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 | 100806837 | G | GTTTATTT others(5): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0004a0002c0002t0008 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0004g0174 others(1): Show |
4 | 67 | 0.0597 | 12 | c.312 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | G | GTTTGTTT others(5): Show |
intron_variant | MODIFIER | HG01346.hp1 HG02257.hp2 HG02818.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0008 | a0002c0002t0002g0010 a0002c0002t0008g0005 a0002c0002t0008g0230 |
3 | 66 | 0.0455 | 12 | c.312 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG00597.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0009 | a0001c0001t0001a0001c0001t0006a0001c0001t0041others(1): Show | a0001c0001t0001g0074 a0001c0001t0001g0092 a0001c0001t0001g0101 others(11): Show |
14 | 47 | 0.2979 | 12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01346.hp2 HG03239.hp2 HG04199.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0024a0002c0004t0007 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0001g0132 others(6): Show |
9 | 129 | 0.0698 | 12 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0006others(13): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0080 others(57): Show |
60 | 215 | 0.2791 | 12 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01123.hp2 HG01257.hp2 others(39): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(5): Show | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0066 others(39): Show |
42 | 71 | 0.5915 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACAC others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(12): Show |
a0001a0002a0003 | a0001c0008a0002c0002a0002c0004others(2): Show | a0001c0008t0001a0002c0002t0004a0002c0002t0005others(6): Show | a0001c0008t0001g0004 a0002c0002t0004g0113 a0002c0002t0004g0174 others(12): Show |
15 | 54 | 0.2778 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(5): Show |
intron_variant | MODIFIER | HG01928.hp1 HG01934.hp2 HG02165.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0011 a0001c0001t0001g0092 a0001c0001t0001g0098 others(4): Show |
7 | 46 | 0.1522 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCAC others(5): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0238 | 1 | 40 | 0.0250 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01496.hp1 HG01981.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0150 a0002c0002t0002g0194 |
2 | 263 | 0.0076 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02280.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0017 a0002c0002t0002g0090 |
2 | 69 | 0.0290 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0097 | 1 | 68 | 0.0147 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0002 | a0002c0006 | a0002c0006t0011 | a0002c0006t0011g0241 | 1 | 68 | 0.0147 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(5): Show |
intron_variant | MODIFIER | HG00597.hp1 HG01192.hp2 HG03239.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0024 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0104 others(7): Show |
10 | 77 | 0.1299 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100908087 | G | GTAGTAAA others(5): Show |
intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0110 | 1 | 284 | 0.0035 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0085 | 1 | 4 | 0.2500 | 12 | c.486 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACACACA others(5): Show |
intron_variant | MODIFIER | HG01070.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0017a0002c0002t0018a0002c0011t0017 | a0002c0002t0017g0044 a0002c0002t0018g0205 a0002c0002t0018g0206 others(1): Show |
4 | 150 | 0.0267 | 12 | c.703 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100952734 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02976.hp1 HG03688.hp1 |
a0002 | a0002c0002a0002c0004 | a0002c0002t0009a0002c0004t0007 | a0002c0002t0009g0033 a0002c0004t0007g0122 |
2 | 21 | 0.0952 | 12 | c.116 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100972516 | T | TTGGATGG others(5): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0007 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0002c0004t0007g0014 others(6): Show |
9 | 155 | 0.0581 | 12 | c.155 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(5): Show |
intron_variant | MODIFIER | HG01109.hp1 HG03017.hp2 NA18522.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0005a0002c0002t0008 | a0002c0002t0002g0119 a0002c0002t0005g0117 a0002c0002t0008g0177 |
3 | 26 | 0.1154 | 12 | c.245 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | A | AAAATAAA others(5): Show |
intron_variant | MODIFIER | HG01256.hp2 HG02129.hp2 HG03834.hp1 others(13): Show |
a0001a0006 | a0001c0001a0006c0017 | a0001c0001t0001a0006c0017t0001 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0023 others(13): Show |
16 | 45 | 0.3556 | 12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100987843 | A | AAATAAAT others(5): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0244 | 1 | 284 | 0.0035 | 12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100995655 | G | GAATAAAT others(5): Show |
downstream_gene_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(4): Show | a0001c0001t0001a0001c0008t0010a0002c0002t0002others(12): Show | a0001c0001t0001g0023 a0001c0001t0001g0124 a0001c0001t0001g0187 others(53): Show |
56 | 74 | 0.7568 | 12 | c.*68 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12796136 | A | ATATCTAT others(5): Show |
intron_variant | MODIFIER | HG03139.hp1 HG03486.hp1 NA18906.hp1 |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0003a0001c0005t0001a0001c0006t0003 | a0001c0001t0003g0090 a0001c0005t0001g0173 a0001c0006t0003g0091 |
3 | 4 | 0.7500 | 12 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG03491.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0002g0016 others(6): Show |
9 | 128 | 0.0703 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841577 | G | GTCTGTCT others(5): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01081.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0002t0003 | a0001c0001t0003g0055 a0001c0001t0003g0079 a0001c0001t0003g0080 others(2): Show |
5 | 213 | 0.0235 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841585 | G | GTCTCTCT others(5): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0090 | 1 | 189 | 0.0053 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(5): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00673.hp2 HG01928.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(16): Show |
19 | 142 | 0.1338 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(5): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02886.hp2 HG03453.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(1): Show | a0001c0001t0001g0033 a0001c0001t0010g0032 a0001c0001t0014g0178 others(1): Show |
4 | 127 | 0.0315 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12841639 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0228 | 1 | 226 | 0.0044 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG02071.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0017 others(6): Show |
9 | 112 | 0.0804 | 12 | c.54- others(29): 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(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(30): Show |
33 | 193 | 0.1710 | 12 | c.54- others(29): 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(5): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03831.hp2 HG03942.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0002g0019 others(4): Show |
7 | 167 | 0.0419 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATATAT others(5): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02572.hp1 HG03239.hp2 |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0003t0001a0001c0008t0020 | a0001c0001t0001g0187 a0001c0003t0001g0211 a0001c0008t0020g0185 |
3 | 132 | 0.0227 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GGAGAGAG others(5): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0177 | 1 | 143 | 0.0070 | 12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 107 | 0.0093 | 12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0070 | 1 | 40 | 0.0250 | 12 | c.582 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02451.hp1 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0025others(1): Show | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0003g0090 others(2): Show |
5 | 44 | 0.1136 | 12 | c.582 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG03942.hp2 NA18989.hp1 |
a0001a0004 | a0001c0009a0004c0017 | a0001c0009t0002a0004c0017t0003 | a0001c0009t0002g0104 a0004c0017t0003g0050 |
2 | 44 | 0.0455 | 12 | c.862 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0130 | 1 | 131 | 0.0076 | 12 | c.176 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02145.hp2 HG03486.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0027a0001c0006t0003 | a0001c0001t0027g0222 a0001c0006t0003g0091 |
2 | 14 | 0.1429 | 12 | c.176 others(31): 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(5): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0208 | 1 | 136 | 0.0074 | 12 | c.231 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCAAAAA others(5): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0222 | 1 | 67 | 0.0149 | 12 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCCAAAA others(5): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02300.hp1 HG04228.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0147 others(1): Show |
4 | 70 | 0.0571 | 12 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32148163 | A | AATCTATC others(5): Show |
intron_variant | MODIFIER | HG02738.hp2 HG03516.hp1 HG03654.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0050 a0001c0001t0001g0128 a0001c0001t0001g0175 others(1): Show |
4 | 60 | 0.0667 | 12 | c.394 others(31): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTCCTT others(5): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02145.hp1 HG02300.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0003c0007t0012 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0120 others(1): Show |
4 | 77 | 0.0519 | 12 | c.162 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATATATA others(5): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG02622.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0067 others(8): Show |
11 | 43 | 0.2558 | 12 | c.162 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | C | CATATATA others(5): Show |
intron_variant | MODIFIER | HG02809.hp2 NA18961.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0093 a0001c0001t0013g0050 |
2 | 14 | 0.1429 | 12 | c.162 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | C | CTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01261.hp1 HG02132.hp1 others(8): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(3): Show | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0057 others(8): Show |
11 | 18 | 0.6111 | 12 | c.749 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11266033 | C | CTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0047 | 1 | 92 | 0.0109 | 12 | c.589 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |