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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF10_chr8_1818926_1963641 | 1888397 | C | CACTG | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0059a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0059g0105 a0002c0028t0001g0223 a0002c0033t0002g0006 others(4): Show |
7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888410 | G | GGGGT | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0059a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0059g0105 a0002c0028t0001g0223 a0002c0033t0002g0006 others(4): Show |
7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1888919 | C | CACTG | intron_variant | MODIFIER | HG00621.hp2 HG02074.hp2 NA18942.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0028a0002c0033others(4): Show | a0001c0001t0002a0001c0001t0004a0002c0028t0001others(5): Show | a0001c0001t0002g0224 a0001c0001t0004g0141 a0002c0028t0001g0223 others(5): Show |
8 | 363 | 0.0220 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888982 | A | AGTGG | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(4): Show | a0001c0001t0019g0278 a0001c0002t0001g0037 a0001c0002t0010g0212 others(4): Show |
7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889386 | C | CACTG | intron_variant | MODIFIER | HG01081.hp2 HG02647.hp2 HG02723.hp2 |
a0001a0010 | a0001c0016a0010c0099a0010c0100 | a0001c0016t0004a0010c0099t0014a0010c0100t0003 | a0001c0016t0004g0176 a0010c0099t0014g0205 a0010c0100t0003g0203 |
3 | 363 | 0.0083 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889386 | C | CGCTG | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(15): Show |
a0002a0017a0026 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0059a0002c0028t0001a0002c0032t0004others(14): Show | a0002c0025t0059g0105 a0002c0028t0001g0223 a0002c0032t0004g0173 others(15): Show |
18 | 363 | 0.0496 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1889688 | C | CACTG | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(7): Show |
a0001a0027 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(5): Show | a0001c0001t0002g0271 a0001c0001t0019g0278 a0001c0002t0001g0037 others(7): Show |
10 | 363 | 0.0276 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTG | intron_variant | MODIFIER | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
a0001a0020a0024 | a0001c0001a0001c0002a0001c0008others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(11): Show | a0001c0001t0002g0069 a0001c0001t0004g0158 a0001c0001t0004g0159 others(13): Show |
16 | 363 | 0.0441 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | C | CTGTG | intron_variant | MODIFIER | HG00323.hp1 HG00738.hp1 HG01106.hp1 others(13): Show |
a0001a0003a0017 | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0004a0001c0001t0012a0001c0001t0043others(12): Show | a0001c0001t0004g0141 a0001c0001t0004g0158 a0001c0001t0012g0207 others(13): Show |
16 | 363 | 0.0441 | 4 | c.214 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1949018 | A | ATGTG | intron_variant | MODIFIER | HG00741.hp2 HG01109.hp2 HG03239.hp1 |
a0006a0015a0022 | a0006c0089a0015c0087a0022c0128 | a0006c0089t0001a0015c0087t0030a0022c0128t0007 | a0006c0089t0001g0070 a0015c0087t0030g0139 a0022c0128t0007g0113 |
3 | 363 | 0.0083 | 4 | c.339 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1950519 | A | ATTAT | intron_variant | MODIFIER | HG01081.hp1 HG01261.hp1 HG02451.hp2 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0003a0001c0051others(6): Show | a0001c0002t0001a0001c0003t0003a0001c0051t0032others(8): Show | a0001c0002t0001g0274 a0001c0002t0001g0327 a0001c0003t0003g0362 others(9): Show |
12 | 363 | 0.0331 | 4 | c.339 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTC | downstream_gene_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
a0002a0011 | a0002c0004a0011c0008 | a0002c0004t0005a0002c0004t0009a0002c0004t0025others(2): Show | a0002c0004t0005g0052 a0002c0004t0005g0054 a0002c0004t0005g0111 others(15): Show |
19 | 362 | 0.0525 | 4 | c.*59 others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATAT | intron_variant | MODIFIER | HG01167.hp1 HG02074.hp1 HG02602.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0035 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0290 others(4): Show |
7 | 362 | 0.0193 | 4 | c.463 others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156992379 | T | TCCTG | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
a0001a0002a0011 | a0001c0001a0002c0004a0011c0008 | a0001c0001t0006a0002c0004t0005a0002c0004t0009others(2): Show | a0001c0001t0006g0110 a0001c0001t0006g0112 a0001c0001t0006g0122 others(18): Show |
22 | 362 | 0.0608 | 4 | c.33- others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | C | CAAAA | intron_variant | MODIFIER | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(20): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0006others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0012others(4): Show | a0001c0001t0001g0347 a0002c0002t0002g0034 a0002c0002t0002g0035 others(20): Show |
23 | 362 | 0.0635 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156996859 | A | ATTTT | intron_variant | MODIFIER | HG00621.hp2 HG01361.hp2 HG02083.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0010a0001c0001t0036others(2): Show | a0001c0001t0001g0279 a0001c0001t0001g0310 a0001c0001t0001g0312 others(9): Show |
12 | 362 | 0.0332 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157008406 | G | GCACA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(66): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(3): Show | a0001c0001t0006a0002c0002t0002a0002c0002t0011others(7): Show | a0001c0001t0006g0088 a0002c0002t0002g0001 a0002c0002t0002g0005 others(65): Show |
69 | 362 | 0.1906 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACA | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(6): Show | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(48): Show |
51 | 362 | 0.1409 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013263 | T | TCACA | intron_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0006a0002c0002t0002a0002c0002t0011others(3): Show | a0001c0001t0006g0088 a0002c0002t0002g0005 a0002c0002t0002g0030 others(48): Show |
51 | 362 | 0.1409 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACC | intron_variant | MODIFIER | HG00741.hp2 HG01175.hp1 HG02015.hp1 others(18): Show |
a0001a0002a0014 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0006a0002c0002t0002a0002c0004t0005others(1): Show | a0001c0001t0006g0112 a0001c0001t0006g0122 a0001c0001t0006g0125 others(18): Show |
21 | 362 | 0.0580 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157016798 | A | ATTAT | intron_variant | MODIFIER | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0004a0002c0004t0022 | a0001c0001t0004g0130 a0002c0004t0022g0131 a0002c0004t0022g0132 |
3 | 362 | 0.0083 | 4 | c.32+ others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157038278 | G | GGAGA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0005a0001c0014others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(353): Show |
358 | 362 | 0.9890 | 4 | c.32+ others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347179 | C | CCTTT | intron_variant | MODIFIER | HG00597.hp1 HG00673.hp2 HG01106.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0021a0001c0001t0023 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(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 | 120347183 | C | CCTTT | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
a0001a0003a0004 | a0001c0001a0003c0005a0004c0009 | a0001c0001t0001a0003c0005t0001a0004c0009t0010 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0003c0005t0001g0002 others(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 | 120347270 | C | CTGTG | intron_variant | MODIFIER | HG01934.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | 308 | 0.0130 | 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 | 120351341 | C | CAAAA | intron_variant | MODIFIER | HG02155.hp1 HG02273.hp1 HG02572.hp2 others(8): Show |
a0001a0007 | a0001c0001a0001c0004a0007c0016 | a0001c0001t0006a0001c0001t0009a0001c0001t0029others(3): Show | a0001c0001t0006g0094 a0001c0001t0006g0138 a0001c0001t0009g0006 others(8): Show |
11 | 308 | 0.0357 | 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 | 120399321 | C | CAAAA | intron_variant | MODIFIER | HG01099.hp2 HG02056.hp2 HG02572.hp2 others(8): Show |
a0001a0002a0007 | a0001c0001a0002c0003a0007c0016 | a0001c0001t0001a0001c0001t0002a0001c0001t0033others(2): Show | a0001c0001t0001g0249 a0001c0001t0002g0097 a0001c0001t0002g0110 others(8): Show |
11 | 308 | 0.0357 | 4 | c.33- others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF15_chr17_8305241_8327511 | 8307456 | T | TCTCA | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(196): Show |
a0001a0003a0005others(9): Show | a0001c0001a0001c0004a0001c0006others(17): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(82): Show |
199 | 428 | 0.4650 | 4 | c.-29 others(15): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 2784 | chr17 | TogoVar | |||||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | A | AACAC | upstream_gene_variant | MODIFIER | HG00733.hp2 HG01175.hp1 HG01433.hp2 others(33): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0013others(8): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(11): Show | a0001c0001t0002g0025 a0001c0001t0002g0049 a0001c0001t0003g0028 others(18): Show |
36 | 428 | 0.0841 | 4 | c.-27 others(13): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | |||||||
ARHGEF15_chr17_8305241_8327511 | 8323103 | C | CAAAA | downstream_gene_variant | MODIFIER | HG01123.hp2 HG01192.hp1 HG01256.hp2 others(9): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0003 | a0001c0001t0003g0007 a0001c0001t0003g0035 a0001c0004t0003g0014 others(2): Show |
12 | 428 | 0.0280 | 4 | c.*21 others(15): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 593 | chr17 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3450012 | C | CGTGT | upstream_gene_variant | MODIFIER | HG02451.hp2 HG02559.hp1 HG03516.hp1 |
a0003a0019 | a0003c0015a0019c0023 | a0003c0015t0002a0003c0015t0007a0019c0023t0012 | a0003c0015t0002g0293 a0003c0015t0007g0294 a0019c0023t0012g0292 |
3 | 334 | 0.0090 | 4 | c.-48 others(15): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4652 | chr1 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3463216 | T | TAGAG | frameshift_variant | HIGH | NA18991.hp1 | a0024 | a0024c0049 | a0024c0049t0002 | a0024c0049t0002g0081 | 1 | 334 | 0.0030 | 4 | c.134 others(11): Show |
p.Asp others(4): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 304/2822 | 138/2130 | 46/709 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||
ARHGEF16_chr1_3449665_3486113 | 3484364 | C | CCCTT | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
a0005a0016 | a0005c0013a0016c0040 | a0005c0013t0005a0016c0040t0005 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(1): Show |
4 | 334 | 0.0120 | 4 | c.*37 others(15): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3252 | chr1 | TogoVar | |||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | C | CGTGT | intron_variant | MODIFIER | HG00423.hp2 HG04204.hp1 NA18952.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | 228 | 0.0219 | 4 | c.319 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | C | CGTGT | upstream_gene_variant | MODIFIER | HG01934.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
a0001a0002a0008others(4): Show | a0001c0013a0002c0005a0008c0061others(4): Show | a0001c0013t0001a0002c0005t0001a0008c0061t0004others(4): Show | a0001c0013t0001g0010 a0002c0005t0001g0259 a0002c0005t0001g0260 others(6): Show |
9 | 298 | 0.0302 | 4 | c.-28 others(15): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | |||||||
ARHGEF18_chr19_7343937_7477478 | 7351305 | T | TTTTG | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0021others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(22): Show | a0001c0001t0001g0216 a0001c0001t0002g0143 a0001c0001t0002g0188 others(52): Show |
55 | 298 | 0.1846 | 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 | 7352531 | C | CTTTT | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
a0001a0002a0019 | a0001c0001a0002c0004a0002c0006others(1): Show | a0001c0001t0005a0002c0004t0004a0002c0004t0021others(2): Show | a0001c0001t0005g0292 a0002c0004t0004g0261 a0002c0004t0021g0277 others(7): Show |
10 | 298 | 0.0336 | 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 | 7352832 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(21): Show | a0001c0001t0001g0140 a0001c0001t0002g0042 a0001c0001t0002g0043 others(65): Show |
68 | 298 | 0.2282 | 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 | T | TCACA | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
a0001a0002 | a0001c0044a0002c0004 | a0001c0044t0025a0002c0004t0004 | a0001c0044t0025g0250 a0002c0004t0004g0018 a0002c0004t0004g0019 |
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 | 7358271 | T | TTCCA | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(57): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0013a0001c0016others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0216 a0001c0001t0002g0012 a0001c0001t0002g0042 others(57): Show |
60 | 298 | 0.2013 | 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 | 7358551 | C | CCCAT | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(7): Show |
a0005a0007 | a0005c0008a0007c0009 | a0005c0008t0002a0005c0008t0032a0007c0009t0001others(1): Show | a0005c0008t0002g0281 a0005c0008t0002g0282 a0005c0008t0002g0283 others(7): Show |
10 | 298 | 0.0336 | 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 | 7364365 | A | AAAGG | intron_variant | MODIFIER | HG01109.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
a0001a0002a0006 | a0001c0019a0002c0004a0002c0006others(3): Show | a0001c0019t0006a0002c0004t0002a0002c0006t0007others(3): Show | a0001c0019t0006g0078 a0002c0004t0002g0251 a0002c0006t0007g0274 others(6): Show |
9 | 298 | 0.0302 | 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 | 7364402 | A | AAGGC | intron_variant | MODIFIER | HG01106.hp1 HG03225.hp2 HG03831.hp1 others(4): Show |
a0001a0002a0037 | a0001c0001a0001c0002a0001c0044others(3): Show | a0001c0001t0002a0001c0002t0003a0001c0044t0025others(3): Show | a0001c0001t0002g0252 a0001c0002t0003g0194 a0001c0002t0003g0280 others(4): Show |
7 | 298 | 0.0235 | 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 | 7367875 | T | TACAC | intron_variant | MODIFIER | HG02622.hp2 HG02886.hp1 NA18943.hp2 |
a0002a0003 | a0002c0005a0003c0003 | a0002c0005t0001a0003c0003t0026 | a0002c0005t0001g0259 a0002c0005t0001g0260 a0003c0003t0026g0208 |
3 | 298 | 0.0101 | 4 | c.16- others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367977 | A | AAGAG | intron_variant | MODIFIER | HG00609.hp2 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002a0008others(4): Show | a0001c0001a0001c0002a0002c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0036others(7): Show | a0001c0001t0001g0082 a0001c0001t0001g0090 a0001c0001t0001g0091 others(15): Show |
18 | 298 | 0.0604 | 4 | c.16- others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7373483 | G | GTTTT | intron_variant | MODIFIER | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(16): Show |
a0001a0002a0006others(4): Show | a0001c0019a0002c0004a0006c0010others(6): Show | a0001c0019t0006a0002c0004t0004a0006c0010t0009others(6): Show | a0001c0019t0006g0078 a0002c0004t0004g0018 a0002c0004t0004g0019 others(16): Show |
19 | 298 | 0.0638 | 4 | c.275 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7373485 | T | TTTTG | intron_variant | MODIFIER | HG00408.hp1 HG01099.hp2 HG02040.hp1 others(17): Show |
a0002a0005a0007others(2): Show | a0002c0007a0005c0008a0007c0009others(2): Show | a0002c0007t0001a0005c0008t0001a0005c0008t0002others(5): Show | a0002c0007t0001g0011 a0002c0007t0001g0016 a0002c0007t0001g0017 others(17): Show |
20 | 298 | 0.0671 | 4 | c.275 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7373849 | A | ATTTT | intron_variant | MODIFIER | HG03098.hp1 HG03098.hp2 HG03486.hp2 others(4): Show |
a0002a0006a0038 | a0002c0004a0002c0005a0002c0036others(2): Show | a0002c0004t0002a0002c0004t0004a0002c0005t0001others(3): Show | a0002c0004t0002g0244 a0002c0004t0004g0261 a0002c0004t0004g0262 others(4): Show |
7 | 298 | 0.0235 | 4 | c.275 others(19): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7381691 | T | TAATA | intron_variant | MODIFIER | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(27): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0002a0002c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0002g0074 others(27): Show |
30 | 298 | 0.1007 | 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 | A | ATCTC | intron_variant | MODIFIER | HG00438.hp2 HG01074.hp2 HG01169.hp2 others(6): Show |
a0001a0003a0004 | a0001c0001a0001c0013a0003c0003others(2): Show | a0001c0001t0002a0001c0013t0001a0003c0003t0027others(2): Show | a0001c0001t0002g0055 a0001c0001t0002g0164 a0001c0001t0002g0165 others(6): Show |
9 | 298 | 0.0302 | 4 | c.967 others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |