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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142949165 | C | CAGAGAGA others(11): Show |
intron_variant | MODIFIER | HG01243.hp2 HG06807.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0046a0001c0003t0004 | a0001c0001t0046g0166 a0001c0003t0004g0092 |
2 | 91 | 0.0220 | 18 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949192 | A | AGAGAGAG others(11): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 193 | 0.0052 | 18 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949194 | A | AGAGAGAG others(11): Show |
intron_variant | MODIFIER | HG02897.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0091 | 1 | 191 | 0.0052 | 18 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATGTGT others(11): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0087 | 1 | 144 | 0.0069 | 18 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG00408.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0007a0001c0001t0025others(2): Show | a0001c0001t0002g0046 a0001c0001t0007g0068 a0001c0001t0025g0071 others(2): Show |
5 | 52 | 0.0962 | 18 | c.110 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012576 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0007 | 1 | 175 | 0.0057 | 18 | c.110 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0161 | 1 | 46 | 0.0217 | 18 | c.153 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | NA18957.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 25 | 0.0400 | 18 | c.198 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG02258.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0016a0001c0003t0003others(1): Show | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0016g0081 others(4): Show |
7 | 127 | 0.0551 | 18 | c.122 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(11): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0116 a0001c0001t0007g0117 |
2 | 122 | 0.0164 | 18 | c.122 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94166813 | G | GCACACAC others(11): Show |
downstream_gene_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0011 | a0001c0011t0040 | a0001c0011t0040g0180 | 1 | 225 | 0.0044 | 18 | c.*70 others(29): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2091 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | HG01243.hp2 HG03471.hp1 |
a0001a0009 | a0001c0005a0009c0011 | a0001c0005t0001a0009c0011t0015 | a0001c0005t0001g0013 a0009c0011t0015g0014 |
2 | 118 | 0.0169 | 18 | c.100 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0006 | a0001c0001t0018a0001c0005t0001a0003c0006t0001 | a0001c0001t0018g0210 a0001c0005t0001g0161 a0001c0005t0001g0164 others(1): Show |
4 | 11 | 0.3636 | 18 | c.100 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(11): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03195.hp2 HG03927.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(5): Show | a0001c0001t0006g0026 a0001c0001t0008g0179 a0001c0001t0008g0272 others(9): Show |
12 | 110 | 0.1091 | 18 | c.683 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128976078 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0189 | 1 | 177 | 0.0056 | 18 | c.219 others(35): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 20/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCACACAC others(11): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0005 | a0005c0011 | a0005c0011t0021 | a0005c0011t0021g0071 | 1 | 131 | 0.0076 | 18 | c.119 others(37): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0002a0002c0004t0001a0002c0004t0010others(2): Show | a0001c0001t0002g0113 a0002c0004t0001g0211 a0002c0004t0001g0215 others(7): Show |
10 | 112 | 0.0893 | 18 | c.226 others(37): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(11): Show |
upstream_gene_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(20): Show |
a0001 | a0001c0002a0001c0024 | a0001c0002t0001a0001c0024t0001 | a0001c0002t0001g0001 a0001c0002t0001g0017 a0001c0002t0001g0030 others(2): Show |
23 | 24 | 0.9583 | 18 | c.-36 others(29): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46936310 | T | TTGCTGCT others(11): Show |
intron_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0242 | 1 | 296 | 0.0034 | 18 | c.368 others(35): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46978686 | G | GATGTGTG others(11): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(182): Show |
185 | 296 | 0.6250 | 18 | c.382 others(37): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02630.hp1 HG03453.hp1 |
a0001a0005 | a0001c0001a0005c0011 | a0001c0001t0021a0005c0011t0001 | a0001c0001t0021g0057 a0005c0011t0001g0067 |
2 | 7 | 0.2857 | 18 | c.-82 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38627633 | G | GGGTGTGT others(11): Show |
intron_variant | MODIFIER | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
a0008 | a0008c0006 | a0008c0006t0002 | a0008c0006t0002g0028 a0008c0006t0002g0086 a0008c0006t0002g0105 others(1): Show |
5 | 274 | 0.0182 | 18 | c.558 others(33): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100788633 | G | GGTTGCAG others(11): Show |
intron_variant | MODIFIER | NA18966.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 284 | 0.0035 | 18 | c.251 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG00544.hp1 HG02055.hp1 HG03139.hp2 |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0039a0002c0005t0016 | a0001c0001t0001g0154 a0002c0002t0039g0200 a0002c0005t0016g0032 |
3 | 36 | 0.0833 | 18 | c.313 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG02922.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0035 | a0002c0002t0002g0034 a0002c0002t0002g0222 a0002c0002t0002g0245 others(2): Show |
5 | 160 | 0.0313 | 18 | c.313 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACAC others(11): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0041 | 1 | 40 | 0.0250 | 18 | c.385 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(11): Show |
intron_variant | MODIFIER | HG01358.hp1 HG01975.hp2 HG02056.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0001t0013a0001c0008t0001others(1): Show | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0074 others(5): Show |
8 | 47 | 0.1702 | 18 | c.385 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(11): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00673.hp1 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0078 a0001c0001t0019g0181 |
2 | 41 | 0.0488 | 18 | c.385 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0211 | 1 | 68 | 0.0147 | 18 | c.385 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(11): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01358.hp2 NA21309.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0020 | a0001c0001t0001g0011 a0002c0002t0002g0019 a0002c0002t0020g0106 |
3 | 26 | 0.1154 | 18 | c.245 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02074.hp2 NA19088.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0179 a0001c0001t0001g0220 |
2 | 25 | 0.0800 | 18 | c.245 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(11): Show |
intron_variant | MODIFIER | HG02027.hp2 NA18963.hp1 NA19010.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0034 | a0001c0001t0003g0087 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | 127 | 0.0315 | 18 | c.53+ others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(11): Show |
intron_variant | MODIFIER | HG02717.hp1 HG02809.hp2 NA19060.hp1 |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0002t0003a0001c0006t0001 | a0001c0001t0001g0212 a0001c0002t0003g0082 a0001c0006t0001g0175 |
3 | 126 | 0.0238 | 18 | c.53+ others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(11): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009 a0001c0001t0003g0072 |
2 | 125 | 0.0160 | 18 | c.53+ others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0148 others(14): Show |
17 | 125 | 0.1360 | 18 | c.54- others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | NA18942.hp2 NA19010.hp1 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0028 | a0001c0001t0004g0002 a0001c0001t0004g0170 a0001c0001t0028g0123 |
3 | 42 | 0.0714 | 18 | c.582 others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG02895.hp2 NA21309.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0005 | a0001c0001t0001g0176 a0001c0001t0001g0213 a0001c0005t0005g0088 |
3 | 45 | 0.0667 | 18 | c.862 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01106.hp2 HG01928.hp2 HG01981.hp1 others(16): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0140 others(16): Show |
19 | 149 | 0.1275 | 18 | c.176 others(37): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0008 | a0001c0008t0020 | a0001c0008t0020g0185 | 1 | 13 | 0.0769 | 18 | c.176 others(37): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0009 | a0009c0023 | a0009c0023t0002 | a0009c0023t0002g0207 | 1 | 123 | 0.0081 | 18 | c.118 others(37): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174565 | C | CCTTTCTT others(11): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 135 | 0.0074 | 18 | c.162 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0106 | 1 | 33 | 0.0303 | 18 | c.162 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354325 | C | CTATATAT others(11): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0010 | 1 | 104 | 0.0096 | 18 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354327 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117 | 1 | 75 | 0.0133 | 18 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11358487 | T | TTCTTTCT others(11): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 139 | 0.0072 | 18 | c.589 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | HG00673.hp1 NA18952.hp1 NA18971.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | 22 | 0.1818 | 18 | c.589 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 | 1 | 125 | 0.0080 | 18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG03486.hp1 NA18906.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0008a0001c0004t0005 | a0001c0001t0008g0049 a0001c0004t0005g0047 |
2 | 126 | 0.0159 | 18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | A | AAATAATA others(11): Show |
intron_variant | MODIFIER | HG00280.hp1 HG02451.hp1 HG02895.hp1 others(5): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0009 | a0001c0001t0001a0002c0002t0003a0004c0009t0001 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0052 others(5): Show |
8 | 98 | 0.0816 | 18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11563742 | G | GTGAAGTT others(11): Show |
intron_variant | MODIFIER | HG02735.hp1 HG03098.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0006 | a0001c0001t0001g0024 a0002c0002t0003g0016 a0002c0002t0006g0031 |
3 | 144 | 0.0208 | 18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |