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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP8_chr22_44747575_44867784 | 44803743 | TCTCCCAT others(11): Show |
T | intron_variant | MODIFIER | HG00639.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0003a0003c0005t0002 | a0001c0001t0003g0376 a0003c0005t0002g0083 a0003c0005t0002g0121 others(2): Show |
5 | 390 | 0.0128 | -18 | c.167 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44836541 | GCACAGTA others(11): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(26): Show | a0001c0001t0001g0097 a0001c0001t0001g0370 a0001c0001t0003g0063 others(89): Show |
92 | 390 | 0.2359 | -18 | c.597 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
a0002a0003a0007 | a0002c0019a0003c0002a0007c0022others(1): Show | a0002c0019t0008a0003c0002t0002a0007c0022t0006others(1): Show | a0002c0019t0008g0040 a0002c0019t0008g0046 a0002c0019t0008g0313 others(5): Show |
8 | 390 | 0.0205 | -18 | c.877 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG02647.hp1 HG03225.hp1 |
a0002 | a0002c0019a0002c0068 | a0002c0019t0008a0002c0068t0008 | a0002c0019t0008g0040 a0002c0019t0008g0313 a0002c0068t0008g0044 |
3 | 390 | 0.0077 | -18 | c.878 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 282903 | TCCCCTGC others(11): Show |
T | 3_prime_UTR_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0028 | 1 | 442 | 0.0023 | -18 | c.*10 others(27): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 6/6 | 107 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17552571 | GTTTTTTT others(11): Show |
G | intron_variant | MODIFIER | HG01081.hp1 HG01123.hp1 HG01169.hp2 others(4): Show |
a0001a0003a0005others(1): Show | a0001c0012a0003c0002a0005c0015others(2): Show | a0001c0012t0001a0003c0002t0001a0005c0015t0002others(3): Show | a0001c0012t0001g0072 a0003c0002t0001g0144 a0005c0015t0002g0067 others(4): Show |
7 | 168 | 0.0417 | -18 | c.-44 others(37): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | AGTGTGTG others(11): Show |
A | intron_variant | MODIFIER | HG02109.hp1 | a0014 | a0014c0029 | a0014c0029t0001 | a0014c0029t0001g0121 | 1 | 168 | 0.0060 | -18 | c.257 others(33): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1823980 | TCGCGGGG others(11): Show |
T | 5_prime_UTR_variant | MODIFIER | HG01255.hp1 HG02818.hp2 HG03139.hp1 |
a0001 | a0001c0002a0001c0003a0001c0012 | a0001c0002t0026a0001c0003t0026a0001c0012t0074 | a0001c0002t0026g0192 a0001c0003t0026g0190 a0001c0012t0074g0191 |
3 | 363 | 0.0083 | -18 | c.-16 others(27): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19391 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1825067 | CCCCCCGC others(11): Show |
C | intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0009 | a0001c0009t0005 | a0001c0009t0005g0326 | 1 | 363 | 0.0028 | -18 | c.-48 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1825220 | CCCCCCGC others(11): Show |
C | intron_variant | MODIFIER | HG00597.hp1 HG01192.hp1 HG01243.hp1 others(2): Show |
a0001a0004a0006 | a0001c0003a0001c0009a0004c0136others(1): Show | a0001c0003t0001a0001c0003t0008a0001c0009t0005others(2): Show | a0001c0003t0001g0306 a0001c0003t0008g0288 a0001c0009t0005g0287 others(2): Show |
5 | 363 | 0.0138 | -18 | c.-48 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832740 | GCAGAGGC others(11): Show |
G | intron_variant | MODIFIER | HG03239.hp1 HG03710.hp1 NA20905.hp1 |
a0002a0005a0021 | a0002c0017a0005c0137a0021c0126 | a0002c0017t0006a0005c0137t0021a0021c0126t0007 | a0002c0017t0006g0114 a0005c0137t0021g0112 a0021c0126t0007g0113 |
3 | 363 | 0.0083 | -18 | c.-48 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833394 | GGGCAGAG others(11): Show |
G | intron_variant | MODIFIER | HG02258.hp1 | a0018 | a0018c0094 | a0018c0094t0016 | a0018c0094t0016g0103 | 1 | 363 | 0.0028 | -18 | c.-48 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841818 | GCGGGAAC others(11): Show |
G | intron_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0005others(16): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(18): Show | a0001c0001t0002g0069 a0001c0001t0002g0271 a0001c0002t0001g0198 others(23): Show |
26 | 363 | 0.0716 | -18 | c.-47 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841836 | ACGGGAAC others(11): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG01515.hp2 HG01934.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(11): Show | a0001c0001t0002g0030 a0001c0001t0004g0165 a0001c0001t0004g0168 others(12): Show |
15 | 363 | 0.0413 | -18 | c.-47 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841928 | GGGAACTG others(11): Show |
G | intron_variant | MODIFIER | HG01175.hp1 HG01192.hp1 NA18952.hp1 others(1): Show |
a0001a0002 | a0001c0004a0001c0009a0002c0121 | a0001c0004t0039a0001c0009t0005a0002c0121t0013 | a0001c0004t0039g0076 a0001c0009t0005g0287 a0001c0009t0005g0326 others(1): Show |
4 | 363 | 0.0110 | -18 | c.-47 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841962 | ACCGGAAC others(11): Show |
A | intron_variant | MODIFIER | HG06807.hp1 | a0003 | a0003c0040 | a0003c0040t0065 | a0003c0040t0065g0181 | 1 | 363 | 0.0028 | -18 | c.-47 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841964 | CGGAACTG others(11): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(18): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0014a0001c0004t0005a0001c0007t0003others(17): Show | a0001c0001t0014g0361 a0001c0004t0005g0299 a0001c0007t0003g0346 others(18): Show |
21 | 363 | 0.0579 | -18 | c.-47 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1941862 | TCAACAGG others(11): Show |
T | intron_variant | MODIFIER | HG02258.hp1 NA19010.hp1 |
a0001a0018 | a0001c0050a0018c0094 | a0001c0050t0002a0018c0094t0016 | a0001c0050t0002g0255 a0018c0094t0016g0103 |
2 | 363 | 0.0055 | -18 | c.322 others(37): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120334861 | GTGTATAT others(11): Show |
G | upstream_gene_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0183 | 1 | 308 | 0.0033 | -18 | c.-23 others(29): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1551 | chr11 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120351408 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG02698.hp2 HG03942.hp2 HG04184.hp2 others(3): Show |
a0001 | a0001c0004 | a0001c0004t0005a0001c0004t0012 | a0001c0004t0005g0049 a0001c0004t0005g0053 a0001c0004t0005g0056 others(3): Show |
6 | 308 | 0.0195 | -18 | c.32+ others(35): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG02257.hp1 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | 308 | 0.0065 | -18 | c.33- others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3485931 | CAAAAAAA others(11): Show |
C | downstream_gene_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 | 1 | 334 | 0.0030 | -18 | c.*53 others(29): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4819 | chr1 | TogoVar | |||||||
ARHGEF17_chr11_73303276_73374388 | 73329322 | CATATATA others(11): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
a0001a0003a0006others(5): Show | a0001c0001a0001c0028a0003c0009others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0028t0001others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(38): Show |
42 | 228 | 0.1842 | -18 | c.319 others(39): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329357 | ATATATAT others(11): Show |
A | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0021 | a0001c0021t0001 | a0001c0021t0001g0077 | 1 | 228 | 0.0044 | -18 | c.319 others(39): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | CGTGTGTG others(11): Show |
C | intron_variant | MODIFIER | HG02109.hp1 | a0002 | a0002c0016 | a0002c0016t0003 | a0002c0016t0003g0222 | 1 | 228 | 0.0044 | -18 | c.319 others(39): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332391 | GTGTGTGT others(11): Show |
G | intron_variant | MODIFIER | HG01071.hp2 | a0009 | a0009c0017 | a0009c0017t0004 | a0009c0017t0004g0097 | 1 | 228 | 0.0044 | -18 | c.319 others(39): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73369504 | ACAATGTT others(11): Show |
A | downstream_gene_variant | MODIFIER | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
a0002 | a0002c0008a0002c0035 | a0002c0008t0002a0002c0008t0006a0002c0035t0006 | a0002c0008t0002g0139 a0002c0008t0006g0140 a0002c0008t0006g0142 others(1): Show |
4 | 228 | 0.0175 | -18 | c.*17 others(29): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 117 | chr11 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7347395 | CAAAAAAA others(11): Show |
C | upstream_gene_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0060 | 1 | 298 | 0.0034 | -18 | c.-19 others(29): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1541 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(11): Show |
G | intron_variant | MODIFIER | HG00544.hp1 HG02615.hp2 NA18999.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0017a0003c0003t0001 | a0001c0001t0017g0014 a0003c0003t0001g0219 a0003c0003t0001g0220 |
3 | 298 | 0.0101 | -18 | c.-11 others(37): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7355068 | TCACACAC others(11): Show |
T | intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02145.hp2 others(11): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0013a0001c0047others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(7): Show | a0001c0001t0002g0012 a0001c0001t0002g0070 a0001c0001t0004g0004 others(11): Show |
14 | 298 | 0.0470 | -18 | c.-11 others(37): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362155 | GAGGAGAA others(11): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(25): Show |
a0001a0003a0008others(2): Show | a0001c0001a0001c0002a0001c0023others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(8): Show | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0081 others(25): Show |
28 | 298 | 0.0940 | -18 | c.-11 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385819 | ATCTATCT others(11): Show |
A | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0042 | a0001c0042t0025 | a0001c0042t0025g0250 | 1 | 298 | 0.0034 | -18 | c.967 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385907 | CCTCTCTC others(11): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
a0002a0003a0022 | a0002c0004a0003c0003a0022c0051 | a0002c0004t0004a0003c0003t0001a0022c0051t0006 | a0002c0004t0004g0018 a0002c0004t0004g0019 a0002c0004t0004g0064 others(4): Show |
7 | 298 | 0.0235 | -18 | c.967 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7416530 | CGTGTGTG others(11): Show |
C | intron_variant | MODIFIER | HG02559.hp2 HG06807.hp1 |
a0001 | a0001c0002a0001c0043 | a0001c0002t0036a0001c0043t0015 | a0001c0002t0036g0015 a0001c0043t0015g0278 |
2 | 298 | 0.0067 | -18 | c.968 others(37): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239287 | AGAGAGAG others(11): Show |
A | intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0003 | a0002c0003t0045 | a0002c0003t0045g0095 | 1 | 283 | 0.0035 | -18 | c.209 others(37): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239289 | AGAGAGAG others(11): Show |
A | intron_variant | MODIFIER | HG02145.hp1 HG03516.hp1 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0037a0002c0007t0018 | a0001c0001t0037g0256 a0002c0007t0018g0091 |
2 | 283 | 0.0071 | -18 | c.209 others(37): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239291 | AGAGAGAG others(11): Show |
A | intron_variant | MODIFIER | NA18965.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0215 | 1 | 283 | 0.0035 | -18 | c.209 others(37): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239293 | AGAGAGAG others(11): Show |
A | intron_variant | MODIFIER | HG00544.hp2 NA18950.hp2 NA19084.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0004a0001c0001t0034a0002c0003t0006 | a0001c0001t0004g0278 a0001c0001t0034g0202 a0002c0003t0006g0115 |
3 | 283 | 0.0106 | -18 | c.209 others(37): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239295 | AGAGAGTG others(11): Show |
A | intron_variant | MODIFIER | HG02258.hp2 | a0002 | a0002c0003 | a0002c0003t0019 | a0002c0003t0019g0102 | 1 | 283 | 0.0035 | -18 | c.209 others(37): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73679796 | TACATGTT others(11): Show |
T | intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0025 | a0001c0025t0005 | a0001c0025t0005g0131 | 1 | 188 | 0.0053 | -18 | c.-11 others(35): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741385 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG01934.hp2 HG03490.hp2 HG03492.hp1 |
a0003a0018 | a0003c0005a0018c0019 | a0003c0005t0002a0018c0019t0002 | a0003c0005t0002g0016 a0003c0005t0002g0084 a0018c0019t0002g0010 |
3 | 188 | 0.0160 | -18 | c.34- others(33): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73938160 | CCACACAC others(11): Show |
C | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(9): Show |
a0001a0002a0003others(6): Show | a0001c0021a0002c0002a0003c0007others(6): Show | a0001c0021t0008a0002c0002t0001a0002c0002t0002others(7): Show | a0001c0021t0008g0102 a0002c0002t0001g0130 a0002c0002t0002g0159 others(9): Show |
12 | 188 | 0.0638 | -18 | c.494 others(37): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155945280 | GGTGTGTG others(11): Show |
G | downstream_gene_variant | MODIFIER | HG02258.hp1 HG02818.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | 284 | 0.0070 | -18 | c.*26 others(29): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1573 | chr1 | TogoVar | |||||||
ARHGEF2_chr1_155941854_155983547 | 155964159 | AAAAAAAA others(11): Show |
A | intron_variant | MODIFIER | HG00621.hp2 HG02083.hp1 NA19004.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0058 |
4 | 284 | 0.0141 | -18 | c.724 others(33): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | |||||||
ARHGEF33_chr2_38884875_38980454 | 38931809 | CTTTGTAT others(11): Show |
C | intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0208 | 1 | 278 | 0.0036 | -18 | c.505 others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF35_chr7_144181083_144200833 | 144185646 | ATGAGAAG others(11): Show |
A | downstream_gene_variant | MODIFIER | NA18992.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0082 | 1 | 383 | 0.0026 | -18 | c.*12 others(29): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 436 | chr7 | TogoVar | |||||||
ARHGEF37_chr5_149576498_149639968 | 149598747 | TATCTATA others(11): Show |
T | intron_variant | MODIFIER | NA18941.hp1 NA18994.hp2 |
a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0229 a0004c0004t0004g0230 |
2 | 394 | 0.0051 | -18 | c.186 others(33): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105661474 | TTTATTAT others(11): Show |
T | intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0009 | a0001c0009t0007 | a0001c0009t0007g0086 | 1 | 186 | 0.0054 | -18 | c.154 others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56789020 | ATGCTGCT others(11): Show |
A | intron_variant | MODIFIER | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
a0001a0002 | a0001c0002a0002c0001 | a0001c0002t0008a0001c0002t0010a0002c0001t0001 | a0001c0002t0008g0145 a0001c0002t0010g0009 a0002c0001t0001g0015 others(3): Show |
6 | 358 | 0.0168 | -18 | c.96+ others(35): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | TogoVar | |||||||
ARHGEF40_chr14_21065304_21095248 | 21080199 | GACACACA others(11): Show |
G | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 386 | 0.0026 | -18 | c.237 others(35): Show |
ARHGEF40 | ENSG00000165801.10 | transcript | ENST00000298694.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |