regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85655810 | G | GAGAGAGA others(10): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0051 | 1 | 108 | 0.0093 | 17 | c.181 others(36): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655812 | G | GAGAGAGA others(10): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02717.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0016 | a0001c0001t0001g0067a0001c0002t0016g0055 | 2 | 108 | 0.0185 | 17 | c.181 others(36): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(10): Show |
intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0003 | a0001c0003t0038 | a0001c0003t0038g0155 | 1 | 198 | 0.0051 | 17 | c.487 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(10): Show |
intron_variant | MODIFIER | NA18990.hp1 NA19082.hp1 |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0010 | a0001c0003t0003g0140a0001c0003t0010g0077 | 2 | 198 | 0.0101 | 17 | c.487 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949178 | A | AGAGAGAG others(10): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0094 | 1 | 198 | 0.0051 | 17 | c.110 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949180 | A | AGAGAGAG others(10): Show |
intron_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0150 | 1 | 198 | 0.0051 | 17 | c.110 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(10): Show |
intron_variant | MODIFIER | HG03654.hp2 NA18972.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0034a0001c0003t0003 | a0001c0001t0034g0192a0001c0003t0003g0132 | 2 | 198 | 0.0101 | 17 | c.110 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(10): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0098 | 1 | 198 | 0.0051 | 17 | c.110 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 |
a0001 | a0001c0001 | a0001c0001t0015a0001c0001t0025 | a0001c0001t0015g0123a0001c0001t0025g0103 | 2 | 198 | 0.0101 | 17 | c.198 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143232630 | C | CTTTTTTT others(10): Show |
downstream_gene_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0141a0001c0001t0002g0007a0001c0001t0002g0013others(26): Show | 29 | 198 | 0.1465 | 17 | c.*10 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94219259 | A | ACCCTGCA others(10): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0002a0001c0005others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 337 | 356 | 0.9466 | 17 | c.340 others(32): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG03834.hp2 HG04228.hp1 |
a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0207a0001c0001t0018g0208 | 2 | 310 | 0.0065 | 17 | c.100 others(36): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(10): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(14): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001a0001c0002t0001g0028 | 17 | 420 | 0.0405 | 17 | c.-36 others(28): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02976.hp1 NA18906.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0006 | a0001c0001t0003g0071a0001c0004t0006g0070 | 2 | 246 | 0.0081 | 17 | c.-82 others(36): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG01891.hp1 NA19084.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0013a0002c0005t0010 | a0001c0001t0013g0168a0002c0005t0010g0044 | 2 | 286 | 0.0070 | 17 | c.313 others(36): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0174 | 1 | 286 | 0.0035 | 17 | c.385 others(34): 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(10): Show |
intron_variant | MODIFIER | HG01258.hp1 HG01891.hp2 NA20752.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0004 | a0002c0002t0002g0021a0002c0002t0002g0067a0002c0002t0004g0107 | 3 | 286 | 0.0105 | 17 | c.245 others(36): 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(10): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0119 | 1 | 286 | 0.0035 | 17 | c.245 others(36): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(65): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0114others(65): Show | 68 | 230 | 0.2957 | 17 | c.54- others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12926405 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0090 | 1 | 230 | 0.0044 | 17 | c.465 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(10): Show |
intron_variant | MODIFIER | NA18963.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0014 | 1 | 230 | 0.0044 | 17 | c.582 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02735.hp2 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005 | a0001c0001t0003g0069a0001c0001t0005g0057 | 2 | 230 | 0.0087 | 17 | c.176 others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0008 | a0001c0008t0015 | a0001c0008t0015g0134 | 1 | 230 | 0.0044 | 17 | c.176 others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0221 | 1 | 230 | 0.0044 | 17 | c.231 others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1085623 | T | TGTCTGTC others(10): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0020 | a0020c0051 | a0020c0051t0009 | a0020c0051t0009g0146 | 1 | 418 | 0.0024 | 17 | c.306 others(32): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32117947 | C | CTTAACCA others(10): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0001t0022a0001c0002t0005 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(5): Show | 9 | 186 | 0.0484 | 17 | c.386 others(34): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11411223 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 144 | 0.0069 | 17 | c.589 others(38): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAAAGAAA others(10): Show |
intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 144 | 0.0069 | 17 | c.588 others(36): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44751549 | T | TACAAAAT others(10): Show |
upstream_gene_variant | MODIFIER | HG02630.hp1 | a0002 | a0002c0011 | a0002c0011t0005 | a0002c0011t0005g0333 | 1 | 390 | 0.0026 | 17 | c.-11 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1025 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02572.hp1 HG02572.hp2 others(4): Show |
a0001a0002a0005others(2): Show | a0001c0008a0002c0028a0005c0015others(3): Show | a0001c0008t0001a0002c0028t0005a0005c0015t0001others(3): Show | a0001c0008t0001g0057a0002c0028t0005g0018a0005c0015t0001g0357others(4): Show | 7 | 390 | 0.0180 | 17 | c.386 others(34): 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(10): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0014 | a0014c0031 | a0014c0031t0003 | a0014c0031t0003g0290 | 1 | 390 | 0.0026 | 17 | c.596 others(34): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44867283 | C | CAAAAAAA others(10): Show |
downstream_gene_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0051 | 1 | 390 | 0.0026 | 17 | c.*46 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4500 | chr22 | TogoVar | ||||||
ARHGAP9_chr12_57467269_57484866 | 57479821 | A | AAGAATCA others(10): Show |
5_prime_UTR_variant | MODIFIER | HG03704.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0040 | 1 | 406 | 0.0025 | 17 | c.-12 others(26): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 1/18 | 416 | chr12 | TogoVar | |||||
ARHGDIG_chr16_275591_288010 | 285835 | A | ATTCTCCC others(10): Show |
downstream_gene_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0028 | 1 | 442 | 0.0023 | 17 | c.*30 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2826 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285937 | C | CCCCAACC others(10): Show |
downstream_gene_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0003 | 1 | 442 | 0.0023 | 17 | c.*31 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2928 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285943 | C | CCCCAACC others(10): Show |
downstream_gene_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0043 | 1 | 442 | 0.0023 | 17 | c.*31 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2934 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285949 | C | CCCCAACC others(10): Show |
downstream_gene_variant | MODIFIER | HG01109.hp1 HG01496.hp2 HG01515.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(1): Show | a0001c0001t0001g0002a0001c0001t0002g0009a0001c0001t0009g0001others(1): Show | 6 | 442 | 0.0136 | 17 | c.*31 others(28): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2940 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1824808 | T | TCCCCCGC others(10): Show |
intron_variant | MODIFIER | HG00738.hp1 HG03831.hp1 HG03927.hp1 others(1): Show |
a0001a0003 | a0001c0003a0001c0009a0001c0026others(1): Show | a0001c0003t0021a0001c0009t0006a0001c0026t0007others(1): Show | a0001c0003t0021g0318a0001c0009t0006g0120a0001c0026t0007g0129others(1): Show | 4 | 363 | 0.0110 | 17 | c.-48 others(32): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839389 | G | GGACTGTC others(10): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(27): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0003a0001c0004others(19): Show | a0001c0002t0026a0001c0003t0001a0001c0003t0026others(23): Show | a0001c0002t0026g0192a0001c0003t0001g0081a0001c0003t0001g0306others(27): Show | 30 | 363 | 0.0826 | 17 | c.-47 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839390 | A | AGCTGTCT others(10): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0024 | a0024c0094 | a0024c0094t0016 | a0024c0094t0016g0103 | 1 | 363 | 0.0028 | 17 | c.-47 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1945873 | A | AAGGAGCC others(10): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
a0001a0002a0003others(21): Show | a0001c0001a0001c0002a0001c0003others(147): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(227): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0069others(332): Show | 336 | 363 | 0.9256 | 17 | c.339 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1945882 | C | CGTGCTGG others(10): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0165 | 1 | 363 | 0.0028 | 17 | c.339 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1945900 | G | GTGCTGGG others(10): Show |
intron_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0051 | 1 | 363 | 0.0028 | 17 | c.339 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1945915 | G | GCGTGCTG others(10): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0036 | a0001c0036t0004 | a0001c0036t0004g0177 | 1 | 363 | 0.0028 | 17 | c.339 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0156 | 1 | 362 | 0.0028 | 17 | c.463 others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013300 | C | CACACACA others(10): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0167 | 1 | 362 | 0.0028 | 17 | c.33- others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347143 | C | CCTTTCCT others(10): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0008 | a0008c0014 | a0008c0014t0019 | a0008c0014t0019g0011 | 1 | 308 | 0.0033 | 17 | c.32+ others(32): 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(10): Show |
intron_variant | MODIFIER | NA18960.hp1 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0086 | 1 | 308 | 0.0033 | 17 | c.32+ others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0065 | 1 | 308 | 0.0033 | 17 | c.33- others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0193 | 1 | 228 | 0.0044 | 17 | c.319 others(38): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |