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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP17_chr16_24914389_25020369 | 24961968 | G | GTTTTT | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | 216 | 0.0324 | 5 | c.574 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961972 | G | GTTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(72): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(67): Show |
75 | 182 | 0.4121 | 5 | c.574 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982997 | T | TATATA | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0055 others(13): Show |
19 | 166 | 0.1145 | 5 | c.54- others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625136 | T | TATATG | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 HG03195.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(1): Show | a0001c0001t0002g0145 a0001c0001t0007g0077 a0001c0001t0010g0136 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 | 129625178 | T | TATTTA | intron_variant | MODIFIER | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0011t0001others(1): Show | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | 226 | 0.0221 | 5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625386 | T | TATATG | intron_variant | MODIFIER | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0002c0002t0005 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | 236 | 0.0127 | 5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97250747 | A | ATATAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(225): Show |
228 | 239 | 0.9540 | 5 | c.928 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97251539 | A | AAGGGG | intron_variant | MODIFIER | NA19012.hp2 NA19064.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 a0001c0001t0001g0198 |
2 | 240 | 0.0083 | 5 | c.927 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97259828 | C | CTGTTT | intron_variant | MODIFIER | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | 62 | 0.1290 | 5 | c.614 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110711005 | C | CAAAAA | intron_variant | MODIFIER | HG00621.hp1 HG03098.hp1 HG03834.hp1 others(2): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0002 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | 126 | 0.0397 | 5 | c.105 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24600132 | C | CAAAAA | intron_variant | MODIFIER | HG02129.hp2 HG02523.hp2 HG02818.hp1 others(4): Show |
a0001a0006a0020 | a0001c0001a0006c0007a0006c0029others(1): Show | a0001c0001t0001a0006c0007t0006a0006c0007t0015others(2): Show | a0001c0001t0001g0144 a0006c0007t0006g0292 a0006c0007t0006g0293 others(4): Show |
7 | 173 | 0.0405 | 5 | c.313 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24625050 | T | TGGGGG | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0188 others(16): Show |
19 | 158 | 0.1203 | 5 | c.496 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24627464 | A | AAGGAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
a0001a0002a0004others(12): Show | a0001c0001a0001c0014a0002c0002others(19): Show | a0001c0001t0001a0001c0001t0004a0001c0014t0004others(26): Show | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | 350 | 0.6143 | 5 | c.495 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATA | intron_variant | MODIFIER | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0324 a0002c0002t0001g0019 a0002c0002t0001g0030 others(11): Show |
14 | 308 | 0.0455 | 5 | c.495 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24631418 | A | ACTATT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
a0002a0004a0005others(8): Show | a0002c0002a0002c0015a0002c0017others(13): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(17): Show | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(148): Show |
151 | 350 | 0.4314 | 5 | c.441 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24660386 | T | TAAAAA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0002c0017others(10): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(16): Show | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0187 others(105): Show |
108 | 154 | 0.7013 | 5 | c.268 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24687127 | G | GATCGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0014a0002c0002others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | 350 | 0.8343 | 5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48472524 | A | AAAAAT | intron_variant | MODIFIER | HG00558.hp2 HG00735.hp1 HG01069.hp2 others(35): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0005a0001c0001t0008a0001c0001t0014others(16): Show | a0001c0001t0005g0216 a0001c0001t0008g0187 a0001c0001t0014g0256 others(34): Show |
38 | 268 | 0.1418 | 5 | c.451 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48530236 | C | CAAAAA | intron_variant | MODIFIER | HG01361.hp2 HG02071.hp1 HG02258.hp1 others(14): Show |
a0001a0003a0007others(1): Show | a0001c0001a0001c0003a0003c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0051 others(14): Show |
17 | 102 | 0.1667 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48539290 | C | CTTTTT | intron_variant | MODIFIER | HG02965.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0005 | a0001c0002t0001a0001c0003t0006a0001c0005t0004 | a0001c0002t0001g0129 a0001c0002t0001g0160 a0001c0003t0006g0252 others(1): Show |
4 | 105 | 0.0381 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48539291 | A | ATTTTT | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(2): Show | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0003g0242 others(4): Show |
7 | 76 | 0.0921 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48563187 | A | ATTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
a0001a0004a0006others(2): Show | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0050 others(71): Show |
74 | 81 | 0.9136 | 5 | c.235 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAA | upstream_gene_variant | MODIFIER | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0014 | a0001c0001t0001a0003c0014t0001 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0150 others(4): Show |
7 | 134 | 0.0522 | 5 | c.-19 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38448858 | C | CTTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(33): Show |
a0001a0002a0003others(1): Show | a0001c0004a0001c0005a0001c0009others(10): Show | a0001c0004t0001a0001c0005t0001a0001c0005t0006others(11): Show | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(33): Show |
36 | 281 | 0.1281 | 5 | c.64- others(20): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85612792 | C | CTTTTT | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG04199.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0010others(1): Show | a0001c0001t0001g0020 a0001c0002t0002g0080 a0001c0003t0010g0083 others(1): Show |
4 | 19 | 0.2105 | 5 | c.180 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | C | CAAAAA | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0008a0001c0003t0011a0001c0004t0004others(2): Show | a0001c0002t0008g0052 a0001c0002t0008g0053 a0001c0003t0011g0095 others(3): Show |
6 | 9 | 0.6667 | 5 | c.181 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85734636 | A | ATTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(20): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(20): Show |
23 | 40 | 0.5750 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85743546 | T | TGACAG | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0046 others(10): Show |
13 | 108 | 0.1204 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85755626 | G | GTTTTT | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(13): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0032 others(13): Show |
16 | 54 | 0.2963 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85840150 | C | CCACCA | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0004 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0046 others(2): Show |
5 | 108 | 0.0463 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85856471 | C | CTTTTT | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0004 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0046 others(2): Show |
5 | 34 | 0.1471 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85894099 | T | TAAAAA | intron_variant | MODIFIER | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004a0001c0008 | a0001c0001t0001a0001c0004t0003a0001c0004t0004others(1): Show | a0001c0001t0001g0026 a0001c0004t0003g0051 a0001c0004t0003g0092 others(3): Show |
6 | 15 | 0.4000 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(29): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | 63 | 0.5079 | 5 | c.733 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85982373 | T | TTTTTG | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
a0001 | a0001c0004a0001c0008 | a0001c0004t0003a0001c0004t0004a0001c0008t0014others(1): Show | a0001c0004t0003g0044 a0001c0004t0003g0051 a0001c0004t0003g0062 others(6): Show |
9 | 27 | 0.3333 | 5 | c.928 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142839893 | A | AGGAGG | intron_variant | MODIFIER | HG02622.hp1 HG03130.hp2 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0032a0001c0001t0054 | a0001c0001t0005g0101 a0001c0001t0032g0053 a0001c0001t0054g0082 |
3 | 196 | 0.0153 | 5 | c.155 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAT | intron_variant | MODIFIER | HG01167.hp1 HG02155.hp2 HG02165.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0116 a0001c0001t0002g0023 a0001c0001t0003g0019 others(3): Show |
6 | 121 | 0.0496 | 5 | c.487 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142947095 | T | TAAAAA | intron_variant | MODIFIER | HG00323.hp2 HG02132.hp1 HG02165.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0012 a0001c0001t0001g0196 a0001c0001t0002g0043 others(15): Show |
18 | 57 | 0.3158 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949206 | A | AGAGAG | intron_variant | MODIFIER | HG01071.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0018 | a0001c0001t0004g0098 a0001c0001t0018g0011 |
2 | 184 | 0.0109 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTAT | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0017 a0001c0001t0001g0153 a0001c0001t0002g0005 others(87): Show |
90 | 106 | 0.8491 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTCTT | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(5): Show | a0001c0001t0001g0012 a0001c0001t0001g0196 a0001c0001t0003g0165 others(7): Show |
10 | 55 | 0.1818 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTT | intron_variant | MODIFIER | HG00438.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(7): Show | a0001c0001t0002g0023 a0001c0001t0002g0027 a0001c0001t0002g0190 others(9): Show |
12 | 57 | 0.2105 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143106466 | C | CTTTTT | intron_variant | MODIFIER | HG02074.hp2 HG02523.hp2 HG03540.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0005a0001c0001t0016others(4): Show | a0001c0001t0001g0020 a0001c0001t0005g0066 a0001c0001t0016g0024 others(5): Show |
8 | 55 | 0.1455 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143142134 | C | CTTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0034 others(54): Show |
57 | 132 | 0.4318 | 5 | c.183 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143154160 | T | TAAAAA | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0131 others(32): Show |
35 | 112 | 0.3125 | 5 | c.198 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143232630 | C | CTTTTT | downstream_gene_variant | MODIFIER | HG01167.hp1 HG02615.hp2 HG02809.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0013a0001c0001t0019others(1): Show | a0001c0001t0006g0064 a0001c0001t0006g0084 a0001c0001t0006g0086 others(7): Show |
10 | 39 | 0.2564 | 5 | c.*10 others(18): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | A | ATTTTT | intron_variant | MODIFIER | HG01943.hp2 HG02080.hp1 HG02602.hp1 others(10): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0017a0001c0003t0003others(5): Show | a0001c0001t0001g0034 a0001c0001t0001g0186 a0001c0001t0017g0118 others(10): Show |
13 | 25 | 0.5200 | 5 | c.123 others(24): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841180 | C | CTCTCT | intron_variant | MODIFIER | HG02559.hp2 HG03239.hp2 NA19003.hp1 |
a0001a0002 | a0001c0001a0001c0012a0002c0005 | a0001c0001t0001a0001c0012t0014a0002c0005t0002 | a0001c0001t0001g0042 a0001c0012t0014g0159 a0002c0005t0002g0018 |
3 | 199 | 0.0151 | 5 | c.543 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841188 | T | TCTCTC | intron_variant | MODIFIER | HG00280.hp1 HG04228.hp1 NA19011.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0071 a0001c0001t0001g0210 a0003c0004t0001g0188 |
3 | 242 | 0.0124 | 5 | c.543 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6908125 | G | GTTTTA | intron_variant | MODIFIER | HG00280.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
a0001a0003 | a0001c0003a0001c0015a0001c0020others(1): Show | a0001c0003t0003a0001c0003t0015a0001c0015t0003others(2): Show | a0001c0003t0003g0002 a0001c0003t0003g0013 a0001c0003t0003g0055 others(32): Show |
35 | 240 | 0.1458 | 5 | c.203 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6911450 | C | CTTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0010others(16): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(29): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
181 | 245 | 0.7388 | 5 | c.209 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar |