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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAA | intron_variant | MODIFIER | HG00639.hp2 HG00673.hp1 HG00738.hp2 others(70): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0008t0005others(10): Show | a0001c0001t0004g0067 a0001c0001t0005g0041 a0001c0008t0005g0073 others(70): Show |
73 | 210 | 0.3476 | 3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAA | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
a0001a0002 | a0001c0001a0001c0008a0001c0010others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(8): Show | a0001c0001t0004g0032 a0001c0001t0004g0035 a0001c0001t0004g0036 others(31): Show |
34 | 172 | 0.1977 | 3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31928535 | G | GCGC | intron_variant | MODIFIER | HG00673.hp2 HG01934.hp2 NA21309.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0007 | a0001c0001t0001g0235 a0001c0001t0005g0234 a0002c0002t0007g0319 |
3 | 320 | 0.0094 | 3 | c.-11 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31931501 | T | TTTG | upstream_gene_variant | MODIFIER | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(7): Show |
10 | 320 | 0.0313 | 3 | c.-29 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2671 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143153828 | T | TTCC | intron_variant | MODIFIER | HG00621.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | 144 | 0.0347 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153831 | T | TTCC | intron_variant | MODIFIER | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0061 others(7): Show |
10 | 149 | 0.0671 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153834 | T | TTCC | intron_variant | MODIFIER | HG02074.hp1 HG02074.hp2 HG02129.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(6): Show |
9 | 130 | 0.0692 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153840 | T | TTCC | intron_variant | MODIFIER | HG02280.hp1 HG02602.hp1 HG02886.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0123 others(3): Show |
6 | 76 | 0.0789 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153873 | T | TTCC | intron_variant | MODIFIER | NA18962.hp2 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 a0001c0001t0001g0153 |
2 | 116 | 0.0172 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153876 | C | CTCT | intron_variant | MODIFIER | HG00738.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 a0001c0001t0001g0120 a0001c0001t0001g0128 others(1): Show |
4 | 127 | 0.0315 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | C | CATT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0021 others(23): Show |
26 | 59 | 0.4407 | 3 | c.166 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143218277 | C | CTTT | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0001g0100 others(3): Show |
6 | 95 | 0.0632 | 3 | c.296 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143235242 | G | GTTT | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0034 others(20): Show |
23 | 148 | 0.1554 | 3 | c.384 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAA | intron_variant | MODIFIER | HG02698.hp1 HG02698.hp2 NA18970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 a0001c0001t0001g0066 a0001c0001t0001g0071 others(2): Show |
5 | 21 | 0.2381 | 3 | c.385 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143270963 | C | CTGA | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(53): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(53): Show |
56 | 160 | 0.3500 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143291452 | G | GTTC | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(104): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
107 | 160 | 0.6688 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143296776 | G | GTAT | intron_variant | MODIFIER | HG02109.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0055 others(5): Show |
8 | 160 | 0.0500 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | C | CTTT | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | 75 | 0.0800 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143323894 | C | CAAA | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01261.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0106 others(3): Show |
6 | 49 | 0.1224 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143330094 | C | CAAA | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG01358.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0112 others(4): Show |
7 | 94 | 0.0745 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143330132 | C | CAAA | intron_variant | MODIFIER | HG02886.hp2 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003 a0001c0002t0001g0105 |
2 | 55 | 0.0364 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143345252 | A | AGAG | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(143): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
146 | 160 | 0.9125 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143389106 | C | CATT | intron_variant | MODIFIER | HG03139.hp1 HG06807.hp2 NA18947.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0048 others(7): Show |
10 | 121 | 0.0826 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143390008 | T | TAAA | intron_variant | MODIFIER | HG02976.hp1 HG03491.hp2 NA18991.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 a0001c0001t0001g0067 a0001c0001t0001g0083 others(2): Show |
5 | 116 | 0.0431 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143428780 | G | GTAA | intron_variant | MODIFIER | HG00621.hp2 HG01496.hp1 HG02148.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0073 others(4): Show |
7 | 160 | 0.0438 | 3 | c.475 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143433739 | A | ATGT | intron_variant | MODIFIER | HG01261.hp1 HG02071.hp1 HG02109.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(13): Show |
16 | 160 | 0.1000 | 3 | c.475 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143445153 | A | ATTT | intron_variant | MODIFIER | HG00621.hp1 HG01243.hp1 HG02074.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0083 others(7): Show |
10 | 16 | 0.6250 | 3 | c.703 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143461281 | C | CAAA | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0033 others(14): Show |
17 | 22 | 0.7727 | 3 | c.703 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143465706 | A | AAAT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(141): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | 160 | 0.9000 | 3 | c.704 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143484365 | C | CAAA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0019 others(29): Show |
32 | 71 | 0.4507 | 3 | c.704 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143506460 | A | AATT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(59): Show |
62 | 160 | 0.3875 | 3 | c.827 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAA | intron_variant | MODIFIER | HG01261.hp1 HG02129.hp2 HG02258.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | 101 | 0.1188 | 3 | c.100 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143625465 | T | TTGC | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(30): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | 160 | 0.2063 | 3 | c.113 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143721061 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG02258.hp1 HG03491.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0046 others(2): Show |
5 | 34 | 0.1471 | 3 | c.124 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143732910 | G | GTTT | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0098 others(2): Show |
5 | 96 | 0.0521 | 3 | c.124 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | C | CTTT | downstream_gene_variant | MODIFIER | HG01074.hp1 HG01123.hp1 HG02257.hp1 others(7): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0028 others(7): Show |
10 | 55 | 0.1818 | 3 | c.*37 others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24926109 | G | GAAA | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0031 a0001c0001t0005g0004 a0001c0001t0005g0228 others(1): Show |
5 | 192 | 0.0260 | 3 | c.251 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24942767 | C | CAAA | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0023 a0001c0001t0001g0119 a0001c0003t0003g0208 others(7): Show |
10 | 194 | 0.0515 | 3 | c.133 others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961968 | G | GTTT | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | 231 | 0.0952 | 3 | c.574 others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982997 | T | TATA | intron_variant | MODIFIER | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0001g0172 others(8): Show |
11 | 158 | 0.0696 | 3 | c.54- others(18): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25003038 | C | CAAA | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0001a0001c0001t0006a0003c0006t0005 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(46): Show |
52 | 170 | 0.3059 | 3 | c.53+ others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25003230 | C | CTTT | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0005a0001c0003t0003 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0003t0003g0208 others(1): Show |
5 | 120 | 0.0417 | 3 | c.53+ others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25008963 | G | GGAC | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
a0001 | a0001c0003a0001c0005 | a0001c0003t0003a0001c0005t0001 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(7): Show |
10 | 238 | 0.0420 | 3 | c.53+ others(18): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129571677 | G | GCAC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(67): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0009a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(67): Show |
70 | 236 | 0.2966 | 3 | c.*68 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4454 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129575104 | T | TAAA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(56): Show |
a0001a0002a0006 | a0001c0001a0001c0009a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(56): Show |
59 | 228 | 0.2588 | 3 | c.*34 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1027 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129588121 | C | CTTT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0071 others(75): Show |
78 | 185 | 0.4216 | 3 | c.171 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129588454 | T | TCCA | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(1): Show | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(8): Show |
11 | 236 | 0.0466 | 3 | c.171 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129613844 | G | GTTT | intron_variant | MODIFIER | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(9): Show | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(22): Show |
25 | 236 | 0.1059 | 3 | c.104 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129622716 | T | TAAG | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | 236 | 0.2415 | 3 | c.787 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625054 | T | TATA | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0011a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(91): Show |
95 | 224 | 0.4241 | 3 | c.786 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar |