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 | 31855108 | GAGGGA | G | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0017others(1): Show | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(15): Show |
18 | 319 | 0.0564 | -5 | c.949 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31880490 | GTTTAA | G | intron_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG01071.hp2 others(50): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0007a0002c0002t0014others(5): Show | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0249 others(50): Show |
53 | 320 | 0.1656 | -5 | c.685 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31924702 | TCATAA | T | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(7): Show | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0094 others(66): Show |
69 | 320 | 0.2156 | -5 | c.-11 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143209945 | CTAGAG | C | intron_variant | MODIFIER | HG01361.hp1 HG01515.hp2 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 a0001c0001t0001g0126 a0001c0001t0001g0143 |
3 | 160 | 0.0188 | -5 | c.235 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143213514 | AAAAAT | A | intron_variant | MODIFIER | HG00642.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0107 others(3): Show |
6 | 160 | 0.0375 | -5 | c.235 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143261325 | CTTTTT | C | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02886.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 a0001c0001t0001g0096 a0001c0001t0001g0101 others(3): Show |
6 | 69 | 0.0870 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTTTT | C | intron_variant | MODIFIER | HG00738.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0045 others(13): Show |
16 | 36 | 0.4444 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143317930 | TTTTTG | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
14 | 160 | 0.0875 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | CTTTTT | C | intron_variant | MODIFIER | HG01071.hp2 HG02698.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0027 others(3): Show |
6 | 75 | 0.0800 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143364219 | ACATTC | A | intron_variant | MODIFIER | HG02074.hp2 HG02129.hp1 HG02523.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
10 | 160 | 0.0625 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143411425 | TCAAAA | T | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0101 others(2): Show |
5 | 160 | 0.0313 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143419583 | ATATGT | A | intron_variant | MODIFIER | HG02258.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0106 |
2 | 160 | 0.0125 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143439422 | CAAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(42): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(42): Show |
45 | 52 | 0.8654 | -5 | 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 | 143453075 | TTAATC | T | intron_variant | MODIFIER | HG01261.hp1 HG02071.hp1 HG02280.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(7): Show |
10 | 160 | 0.0625 | -5 | c.703 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143457974 | GATAAA | G | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | 160 | 0.0250 | -5 | c.703 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143495705 | ATTGAG | A | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(22): Show |
25 | 160 | 0.1563 | -5 | c.826 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143555860 | AAGAAT | A | intron_variant | MODIFIER | HG01069.hp2 HG01358.hp1 HG01361.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0056 others(16): Show |
19 | 41 | 0.4634 | -5 | c.926 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143601668 | TTTCTA | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0137 |
3 | 160 | 0.0188 | -5 | c.100 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143667629 | GTTAAT | G | intron_variant | MODIFIER | HG01071.hp2 HG02071.hp2 HG02698.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(3): Show |
6 | 160 | 0.0375 | -5 | c.113 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAA | C | intron_variant | MODIFIER | HG02129.hp1 NA18947.hp1 NA18962.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0115 others(4): Show |
7 | 18 | 0.3889 | -5 | c.113 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143710154 | CTCTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(34): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0020 others(34): Show |
37 | 160 | 0.2313 | -5 | 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 | 24982996 | ATTTTT | A | intron_variant | MODIFIER | HG00642.hp2 HG01261.hp1 HG01358.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0133 others(2): Show |
5 | 185 | 0.0270 | -5 | c.54- others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129580322 | TTAAAA | T | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0004a0004c0008t0004 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | 236 | 0.0169 | -5 | c.183 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129585301 | AAAAAT | A | intron_variant | MODIFIER | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | 236 | 0.0127 | -5 | c.171 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129607593 | CTATTA | C | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | 236 | 0.0339 | -5 | c.128 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625091 | TATATG | T | intron_variant | MODIFIER | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(17): Show |
20 | 236 | 0.0847 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625311 | TATGTA | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | 236 | 0.0085 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625327 | TATATG | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | 236 | 0.0085 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625364 | TATTTA | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | 235 | 0.0085 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625729 | TATTTA | T | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | 236 | 0.2119 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625935 | ATATAT | A | intron_variant | MODIFIER | HG02451.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0010a0003c0004t0001others(1): Show | a0001c0001t0002g0145 a0001c0001t0010g0136 a0003c0004t0001g0151 others(1): Show |
4 | 236 | 0.0169 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129655337 | AAAAAG | A | intron_variant | MODIFIER | HG02004.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(1): Show | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0091 others(5): Show |
8 | 171 | 0.0468 | -5 | c.114 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129659456 | TTTTTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(109): Show |
113 | 235 | 0.4809 | -5 | c.114 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129683050 | TTTTTC | T | intron_variant | MODIFIER | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | 236 | 0.0254 | -5 | c.113 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129695821 | TAAAAG | T | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
67 | 236 | 0.2839 | -5 | c.113 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97251753 | AGAAGG | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(27): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(27): Show |
30 | 228 | 0.1316 | -5 | c.927 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97259828 | CTGTTT | C | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0002a0001c0001t0006a0005c0007t0006 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | 60 | 0.1000 | -5 | c.614 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110596975 | GTTCAT | G | intron_variant | MODIFIER | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
a0007a0011a0013 | a0007c0018a0011c0015a0013c0019 | a0007c0018t0015a0011c0015t0004a0013c0019t0004 | a0007c0018t0015g0009 a0011c0015t0004g0151 a0013c0019t0004g0149 |
3 | 224 | 0.0134 | -5 | c.965 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110628742 | AAAGTT | A | intron_variant | MODIFIER | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
a0001a0003a0012 | a0001c0001a0003c0004a0012c0017 | a0001c0001t0001a0003c0004t0002a0012c0017t0002 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | 224 | 0.0179 | -5 | c.353 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110689521 | ATAAAT | A | intron_variant | MODIFIER | HG02622.hp2 HG03540.hp2 |
a0005 | a0005c0007 | a0005c0007t0010 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | 224 | 0.0089 | -5 | c.188 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAA | C | downstream_gene_variant | MODIFIER | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0169 others(3): Show |
6 | 32 | 0.1875 | -5 | c.*35 others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24587827 | TTACTC | T | intron_variant | MODIFIER | HG02145.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
a0001a0005 | a0001c0001a0001c0014a0005c0005 | a0001c0001t0001a0001c0014t0004a0005c0005t0004 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | 350 | 0.0171 | -5 | c.418 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24598528 | TAAGAG | T | intron_variant | MODIFIER | HG00642.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | 350 | 0.0171 | -5 | c.313 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24615771 | ATTATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
a0002a0005a0015others(3): Show | a0002c0002a0002c0015a0002c0017others(8): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(12): Show | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(131): Show |
134 | 350 | 0.3829 | -5 | c.242 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24649962 | AAACTT | A | intron_variant | MODIFIER | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
a0002a0015 | a0002c0002a0002c0017a0015c0020 | a0002c0002t0001a0002c0002t0014a0002c0017t0001others(1): Show | a0002c0002t0001g0020 a0002c0002t0001g0107 a0002c0002t0001g0108 others(14): Show |
17 | 350 | 0.0486 | -5 | c.269 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24683095 | CAAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
a0001a0002a0004others(4): Show | a0001c0001a0002c0002a0002c0021others(5): Show | a0001c0001t0001a0001c0001t0013a0002c0002t0001others(8): Show | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(62): Show |
65 | 338 | 0.1923 | -5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAA | C | intron_variant | MODIFIER | HG01081.hp1 HG01258.hp2 HG01928.hp2 others(11): Show |
a0001a0003a0013 | a0001c0001a0003c0006a0013c0026 | a0001c0001t0002a0001c0001t0016a0003c0006t0002others(1): Show | a0001c0001t0002g0001 a0001c0001t0002g0308 a0001c0001t0002g0309 others(10): Show |
14 | 16 | 0.8750 | -5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24702127 | CTTTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
a0002a0004a0012others(1): Show | a0002c0002a0004c0004a0012c0019others(1): Show | a0002c0002t0001a0004c0004t0001a0012c0019t0001others(1): Show | a0002c0002t0001g0071 a0002c0002t0001g0086 a0002c0002t0001g0137 others(10): Show |
13 | 75 | 0.1733 | -5 | c.63+ others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48441421 | CAGAAG | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0055 others(113): Show |
117 | 268 | 0.4366 | -5 | c.*49 others(16): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4614 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38446181 | ATTTTT | A | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
a0001a0003a0007 | a0001c0004a0001c0009a0001c0010others(3): Show | a0001c0004t0001a0001c0009t0003a0001c0010t0001others(3): Show | a0001c0004t0001g0059 a0001c0004t0001g0071 a0001c0004t0001g0170 others(8): Show |
11 | 75 | 0.1467 | -5 | c.64- others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |