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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP25_chr2_68729811_68831833 | 68824265 | TGTCAGA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0020a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(215): Show |
232 | 366 | 0.6339 | -6 | c.173 others(25): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142783525 | AGCTGTT | A | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 NA18952.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0048a0001c0002t0001others(1): Show | a0001c0001t0002g0001 a0001c0001t0002g0128 a0001c0001t0048g0127 others(2): Show |
5 | 196 | 0.0255 | -6 | c.154 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142796054 | CTGTGTG | C | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0141 a0001c0001t0002g0142 a0001c0001t0002g0195 others(23): Show |
26 | 119 | 0.2185 | -6 | c.154 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142806473 | ATGTGTG | A | intron_variant | MODIFIER | HG02615.hp2 HG02698.hp1 HG02723.hp1 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0034 a0001c0001t0002g0036 a0001c0001t0003g0033 others(7): Show |
10 | 19 | 0.5263 | -6 | c.154 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAA | G | intron_variant | MODIFIER | HG00558.hp1 HG01167.hp1 HG02165.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0020 a0001c0001t0001g0116 a0001c0001t0002g0007 others(16): Show |
19 | 21 | 0.9048 | -6 | c.154 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | GGTGTGT | G | intron_variant | MODIFIER | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0002g0117 a0001c0001t0003g0143 a0001c0001t0004g0056 others(11): Show |
14 | 59 | 0.2373 | -6 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142876776 | CAAAAAA | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG03041.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(3): Show | a0001c0001t0004g0098 a0001c0001t0006g0095 a0001c0001t0006g0096 others(5): Show |
8 | 73 | 0.1096 | -6 | c.312 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142936108 | AACACAC | A | intron_variant | MODIFIER | HG02258.hp1 HG02647.hp1 HG02818.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010a0001c0001t0025 | a0001c0001t0006g0086 a0001c0001t0010g0080 a0001c0001t0025g0071 |
3 | 77 | 0.0390 | -6 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142950994 | CCTTTCT | C | intron_variant | MODIFIER | HG00408.hp1 HG02056.hp1 HG02074.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0042 | a0001c0001t0002g0195 a0001c0001t0007g0068 a0001c0001t0042g0163 |
3 | 196 | 0.0153 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963217 | TGTGCGC | T | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01433.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0005a0001c0002t0004a0001c0002t0017others(1): Show | a0001c0001t0005g0101 a0001c0001t0005g0108 a0001c0001t0005g0109 others(3): Show |
6 | 196 | 0.0306 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142997090 | TTTCCAA | T | intron_variant | MODIFIER | HG01071.hp1 HG01167.hp2 HG01433.hp1 others(4): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0002a0001c0003t0003 | a0001c0003t0001g0149 a0001c0003t0002g0183 a0001c0003t0003g0050 others(4): Show |
7 | 196 | 0.0357 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTTTT | G | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0021a0001c0001t0024others(1): Show | a0001c0001t0006g0064 a0001c0001t0006g0104 a0001c0001t0021g0081 others(2): Show |
5 | 52 | 0.0962 | -6 | c.114 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143085044 | CAAAAAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00597.hp2 HG02056.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0131 a0001c0001t0001g0158 a0001c0001t0002g0001 others(30): Show |
33 | 171 | 0.1930 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143097360 | GAAAAAA | G | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(7): Show | a0001c0001t0001g0012 a0001c0001t0001g0196 a0001c0001t0003g0165 others(9): Show |
12 | 132 | 0.0909 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143098854 | GGTTAGT | G | intron_variant | MODIFIER | HG01243.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0024a0001c0001t0055a0001c0003t0002others(1): Show | a0001c0001t0024g0103 a0001c0001t0055g0072 a0001c0003t0002g0044 others(1): Show |
4 | 196 | 0.0204 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATA | G | intron_variant | MODIFIER | HG01256.hp2 HG01358.hp2 HG01891.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0009a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0009t0012others(5): Show | a0001c0001t0001g0185 a0001c0001t0001g0304 a0001c0001t0006g0021 others(12): Show |
16 | 63 | 0.2540 | -6 | c.657 others(25): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729481 | CACAGGT | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0016a0001c0003t0001others(13): Show | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0026 others(60): Show |
63 | 246 | 0.2561 | -6 | c.-34 others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 234 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841202 | TCCTCTC | T | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0002others(3): Show | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0180 others(13): Show |
16 | 218 | 0.0734 | -6 | c.543 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909295 | CTTTTCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0005others(3): Show | a0001c0001t0001a0001c0001t0009a0001c0003t0003others(5): Show | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0035 others(67): Show |
70 | 246 | 0.2846 | -6 | c.209 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94209812 | TATATAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0002a0001c0005others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | 354 | 0.9322 | -6 | c.341 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94210606 | CAAAAAG | C | intron_variant | MODIFIER | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
a0001a0006 | a0001c0002a0006c0016 | a0001c0002t0016a0006c0016t0016 | a0001c0002t0016g0145 a0001c0002t0016g0162 a0001c0002t0016g0163 others(1): Show |
4 | 354 | 0.0113 | -6 | c.341 others(23): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTC | T | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0007t0001a0002c0002t0001others(2): Show | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0093 others(24): Show |
29 | 56 | 0.5179 | -6 | c.537 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055890 | TAAAATA | T | intron_variant | MODIFIER | NA18960.hp1 NA18979.hp2 NA18982.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 a0001c0001t0001g0200 a0001c0001t0001g0236 |
3 | 383 | 0.0078 | -6 | c.345 others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055915 | TAAAATA | T | intron_variant | MODIFIER | HG01175.hp2 HG01433.hp2 HG01515.hp1 others(10): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0159 others(9): Show |
13 | 297 | 0.0438 | -6 | c.345 others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064773 | GAAAGAA | G | intron_variant | MODIFIER | HG01099.hp2 HG01358.hp1 HG02717.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0121 others(2): Show |
5 | 388 | 0.0129 | -6 | c.97+ others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064825 | AAGAAAG | A | intron_variant | MODIFIER | HG02559.hp2 HG02897.hp2 HG03471.hp1 others(4): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0003c0004t0001 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0240 others(4): Show |
7 | 388 | 0.0180 | -6 | c.97+ others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119321557 | TTATATA | T | intron_variant | MODIFIER | NA18960.hp2 NA18969.hp1 NA19003.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0006a0001c0002t0001a0001c0004t0003 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0002t0001g0106 others(1): Show |
4 | 308 | 0.0130 | -6 | c.100 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332631 | TCTCTCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(7): Show | a0001c0001t0005g0084 a0001c0001t0005g0085 a0001c0001t0006g0074 others(13): Show |
16 | 269 | 0.0595 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119336632 | GTTTTAT | G | intron_variant | MODIFIER | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0039 a0001c0004t0003g0040 a0001c0004t0003g0041 |
3 | 308 | 0.0097 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119354846 | CTATATT | C | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp1 HG02818.hp2 others(4): Show |
a0001a0003 | a0001c0004a0001c0005a0003c0006 | a0001c0004t0003a0001c0005t0001a0001c0005t0014others(2): Show | a0001c0004t0003g0010 a0001c0004t0003g0148 a0001c0005t0001g0013 others(4): Show |
7 | 308 | 0.0227 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | TTTTATA | T | intron_variant | MODIFIER | HG01099.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
a0001a0014 | a0001c0004a0001c0005a0014c0021 | a0001c0004t0058a0001c0005t0001a0014c0021t0001 | a0001c0004t0058g0016 a0001c0005t0001g0068 a0001c0005t0001g0070 others(1): Show |
4 | 102 | 0.0392 | -6 | c.683 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | TTTATTA | T | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(119): Show |
123 | 207 | 0.5942 | -6 | c.212 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985831 | CGTGTGT | C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0202 a0001c0003t0006g0203 a0001c0003t0006g0204 others(1): Show |
4 | 296 | 0.0135 | -6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129058188 | TACACAC | T | intron_variant | MODIFIER | HG02602.hp1 HG02735.hp2 HG03704.hp2 |
a0001a0002 | a0001c0003a0002c0004 | a0001c0003t0003a0002c0004t0001 | a0001c0003t0003g0321 a0001c0003t0003g0322 a0002c0004t0001g0210 |
3 | 211 | 0.0142 | -6 | c.963 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129058217 | ACACACT | A | intron_variant | MODIFIER | HG02280.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
a0001a0005 | a0001c0001a0001c0010a0005c0011 | a0001c0001t0016a0001c0001t0033a0001c0010t0014others(1): Show | a0001c0001t0016g0198 a0001c0001t0033g0301 a0001c0010t0014g0200 others(1): Show |
4 | 395 | 0.0101 | -6 | c.963 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129082882 | AAACAAC | A | intron_variant | MODIFIER | HG01123.hp1 HG02602.hp2 HG02683.hp2 others(1): Show |
a0001 | a0001c0003a0001c0010 | a0001c0003t0005a0001c0010t0008 | a0001c0003t0005g0188 a0001c0003t0005g0189 a0001c0010t0008g0193 others(1): Show |
4 | 383 | 0.0104 | -6 | c.531 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129183766 | ACCCACC | A | intron_variant | MODIFIER | HG00642.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
a0001a0002a0013 | a0001c0001a0001c0002a0002c0008others(1): Show | a0001c0001t0002a0001c0002t0001a0002c0008t0001others(1): Show | a0001c0001t0002g0190 a0001c0002t0001g0207 a0001c0002t0001g0208 others(3): Show |
6 | 396 | 0.0152 | -6 | c.116 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1/22 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTT | C | upstream_gene_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(21): Show |
a0001a0002a0009 | a0001c0002a0001c0030a0002c0013others(1): Show | a0001c0002t0001a0001c0030t0001a0002c0013t0001others(1): Show | a0001c0002t0001g0005 a0001c0002t0001g0020 a0001c0002t0001g0079 others(3): Show |
24 | 105 | 0.2286 | -6 | c.-16 others(17): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46877569 | AAATAAC | A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0024a0001c0001t0036 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | 296 | 0.0135 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATAT | A | intron_variant | MODIFIER | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(30): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(30): Show |
33 | 65 | 0.5077 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46898775 | AGCTGCT | A | intron_variant | MODIFIER | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0289 |
3 | 236 | 0.0127 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131065041 | TTGTGTG | T | intron_variant | MODIFIER | HG02109.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0047 others(1): Show |
4 | 18 | 0.2222 | -6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATAT | C | intron_variant | MODIFIER | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005 | a0001c0001t0001g0081 a0001c0001t0001g0126 a0001c0001t0003g0202 others(1): Show |
4 | 8 | 0.5000 | -6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144603896 | ACAGGAT | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
a0001a0003a0005 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(5): Show | a0001c0001t0001g0228 a0001c0003t0001g0004 a0001c0003t0001g0011 others(10): Show |
13 | 244 | 0.0533 | -6 | c.80+ others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144619394 | CCATGTG | C | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0001t0002a0001c0018t0001 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(9): Show |
12 | 244 | 0.0492 | -6 | c.-81 others(25): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38617577 | CCACCTA | C | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
a0001a0005a0021 | a0001c0008a0001c0021a0001c0038others(2): Show | a0001c0008t0004a0001c0008t0006a0001c0021t0002others(3): Show | a0001c0008t0004g0025 a0001c0008t0004g0305 a0001c0008t0006g0282 others(5): Show |
9 | 348 | 0.0259 | -6 | c.138 others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100691921 | AATATAT | A | intron_variant | MODIFIER | HG02280.hp2 HG02723.hp2 HG02809.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0008t0001a0002c0002t0002others(4): Show | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0008t0001g0004 others(9): Show |
12 | 284 | 0.0423 | -6 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100704644 | GATGTCA | G | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002others(1): Show | a0001c0001t0001a0001c0010t0001a0002c0002t0028others(2): Show | a0001c0001t0001g0002 a0001c0010t0001g0238 a0002c0002t0028g0001 others(5): Show |
8 | 284 | 0.0282 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(92): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(21): Show | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0185 others(92): Show |
95 | 164 | 0.5793 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATAT | C | intron_variant | MODIFIER | HG00639.hp1 HG00673.hp2 HG01257.hp2 others(26): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(9): Show | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0001t0001g0180 others(26): Show |
29 | 159 | 0.1824 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar |