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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP18_chr6_129571132_129715177 | 129625728 | A | ATATTAAT others(29): Show |
intron_variant | MODIFIER | HG02486.hp1 NA20300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | 234 | 0.0085 | 36 | c.786 others(53): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(29): Show |
downstream_gene_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(25): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0011a0001c0004t0001others(7): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0083 others(25): Show |
28 | 79 | 0.3544 | 36 | c.*21 others(47): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(29): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0053 | a0001c0001t0053g0078 | 1 | 76 | 0.0132 | 36 | c.110 others(57): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGGAG others(29): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0037 | 1 | 100 | 0.0100 | 36 | c.110 others(57): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0061 | 1 | 144 | 0.0069 | 36 | c.110 others(57): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(29): Show |
intron_variant | MODIFIER | HG02155.hp2 NA18990.hp2 NA19009.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0048a0001c0003t0005 | a0001c0001t0003g0019 a0001c0001t0048g0127 a0001c0003t0005g0060 |
3 | 50 | 0.0600 | 36 | c.110 others(55): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012557 | A | ACATATAT others(29): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0055 | a0001c0001t0055g0072 | 1 | 196 | 0.0051 | 36 | c.110 others(55): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(29): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0123 | 1 | 121 | 0.0083 | 36 | c.122 others(51): 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(29): Show |
intron_variant | MODIFIER | HG00408.hp1 HG02735.hp2 NA18747.hp1 others(2): Show |
a0002a0003 | a0002c0002a0002c0005a0003c0022 | a0002c0002t0002a0002c0005t0002a0003c0022t0003 | a0002c0002t0002g0131 a0002c0002t0002g0134 a0002c0002t0002g0135 others(2): Show |
5 | 125 | 0.0400 | 36 | c.122 others(51): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0050 | 1 | 201 | 0.0050 | 36 | c.-12 others(47): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(29): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0034others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0003t0005others(2): Show | a0001c0001t0002g0098 a0001c0001t0002g0105 a0001c0001t0002g0156 others(10): Show |
13 | 115 | 0.1130 | 36 | c.226 others(55): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193575 | T | TAATATAT others(29): Show |
upstream_gene_variant | MODIFIER | HG01361.hp2 HG03669.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0002 | a0001c0001t0002g0103 a0001c0002t0002g0104 |
2 | 93 | 0.0215 | 36 | c.-13 others(47): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1251 | chr11 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144686873 | T | TGTGACCA others(29): Show |
upstream_gene_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0185 | 1 | 244 | 0.0041 | 36 | c.-12 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1028 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144686879 | A | AACACACT others(29): Show |
upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(164): Show |
167 | 239 | 0.6987 | 36 | c.-12 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1034 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687010 | C | CCACCCCC others(29): Show |
upstream_gene_variant | MODIFIER | NA18943.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0113 | 1 | 242 | 0.0041 | 36 | c.-14 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1165 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687084 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG01074.hp1 NA18963.hp1 NA18979.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0244 a0001c0002t0001g0061 a0001c0002t0001g0093 |
3 | 176 | 0.0170 | 36 | c.-14 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1239 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687263 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0161 | 1 | 195 | 0.0051 | 36 | c.-16 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1418 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687281 | G | GGCGGTGA others(29): Show |
upstream_gene_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0057 | 1 | 183 | 0.0055 | 36 | c.-16 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1436 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687321 | C | CGAGCACT others(29): Show |
upstream_gene_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0160 | 1 | 141 | 0.0071 | 36 | c.-17 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1476 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687405 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0168 | 1 | 211 | 0.0047 | 36 | c.-18 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1560 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687405 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0017 | 1 | 211 | 0.0047 | 36 | c.-18 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1560 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687440 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0162 | 1 | 220 | 0.0045 | 36 | c.-18 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1595 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687515 | C | CGTGACCA others(29): Show |
upstream_gene_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0011 | 1 | 233 | 0.0043 | 36 | c.-19 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1670 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687585 | C | CGTGACCA others(29): Show |
upstream_gene_variant | MODIFIER | HG01168.hp2 HG01192.hp1 HG01952.hp1 |
a0001 | a0001c0005a0001c0010 | a0001c0005t0001a0001c0010t0001 | a0001c0005t0001g0005 a0001c0005t0001g0008 a0001c0010t0001g0010 |
3 | 240 | 0.0125 | 36 | c.-19 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1740 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687616 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 220 | 0.0045 | 36 | c.-20 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1771 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144687687 | A | ACCCCGTG others(29): Show |
upstream_gene_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0004 | 1 | 172 | 0.0058 | 36 | c.-20 others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1842 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100779498 | A | ACATATAT others(29): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0006 | 1 | 279 | 0.0036 | 36 | c.250 others(53): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100779551 | C | CATATATA others(29): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0010 | 1 | 277 | 0.0036 | 36 | c.250 others(53): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(29): Show |
intron_variant | MODIFIER | NA18989.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 24 | 0.0417 | 36 | c.245 others(55): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(29): Show |
intron_variant | MODIFIER | HG02300.hp1 NA20129.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0002g0156 |
3 | 45 | 0.0667 | 36 | c.862 others(51): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153903420 | T | TGGTGTGG others(29): Show |
downstream_gene_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 306 | 0.0033 | 36 | c.*43 others(47): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3957 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11190464 | T | TATATTTA others(29): Show |
intron_variant | MODIFIER | HG01515.hp1 HG02698.hp1 HG03492.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0006a0002c0002t0014 | a0002c0002t0003g0005 a0002c0002t0003g0008 a0002c0002t0003g0009 others(3): Show |
6 | 135 | 0.0444 | 36 | c.821 others(53): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(29): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 52 | 0.0192 | 36 | c.589 others(55): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44803661 | A | ATGCACAC others(29): Show |
intron_variant | MODIFIER | HG03041.hp1 HG03139.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0074 a0001c0001t0003g0201 |
2 | 274 | 0.0073 | 36 | c.167 others(53): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44803679 | G | GTGCACAC others(29): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01256.hp1 HG01358.hp2 others(18): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0007a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(12): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0003g0023 others(18): Show |
21 | 246 | 0.0854 | 36 | c.167 others(53): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 281311 | G | GGGGGGCC others(29): Show |
intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(4): Show |
10 | 436 | 0.0229 | 36 | c.74- others(49): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285966 | T | TCCCAACC others(29): Show |
downstream_gene_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 414 | 0.0024 | 36 | c.*31 others(47): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2957 | chr16 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1841802 | A | AGGAACTG others(29): Show |
intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0002 | a0001c0002t0020 | a0001c0002t0020g0264 | 1 | 333 | 0.0030 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841802 | A | AGGAACTG others(29): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0052 | a0001c0052t0045 | a0001c0052t0045g0336 | 1 | 333 | 0.0030 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841836 | A | ACGGGAAC others(29): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01516.hp1 |
a0001 | a0001c0003 | a0001c0003t0008a0001c0003t0029 | a0001c0003t0008g0117 a0001c0003t0029g0168 |
2 | 166 | 0.0120 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841910 | G | GGGAACTG others(29): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0010 | a0010c0098 | a0010c0098t0008 | a0010c0098t0008g0258 | 1 | 297 | 0.0034 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841928 | G | GGGAACTG others(29): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0189 | 1 | 280 | 0.0036 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841946 | C | CGGAACTG others(29): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 NA19010.hp1 |
a0001a0005 | a0001c0008a0001c0050a0005c0087 | a0001c0008t0002a0001c0050t0002a0005c0087t0002 | a0001c0008t0002g0199 a0001c0050t0002g0234 a0005c0087t0002g0254 |
3 | 264 | 0.0114 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841956 | G | GCCGCGGC others(29): Show |
intron_variant | MODIFIER | HG02129.hp1 HG02129.hp2 NA18612.hp1 |
a0001 | a0001c0005a0001c0014 | a0001c0005t0001a0001c0005t0008a0001c0014t0002 | a0001c0005t0001g0080 a0001c0005t0008g0126 a0001c0014t0002g0229 |
3 | 326 | 0.0092 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841974 | G | GCCGCGGC others(29): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02258.hp2 HG04184.hp1 others(2): Show |
a0001 | a0001c0002a0001c0006a0001c0037others(1): Show | a0001c0002t0001a0001c0006t0039a0001c0037t0004others(1): Show | a0001c0002t0001g0071 a0001c0002t0001g0341 a0001c0006t0039g0160 others(2): Show |
5 | 287 | 0.0174 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841992 | G | GCCGCGAC others(29): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0004 | a0004c0038 | a0004c0038t0019 | a0004c0038t0019g0243 | 1 | 273 | 0.0037 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841992 | G | GCCGCGGC others(29): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0179 | 1 | 273 | 0.0037 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1842028 | G | GCCGCGAC others(29): Show |
intron_variant | MODIFIER | NA18959.hp2 NA18963.hp2 |
a0001a0002 | a0001c0001a0002c0031 | a0001c0001t0014a0002c0031t0001 | a0001c0001t0014g0185 a0002c0031t0001g0247 |
2 | 311 | 0.0064 | 36 | c.-47 others(53): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAAAAAA others(29): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0109 | 1 | 78 | 0.0128 | 36 | c.463 others(53): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7362020 | A | AAGAAGAA others(29): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03516.hp1 |
a0002 | a0002c0004 | a0002c0004t0004 | a0002c0004t0004g0235 a0002c0004t0004g0236 |
2 | 281 | 0.0071 | 36 | c.-11 others(53): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |