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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACAC others(9): Show |
intron_variant | MODIFIER | HG02738.hp1 NA18943.hp1 NA18987.hp1 others(2): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0012a0002c0004t0005a0002c0004t0025 | a0002c0002t0012g0192a0002c0004t0005g0111a0002c0004t0005g0120others(2): Show | 5 | 362 | 0.0138 | 16 | c.33- others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347151 | C | CCTTTCTT others(9): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0002 | a0001c0002t0034 | a0001c0002t0034g0013 | 1 | 308 | 0.0033 | 16 | c.32+ others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347175 | C | CCTTTCTT others(9): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | 308 | 0.0065 | 16 | c.32+ others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347179 | C | CCTTTCTT others(9): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01069.hp2 HG02155.hp2 others(8): Show |
a0001a0009 | a0001c0001a0001c0010a0009c0015 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(2): Show | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0004g0243others(8): Show | 11 | 308 | 0.0357 | 16 | c.32+ others(31): 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(9): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0296 | 1 | 308 | 0.0033 | 16 | c.32+ others(31): 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(9): Show |
intron_variant | MODIFIER | HG03540.hp1 NA19070.hp2 NA19081.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0290a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 4 | 308 | 0.0130 | 16 | c.32+ others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347266 | C | CTCTGTGT others(9): Show |
intron_variant | MODIFIER | NA19080.hp1 | a0001 | a0001c0004 | a0001c0004t0012 | a0001c0004t0012g0060 | 1 | 308 | 0.0033 | 16 | c.32+ others(31): 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(9): Show |
intron_variant | MODIFIER | HG00597.hp2 HG00738.hp1 HG03486.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0006 | a0001c0001t0002a0001c0001t0035a0001c0004t0005others(1): Show | a0001c0001t0002g0121a0001c0001t0035g0088a0001c0004t0005g0048others(1): Show | 4 | 308 | 0.0130 | 16 | c.32+ others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | A | AACACACA others(9): Show |
upstream_gene_variant | MODIFIER | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0006others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(6): Show | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0047others(17): Show | 29 | 428 | 0.0678 | 16 | c.-27 others(25): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3450012 | C | CGTGTGTG others(9): Show |
upstream_gene_variant | MODIFIER | HG00423.hp1 HG00597.hp2 HG00642.hp2 others(6): Show |
a0001a0002a0004others(1): Show | a0001c0005a0002c0002a0002c0003others(2): Show | a0001c0005t0001a0002c0002t0002a0002c0003t0002others(2): Show | a0001c0005t0001g0024a0001c0005t0001g0027a0002c0002t0002g0039others(6): Show | 9 | 334 | 0.0270 | 16 | c.-48 others(27): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4652 | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3475413 | G | GCGCTGAC others(9): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0002 | a0002c0007 | a0002c0007t0002 | a0002c0007t0002g0159 | 1 | 334 | 0.0030 | 16 | c.138 others(33): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3482315 | G | GGGGGGGG others(9): Show |
downstream_gene_variant | MODIFIER | HG00621.hp1 HG00673.hp2 HG01099.hp1 others(17): Show |
a0001a0007 | a0001c0001a0001c0005a0007c0018 | a0001c0001t0001a0001c0001t0004a0001c0005t0001others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0098a0001c0001t0001g0113others(17): Show | 20 | 334 | 0.0599 | 16 | c.*17 others(27): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1203 | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATAT others(9): Show |
intron_variant | MODIFIER | HG01978.hp2 NA18612.hp1 |
a0001a0007 | a0001c0001a0007c0010 | a0001c0001t0001a0007c0010t0001 | a0001c0001t0001g0188a0007c0010t0001g0187 | 2 | 228 | 0.0088 | 16 | c.319 others(37): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATAT others(9): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 228 | 0.0044 | 16 | c.319 others(37): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATATTT others(9): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0025 | 1 | 228 | 0.0044 | 16 | c.319 others(37): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73329373 | A | ATATTTTT others(9): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0026 | 1 | 228 | 0.0044 | 16 | c.319 others(37): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | C | CGTGTGTG others(9): Show |
intron_variant | MODIFIER | NA18939.hp2 NA19002.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0211a0001c0001t0010g0217 | 2 | 228 | 0.0088 | 16 | c.319 others(37): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | C | CGTGTGTG others(9): Show |
upstream_gene_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02896.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0047a0002c0007 | a0001c0001t0004a0001c0047t0002a0002c0007t0001 | a0001c0001t0004g0007a0001c0047t0002g0005a0002c0007t0001g0023others(1): Show | 4 | 298 | 0.0134 | 16 | c.-28 others(27): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7358215 | T | TTCCATCC others(9): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(23): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(9): Show | a0001c0001t0002a0001c0002t0003a0001c0013t0001others(12): Show | a0001c0001t0002g0028a0001c0001t0002g0130a0001c0001t0002g0159others(23): Show | 26 | 298 | 0.0873 | 16 | c.-11 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7358240 | T | TCCATCCA others(9): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0219 | 1 | 298 | 0.0034 | 16 | c.-11 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364365 | A | AAAGGAAG others(9): Show |
intron_variant | MODIFIER | HG01496.hp1 HG03486.hp1 NA18954.hp2 others(1): Show |
a0004a0006a0008others(1): Show | a0004c0015a0006c0008a0008c0010others(1): Show | a0004c0015t0003a0006c0008t0002a0008c0010t0033others(1): Show | a0004c0015t0003g0166a0006c0008t0002g0281a0008c0010t0033g0286others(1): Show | 4 | 298 | 0.0134 | 16 | c.15+ others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364390 | A | AAGGAAGG others(9): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0047a0002c0004others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(3): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(5): Show | 8 | 298 | 0.0269 | 16 | c.15+ others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(9): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(58): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0021others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(16): Show | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0216others(58): Show | 61 | 298 | 0.2047 | 16 | c.15+ others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364402 | A | AAGGAAGG others(9): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(4): Show |
a0002a0012a0016others(1): Show | a0002c0007a0012c0028a0016c0026others(1): Show | a0002c0007t0001a0012c0028t0018a0016c0026t0019others(1): Show | a0002c0007t0001g0021a0002c0007t0001g0022a0002c0007t0001g0023others(4): Show | 7 | 298 | 0.0235 | 16 | c.15+ others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7368007 | G | GAGGAAGG others(9): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0011 | a0011c0025 | a0011c0025t0005 | a0011c0025t0005g0013 | 1 | 298 | 0.0034 | 16 | c.16- others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7368020 | C | CGGAAGGA others(9): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(34): Show |
a0001a0003a0024 | a0001c0001a0003c0003a0024c0052 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(7): Show | a0001c0001t0001g0216a0001c0001t0002g0188a0001c0001t0002g0189others(34): Show | 37 | 298 | 0.1242 | 16 | c.16- others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7381691 | T | TAAATAAT others(9): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02717.hp2 others(1): Show |
a0001a0009 | a0001c0001a0001c0047a0009c0012 | a0001c0001t0004a0001c0047t0002a0009c0012t0010 | a0001c0001t0004g0004a0001c0001t0004g0007a0001c0047t0002g0005others(1): Show | 4 | 298 | 0.0134 | 16 | c.722 others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7381691 | T | TAATAAAT others(9): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0002 | a0002c0006 | a0002c0006t0007 | a0002c0006t0007g0270 | 1 | 298 | 0.0034 | 16 | c.722 others(31): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7389501 | T | TCCTTCCT others(9): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
a0002a0003a0017 | a0002c0004a0003c0003a0017c0051 | a0002c0004t0004a0003c0003t0001a0017c0051t0006 | a0002c0004t0004g0018a0002c0004t0004g0019a0002c0004t0004g0064others(4): Show | 7 | 298 | 0.0235 | 16 | c.967 others(33): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7407983 | A | AAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
a0002a0007a0025 | a0002c0004a0002c0006a0007c0014others(1): Show | a0002c0004t0021a0002c0006t0007a0007c0014t0004others(1): Show | a0002c0004t0021g0277a0002c0006t0007g0274a0007c0014t0004g0051others(2): Show | 5 | 298 | 0.0168 | 16 | c.967 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | A | AGTGAGTG others(9): Show |
downstream_gene_variant | MODIFIER | HG03209.hp2 | a0011 | a0011c0024 | a0011c0024t0015 | a0011c0024t0015g0009 | 1 | 298 | 0.0034 | 16 | c.*44 others(27): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | A | AGTGTGTG others(9): Show |
downstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(26): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0019others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0003others(14): Show | a0001c0001t0001g0053a0001c0001t0002g0193a0001c0002t0003g0060others(26): Show | 29 | 298 | 0.0973 | 16 | c.*44 others(27): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7475530 | A | ACACACAC others(9): Show |
downstream_gene_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0021 | a0001c0021t0006 | a0001c0021t0006g0088 | 1 | 298 | 0.0034 | 16 | c.*52 others(27): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3053 | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154161312 | C | CAAATATA others(9): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0009a0001c0015others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(64): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | 283 | 0.9541 | 16 | c.148 others(35): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154186136 | G | GACACACA others(9): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204 | 1 | 283 | 0.0035 | 16 | c.148 others(35): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154186886 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0003 | a0002c0003t0045 | a0002c0003t0045g0095 | 1 | 283 | 0.0035 | 16 | c.148 others(33): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | T | TACACACA others(9): Show |
intron_variant | MODIFIER | HG02074.hp2 NA19007.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0161a0001c0001t0002g0217 | 2 | 283 | 0.0071 | 16 | c.209 others(33): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154237538 | T | TCACACAC others(9): Show |
intron_variant | MODIFIER | HG02015.hp2 HG02165.hp2 NA18942.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0005 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0194others(3): Show | 6 | 283 | 0.0212 | 16 | c.209 others(35): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73631782 | G | GATCTCAA others(9): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(46): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0021a0001c0025others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(35): Show | a0001c0001t0001g0063a0001c0001t0002g0050a0001c0001t0002g0058others(46): Show | 49 | 188 | 0.2606 | 16 | c.-12 others(33): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73703647 | T | TTGTGTGT others(9): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0003 | a0003c0058 | a0003c0058t0001 | a0003c0058t0001g0139 | 1 | 188 | 0.0053 | 16 | c.33+ others(33): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | C | CTTCTCTT others(9): Show |
intron_variant | MODIFIER | NA19010.hp2 | a0020 | a0020c0078 | a0020c0078t0004 | a0020c0078t0004g0051 | 1 | 188 | 0.0053 | 16 | c.34- others(33): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73938160 | C | CCACACAC others(9): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0002 | a0002c0029 | a0002c0029t0001 | a0002c0029t0001g0091 | 1 | 188 | 0.0053 | 16 | c.494 others(35): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF2_chr1_155941854_155983547 | 155945280 | G | GGTGTGTG others(9): Show |
downstream_gene_variant | MODIFIER | HG02559.hp1 NA18984.hp2 NA19057.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048a0001c0001t0001g0156a0001c0001t0001g0175others(1): Show | 4 | 284 | 0.0141 | 16 | c.*26 others(27): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1573 | chr1 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38917102 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0010 | 1 | 278 | 0.0036 | 16 | c.-85 others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149599434 | C | CTTATTTA others(9): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0284 | 1 | 394 | 0.0025 | 16 | c.186 others(33): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105590074 | A | AGAAGGAA others(9): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0096 | 1 | 186 | 0.0054 | 16 | c.384 others(31): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF3_chr3_56722420_56806949 | 56764637 | C | CGATATGA others(9): Show |
intron_variant | MODIFIER | NA18956.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0218 | 1 | 358 | 0.0028 | 16 | c.204 others(33): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926008 | T | TTTTCTTT others(9): Show |
intron_variant | MODIFIER | HG02698.hp2 HG03130.hp2 HG03704.hp1 others(6): Show |
a0001a0011 | a0001c0001a0001c0002a0011c0049 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0046others(6): Show | 9 | 144 | 0.0625 | 16 | c.355 others(35): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130926014 | C | CTCTTTCT others(9): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02257.hp1 HG02559.hp1 |
a0001a0006 | a0001c0025a0001c0026a0006c0050 | a0001c0025t0005a0001c0026t0001a0006c0050t0001 | a0001c0025t0005g0067a0001c0026t0001g0080a0006c0050t0001g0142 | 3 | 144 | 0.0208 | 16 | c.355 others(35): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130926048 | C | CTTTCTCT others(9): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01258.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0007 | a0001c0007t0004 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(1): Show | 4 | 144 | 0.0278 | 16 | c.355 others(35): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |