | T | intron_variant | MODIFIER | HG01517.hp2 NA19012.hp1 NA19084.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0219a0001c0001t0001g0236a0001c0001t0001g0259 | 3 | 308 | 0.0097 | -7 | c.32+ others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7347395 | CAAAAAAA | C | upstream_gene_variant | MODIFIER | HG02602.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0012 | a0001c0001t0002a0001c0001t0030a0001c0002t0003others(1): Show | a0001c0001t0002g0070a0001c0001t0030g0008a0001c0002t0003g0121others(3): Show | 6 | 298 | 0.0201 | -7 | c.-19 others(18): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1541 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7350762 | GGGTGGGT | G | intron_variant | MODIFIER | HG01952.hp1 HG03688.hp2 HG03704.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0247a0001c0002t0003g0248a0001c0002t0003g0249 | 3 | 298 | 0.0101 | -7 | c.-11 others(26): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7375354 | AAAGGAAG | A | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
a0001a0009 | a0001c0001a0001c0047a0009c0012 | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(1): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(4): Show | 7 | 298 | 0.0235 | -7 | c.276 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7428384 | GGCCTGTT | G | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp1 HG02622.hp2 others(5): Show |
a0001a0002a0014others(1): Show | a0001c0001a0001c0013a0002c0005others(3): Show | a0001c0001t0030a0001c0013t0001a0002c0005t0001others(3): Show | a0001c0001t0030g0008a0001c0013t0001g0010a0002c0005t0001g0259others(5): Show | 8 | 298 | 0.0269 | -7 | c.968 others(26): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF19_chr1_16192854_16217652 | 16196103 | AAAAAAAC | A | downstream_gene_variant | MODIFIER | HG00544.hp2 HG00741.hp1 HG01069.hp1 others(76): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0002c0009others(1): Show | a0001c0001t0002a0002c0002t0002a0002c0002t0010others(2): Show | a0001c0001t0002g0060a0002c0002t0002g0002a0002c0002t0002g0030others(10): Show | 79 | 362 | 0.2182 | -7 | c.*24 others(18): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1750 | chr1 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154161099 | TTTGTGTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(39): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0207others(37): Show | 42 | 283 | 0.1484 | -7 | c.148 others(26): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73806392 | ATATATAC | A | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02602.hp1 others(4): Show |
a0002a0007a0013others(2): Show | a0002c0002a0002c0006a0007c0009others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(4): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(4): Show | 7 | 188 | 0.0372 | -7 | c.102 others(28): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73828597 | TTCCTTTC | T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA18949.hp1 |
a0004a0022 | a0004c0004a0022c0044 | a0004c0004t0001a0022c0044t0001 | a0004c0004t0001g0187a0004c0004t0001g0188a0022c0044t0001g0123 | 3 | 188 | 0.0160 | -7 | c.102 others(26): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598326 | TTTCTTCC | T | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(35): Show |
a0001a0002a0003others(6): Show | a0001c0002a0002c0001a0003c0003others(6): Show | a0001c0002t0006a0001c0002t0008a0002c0001t0001others(11): Show | a0001c0002t0006g0020a0001c0002t0006g0046a0001c0002t0006g0123others(35): Show | 38 | 394 | 0.0965 | -7 | c.186 others(22): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |