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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 147798781 | CTATATA | C | intron_variant | MODIFIER | HG03130.hp2 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 a0001c0001t0001g0042 |
2 | 57 | 0.0351 | -6 | c.155 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147830512 | CTTTTTT | C | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(33): Show |
36 | 54 | 0.6667 | -6 | c.312 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147843517 | TTTTTTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0046 others(8): Show |
11 | 103 | 0.1068 | -6 | c.313 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147852725 | TTTTTTA | T | intron_variant | MODIFIER | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0038 a0001c0001t0001g0076 a0001c0004t0001g0045 others(1): Show |
4 | 104 | 0.0385 | -6 | c.385 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | TTGTGTG | T | intron_variant | MODIFIER | HG01243.hp2 HG01261.hp2 HG01993.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0023 others(7): Show |
10 | 73 | 0.1370 | -6 | c.702 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | CTGTGTG | C | intron_variant | MODIFIER | HG03098.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0081 a0001c0004t0001g0102 |
2 | 14 | 0.1429 | -6 | c.703 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147899339 | GTGTGTC | G | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 a0001c0001t0001g0093 a0001c0001t0001g0099 others(2): Show |
5 | 104 | 0.0481 | -6 | c.103 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AATATAT | A | intron_variant | MODIFIER | HG02145.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0061 others(1): Show |
4 | 6 | 0.6667 | -6 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148039368 | ATTTTTT | A | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0011others(2): Show | a0001c0001t0001a0001c0006t0001a0001c0011t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0046 others(17): Show |
20 | 63 | 0.3175 | -6 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | AATATAT | A | intron_variant | MODIFIER | HG02895.hp1 NA18983.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0006 a0001c0002t0001g0012 |
2 | 11 | 0.1818 | -6 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | AGTGTGT | A | downstream_gene_variant | MODIFIER | HG01081.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0002c0002t0001g0009 |
6 | 72 | 0.0833 | -6 | c.*12 others(17): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | TCACACA | T | 3_prime_UTR_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(18): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0005a0001c0001t0011a0001c0008t0005 | a0001c0001t0005g0041 a0001c0001t0005g0043 a0001c0001t0005g0044 others(18): Show |
21 | 50 | 0.4200 | -6 | c.*20 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2004 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31820712 | TTATATA | T | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(62): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(14): Show | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(61): Show |
65 | 126 | 0.5159 | -6 | c.153 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862699 | CACACAG | C | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG01346.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(1): Show | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0102 others(10): Show |
13 | 320 | 0.0406 | -6 | c.685 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | GACACAC | G | intron_variant | MODIFIER | HG01167.hp2 HG01168.hp1 HG01175.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(3): Show | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | 140 | 0.0786 | -6 | c.685 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | TCACACA | T | intron_variant | MODIFIER | HG01106.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(4): Show | a0001c0001t0003g0186 a0001c0001t0006g0151 a0001c0001t0006g0156 others(7): Show |
10 | 69 | 0.1449 | -6 | c.-11 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | CATATAT | C | upstream_gene_variant | MODIFIER | HG00597.hp1 HG00673.hp1 HG00738.hp2 others(46): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0043others(8): Show | a0001c0001t0001g0202 a0001c0001t0003g0193 a0001c0001t0043g0024 others(46): Show |
49 | 143 | 0.3427 | -6 | c.-46 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143127149 | AAAAAAG | A | upstream_gene_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(46): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0110 others(46): Show |
49 | 160 | 0.3063 | -6 | c.-23 others(17): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2269 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143145839 | GGTGTGT | G | intron_variant | MODIFIER | HG01071.hp2 HG01255.hp1 HG01255.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(22): Show |
25 | 49 | 0.5102 | -6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153777 | ATCTTCT | A | intron_variant | MODIFIER | HG00642.hp2 HG01496.hp1 HG01515.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 a0001c0001t0001g0087 a0001c0001t0001g0092 others(5): Show |
8 | 130 | 0.0615 | -6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | CATTATT | C | intron_variant | MODIFIER | HG00733.hp1 HG01243.hp1 HG01256.hp1 others(28): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(28): Show |
31 | 64 | 0.4844 | -6 | c.166 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143207495 | AACACAC | A | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(25): Show |
28 | 93 | 0.3011 | -6 | c.234 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143225705 | TTAAATC | T | intron_variant | MODIFIER | HG02886.hp1 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 a0001c0001t0001g0101 |
2 | 160 | 0.0125 | -6 | c.297 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTTTTT | C | intron_variant | MODIFIER | HG00733.hp2 HG01071.hp2 HG01081.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0030 others(10): Show |
13 | 33 | 0.3939 | -6 | c.474 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143308935 | CAAAAAA | C | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0103 others(2): Show |
5 | 37 | 0.1351 | -6 | c.474 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | CTTTTTT | C | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(13): Show |
16 | 85 | 0.1882 | -6 | c.474 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346170 | ACACTCT | A | intron_variant | MODIFIER | HG00741.hp2 HG01496.hp2 HG02148.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0052 others(9): Show |
12 | 160 | 0.0750 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346216 | TCTCTCA | T | intron_variant | MODIFIER | HG02723.hp2 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | 160 | 0.0125 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | ATGTGTG | A | intron_variant | MODIFIER | HG02886.hp2 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003 a0001c0002t0001g0105 |
2 | 51 | 0.0392 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143390731 | GCACACA | G | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
52 | 56 | 0.9286 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | GTATATA | G | intron_variant | MODIFIER | HG00609.hp1 HG03139.hp2 NA18955.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0100 |
3 | 59 | 0.0508 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143416831 | CCCCACG | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(46): Show |
49 | 160 | 0.3063 | -6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143478706 | TTATAAA | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG01071.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(25): Show |
28 | 160 | 0.1750 | -6 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143510018 | TAAAAAA | T | intron_variant | MODIFIER | HG01243.hp2 HG03139.hp2 NA18970.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0100 others(2): Show |
5 | 41 | 0.1220 | -6 | c.827 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143605858 | CAAAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00733.hp2 HG01358.hp2 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
23 | 41 | 0.5610 | -6 | c.100 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143607548 | CGAGAGA | C | intron_variant | MODIFIER | NA18970.hp1 NA18975.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 a0001c0001t0001g0066 |
2 | 100 | 0.0200 | -6 | c.100 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143631861 | GACTAAT | G | intron_variant | MODIFIER | HG00741.hp1 HG01071.hp2 HG01255.hp1 others(25): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(25): Show |
28 | 160 | 0.1750 | -6 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | GGTGTGT | G | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(25): Show |
28 | 37 | 0.7568 | -6 | c.113 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143679654 | CGTGTGT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(42): Show |
45 | 75 | 0.6000 | -6 | c.113 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143713695 | AAGTGGG | A | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01071.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(26): Show |
29 | 160 | 0.1813 | -6 | c.124 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143763722 | GTATGTA | G | intron_variant | MODIFIER | HG02109.hp1 HG03225.hp2 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0106 |
3 | 160 | 0.0188 | -6 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | CTTTTTT | C | downstream_gene_variant | MODIFIER | HG01928.hp1 HG02293.hp2 HG02300.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0001 | a0001c0001t0005g0114 a0001c0001t0005g0228 a0001c0002t0001g0032 others(4): Show |
7 | 52 | 0.1346 | -6 | c.*37 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916784 | GTATATA | G | downstream_gene_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
45 | 191 | 0.2356 | -6 | c.*33 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2604 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916818 | GCACACA | G | downstream_gene_variant | MODIFIER | HG00597.hp2 HG01069.hp1 HG01099.hp1 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(30): Show |
34 | 121 | 0.2810 | -6 | c.*33 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2570 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24952113 | AATAATT | A | intron_variant | MODIFIER | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | 238 | 0.0210 | -6 | c.104 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982996 | ATTTTTT | A | intron_variant | MODIFIER | HG02040.hp1 HG02074.hp2 HG02622.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0122 others(2): Show |
5 | 185 | 0.0270 | -6 | c.54- others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25015910 | GAAAAAA | G | upstream_gene_variant | MODIFIER | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0226 a0001c0001t0005g0004 a0001c0001t0005g0228 others(1): Show |
5 | 106 | 0.0472 | -6 | c.-65 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 542 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020123 | AAGAGAG | A | upstream_gene_variant | MODIFIER | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
7 | 118 | 0.0593 | -6 | c.-48 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4755 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625419 | AATATAT | A | intron_variant | MODIFIER | HG01071.hp1 HG01169.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | 182 | 0.0110 | -6 | c.786 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625957 | ATATATT | A | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0002c0002t0001others(1): Show | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(10): Show |
13 | 236 | 0.0551 | -6 | c.786 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar |