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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143153843 | T | TTCTTCTT others(14): Show |
intron_variant | MODIFIER | HG02071.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 a0001c0001t0001g0137 |
2 | 39 | 0.0513 | 21 | c.-14 others(38): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143382079 | T | TCCTTTCC others(14): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 68 | 0.0147 | 21 | c.475 others(40): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143419461 | T | TATCATGA others(14): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(141): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | 160 | 0.9000 | 21 | c.475 others(40): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GTGTGTGT others(14): Show |
intron_variant | MODIFIER | NA18962.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 | 1 | 10 | 0.1000 | 21 | c.113 others(42): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143686270 | G | GTGGCACA others(14): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(88): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
91 | 160 | 0.5688 | 21 | c.113 others(42): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | chr2 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625415 | A | ATATTATA others(14): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0056 | 1 | 235 | 0.0043 | 21 | c.786 others(38): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24593590 | T | TGAAAGAT others(14): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0014a0002c0002others(10): Show | a0001c0001t0008a0001c0014t0004a0002c0002t0001others(14): Show | a0001c0001t0008g0325 a0001c0014t0004g0287 a0002c0002t0001g0011 others(130): Show |
133 | 346 | 0.3844 | 21 | c.387 others(40): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24593590 | T | TGAAAGAT others(14): Show |
intron_variant | MODIFIER | HG00741.hp1 HG01975.hp1 HG02738.hp2 others(1): Show |
a0002a0019 | a0002c0002a0019c0023 | a0002c0002t0001a0019c0023t0001 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 others(1): Show |
4 | 217 | 0.0184 | 21 | c.387 others(40): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG01517.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0124 | 1 | 140 | 0.0071 | 21 | c.495 others(38): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02698.hp2 HG03491.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0184 a0001c0001t0001g0239 a0001c0001t0001g0241 others(1): Show |
4 | 143 | 0.0280 | 21 | c.495 others(38): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48539291 | A | ATTTTTTT others(14): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0039 | 1 | 70 | 0.0143 | 21 | c.322 others(40): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(14): Show |
upstream_gene_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0009 | a0001c0009t0003 | a0001c0009t0003g0173 | 1 | 128 | 0.0078 | 21 | c.-19 others(32): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | AAATAATA others(14): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 HG02071.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0006t0002others(4): Show | a0001c0001t0001g0145 a0001c0001t0001g0268 a0001c0001t0001g0290 others(13): Show |
16 | 60 | 0.2667 | 21 | c.344 others(40): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38507300 | T | TAATAATA others(14): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01169.hp1 HG01433.hp1 others(1): Show |
a0001 | a0001c0002a0001c0040a0001c0048 | a0001c0002t0002a0001c0040t0002a0001c0048t0002 | a0001c0002t0002g0015 a0001c0002t0002g0251 a0001c0040t0002g0137 others(1): Show |
4 | 307 | 0.0130 | 21 | c.344 others(40): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02080.hp1 HG02258.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(1): Show | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0005g0074 others(2): Show |
5 | 19 | 0.2632 | 21 | c.268 others(40): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949180 | A | AGAGAGAG others(14): Show |
intron_variant | MODIFIER | HG01175.hp1 HG02080.hp1 HG02257.hp1 others(4): Show |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0003t0003a0001c0003t0008others(2): Show | a0001c0003t0001g0130 a0001c0003t0001g0156 a0001c0003t0001g0181 others(4): Show |
7 | 194 | 0.0361 | 21 | c.110 others(42): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GGAGAGAG others(14): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 1 | 76 | 0.0132 | 21 | c.110 others(42): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(14): Show |
intron_variant | MODIFIER | HG02280.hp2 HG03139.hp1 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0024a0001c0001t0049 | a0001c0001t0006g0064 a0001c0001t0024g0103 a0001c0001t0049g0047 |
3 | 102 | 0.0294 | 21 | c.110 others(42): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(14): Show |
intron_variant | MODIFIER | HG00597.hp2 HG00741.hp2 HG01106.hp1 others(19): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(8): Show | a0001c0001t0005g0059 a0001c0001t0005g0118 a0001c0001t0005g0120 others(19): Show |
22 | 29 | 0.7586 | 21 | c.100 others(40): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193575 | T | TATATATT others(14): Show |
upstream_gene_variant | MODIFIER | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0004 | a0001c0001t0038a0001c0003t0003a0002c0004t0001others(6): Show | a0001c0001t0038g0393 a0001c0003t0003g0213 a0002c0004t0001g0210 others(18): Show |
21 | 112 | 0.1875 | 21 | c.-13 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1251 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193696 | A | ATATATAT others(14): Show |
upstream_gene_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0115 | 1 | 390 | 0.0026 | 21 | c.-14 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1372 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193703 | A | ATATATAT others(14): Show |
upstream_gene_variant | MODIFIER | HG01496.hp2 HG03471.hp1 NA21309.hp1 |
a0001a0014 | a0001c0016a0014c0036 | a0001c0016t0002a0001c0016t0014a0014c0036t0020 | a0001c0016t0002g0192 a0001c0016t0014g0191 a0014c0036t0020g0195 |
3 | 218 | 0.0138 | 21 | c.-15 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1379 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193710 | T | TTATATAT others(14): Show |
upstream_gene_variant | MODIFIER | HG03942.hp1 NA18955.hp2 NA19002.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0171 a0001c0001t0004g0174 a0001c0001t0004g0183 others(1): Show |
4 | 391 | 0.0102 | 21 | c.-15 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1386 | chr11 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38653169 | G | GGCGTTGA others(14): Show |
downstream_gene_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040 | 1 | 42 | 0.0238 | 21 | c.*33 others(32): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2517 | chr20 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAAAAAA others(14): Show |
intron_variant | MODIFIER | HG03139.hp1 HG03516.hp1 |
a0002 | a0002c0002 | a0002c0002t0018 | a0002c0002t0018g0205 a0002c0002t0018g0206 |
2 | 15 | 0.1333 | 21 | c.251 others(37): 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(14): Show |
intron_variant | MODIFIER | NA19057.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 34 | 0.0294 | 21 | c.313 others(40): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0128 | 1 | 24 | 0.0417 | 21 | c.245 others(40): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(14): Show |
intron_variant | MODIFIER | HG02071.hp2 HG06807.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 a0001c0001t0001g0101 |
2 | 132 | 0.0152 | 21 | c.176 others(40): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP45_chr19_1062167_1091628 | 1085529 | C | CTCCATCT others(14): Show |
intron_variant | MODIFIER | HG01978.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
a0001 | a0001c0004a0001c0017 | a0001c0004t0006a0001c0017t0006 | a0001c0004t0006g0024 a0001c0004t0006g0192 a0001c0004t0006g0194 others(2): Show |
6 | 391 | 0.0153 | 21 | c.306 others(38): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | chr19 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32143227 | G | GTTATTAT others(14): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0160 | 1 | 180 | 0.0056 | 21 | c.386 others(40): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32143236 | G | GTTATTAT others(14): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0163 | 1 | 174 | 0.0057 | 21 | c.386 others(40): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | A | AAATAATA others(14): Show |
intron_variant | MODIFIER | HG03516.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0117 a0001c0001t0008g0049 |
2 | 92 | 0.0217 | 21 | c.588 others(42): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11567566 | A | AAAAAAAA others(14): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 112 | 0.0089 | 21 | c.588 others(40): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(14): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0202 | 1 | 260 | 0.0038 | 21 | c.386 others(38): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44833096 | C | CTTTTCTT others(14): Show |
intron_variant | MODIFIER | HG01496.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0269 | 1 | 223 | 0.0045 | 21 | c.596 others(38): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1825162 | T | TCCCCCCC others(14): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0017 | a0017c0072 | a0017c0072t0007 | a0017c0072t0007g0330 | 1 | 360 | 0.0028 | 21 | c.-48 others(38): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1881263 | C | CTGGGGTC others(14): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02717.hp2 HG02897.hp2 others(2): Show |
a0001a0008a0012others(1): Show | a0001c0002a0008c0138a0012c0084others(2): Show | a0001c0002t0020a0008c0138t0018a0012c0084t0008others(2): Show | a0001c0002t0020g0264 a0008c0138t0018g0346 a0012c0084t0008g0352 others(2): Show |
5 | 362 | 0.0138 | 21 | c.960 others(38): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 9/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1888234 | G | GAGGTGAT others(14): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01243.hp1 HG02683.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0001others(9): Show | a0001c0001t0002g0249 a0001c0001t0003g0102 a0001c0002t0001g0248 others(11): Show |
14 | 357 | 0.0392 | 21 | c.118 others(40): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936493 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG00609.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0286 | 1 | 331 | 0.0030 | 21 | c.463 others(38): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0002 | a0002c0004 | a0002c0004t0013 | a0002c0004t0013g0188 | 1 | 78 | 0.0128 | 21 | c.463 others(38): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120367353 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0112 | 1 | 72 | 0.0139 | 21 | c.32+ others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3459995 | A | ATGCTAAG others(14): Show |
intron_variant | MODIFIER | HG01515.hp1 | a0004 | a0004c0010 | a0004c0010t0002 | a0004c0010t0002g0059 | 1 | 332 | 0.0030 | 21 | c.-19 others(38): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATTT others(14): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0044 | 1 | 45 | 0.0222 | 21 | c.319 others(42): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362008 | A | AAGAAGAA others(14): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0210 | 1 | 286 | 0.0035 | 21 | c.-11 others(38): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362104 | A | AAGGAGGA others(14): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0002 | a0002c0004 | a0002c0004t0004 | a0002c0004t0004g0023 | 1 | 283 | 0.0035 | 21 | c.-11 others(38): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385870 | T | TCTCTCTC others(14): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0055 | 1 | 255 | 0.0039 | 21 | c.967 others(38): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149598263 | C | CTCTTCTT others(14): Show |
intron_variant | MODIFIER | NA18946.hp2 | a0005 | a0005c0007 | a0005c0007t0003 | a0005c0007t0003g0145 | 1 | 229 | 0.0044 | 21 | c.186 others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56787718 | G | GATAATAA others(14): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0160 | 1 | 279 | 0.0036 | 21 | c.97- others(38): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | TogoVar | |||||||
ARHGEF4_chr2_130831914_131052253 | 130872938 | C | CTGGGGCA others(14): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0026 | a0001c0026t0001 | a0001c0026t0001g0107 | 1 | 142 | 0.0070 | 21 | c.39+ others(38): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26708266 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0085 | 1 | 15 | 0.0667 | 21 | c.113 others(42): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |