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 | 100980559 | C | CTTCTTTT others(4): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01361.hp2 |
a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0116 a0002c0002t0005g0146 |
2 | 25 | 0.0800 | 11 | c.245 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | NA18957.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0279 | 1 | 24 | 0.0417 | 11 | c.245 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 109 | 0.0092 | 11 | c.54- others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12861653 | T | TTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(13): Show |
a0001 | a0001c0001a0001c0004a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | 176 | 0.0909 | 11 | c.54- others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12861653 | T | TTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0001g0174 a0001c0001t0001g0187 a0001c0001t0003g0028 others(9): Show |
12 | 172 | 0.0698 | 11 | c.54- others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0004 | a0004c0017 | a0004c0017t0003 | a0004c0017t0003g0050 | 1 | 130 | 0.0077 | 11 | c.54- others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12913916 | C | CCAAGTAC others(4): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0010a0001c0008t0020 | a0001c0001t0001g0187 a0001c0001t0010g0186 a0001c0008t0020g0185 |
3 | 228 | 0.0132 | 11 | c.276 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02602.hp1 HG02717.hp1 others(3): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0127 others(3): Show |
6 | 18 | 0.3333 | 11 | c.176 others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01258.hp2 HG02647.hp1 |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0011t0001 | a0001c0001t0001g0188 a0001c0011t0001g0215 |
2 | 137 | 0.0146 | 11 | c.231 others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCCAAAA others(4): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01070.hp2 HG01258.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0003a0003c0013 | a0001c0001t0001a0001c0003t0001a0003c0013t0003 | a0001c0001t0001g0044 a0001c0001t0001g0093 a0001c0001t0001g0118 others(4): Show |
7 | 73 | 0.0959 | 11 | c.231 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCCCAAA others(4): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146 | 1 | 67 | 0.0149 | 11 | c.231 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCGAAAAA others(4): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02647.hp1 |
a0001 | a0001c0006a0001c0011 | a0001c0006t0001a0001c0011t0001 | a0001c0006t0001g0221 a0001c0011t0001g0215 |
2 | 68 | 0.0294 | 11 | c.231 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0021 | a0021c0037 | a0021c0037t0022 | a0021c0037t0022g0173 | 1 | 123 | 0.0081 | 11 | c.118 others(30): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1084625 | C | CCAGGTCA others(4): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0067 | 1 | 416 | 0.0024 | 11 | c.306 others(28): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0160 | 1 | 23 | 0.0435 | 11 | c.418 others(28): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11444740 | A | ACCTTGTT others(4): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01433.hp1 others(19): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0002 | a0001c0001t0001a0001c0006t0001a0002c0002t0003others(2): Show | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(19): Show |
22 | 144 | 0.1528 | 11 | c.589 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11499374 | T | TCTCAACT others(4): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0008a0001c0004t0005others(5): Show | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(22): Show |
25 | 144 | 0.1736 | 11 | c.588 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11518504 | A | AATTTAAG others(4): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02258.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0015 | a0001c0001t0001g0028 a0002c0002t0015g0029 |
2 | 144 | 0.0139 | 11 | c.588 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11526443 | G | GCACCTGC others(4): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(3): Show | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0052 others(6): Show |
9 | 144 | 0.0625 | 11 | c.588 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAGGAAAG others(4): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0001 | 1 | 68 | 0.0147 | 11 | c.588 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590910 | G | GAAAAGAA others(4): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0126 | 1 | 138 | 0.0072 | 11 | c.588 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02698.hp2 HG03710.hp1 NA19011.hp2 |
a0001a0003 | a0001c0008a0001c0010a0003c0002 | a0001c0008t0003a0001c0010t0001a0003c0002t0002 | a0001c0008t0003g0299 a0001c0010t0001g0244 a0003c0002t0002g0329 |
3 | 66 | 0.0455 | 11 | c.-72 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02886.hp1 NA19000.hp2 others(2): Show |
a0002a0003a0008 | a0002c0003a0003c0005a0008c0027 | a0002c0003t0004a0003c0005t0002a0008c0027t0001 | a0002c0003t0004g0120 a0002c0003t0004g0184 a0002c0003t0004g0251 others(2): Show |
5 | 264 | 0.0189 | 11 | c.386 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0009 | a0009c0026 | a0009c0026t0005 | a0009c0026t0005g0262 | 1 | 13 | 0.0769 | 11 | c.596 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44833096 | C | CTTTTCTT others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0024others(15): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(18): Show | a0001c0001t0003g0089 a0001c0001t0003g0157 a0001c0001t0003g0159 others(60): Show |
63 | 285 | 0.2211 | 11 | c.596 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | NA18982.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 59 | 0.0169 | 11 | c.877 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00735.hp2 HG00741.hp1 HG01261.hp2 others(3): Show |
a0001a0005 | a0001c0004a0001c0007a0001c0008others(2): Show | a0001c0004t0001a0001c0007t0001a0001c0008t0001others(2): Show | a0001c0004t0001g0007 a0001c0007t0001g0051 a0001c0008t0001g0275 others(3): Show |
6 | 42 | 0.1429 | 11 | c.878 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858734 | T | TGGGGGGG others(4): Show |
intron_variant | MODIFIER | HG02717.hp1 HG02723.hp2 HG03130.hp1 |
a0002a0009 | a0002c0011a0002c0013a0009c0026 | a0002c0011t0005a0002c0013t0005a0009c0026t0005 | a0002c0011t0005g0086 a0002c0013t0005g0364 a0009c0026t0005g0019 |
3 | 357 | 0.0084 | 11 | c.878 others(26): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44867283 | C | CAAAAAAA others(4): Show |
downstream_gene_variant | MODIFIER | HG03239.hp2 HG03927.hp2 HG04204.hp1 |
a0001a0003a0024 | a0001c0010a0003c0070a0024c0048 | a0001c0010t0001a0003c0070t0002a0024c0048t0001 | a0001c0010t0001g0103 a0003c0070t0002g0146 a0024c0048t0001g0310 |
3 | 133 | 0.0226 | 11 | c.*46 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4500 | chr22 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 285937 | C | CCCCGCGG others(4): Show |
downstream_gene_variant | MODIFIER | HG01952.hp1 NA18989.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001 a0001c0001t0002g0031 |
2 | 391 | 0.0051 | 11 | c.*31 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2928 | chr16 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 285943 | C | CCCCGCGG others(4): Show |
downstream_gene_variant | MODIFIER | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0003 a0001c0001t0003g0005 a0001c0001t0003g0011 others(4): Show |
10 | 434 | 0.0230 | 11 | c.*31 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2934 | chr16 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 285949 | C | CCCCGCGG others(4): Show |
downstream_gene_variant | MODIFIER | HG00738.hp2 HG01943.hp1 HG01981.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0019 | a0001c0001t0001g0002 a0001c0001t0019g0003 |
3 | 392 | 0.0077 | 11 | c.*31 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2940 | chr16 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 286209 | T | TCCCCCCC others(4): Show |
downstream_gene_variant | MODIFIER | HG00323.hp2 HG01074.hp1 HG01981.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0002 a0001c0001t0002g0002 a0001c0001t0002g0033 others(6): Show |
13 | 437 | 0.0297 | 11 | c.*33 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3200 | chr16 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 286212 | C | CCCCCACC others(4): Show |
downstream_gene_variant | MODIFIER | NA18956.hp1 NA19005.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005 | a0001c0001t0004g0006 a0001c0001t0005g0002 |
2 | 440 | 0.0045 | 11 | c.*33 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3203 | chr16 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 287123 | T | TGTCACCC others(4): Show |
downstream_gene_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 440 | 0.0023 | 11 | c.*43 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4114 | chr16 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1823999 | C | CGGCGGGG others(4): Show |
5_prime_UTR_variant | MODIFIER | HG04228.hp2 NA18959.hp1 NA18960.hp1 |
a0001a0002 | a0001c0018a0002c0061 | a0001c0018t0025a0001c0018t0028a0002c0061t0025 | a0001c0018t0025g0297 a0001c0018t0028g0108 a0002c0061t0025g0286 |
3 | 318 | 0.0094 | 11 | c.-16 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19399 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1833315 | A | AGCAGAGG others(4): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(65): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(98): Show | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0002g0069 others(135): Show |
138 | 362 | 0.3812 | 11 | c.-48 others(28): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0296 | 1 | 158 | 0.0063 | 11 | c.679 others(28): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1908227 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0002 | a0002c0024 | a0002c0024t0044 | a0002c0024t0044g0115 | 1 | 143 | 0.0070 | 11 | c.196 others(30): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG01517.hp1 NA18955.hp2 NA18978.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0002 | a0001c0001t0004g0158 a0002c0002t0002g0002 a0002c0002t0002g0050 others(1): Show |
4 | 224 | 0.0179 | 11 | c.463 others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01258.hp1 NA18943.hp1 |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0009 | a0002c0004t0005g0114 a0002c0004t0009g0004 |
3 | 80 | 0.0375 | 11 | c.463 others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAAAAAT others(4): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0002 | a0002c0004 | a0002c0004t0009 | a0002c0004t0009g0121 | 1 | 78 | 0.0128 | 11 | c.463 others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAATATAT others(4): Show |
intron_variant | MODIFIER | HG01169.hp1 HG02071.hp1 NA19011.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0001c0001t0010a0002c0002t0002 | a0001c0001t0004g0154 a0001c0001t0010g0345 a0002c0002t0002g0093 |
3 | 80 | 0.0375 | 11 | c.463 others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | NA19009.hp1 NA19060.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0016 | a0002c0002t0002g0078 a0002c0002t0016g0254 |
2 | 79 | 0.0253 | 11 | c.463 others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156980833 | C | CGGGGGGG others(4): Show |
intron_variant | MODIFIER | HG02258.hp1 NA19030.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0004a0002c0004t0022 | a0001c0001t0004g0133 a0002c0004t0022g0134 |
2 | 154 | 0.0130 | 11 | c.224 others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156991710 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02723.hp2 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0125 a0001c0001t0006g0128 |
2 | 137 | 0.0146 | 11 | c.33- others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347151 | C | CTTTCTTT others(4): Show |
intron_variant | MODIFIER | HG01123.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0007a0001c0002t0016 | a0001c0002t0003g0063 a0001c0002t0007g0042 a0001c0002t0007g0045 others(1): Show |
4 | 260 | 0.0154 | 11 | c.32+ others(26): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120367353 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02040.hp1 HG02155.hp1 HG02647.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0008a0001c0002t0019a0001c0004t0005others(3): Show | a0001c0001t0008g0093 a0001c0002t0019g0012 a0001c0004t0005g0049 others(9): Show |
12 | 83 | 0.1446 | 11 | c.32+ others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00099.hp1 HG01515.hp2 HG01517.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003a0001c0002t0016 | a0001c0001t0002g0102 a0001c0002t0003g0001 a0001c0002t0003g0062 others(3): Show |
7 | 78 | 0.0897 | 11 | c.33- others(26): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120464366 | G | GTCAGGAG others(4): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0190 | 1 | 306 | 0.0033 | 11 | c.261 others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |