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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF12_chr11_120331413_120494937 | 120334861 | GTGTA | G | upstream_gene_variant | MODIFIER | HG01496.hp2 HG01975.hp2 HG01993.hp2 others(17): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0001a0001c0001t0021a0001c0001t0022others(1): Show | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0145others(17): Show | 20 | 308 | 0.0649 | -4 | c.-23 others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1551 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120334863 | GTATA | G | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(22): Show |
a0001a0006a0009 | a0001c0001a0001c0010a0006c0013others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(6): Show | a0001c0001t0001g0193a0001c0001t0001g0196a0001c0001t0001g0201others(22): Show | 25 | 308 | 0.0812 | -4 | c.-23 others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1549 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120337293 | CTTCG | C | intron_variant | MODIFIER | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | 308 | 0.0162 | -4 | c.32+ others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120344265 | CAAAA | C | intron_variant | MODIFIER | HG01257.hp2 HG02451.hp1 HG02976.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0006a0001c0002t0003others(2): Show | a0001c0001t0002g0133a0001c0001t0006g0122a0001c0002t0003g0045others(5): Show | 8 | 308 | 0.0260 | -4 | c.32+ others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347132 | TTTCC | T | intron_variant | MODIFIER | HG00099.hp1 HG00735.hp1 HG01358.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(1): Show | a0001c0001t0001g0146a0001c0001t0001g0255a0001c0001t0001g0287others(6): Show | 10 | 308 | 0.0325 | -4 | c.32+ others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347264 | CTCTG | C | intron_variant | MODIFIER | HG00597.hp2 HG01123.hp2 HG01884.hp1 others(1): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0003a0001c0002t0007a0001c0004t0005 | a0001c0002t0003g0035a0001c0002t0007g0041a0001c0002t0007g0043others(1): Show | 4 | 308 | 0.0130 | -4 | c.32+ others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120349463 | GTATT | G | intron_variant | MODIFIER | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
a0001 | a0001c0007 | a0001c0007t0015 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | 308 | 0.0097 | -4 | c.32+ others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120350631 | ACTGT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0007a0001c0002t0016 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(28): Show | 32 | 308 | 0.1039 | -4 | c.32+ others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120442427 | TACAC | T | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0023a0001c0001t0026others(1): Show | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0175others(4): Show | 7 | 308 | 0.0227 | -4 | c.130 others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120442453 | CACAT | C | intron_variant | MODIFIER | HG03486.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0012others(1): Show | a0001c0001t0035a0001c0002t0019a0001c0012t0001others(1): Show | a0001c0001t0035g0088a0001c0002t0019g0012a0001c0012t0001g0296others(1): Show | 4 | 308 | 0.0130 | -4 | c.130 others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120492501 | ATTCT | A | downstream_gene_variant | MODIFIER | HG01952.hp2 HG02273.hp1 NA18940.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009a0001c0001t0014 | a0001c0001t0002g0113a0001c0001t0002g0132a0001c0001t0009g0005others(4): Show | 7 | 308 | 0.0227 | -4 | c.*74 others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2565 | chr11 | TogoVar | ||||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | AACAC | A | upstream_gene_variant | MODIFIER | HG02135.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0001a0002c0002t0001g0013 | 7 | 428 | 0.0164 | -4 | c.-27 others(13): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3450012 | CGTGT | C | upstream_gene_variant | MODIFIER | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
a0001a0003 | a0001c0001a0003c0004a0003c0006others(2): Show | a0001c0001t0001a0003c0004t0002a0003c0006t0002others(3): Show | a0001c0001t0001g0108a0003c0004t0002g0007a0003c0004t0002g0066others(20): Show | 27 | 334 | 0.0808 | -4 | c.-48 others(15): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4652 | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3485931 | CAAAA | C | downstream_gene_variant | MODIFIER | HG01123.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
a0002 | a0002c0003a0002c0014 | a0002c0003t0002a0002c0014t0006 | a0002c0003t0002g0004a0002c0003t0002g0005a0002c0003t0002g0018others(2): Show | 6 | 334 | 0.0180 | -4 | c.*53 others(15): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4819 | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329322 | CATAT | C | intron_variant | MODIFIER | HG00438.hp2 HG01255.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0002 | a0001c0001t0001g0207a0003c0003t0002g0052 | 2 | 228 | 0.0088 | -4 | c.319 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | CGTGT | C | intron_variant | MODIFIER | HG01255.hp1 HG02055.hp2 HG02451.hp1 others(3): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0005 | a0001c0001t0001a0003c0003t0002a0004c0005t0005 | a0001c0001t0001g0181a0001c0001t0001g0198a0003c0003t0002g0043others(3): Show | 6 | 228 | 0.0263 | -4 | c.319 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73361920 | CCACA | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
a0001a0002a0003others(8): Show | a0001c0001a0002c0002a0002c0004others(21): Show | a0001c0001t0004a0002c0002t0001a0002c0002t0008others(28): Show | a0001c0001t0004g0098a0001c0001t0004g0099a0002c0002t0001g0023others(93): Show | 98 | 228 | 0.4298 | -4 | c.449 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7347395 | CAAAA | C | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
a0001a0002a0006others(4): Show | a0001c0001a0002c0004a0002c0005others(6): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(10): Show | a0001c0001t0002g0043a0001c0001t0004g0293a0001c0001t0005g0291others(18): Show | 21 | 298 | 0.0705 | -4 | c.-19 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1541 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7350761 | GGGGT | G | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(23): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0016others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(14): Show | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0035others(23): Show | 26 | 298 | 0.0873 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7350767 | GGTGT | G | intron_variant | MODIFIER | HG02615.hp1 HG03579.hp1 HG03834.hp1 |
a0001a0002 | a0001c0019a0002c0007 | a0001c0019t0006a0002c0007t0001 | a0001c0019t0006g0063a0002c0007t0001g0016a0002c0007t0001g0017 | 3 | 298 | 0.0101 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7351305 | TTTTG | T | intron_variant | MODIFIER | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(27): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0042others(11): Show | a0001c0001t0002a0001c0001t0008a0001c0002t0003others(14): Show | a0001c0001t0002g0138a0001c0001t0002g0252a0001c0001t0008g0137others(27): Show | 30 | 298 | 0.1007 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7351689 | CCTCT | C | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(46): Show |
a0001a0003a0012others(2): Show | a0001c0001a0001c0002a0001c0013others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(17): Show | a0001c0001t0001g0216a0001c0001t0002g0144a0001c0001t0002g0182others(46): Show | 49 | 298 | 0.1644 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7355068 | TCACA | T | intron_variant | MODIFIER | HG02615.hp1 HG03579.hp1 HG03579.hp2 others(3): Show |
a0001a0002a0007others(1): Show | a0001c0002a0001c0019a0002c0007others(2): Show | a0001c0002t0003a0001c0019t0006a0002c0007t0001others(2): Show | a0001c0002t0003g0060a0001c0019t0006g0057a0002c0007t0001g0016others(3): Show | 6 | 298 | 0.0201 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7358159 | TTCCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
a0001a0002a0003others(28): Show | a0001c0001a0001c0002a0001c0013others(46): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(76): Show | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0077others(268): Show | 271 | 298 | 0.9094 | -4 | c.-11 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7363421 | GGAAA | G | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(1): Show |
a0006 | a0006c0008 | a0006c0008t0002a0006c0008t0032 | a0006c0008t0002g0281a0006c0008t0002g0282a0006c0008t0002g0283others(1): Show | 4 | 298 | 0.0134 | -4 | c.15+ others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364041 | AAATG | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
a0001a0002a0003others(25): Show | a0001c0001a0001c0002a0001c0013others(40): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(66): Show | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0077others(232): Show | 235 | 298 | 0.7886 | -4 | c.15+ others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7364365 | AAAGG | A | intron_variant | MODIFIER | HG06807.hp1 NA19030.hp1 NA19043.hp1 |
a0001a0020 | a0001c0002a0001c0043a0020c0044 | a0001c0002t0003a0001c0043t0015a0020c0044t0001 | a0001c0002t0003g0280a0001c0043t0015g0278a0020c0044t0001g0279 | 3 | 298 | 0.0101 | -4 | c.15+ others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7375289 | GAAAA | G | intron_variant | MODIFIER | HG00544.hp1 HG00673.hp2 HG01099.hp1 others(31): Show |
a0001a0003a0015others(1): Show | a0001c0001a0001c0016a0001c0046others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0016t0014others(9): Show | a0001c0001t0001g0216a0001c0001t0002g0181a0001c0001t0002g0182others(31): Show | 34 | 298 | 0.1141 | -4 | c.276 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7375313 | AAAAG | A | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp2 NA19043.hp2 |
a0012a0016 | a0012c0027a0012c0028a0016c0026 | a0012c0027t0005a0012c0028t0018a0016c0026t0019 | a0012c0027t0005g0025a0012c0028t0018g0045a0016c0026t0019g0046 | 3 | 298 | 0.0101 | -4 | c.276 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7375344 | AAAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(48): Show |
a0001a0003a0013others(2): Show | a0001c0001a0001c0016a0001c0046others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(13): Show | a0001c0001t0001g0216a0001c0001t0002g0181a0001c0001t0002g0182others(48): Show | 51 | 298 | 0.1711 | -4 | c.276 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7375354 | AAAGG | A | intron_variant | MODIFIER | HG00408.hp1 HG01099.hp2 HG02040.hp1 others(14): Show |
a0002a0006a0011others(2): Show | a0002c0007a0006c0008a0011c0024others(3): Show | a0002c0007t0001a0006c0008t0001a0006c0008t0002others(5): Show | a0002c0007t0001g0011a0002c0007t0001g0016a0002c0007t0001g0017others(14): Show | 17 | 298 | 0.0571 | -4 | c.276 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7375420 | GAAGA | G | intron_variant | MODIFIER | HG01167.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(1): Show | 4 | 298 | 0.0134 | -4 | c.276 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7377372 | TCTGA | T | intron_variant | MODIFIER | HG01106.hp1 HG01891.hp2 HG03486.hp1 others(1): Show |
a0001a0003a0017 | a0001c0001a0001c0042a0003c0003others(1): Show | a0001c0001t0002a0001c0042t0025a0003c0003t0001others(1): Show | a0001c0001t0002g0252a0001c0042t0025g0250a0003c0003t0001g0263others(1): Show | 4 | 298 | 0.0134 | -4 | c.541 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7377785 | CAAAA | C | intron_variant | MODIFIER | HG01106.hp1 HG01261.hp2 HG01891.hp2 others(6): Show |
a0001a0003a0017 | a0001c0001a0001c0002a0001c0013others(3): Show | a0001c0001t0002a0001c0001t0030a0001c0002t0036others(4): Show | a0001c0001t0002g0012a0001c0001t0002g0252a0001c0001t0030g0008others(6): Show | 9 | 298 | 0.0302 | -4 | c.542 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7381691 | TAATA | T | intron_variant | MODIFIER | HG01106.hp2 HG01928.hp2 HG01934.hp1 others(15): Show |
a0001a0002a0011others(2): Show | a0001c0001a0001c0019a0001c0021others(8): Show | a0001c0001t0002a0001c0019t0006a0001c0021t0006others(9): Show | a0001c0001t0002g0093a0001c0019t0006g0057a0001c0019t0006g0063others(15): Show | 18 | 298 | 0.0604 | -4 | c.722 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385833 | ATCTC | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0016others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(22): Show | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0090others(70): Show | 73 | 298 | 0.2450 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385915 | CCTCT | C | intron_variant | MODIFIER | HG02723.hp1 HG03139.hp1 HG03471.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0005g0292others(2): Show | 5 | 298 | 0.0168 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385981 | CCTCT | C | intron_variant | MODIFIER | HG02922.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
a0002a0005 | a0002c0004a0005c0009 | a0002c0004t0002a0002c0004t0004a0005c0009t0009 | a0002c0004t0002g0050a0002c0004t0002g0251a0002c0004t0004g0002others(1): Show | 4 | 298 | 0.0134 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7389497 | CCCTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
a0001a0002a0003others(21): Show | a0001c0001a0001c0002a0001c0013others(35): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(57): Show | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0077others(190): Show | 193 | 298 | 0.6477 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7389514 | CCTTT | C | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
a0001a0009a0033 | a0001c0001a0001c0047a0009c0012others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(2): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(5): Show | 8 | 298 | 0.0269 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7390521 | AAAAG | A | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01070.hp2 others(42): Show |
a0001a0003a0013others(1): Show | a0001c0001a0001c0046a0003c0003others(2): Show | a0001c0001t0002a0001c0001t0008a0001c0046t0001others(8): Show | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(42): Show | 45 | 298 | 0.1510 | -4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7397097 | GAAAA | G | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
a0001a0009a0018 | a0001c0001a0001c0019a0001c0047others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0019t0006others(3): Show | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0007others(7): Show | 10 | 298 | 0.0336 | -4 | c.967 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7409752 | TTTTC | T | intron_variant | MODIFIER | NA18942.hp2 NA18944.hp1 NA19007.hp2 |
a0003 | a0003c0003 | a0003c0003t0001a0003c0003t0002a0003c0003t0037 | a0003c0003t0001g0203a0003c0003t0002g0207a0003c0003t0037g0186 | 3 | 298 | 0.0101 | -4 | c.967 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7416530 | CGTGT | C | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(33): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0018a0001c0019others(14): Show | a0001c0001t0002a0001c0001t0004a0001c0018t0001others(19): Show | a0001c0001t0002g0202a0001c0001t0004g0004a0001c0018t0001g0101others(33): Show | 36 | 298 | 0.1208 | -4 | c.968 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7424025 | CTTAT | C | intron_variant | MODIFIER | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
a0002 | a0002c0004 | a0002c0004t0004 | a0002c0004t0004g0018a0002c0004t0004g0019a0002c0004t0004g0064others(2): Show | 5 | 298 | 0.0168 | -4 | c.968 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7442124 | CCCTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(19): Show |
a0001a0003a0013others(2): Show | a0001c0001a0003c0003a0013c0022others(2): Show | a0001c0001t0001a0001c0001t0008a0003c0003t0001others(5): Show | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0090others(19): Show | 22 | 298 | 0.0738 | -4 | c.136 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7457353 | CTTTT | C | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(18): Show |
a0001a0002a0005others(3): Show | a0001c0018a0001c0047a0002c0005others(5): Show | a0001c0018t0001a0001c0047t0002a0002c0005t0001others(6): Show | a0001c0018t0001g0101a0001c0047t0002g0005a0002c0005t0001g0221others(18): Show | 21 | 298 | 0.0705 | -4 | c.218 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7473808 | CAAAA | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(104): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0013others(24): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(35): Show | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0082others(104): Show | 107 | 298 | 0.3591 | -4 | c.*35 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1331 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7474754 | AGTGT | A | downstream_gene_variant | MODIFIER | HG02040.hp1 NA18966.hp1 NA18973.hp1 others(2): Show |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0001a0006c0008t0001 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0108others(2): Show | 5 | 298 | 0.0168 | -4 | c.*44 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2277 | chr19 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16194685 | GAAGA | G | downstream_gene_variant | MODIFIER | HG00544.hp2 HG00741.hp1 HG01069.hp1 others(53): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0002a0002c0002t0002a0002c0002t0010others(1): Show | a0001c0001t0002g0060a0002c0002t0002g0002a0002c0002t0002g0030others(9): Show | 56 | 362 | 0.1547 | -4 | c.*38 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 3168 | chr1 | TogoVar |