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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02523.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0076 | 1 | 198 | 0.0051 | 24 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0002 | a0001c0002t0017 | a0001c0002t0017g0175 | 1 | 198 | 0.0051 | 24 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02572.hp1 NA18957.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0008t0020 | a0001c0001t0002g0118a0001c0008t0020g0177 | 2 | 198 | 0.0101 | 24 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATGT others(17): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0047 | a0001c0001t0047g0127 | 1 | 198 | 0.0051 | 24 | c.110 others(45): 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(17): Show |
intron_variant | MODIFIER | HG03130.hp1 NA19082.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0023 | a0001c0001t0002g0126a0001c0001t0023g0055 | 2 | 198 | 0.0101 | 24 | c.110 others(43): 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(17): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(12): Show | a0001c0001t0003g0167a0001c0001t0004g0099a0001c0001t0006g0096others(14): Show | 17 | 198 | 0.0859 | 24 | c.110 others(43): 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(17): Show |
intron_variant | MODIFIER | HG04199.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0141a0001c0001t0002g0118a0001c0001t0005g0058others(1): Show | 4 | 198 | 0.0202 | 24 | c.110 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | NA19002.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0133 | 1 | 198 | 0.0051 | 24 | c.198 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(17): Show |
upstream_gene_variant | MODIFIER | HG02818.hp1 HG03098.hp1 NA20300.hp1 |
a0001a0006 | a0001c0001a0001c0003a0006c0009 | a0001c0001t0001a0001c0003t0003a0006c0009t0009 | a0001c0001t0001g0149a0001c0003t0003g0154a0006c0009t0009g0153 | 3 | 248 | 0.0121 | 24 | c.-24 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCGCACAC others(17): Show |
upstream_gene_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0151 | 1 | 248 | 0.0040 | 24 | c.-24 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(17): Show |
intron_variant | MODIFIER | HG02451.hp1 HG04184.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0020 | a0001c0001t0001a0001c0020t0023 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0020t0023g0101 | 3 | 248 | 0.0121 | 24 | c.122 others(39): 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(17): Show |
upstream_gene_variant | MODIFIER | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0055a0001c0002t0001a0001c0002t0012others(6): Show | a0001c0001t0055g0306a0001c0002t0001g0014a0001c0002t0001g0080others(9): Show | 12 | 310 | 0.0387 | 24 | c.-12 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(17): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0003 | a0003c0006 | a0003c0006t0056 | a0003c0006t0056g0011 | 1 | 310 | 0.0032 | 24 | c.100 others(41): 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(17): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02293.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0007a0002c0003t0026 | a0001c0001t0007g0293a0002c0003t0026g0294 | 2 | 310 | 0.0065 | 24 | c.100 others(43): 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(17): Show |
intron_variant | MODIFIER | HG00639.hp1 HG02135.hp1 HG02717.hp1 others(5): Show |
a0001a0003a0012 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0006a0001c0001t0008a0001c0004t0003others(3): Show | a0001c0001t0006g0092a0001c0001t0006g0124a0001c0001t0008g0199others(5): Show | 8 | 310 | 0.0258 | 24 | c.683 others(41): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(17): Show |
intron_variant | MODIFIER | HG00438.hp1 HG01993.hp2 HG02004.hp1 others(7): Show |
a0001a0007 | a0001c0001a0001c0010a0001c0014others(1): Show | a0001c0001t0002a0001c0010t0008a0001c0014t0004others(1): Show | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(7): Show | 10 | 398 | 0.0251 | 24 | c.226 others(43): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46879587 | A | AAAATAAA others(17): Show |
intron_variant | MODIFIER | HG00597.hp2 HG00735.hp1 HG01255.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0023others(4): Show | a0001c0001t0001g0130a0001c0001t0001g0165a0001c0001t0001g0173others(14): Show | 17 | 298 | 0.0571 | 24 | c.-18 others(45): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46879615 | T | TAAATAAA others(17): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0286 | 1 | 298 | 0.0034 | 24 | c.-18 others(45): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144561755 | A | ATCCAGTG others(17): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0228a0001c0001t0003g0023a0001c0001t0004g0237others(3): Show | 6 | 246 | 0.0244 | 24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561796 | G | GGACTTAC others(17): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(2): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | 246 | 0.0569 | 24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561796 | G | GGACTTAC others(17): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
a0001a0004a0005 | a0001c0003a0001c0005a0001c0007others(3): Show | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(6): Show | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(10): Show | 13 | 246 | 0.0529 | 24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562021 | C | CACTCCAG others(17): Show |
intron_variant | MODIFIER | HG02135.hp1 HG02809.hp2 NA20129.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0001 | a0001c0001t0001g0053a0001c0001t0004g0158a0001c0002t0001g0082 | 3 | 246 | 0.0122 | 24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562764 | T | TCACTCCA others(17): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0023 | 1 | 246 | 0.0041 | 24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | NA19005.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 286 | 0.0035 | 24 | c.313 others(43): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(17): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 286 | 0.0035 | 24 | c.385 others(43): 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(17): Show |
intron_variant | MODIFIER | HG01257.hp2 HG03492.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0012 | a0001c0001t0001g0086a0002c0002t0012g0052 | 2 | 286 | 0.0070 | 24 | c.245 others(43): 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(17): Show |
intron_variant | MODIFIER | NA18992.hp1 NA19081.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0221a0001c0003t0003g0273 | 2 | 286 | 0.0070 | 24 | c.245 others(43): 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(17): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0229 | 1 | 230 | 0.0044 | 24 | c.53+ others(41): 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(17): Show |
intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0230 | 1 | 230 | 0.0044 | 24 | c.53+ others(41): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(17): Show |
intron_variant | MODIFIER | HG01934.hp1 HG01981.hp2 NA19043.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0001t0008a0001c0005t0032 | a0001c0001t0002g0023a0001c0001t0008g0037a0001c0005t0032g0192 | 3 | 230 | 0.0130 | 24 | c.862 others(39): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32076986 | T | TGCGCCGC others(17): Show |
upstream_gene_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 186 | 0.0054 | 24 | c.-61 others(33): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 317 | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(17): Show |
intron_variant | MODIFIER | HG02698.hp1 HG02735.hp1 HG03516.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0117a0002c0002t0003g0005a0002c0002t0003g0016 | 3 | 144 | 0.0208 | 24 | c.589 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | A | AGAGGAGG others(17): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 144 | 0.0069 | 24 | c.589 others(45): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590865 | A | AGAAAAGA others(17): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 | 1 | 144 | 0.0069 | 24 | c.588 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP9_chr12_57467269_57484866 | 57483097 | T | TCAAAAAA others(17): Show |
upstream_gene_variant | MODIFIER | HG01256.hp1 HG02622.hp2 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0080 | 3 | 406 | 0.0074 | 24 | c.-33 others(35): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 3232 | chr12 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285909 | C | CCCAACCC others(17): Show |
downstream_gene_variant | MODIFIER | HG02055.hp2 HG02886.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0007g0026 | 3 | 442 | 0.0068 | 24 | c.*30 others(35): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2900 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285966 | T | TCCCAACC others(17): Show |
downstream_gene_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0024 | 1 | 442 | 0.0023 | 24 | c.*31 others(35): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2957 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1858143 | A | AGTCCCCA others(17): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01255.hp1 HG01346.hp1 others(26): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(24): Show | a0001c0001t0002g0066a0001c0001t0019g0278a0001c0002t0001g0037others(26): Show | 29 | 363 | 0.0799 | 24 | c.193 others(37): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0106 | a0001c0106t0042 | a0001c0106t0042g0330 | 1 | 363 | 0.0028 | 24 | c.118 others(43): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | C | CTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0185 | 1 | 363 | 0.0028 | 24 | c.214 others(43): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0015 | 1 | 362 | 0.0028 | 24 | c.463 others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(17): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(20): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0004a0003c0003others(3): Show | a0001c0001t0007a0001c0001t0020a0002c0004t0008others(5): Show | a0001c0001t0007g0143a0001c0001t0020g0170a0002c0004t0008g0197others(20): Show | 23 | 362 | 0.0635 | 24 | c.33- others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCTCACAC others(17): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0209 | 1 | 362 | 0.0028 | 24 | c.33- others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157036164 | T | TATATATG others(17): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01243.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0167a0001c0001t0004g0168 | 2 | 362 | 0.0055 | 24 | c.32+ others(39): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(17): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0300 | 1 | 308 | 0.0033 | 24 | c.32+ others(39): 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(17): Show |
intron_variant | MODIFIER | HG02922.hp2 HG03195.hp1 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0018 | a0001c0001t0001g0233a0001c0001t0018g0280a0001c0001t0018g0281 | 3 | 308 | 0.0097 | 24 | c.32+ others(39): 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(17): Show |
intron_variant | MODIFIER | HG01993.hp1 HG02683.hp2 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011a0001c0001t0013 | a0001c0001t0001g0198a0001c0001t0011g0192a0001c0001t0013g0197 | 3 | 308 | 0.0097 | 24 | c.32+ others(39): 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(17): Show |
intron_variant | MODIFIER | HG03491.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 | 1 | 308 | 0.0033 | 24 | c.32+ others(39): 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(17): Show |
intron_variant | MODIFIER | HG02135.hp2 NA18942.hp2 NA18967.hp1 others(2): Show |
a0002 | a0002c0003 | a0002c0003t0002a0002c0003t0017 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0073others(2): Show | 5 | 308 | 0.0162 | 24 | c.32+ others(41): 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(17): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0034 | 1 | 308 | 0.0033 | 24 | c.33- others(39): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |