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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF12_chr11_120331413_120494937 | 120399321 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
a0001a0006 | a0001c0001a0001c0008a0006c0013 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(5): Show | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0196 others(24): Show |
27 | 308 | 0.0877 | -2 | c.33- others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120411581 | CTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG01074.hp1 others(11): Show |
a0001a0003a0008 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0002t0003others(5): Show | a0001c0001t0001g0175 a0001c0001t0009g0003 a0001c0001t0009g0004 others(11): Show |
14 | 308 | 0.0455 | -2 | c.199 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120420051 | AAC | A | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0301 a0001c0006t0002g0302 a0001c0006t0002g0303 others(3): Show |
6 | 308 | 0.0195 | -2 | c.200 others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120421440 | TTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00741.hp1 others(30): Show |
a0001a0010 | a0001c0001a0001c0008a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(8): Show | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0193 others(30): Show |
33 | 308 | 0.1071 | -2 | c.299 others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120425760 | TAA | T | intron_variant | MODIFIER | HG00438.hp2 HG01070.hp2 HG02027.hp2 others(8): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0008others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(3): Show | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0102 others(8): Show |
11 | 308 | 0.0357 | -2 | c.406 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120438886 | CAG | C | intron_variant | MODIFIER | NA18960.hp1 NA18977.hp2 NA19005.hp2 others(1): Show |
a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0070 a0002c0003t0002g0079 a0002c0003t0002g0080 others(1): Show |
4 | 308 | 0.0130 | -2 | c.100 others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120442427 | TAC | T | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp1 HG01255.hp2 others(35): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0008others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(9): Show | a0001c0001t0001g0173 a0001c0001t0001g0279 a0001c0001t0008g0020 others(35): Show |
38 | 308 | 0.1234 | -2 | c.130 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120442455 | CAT | C | intron_variant | MODIFIER | HG02965.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
a0001a0005 | a0001c0001a0005c0016 | a0001c0001t0031a0001c0001t0033a0001c0001t0036others(1): Show | a0001c0001t0031g0090 a0001c0001t0033g0131 a0001c0001t0036g0087 others(1): Show |
4 | 308 | 0.0130 | -2 | c.130 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120442463 | TAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
a0001a0008 | a0001c0002a0008c0014 | a0001c0002t0002a0001c0002t0003a0001c0002t0007others(3): Show | a0001c0002t0002g0022 a0001c0002t0002g0024 a0001c0002t0003g0001 others(32): Show |
36 | 308 | 0.1169 | -2 | c.130 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120456477 | CAG | C | intron_variant | MODIFIER | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
a0001a0008 | a0001c0002a0008c0014 | a0001c0002t0019a0001c0002t0034a0008c0014t0019 | a0001c0002t0019g0012 a0001c0002t0034g0013 a0008c0014t0019g0011 |
3 | 308 | 0.0097 | -2 | c.205 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120463525 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
a0001a0002a0008 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0006a0001c0002t0002a0001c0002t0003others(6): Show | a0001c0001t0006g0096 a0001c0001t0006g0138 a0001c0002t0002g0022 others(35): Show |
39 | 308 | 0.1266 | -2 | c.261 others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120475705 | AAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0016 | a0001c0002t0003g0001 a0001c0002t0003g0015 a0001c0002t0003g0023 others(24): Show |
28 | 308 | 0.0909 | -2 | c.327 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120475726 | ATT | A | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
a0001a0003a0007 | a0001c0001a0003c0005a0007c0011 | a0001c0001t0001a0001c0001t0009a0001c0001t0021others(4): Show | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(48): Show |
52 | 308 | 0.1688 | -2 | c.327 others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120487133 | CTT | C | 3_prime_UTR_variant | MODIFIER | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(93): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0006others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(17): Show | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(93): Show |
96 | 308 | 0.3117 | -2 | c.*20 others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2058 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF15_chr17_8305241_8327511 | 8314742 | CAA | C | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp1 HG01123.hp2 others(4): Show |
a0001a0003a0007 | a0001c0004a0003c0009a0007c0018 | a0001c0004t0003a0003c0009t0001a0007c0018t0002 | a0001c0004t0003g0014 a0003c0009t0001g0058 a0007c0018t0002g0059 |
7 | 428 | 0.0164 | -2 | c.990 others(17): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3450012 | CGT | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0009a0002c0007others(14): Show | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(21): Show | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(181): Show |
189 | 334 | 0.5659 | -2 | c.-48 others(13): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4652 | chr1 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3450447 | CAT | C | upstream_gene_variant | MODIFIER | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(16): Show |
a0003 | a0003c0004a0003c0015a0003c0026 | a0003c0004t0002a0003c0015t0002a0003c0026t0001 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(15): Show |
19 | 334 | 0.0569 | -2 | c.-43 others(13): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4217 | chr1 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3459420 | CAG | C | intron_variant | MODIFIER | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
a0002a0012a0013 | a0002c0003a0002c0022a0012c0031others(1): Show | a0002c0003t0002a0002c0022t0002a0012c0031t0002others(1): Show | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | 334 | 0.0659 | -2 | c.-19 others(19): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3464151 | CTG | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0009a0002c0007others(10): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(16): Show | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(192): Show |
203 | 334 | 0.6078 | -2 | c.588 others(17): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3479409 | ACC | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0005a0001c0009others(22): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(31): Show | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
258 | 334 | 0.7725 | -2 | c.181 others(19): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73319065 | CTT | C | intron_variant | MODIFIER | HG01106.hp2 HG01884.hp2 HG02451.hp2 others(25): Show |
a0002a0017 | a0002c0002a0002c0008a0002c0035others(2): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0008others(6): Show | a0002c0002t0001g0023 a0002c0002t0001g0026 a0002c0002t0001g0027 others(25): Show |
28 | 228 | 0.1228 | -2 | c.319 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329322 | CAT | C | intron_variant | MODIFIER | HG02965.hp2 HG03579.hp1 HG03688.hp2 |
a0001a0003a0006 | a0001c0001a0003c0003a0006c0011 | a0001c0001t0001a0003c0003t0002a0006c0011t0001 | a0001c0001t0001g0205 a0003c0003t0002g0054 a0006c0011t0001g0215 |
3 | 228 | 0.0132 | -2 | c.319 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | CGT | C | intron_variant | MODIFIER | HG00099.hp2 HG00609.hp2 HG02027.hp2 others(6): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0003a0003c0015others(2): Show | a0001c0001t0001a0003c0003t0011a0003c0015t0004others(2): Show | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0185 others(6): Show |
9 | 228 | 0.0395 | -2 | c.319 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332407 | GTA | G | intron_variant | MODIFIER | HG02083.hp1 HG02132.hp1 NA19007.hp2 |
a0001 | a0001c0001a0001c0027 | a0001c0001t0001a0001c0027t0001 | a0001c0001t0001g0002 a0001c0027t0001g0088 |
3 | 228 | 0.0132 | -2 | c.319 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73341991 | CCT | C | intron_variant | MODIFIER | HG00140.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
a0001a0005a0011 | a0001c0001a0005c0009a0011c0019 | a0001c0001t0001a0005c0009t0001a0011c0019t0001 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0102 others(14): Show |
17 | 228 | 0.0746 | -2 | c.319 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73352563 | GCT | G | intron_variant | MODIFIER | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
a0003a0009a0015others(1): Show | a0003c0003a0003c0007a0003c0030others(3): Show | a0003c0003t0002a0003c0007t0002a0003c0030t0014others(3): Show | a0003c0003t0002g0043 a0003c0003t0002g0046 a0003c0003t0002g0049 others(27): Show |
30 | 228 | 0.1316 | -2 | c.327 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73357169 | CAG | C | intron_variant | MODIFIER | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
a0002 | a0002c0006 | a0002c0006t0003 | a0002c0006t0003g0008 a0002c0006t0003g0009 a0002c0006t0003g0010 others(3): Show |
6 | 228 | 0.0263 | -2 | c.400 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 8/20 | chr11 | TogoVar | |||||||
ARHGEF17_chr11_73303276_73374388 | 73366140 | TGC | T | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp1 HG03195.hp2 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0023 a0002c0002t0001g0026 a0002c0002t0001g0027 others(2): Show |
5 | 228 | 0.0219 | -2 | c.599 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73372373 | AGT | A | downstream_gene_variant | MODIFIER | HG00621.hp2 HG02074.hp1 |
a0007 | a0007c0010 | a0007c0010t0001 | a0007c0010t0001g0189 a0007c0010t0001g0194 |
2 | 228 | 0.0088 | -2 | c.*45 others(13): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2986 | chr11 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | CGT | C | upstream_gene_variant | MODIFIER | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0003 | a0001c0001t0002a0001c0002t0003a0003c0003t0001 | a0001c0001t0002g0202 a0001c0002t0003g0127 a0003c0003t0001g0169 others(3): Show |
6 | 298 | 0.0201 | -2 | c.-28 others(13): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7350765 | TGG | T | intron_variant | MODIFIER | HG02015.hp2 HG03491.hp1 NA18946.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(2): Show | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(7): Show |
10 | 298 | 0.0336 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7351689 | CCT | C | intron_variant | MODIFIER | HG01496.hp1 HG01891.hp2 HG02280.hp2 |
a0001a0003a0004 | a0001c0013a0003c0003a0004c0015 | a0001c0013t0001a0003c0003t0001a0004c0015t0003 | a0001c0013t0001g0297 a0003c0003t0001g0263 a0004c0015t0003g0166 |
3 | 298 | 0.0101 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7351727 | CAG | C | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
a0002a0026 | a0002c0004a0002c0006a0026c0029 | a0002c0004t0021a0002c0006t0007a0026c0029t0020 | a0002c0004t0021g0277 a0002c0006t0007g0270 a0002c0006t0007g0271 others(5): Show |
8 | 298 | 0.0269 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7353590 | CAA | C | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(7): Show |
a0006a0008 | a0006c0008a0008c0010 | a0006c0008t0002a0006c0008t0032a0008c0010t0001others(1): Show | a0006c0008t0002g0281 a0006c0008t0002g0282 a0006c0008t0002g0283 others(7): Show |
10 | 298 | 0.0336 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7353970 | AAG | A | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(6): Show |
a0006a0008 | a0006c0008a0008c0010 | a0006c0008t0002a0006c0008t0032a0008c0010t0001others(1): Show | a0006c0008t0002g0282 a0006c0008t0002g0283 a0006c0008t0002g0287 others(6): Show |
9 | 298 | 0.0302 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7355068 | TCA | T | intron_variant | MODIFIER | HG01106.hp2 HG03098.hp2 HG06807.hp1 others(2): Show |
a0001a0005 | a0001c0019a0001c0021a0001c0043others(1): Show | a0001c0019t0006a0001c0021t0006a0001c0043t0015others(1): Show | a0001c0019t0006g0078 a0001c0021t0006g0059 a0001c0043t0015g0278 others(2): Show |
5 | 298 | 0.0168 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7356271 | CTT | C | intron_variant | MODIFIER | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(37): Show |
a0001a0002a0007others(5): Show | a0001c0001a0001c0013a0001c0047others(10): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(16): Show | a0001c0001t0002g0012 a0001c0001t0002g0047 a0001c0001t0002g0070 others(37): Show |
40 | 298 | 0.1342 | -2 | c.-11 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367842 | TTA | T | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(13): Show | a0001c0001t0001g0216 a0001c0001t0002g0181 a0001c0001t0002g0182 others(45): Show |
48 | 298 | 0.1611 | -2 | 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 | 7373483 | GTT | G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
a0002a0012a0014others(7): Show | a0002c0004a0002c0005a0002c0006others(12): Show | a0002c0004t0002a0002c0004t0004a0002c0004t0021others(18): Show | a0002c0004t0002g0044 a0002c0004t0002g0050 a0002c0004t0002g0222 others(42): Show |
45 | 298 | 0.1510 | -2 | c.275 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385821 | CTA | C | intron_variant | MODIFIER | HG01099.hp2 HG03579.hp1 NA19000.hp2 |
a0001a0002 | a0001c0019a0002c0007 | a0001c0019t0006a0002c0007t0001 | a0001c0019t0006g0057 a0002c0007t0001g0011 a0002c0007t0001g0016 |
3 | 298 | 0.0101 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385833 | ATC | A | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(10): Show |
a0001a0003a0023 | a0001c0001a0001c0018a0003c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(4): Show | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0138 others(10): Show |
13 | 298 | 0.0436 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385893 | TCC | T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0042a0002c0004a0002c0006others(5): Show | a0001c0042t0025a0002c0004t0004a0002c0006t0007others(5): Show | a0001c0042t0025g0250 a0002c0004t0004g0018 a0002c0004t0004g0019 others(11): Show |
14 | 298 | 0.0470 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385915 | CCT | C | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
a0001a0009 | a0001c0001a0001c0047a0009c0012 | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(1): Show | a0001c0001t0002g0070 a0001c0001t0002g0074 a0001c0001t0004g0004 others(5): Show |
8 | 298 | 0.0269 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7392240 | CAA | C | intron_variant | MODIFIER | HG01257.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0043a0002c0004others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0043t0015others(6): Show | a0001c0001t0002g0035 a0001c0001t0004g0293 a0001c0043t0015g0278 others(8): Show |
11 | 298 | 0.0369 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7393047 | CAA | C | intron_variant | MODIFIER | HG01070.hp2 HG01255.hp2 HG01884.hp1 others(7): Show |
a0002a0003a0012others(3): Show | a0002c0004a0002c0007a0003c0003others(5): Show | a0002c0004t0004a0002c0007t0001a0003c0003t0001others(5): Show | a0002c0004t0004g0261 a0002c0004t0004g0262 a0002c0007t0001g0016 others(7): Show |
10 | 298 | 0.0336 | -2 | c.967 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7408437 | CCA | C | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
a0001a0009 | a0001c0001a0001c0047a0009c0012 | a0001c0001t0002a0001c0001t0004a0001c0047t0002others(1): Show | a0001c0001t0002g0070 a0001c0001t0004g0004 a0001c0001t0004g0007 others(4): Show |
7 | 298 | 0.0235 | -2 | 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 | 7409430 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0001c0013others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(39): Show | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0077 others(160): Show |
163 | 298 | 0.5470 | -2 | 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 | 7409766 | TTC | T | intron_variant | MODIFIER | HG00099.hp1 HG01169.hp2 HG02897.hp1 others(4): Show |
a0001a0002a0017others(1): Show | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0011a0001c0002t0003a0001c0013t0001others(4): Show | a0001c0001t0011g0246 a0001c0002t0003g0106 a0001c0013t0001g0204 others(4): Show |
7 | 298 | 0.0235 | -2 | 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 | 7409768 | CTT | C | intron_variant | MODIFIER | HG02165.hp2 NA18967.hp1 NA18990.hp2 others(3): Show |
a0006a0008 | a0006c0008a0008c0010 | a0006c0008t0002a0008c0010t0001a0008c0010t0033 | a0006c0008t0002g0287 a0008c0010t0001g0285 a0008c0010t0001g0288 others(3): Show |
6 | 298 | 0.0201 | -2 | 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 | 7410809 | CAA | C | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
a0001a0002a0014others(1): Show | a0001c0001a0001c0013a0002c0005others(4): Show | a0001c0001t0030a0001c0013t0001a0002c0005t0001others(4): Show | a0001c0001t0030g0008 a0001c0013t0001g0010 a0002c0005t0001g0259 others(6): Show |
9 | 298 | 0.0302 | -2 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |