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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(13): Show |
intron_variant | MODIFIER | NA18942.hp1 NA18986.hp1 NA18990.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0150 a0001c0001t0001g0164 a0001c0001t0003g0083 |
3 | 133 | 0.0226 | 20 | c.176 others(39): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174518 | T | TTTCCTTC others(13): Show |
intron_variant | MODIFIER | NA18943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 117 | 0.0085 | 20 | c.162 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTCCTT others(13): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 74 | 0.0135 | 20 | c.162 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11190473 | A | ATATATAC others(13): Show |
intron_variant | MODIFIER | HG01243.hp1 HG03098.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0024 a0001c0004t0005g0015 a0001c0004t0005g0047 |
3 | 122 | 0.0246 | 20 | c.821 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(13): Show |
intron_variant | MODIFIER | HG01256.hp1 HG02622.hp2 HG02922.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0003others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0002g0138 others(3): Show |
6 | 57 | 0.1053 | 20 | c.589 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11358431 | A | ATCTTTCT others(13): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0009 | 1 | 45 | 0.0222 | 20 | c.589 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | HG00609.hp1 HG01069.hp1 NA18906.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | 23 | 0.2174 | 20 | c.589 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590775 | C | CGAAAAGA others(13): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0019 | 1 | 129 | 0.0078 | 20 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590869 | G | GGAAAGAA others(13): Show |
intron_variant | MODIFIER | NA18983.hp1 NA18985.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 a0001c0001t0001g0076 |
2 | 29 | 0.0690 | 20 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44754373 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0008 | a0008c0030 | a0008c0030t0001 | a0008c0030t0001g0379 | 1 | 124 | 0.0081 | 20 | c.-72 others(37): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44813686 | T | TACCTACA others(13): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0007a0002c0011others(3): Show | a0001c0001t0009a0001c0007t0001a0002c0011t0005others(3): Show | a0001c0001t0009g0173 a0001c0001t0009g0321 a0001c0007t0001g0324 others(4): Show |
7 | 388 | 0.0180 | 20 | c.300 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0008 | a0008c0074 | a0008c0074t0001 | a0008c0074t0001g0049 | 1 | 260 | 0.0038 | 20 | c.386 others(37): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44863968 | G | GTACAGGG others(13): Show |
downstream_gene_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
a0002a0015a0018others(1): Show | a0002c0003a0002c0006a0002c0016others(7): Show | a0002c0003t0003a0002c0003t0004a0002c0006t0004others(8): Show | a0002c0003t0003g0276 a0002c0003t0004g0002 a0002c0003t0004g0011 others(59): Show |
62 | 387 | 0.1602 | 20 | c.*13 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1185 | chr22 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
a0001a0007a0015 | a0001c0001a0001c0006a0007c0010others(1): Show | a0001c0001t0003a0001c0006t0007a0007c0010t0001others(1): Show | a0001c0001t0003g0131 a0001c0006t0007g0150 a0007c0010t0001g0053 others(1): Show |
4 | 80 | 0.0500 | 20 | c.257 others(35): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1823999 | C | CGCGGGGG others(13): Show |
5_prime_UTR_variant | MODIFIER | HG01952.hp1 HG03209.hp2 |
a0001a0002 | a0001c0009a0002c0025 | a0001c0009t0051a0002c0025t0050 | a0001c0009t0051g0274 a0002c0025t0050g0174 |
2 | 317 | 0.0063 | 20 | c.-14 others(29): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19361 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1824016 | A | AACGGCGG others(13): Show |
5_prime_UTR_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0159 | 1 | 296 | 0.0034 | 20 | c.-13 others(29): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19374 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1824019 | G | GGCGGGGG others(13): Show |
5_prime_UTR_variant | MODIFIER | NA19087.hp2 | a0002 | a0002c0079 | a0002c0079t0001 | a0002c0079t0001g0048 | 1 | 355 | 0.0028 | 20 | c.-99 others(27): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19318 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1824952 | T | TCCCCGCA others(13): Show |
intron_variant | MODIFIER | NA18962.hp2 NA19000.hp2 |
a0001 | a0001c0021a0001c0115 | a0001c0021t0004a0001c0115t0004 | a0001c0021t0004g0312 a0001c0115t0004g0281 |
2 | 193 | 0.0104 | 20 | 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 | 1825173 | T | TCCACCTG others(13): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0008 | a0001c0008t0002 | a0001c0008t0002g0242 | 1 | 143 | 0.0070 | 20 | c.-48 others(37): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1825238 | T | TCCCCCCG others(13): Show |
intron_variant | MODIFIER | HG02145.hp2 NA19030.hp2 |
a0001a0017 | a0001c0005a0017c0072 | a0001c0005t0016a0017c0072t0007 | a0001c0005t0016g0167 a0017c0072t0007g0330 |
2 | 135 | 0.0148 | 20 | c.-48 others(37): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1881572 | G | GGACGTGA others(13): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02717.hp2 HG02897.hp2 others(1): Show |
a0001a0012a0017 | a0001c0002a0012c0084a0012c0130others(1): Show | a0001c0002t0020a0012c0084t0008a0012c0130t0061others(1): Show | a0001c0002t0020g0264 a0012c0084t0008g0352 a0012c0130t0061g0342 others(1): Show |
4 | 362 | 0.0110 | 20 | c.961 others(37): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1919775 | A | ATGGGTGA others(13): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0005 | a0005c0087 | a0005c0087t0002 | a0005c0087t0002g0254 | 1 | 359 | 0.0028 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1919917 | A | ATGATGGA others(13): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
a0001a0002a0022 | a0001c0009a0001c0012a0001c0092others(2): Show | a0001c0009t0004a0001c0012t0008a0001c0092t0011others(2): Show | a0001c0009t0004g0303 a0001c0009t0004g0326 a0001c0012t0008g0348 others(3): Show |
6 | 144 | 0.0417 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1920031 | T | TATGGGTG others(13): Show |
intron_variant | MODIFIER | HG00741.hp1 HG02622.hp2 HG03041.hp1 others(9): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0010a0001c0001t0017a0001c0001t0019others(8): Show | a0001c0001t0010g0344 a0001c0001t0017g0351 a0001c0001t0019g0317 others(9): Show |
12 | 164 | 0.0732 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1920031 | T | TATGGGTG others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(188): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0003others(88): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(128): Show | a0001c0001t0002g0054 a0001c0001t0002g0069 a0001c0001t0002g0072 others(188): Show |
191 | 343 | 0.5569 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1920032 | A | ATGGGTGA others(13): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0002 | a0002c0017 | a0002c0017t0002 | a0002c0017t0002g0044 | 1 | 361 | 0.0028 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1920032 | A | ATGGGTGA others(13): Show |
intron_variant | MODIFIER | NA19011.hp1 | a0001 | a0001c0035 | a0001c0035t0001 | a0001c0035t0001g0050 | 1 | 361 | 0.0028 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1920051 | C | CGTGGGTG others(13): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0004 | a0004c0136 | a0004c0136t0009 | a0004c0136t0009g0283 | 1 | 349 | 0.0029 | 20 | c.214 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936493 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG00558.hp2 NA19055.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0273 a0001c0005t0001g0278 |
2 | 332 | 0.0060 | 20 | c.463 others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0142 | 1 | 78 | 0.0128 | 20 | c.463 others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(13): Show |
intron_variant | MODIFIER | HG01192.hp2 HG01517.hp2 HG01884.hp1 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0004a0003c0003others(1): Show | a0001c0001t0004a0001c0001t0007a0001c0001t0020others(5): Show | a0001c0001t0004g0139 a0001c0001t0004g0181 a0001c0001t0007g0144 others(10): Show |
13 | 153 | 0.0850 | 20 | c.33- others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCTCACAC others(13): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0004a0001c0001t0028a0001c0011t0004 | a0001c0001t0004g0141 a0001c0001t0004g0178 a0001c0001t0028g0183 others(1): Show |
4 | 144 | 0.0278 | 20 | c.33- others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACAC others(13): Show |
intron_variant | MODIFIER | HG00642.hp1 HG04204.hp2 NA18964.hp2 others(2): Show |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0009 | a0002c0004t0005g0116 a0002c0004t0005g0120 a0002c0004t0005g0122 others(2): Show |
5 | 315 | 0.0159 | 20 | c.33- others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347175 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0257 | 1 | 207 | 0.0048 | 20 | 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 | 120347179 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG00280.hp2 HG02027.hp1 NA19067.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0001t0001g0289 |
3 | 81 | 0.0370 | 20 | 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 | 120347183 | C | CCTTCCTT others(13): Show |
intron_variant | MODIFIER | HG01515.hp1 HG02040.hp2 NA18977.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0236 a0001c0001t0004g0248 a0001c0001t0004g0255 |
3 | 9 | 0.3333 | 20 | 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 | 120347183 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00741.hp1 HG01255.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(2): Show | a0001c0001t0001g0231 a0001c0001t0001g0238 a0001c0001t0001g0241 others(6): Show |
9 | 15 | 0.6000 | 20 | 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 | 120367353 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01123.hp1 HG03654.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0002a0001c0006t0002 | a0001c0001t0002g0088 a0001c0006t0002g0301 |
2 | 73 | 0.0274 | 20 | c.32+ others(37): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | A | AACACACA others(13): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 HG01123.hp1 NA18951.hp1 others(3): Show |
a0001a0003a0005 | a0001c0001a0003c0003a0003c0009others(1): Show | a0001c0001t0003a0003c0003t0001a0003c0009t0001others(1): Show | a0001c0001t0003g0048 a0003c0003t0001g0003 a0003c0003t0001g0011 others(3): Show |
6 | 23 | 0.2609 | 20 | c.-27 others(29): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3450012 | C | CGTGTGTG others(13): Show |
upstream_gene_variant | MODIFIER | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0002 | a0001c0001t0001a0001c0005t0001a0001c0005t0019others(2): Show | a0001c0001t0001g0208 a0001c0005t0001g0022 a0001c0005t0001g0026 others(8): Show |
11 | 24 | 0.4583 | 20 | c.-48 others(31): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4652 | chr1 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3470253 | G | GGGGCAGG others(13): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0012 | a0012c0025 | a0012c0025t0012 | a0012c0025t0012g0292 | 1 | 332 | 0.0030 | 20 | c.102 others(37): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0165 | 1 | 45 | 0.0222 | 20 | c.319 others(41): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7364365 | A | AAAGGAAG others(13): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02165.hp2 HG02922.hp1 others(3): Show |
a0002a0003a0005others(2): Show | a0002c0004a0003c0003a0005c0008others(2): Show | a0002c0004t0002a0003c0003t0001a0005c0008t0002others(2): Show | a0002c0004t0002g0049 a0003c0003t0001g0257 a0005c0008t0002g0288 others(3): Show |
6 | 240 | 0.0250 | 20 | c.15+ others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7364390 | A | AAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
a0001a0002a0009 | a0001c0001a0002c0007a0009c0012 | a0001c0001t0002a0001c0001t0030a0002c0007t0001others(1): Show | a0001c0001t0002g0012 a0001c0001t0030g0010 a0002c0007t0001g0009 others(1): Show |
4 | 286 | 0.0140 | 20 | c.15+ others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(29): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0046others(6): Show | a0001c0001t0002a0001c0002t0003a0001c0046t0001others(10): Show | a0001c0001t0002g0063 a0001c0001t0002g0070 a0001c0001t0002g0071 others(29): Show |
32 | 102 | 0.3137 | 20 | c.15+ others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02970.hp2 HG03669.hp2 others(1): Show |
a0001a0002a0003others(1): Show | a0001c0016a0002c0007a0003c0003others(1): Show | a0001c0016t0014a0002c0007t0001a0003c0003t0001others(1): Show | a0001c0016t0014g0268 a0002c0007t0001g0026 a0003c0003t0001g0062 others(1): Show |
4 | 74 | 0.0541 | 20 | c.15+ others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(13): Show |
intron_variant | MODIFIER | NA18977.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0066 | 1 | 71 | 0.0141 | 20 | c.15+ others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7368007 | G | GAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0012 | 1 | 283 | 0.0035 | 20 | c.16- others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7368020 | C | CGGAAGGA others(13): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01169.hp2 HG02055.hp2 |
a0001a0013 | a0001c0013a0013c0027 | a0001c0013t0001a0013c0027t0005 | a0001c0013t0001g0064 a0001c0013t0001g0077 a0013c0027t0005g0016 |
3 | 219 | 0.0137 | 20 | c.16- others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385870 | T | TCTCTCTC others(13): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0047 | a0001c0047t0002 | a0001c0047t0002g0004 | 1 | 255 | 0.0039 | 20 | c.967 others(37): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |