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 | 100798692 | ATATTT | A | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0008a0002c0002t0009others(1): Show | a0002c0002t0002g0139a0002c0002t0008g0028a0002c0002t0008g0029others(3): Show | 6 | 286 | 0.0210 | -5 | c.312 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100816521 | AGATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0005a0002c0002t0006 | a0002c0002t0005g0048a0002c0002t0005g0051a0002c0002t0005g0055others(1): Show | 4 | 286 | 0.0140 | -5 | c.312 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(1): Show | a0001c0001t0001g0136a0001c0001t0001g0279a0001c0001t0002g0025others(19): Show | 22 | 286 | 0.0769 | -5 | c.313 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100863074 | ACACAC | A | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(21): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0010others(5): Show | a0001c0001t0037a0001c0003t0014a0001c0010t0001others(10): Show | a0001c0001t0037g0041a0001c0003t0014g0234a0001c0003t0014g0235others(21): Show | 24 | 286 | 0.0839 | -5 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903710 | ATATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(11): Show |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(2): Show | a0002c0002t0002g0139a0002c0002t0004g0172a0002c0002t0005g0048others(11): Show | 14 | 286 | 0.0490 | -5 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100950288 | ATATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(22): Show |
a0002a0003a0005 | a0002c0002a0002c0006a0003c0007others(1): Show | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(6): Show | a0002c0002t0002g0252a0002c0002t0004g0107a0002c0002t0005g0048others(22): Show | 25 | 286 | 0.0874 | -5 | c.116 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100956595 | AAATAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(50): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(261): Show | 264 | 286 | 0.9231 | -5 | c.116 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTT | C | intron_variant | MODIFIER | HG00733.hp2 HG01109.hp2 HG01978.hp2 others(4): Show |
a0002 | a0002c0002a0002c0006 | a0002c0002t0002a0002c0002t0011a0002c0006t0011 | a0002c0002t0002g0151a0002c0002t0011g0038a0002c0002t0011g0207others(4): Show | 7 | 286 | 0.0245 | -5 | c.245 others(24): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802964 | TATATA | T | intron_variant | MODIFIER | HG02129.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0213a0001c0001t0002g0105 | 2 | 230 | 0.0087 | -5 | c.53+ others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868584 | ATGCAT | A | intron_variant | MODIFIER | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | 230 | 0.0130 | -5 | c.54- others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12886970 | TTTTTG | T | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0136others(48): Show | 51 | 230 | 0.2217 | -5 | 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 | 12900932 | TTTTTA | T | intron_variant | MODIFIER | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0124others(51): Show | 54 | 230 | 0.2348 | -5 | c.198 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGA | G | intron_variant | MODIFIER | HG02074.hp2 HG02129.hp2 NA19074.hp2 |
a0001a0004 | a0001c0004a0004c0016 | a0001c0004t0005a0004c0016t0002 | a0001c0004t0005g0051a0001c0004t0005g0062a0004c0016t0002g0169 | 3 | 230 | 0.0130 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903114 | GAGAGA | G | intron_variant | MODIFIER | HG01070.hp2 HG01258.hp1 HG01517.hp2 others(4): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0028others(1): Show | a0001c0001t0001g0127a0001c0001t0001g0150a0001c0001t0001g0205others(4): Show | 7 | 230 | 0.0304 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903116 | GAGAGA | G | intron_variant | MODIFIER | HG01891.hp2 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009a0001c0001t0003g0074 | 2 | 230 | 0.0087 | -5 | c.199 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12913172 | CAGAAG | C | intron_variant | MODIFIER | HG02071.hp1 HG03831.hp2 HG03942.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0013a0001c0001t0002g0019a0001c0001t0003g0088others(4): Show | 7 | 230 | 0.0304 | -5 | c.276 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1068957 | CTTTAT | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
a0001a0002a0005others(6): Show | a0001c0002a0001c0004a0001c0017others(20): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0013others(34): Show | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0018others(146): Show | 194 | 418 | 0.4641 | -5 | c.421 others(20): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1070505 | TCTTTC | T | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01891.hp1 others(54): Show |
a0002a0004a0005others(8): Show | a0002c0001a0002c0015a0002c0019others(19): Show | a0002c0001t0004a0002c0015t0001a0002c0019t0009others(19): Show | a0002c0001t0004g0006a0002c0001t0004g0010a0002c0001t0004g0032others(44): Show | 57 | 418 | 0.1364 | -5 | c.421 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
a0002a0004a0005others(2): Show | a0002c0001a0002c0015a0002c0021others(8): Show | a0002c0001t0003a0002c0001t0005a0002c0001t0007others(12): Show | a0002c0001t0003g0003a0002c0001t0003g0013a0002c0001t0003g0028others(40): Show | 63 | 418 | 0.1507 | -5 | c.118 others(24): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1077650 | TGCTGG | T | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01978.hp1 others(10): Show |
a0002a0003 | a0002c0001a0002c0015a0002c0031others(2): Show | a0002c0001t0004a0002c0015t0001a0002c0031t0004others(2): Show | a0002c0001t0004g0010a0002c0001t0004g0033a0002c0001t0004g0148others(7): Show | 13 | 418 | 0.0311 | -5 | c.118 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP4_chrX_153902378_153931264 | 153930522 | ACTGGT | A | upstream_gene_variant | MODIFIER | NA19056.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0033 | 1 | 308 | 0.0033 | -5 | c.-43 others(16): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4259 | chrX | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153930725 | CCCCCG | C | upstream_gene_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 308 | 0.0033 | -5 | c.-45 others(16): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4462 | chrX | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32114258 | CTCTTT | C | intron_variant | MODIFIER | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
a0002 | a0002c0003 | a0002c0003t0001a0002c0003t0019 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 3 | 186 | 0.0161 | -5 | c.371 others(24): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32131278 | CTTTAT | C | intron_variant | MODIFIER | HG00609.hp2 HG02809.hp1 |
a0009a0013 | a0009c0014a0013c0017 | a0009c0014t0015a0013c0017t0016 | a0009c0014t0015g0159a0013c0017t0016g0005 | 2 | 186 | 0.0108 | -5 | c.386 others(26): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAA | C | intron_variant | MODIFIER | HG01257.hp2 HG01975.hp1 HG02257.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0115a0001c0001t0002g0039a0001c0001t0002g0103others(3): Show | 6 | 186 | 0.0323 | -5 | c.418 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11138436 | TAAGTG | T | 3_prime_UTR_variant | MODIFIER | HG02895.hp1 | a0003 | a0003c0010 | a0003c0010t0017 | a0003c0010t0017g0119 | 1 | 144 | 0.0069 | -5 | c.*42 others(14): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 13/13 | 422 | chrX | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11174617 | TCTTTC | T | intron_variant | MODIFIER | HG00609.hp1 NA18965.hp1 NA19007.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0019a0002c0002t0009 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(4): Show | 7 | 144 | 0.0486 | -5 | c.162 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11196135 | AAAAAC | A | intron_variant | MODIFIER | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(2): Show | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0043others(5): Show | 8 | 144 | 0.0556 | -5 | c.820 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11210882 | AAAAAC | A | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0141 | 1 | 144 | 0.0069 | -5 | c.749 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11372792 | AAAAAG | A | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 144 | 0.0069 | -5 | c.589 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11464062 | GTTACT | G | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0115 | 1 | 144 | 0.0069 | -5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11484605 | GAAGAA | G | intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0138 | 1 | 144 | 0.0069 | -5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11514161 | CAAAAA | C | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11516199 | GTTTCC | G | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAAA | C | intron_variant | MODIFIER | HG01243.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0004t0005a0002c0002t0006 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0004t0005g0015others(1): Show | 4 | 144 | 0.0278 | -5 | c.588 others(26): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11649982 | CTTTCT | C | intron_variant | MODIFIER | HG03209.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0046a0001c0004t0005g0047 | 2 | 144 | 0.0139 | -5 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11661056 | GAAGAA | G | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0124a0001c0003t0001g0125 | 2 | 144 | 0.0139 | -5 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44749156 | CAAAAA | C | upstream_gene_variant | MODIFIER | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(54): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0007others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(28): Show | a0001c0001t0001g0370a0001c0001t0003g0081a0001c0001t0003g0137others(54): Show | 57 | 390 | 0.1462 | -5 | c.-35 others(16): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3418 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44787321 | CTTTGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(61): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(23): Show | a0001c0001t0001g0097a0001c0001t0003g0006a0001c0001t0003g0063others(61): Show | 64 | 390 | 0.1641 | -5 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44790365 | TTTAAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0004a0001c0007others(56): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(67): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0042others(172): Show | 175 | 390 | 0.4487 | -5 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44790676 | CAAAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG01256.hp1 others(37): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(20): Show | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0003g0074others(37): Show | 40 | 390 | 0.1026 | -5 | c.79+ others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44824607 | GTCTTT | G | intron_variant | MODIFIER | HG02280.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0352a0005c0015t0001g0353a0005c0015t0001g0354others(1): Show | 4 | 390 | 0.0103 | -5 | c.486 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44828425 | ATTTTT | A | intron_variant | MODIFIER | HG01256.hp2 HG02735.hp2 HG02738.hp2 others(8): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0003a0002c0006others(3): Show | a0001c0001t0003a0002c0003t0004a0002c0006t0004others(3): Show | a0001c0001t0003g0089a0002c0003t0004g0055a0002c0003t0004g0234others(8): Show | 11 | 390 | 0.0282 | -5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44830523 | ATTTTC | A | intron_variant | MODIFIER | HG02615.hp2 HG03516.hp2 NA21309.hp2 |
a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0058a0001c0007t0001g0070a0001c0007t0001g0382 | 3 | 390 | 0.0077 | -5 | c.596 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44859222 | GTTGAA | G | intron_variant | MODIFIER | HG02965.hp1 HG03041.hp2 HG03654.hp2 |
a0001a0006 | a0001c0004a0001c0007a0006c0030 | a0001c0004t0001a0001c0007t0001a0006c0030t0001 | a0001c0004t0001g0029a0001c0007t0001g0107a0006c0030t0001g0105 | 3 | 390 | 0.0077 | -5 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP9_chr12_57467269_57484866 | 57473418 | TAAATA | T | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
a0001a0014 | a0001c0001a0001c0008a0014c0017 | a0001c0001t0001a0001c0008t0001a0014c0017t0001 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0070others(3): Show | 11 | 406 | 0.0271 | -5 | c.202 others(22): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 17/17 | chr12 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17537038 | TTTTTA | T | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(147): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0006a0001c0011others(43): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(48): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(147): Show | 150 | 168 | 0.8929 | -5 | c.-29 others(16): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2659 | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17686101 | TCTTTC | T | intron_variant | MODIFIER | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
a0002a0004 | a0002c0034a0002c0041a0004c0005 | a0002c0034t0002a0002c0041t0008a0004c0005t0002 | a0002c0034t0002g0149a0002c0041t0008g0054a0004c0005t0002g0006others(5): Show | 8 | 168 | 0.0476 | -5 | c.301 others(24): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889602 | GAGTGT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(13): Show |
a0001a0005a0006 | a0001c0002a0001c0003a0001c0005others(11): Show | a0001c0002t0001a0001c0003t0020a0001c0005t0001others(12): Show | a0001c0002t0001g0198a0001c0003t0020g0083a0001c0005t0001g0325others(13): Show | 16 | 363 | 0.0441 | -5 | c.118 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1917764 | TTTTTC | T | intron_variant | MODIFIER | HG01074.hp2 HG03486.hp2 HG03540.hp1 |
a0001 | a0001c0003a0001c0020 | a0001c0003t0001a0001c0003t0068a0001c0020t0016 | a0001c0003t0001g0220a0001c0003t0068g0338a0001c0020t0016g0092 | 3 | 363 | 0.0083 | -5 | c.214 others(24): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |