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 | 156936497 | A | AATATAT | intron_variant | MODIFIER | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(25): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0012others(1): Show | a0001c0001t0001g0286a0001c0001t0001g0304a0001c0001t0001g0312others(25): Show | 28 | 362 | 0.0774 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156943065 | C | CTTTTTT | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0008a0002c0004t0009others(2): Show | a0002c0004t0005g0054a0002c0004t0005g0111a0002c0004t0005g0113others(14): Show | 18 | 362 | 0.0497 | 6 | c.323 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157008406 | G | GCACACA | intron_variant | MODIFIER | HG00558.hp1 HG02630.hp2 NA18943.hp2 others(6): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0002t0012a0002c0002t0017others(1): Show | a0002c0002t0002g0031a0002c0002t0002g0061a0002c0002t0002g0083others(6): Show | 9 | 362 | 0.0249 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACA | intron_variant | MODIFIER | HG01074.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0010a0001c0005t0001 | a0001c0001t0001g0273a0001c0001t0001g0291a0001c0001t0001g0292others(16): Show | 19 | 362 | 0.0525 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013263 | T | TCACACA | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0002t0024a0002c0002t0029others(1): Show | a0002c0002t0002g0001a0002c0002t0002g0029a0002c0002t0002g0037others(7): Show | 11 | 362 | 0.0304 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACC | intron_variant | MODIFIER | HG00408.hp1 HG03654.hp2 HG03831.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0044a0002c0002t0002g0062a0002c0002t0002g0095 | 3 | 362 | 0.0083 | 6 | c.33- others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157029261 | T | TTTGTTG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0011a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(167): Show | 171 | 362 | 0.4724 | 6 | c.32+ others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157046231 | G | GCCGCCA | upstream_gene_variant | MODIFIER | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(9): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0005a0003c0003t0006 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(9): Show | 12 | 362 | 0.0332 | 6 | c.-19 others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 490 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120334861 | G | GTATATA | upstream_gene_variant | MODIFIER | HG01243.hp1 HG03225.hp2 HG04115.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0023a0001c0001t0026 | a0001c0001t0001g0185a0001c0001t0023g0178a0001c0001t0026g0230 | 3 | 308 | 0.0097 | 6 | c.-23 others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1551 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAA | intron_variant | MODIFIER | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0031a0001c0002t0002others(1): Show | a0001c0001t0002g0021a0001c0001t0002g0091a0001c0001t0002g0106others(6): Show | 9 | 308 | 0.0292 | 6 | c.33- others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120442412 | T | TTATATA | intron_variant | MODIFIER | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0009 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0009g0003others(3): Show | 6 | 308 | 0.0195 | 6 | c.130 others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120446198 | A | AAATAAT | intron_variant | MODIFIER | HG01099.hp1 HG02559.hp1 HG02723.hp1 |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0029a0001c0002t0034a0001c0008t0020 | a0001c0001t0029g0190a0001c0002t0034g0013a0001c0008t0020g0008 | 3 | 308 | 0.0097 | 6 | c.134 others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF15_chr17_8305241_8327511 | 8310116 | A | AACACAC | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00741.hp1 HG01515.hp2 others(26): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0012others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0004t0002others(8): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(17): Show | 29 | 428 | 0.0678 | 6 | c.-27 others(15): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 124 | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3479714 | T | TGCCCCG | intron_variant | MODIFIER | HG00280.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(4): Show | 7 | 334 | 0.0210 | 6 | c.188 others(21): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | C | CGTGTGT | intron_variant | MODIFIER | HG01106.hp1 HG01255.hp2 HG01346.hp1 others(4): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0017a0002c0002t0001others(1): Show | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0204others(4): Show | 7 | 228 | 0.0307 | 6 | c.319 others(27): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | C | CGTGTGT | upstream_gene_variant | MODIFIER | HG00408.hp2 HG01070.hp1 HG01099.hp2 others(27): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0016others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0109others(27): Show | 30 | 298 | 0.1007 | 6 | c.-28 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7352832 | C | CTTTTTT | intron_variant | MODIFIER | HG00621.hp1 HG01099.hp2 HG01346.hp1 others(39): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0004others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0001g0091others(39): Show | 42 | 298 | 0.1409 | 6 | c.-11 others(25): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7362020 | A | AAGAAGG | intron_variant | MODIFIER | HG00423.hp2 HG03834.hp2 NA19080.hp1 |
a0001a0002 | a0001c0001a0002c0005a0002c0006 | a0001c0001t0011a0002c0005t0001a0002c0006t0001 | a0001c0001t0011g0246a0002c0005t0001g0238a0002c0006t0001g0161 | 3 | 298 | 0.0101 | 6 | 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 | 7362327 | T | TGGAGGA | intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02145.hp2 others(11): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0013a0001c0047others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(7): Show | a0001c0001t0002g0012a0001c0001t0002g0070a0001c0001t0004g0004others(11): Show | 14 | 298 | 0.0470 | 6 | 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 | 7362353 | G | GAGGAGA | intron_variant | MODIFIER | HG01099.hp2 HG01261.hp2 HG02145.hp2 others(15): Show |
a0001a0002a0009others(3): Show | a0001c0001a0001c0002a0001c0013others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(11): Show | a0001c0001t0002g0012a0001c0001t0002g0070a0001c0001t0004g0004others(15): Show | 18 | 298 | 0.0604 | 6 | 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 | 7367977 | A | AAGAGAG | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
a0001a0002a0030 | a0001c0001a0002c0007a0030c0037 | a0001c0001t0017a0002c0007t0001a0030c0037t0001 | a0001c0001t0017g0014a0002c0007t0001g0021a0002c0007t0001g0022others(4): Show | 7 | 298 | 0.0235 | 6 | c.16- others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7367998 | A | AGAGAGG | intron_variant | MODIFIER | HG00621.hp2 NA18939.hp1 NA18977.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0018 | a0001c0001t0002a0001c0001t0011a0001c0001t0035others(2): Show | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0086others(6): Show | 9 | 298 | 0.0302 | 6 | c.16- others(21): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385443 | C | CATTATT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(18): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0018others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(8): Show | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0002g0032others(18): Show | 21 | 298 | 0.0705 | 6 | 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 | 7385833 | A | ATCTCTC | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(2): Show |
a0001a0006 | a0001c0002a0001c0018a0006c0008 | a0001c0002t0003a0001c0018t0001a0006c0008t0002others(1): Show | a0001c0002t0003g0157a0001c0018t0001g0136a0006c0008t0002g0282others(2): Show | 5 | 298 | 0.0168 | 6 | 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 | 7385835 | C | CTCTCTA | intron_variant | MODIFIER | HG02922.hp2 HG03139.hp2 HG03225.hp2 |
a0002 | a0002c0004 | a0002c0004t0002a0002c0004t0004 | a0002c0004t0002g0050a0002c0004t0002g0251a0002c0004t0004g0002 | 3 | 298 | 0.0101 | 6 | 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 | C | CGTGTGT | intron_variant | MODIFIER | HG00673.hp1 HG00735.hp1 HG01074.hp2 others(23): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(10): Show | a0001c0001t0001g0056a0001c0001t0001g0091a0001c0001t0002g0052others(23): Show | 26 | 298 | 0.0873 | 6 | c.968 others(25): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7431510 | C | CAAAAAA | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
a0002a0003a0007others(1): Show | a0002c0004a0002c0007a0003c0003others(2): Show | a0002c0004t0004a0002c0007t0001a0003c0003t0001others(2): Show | a0002c0004t0004g0064a0002c0007t0001g0016a0002c0007t0001g0021others(6): Show | 9 | 298 | 0.0302 | 6 | 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 | 7437322 | G | GGAGGCT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
a0001a0002a0004others(19): Show | a0001c0001a0001c0013a0001c0016others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | a0001c0001t0001g0056a0001c0001t0002g0012a0001c0001t0002g0028others(131): Show | 134 | 298 | 0.4497 | 6 | 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 | 7450794 | C | CTTTCCG | intron_variant | MODIFIER | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0002a0002c0006a0003c0003others(3): Show | a0001c0002t0002a0001c0002t0003a0002c0006t0003others(5): Show | a0001c0002t0002g0129a0001c0002t0003g0041a0001c0002t0003g0075others(21): Show | 24 | 298 | 0.0805 | 6 | c.173 others(23): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7475525 | A | AACACAC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(36): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0084others(36): Show | 39 | 298 | 0.1309 | 6 | c.*52 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3048 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7475527 | C | CACACAT | downstream_gene_variant | MODIFIER | HG01106.hp1 HG02970.hp2 NA19043.hp1 others(1): Show |
a0001a0015a0020 | a0001c0001a0001c0016a0015c0057others(1): Show | a0001c0001t0002a0001c0016t0014a0015c0057t0001others(1): Show | a0001c0001t0002g0252a0001c0016t0014g0096a0015c0057t0001g0269others(1): Show | 4 | 298 | 0.0134 | 6 | c.*52 others(17): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 3050 | chr19 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16213054 | C | CATCCCT | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(6): Show |
a0003a0010 | a0003c0003a0010c0015 | a0003c0003t0001a0010c0015t0001 | a0003c0003t0001g0012a0003c0003t0001g0032a0003c0003t0001g0033others(1): Show | 9 | 362 | 0.0249 | 6 | c.-58 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 403 | chr1 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41894135 | A | AGTGTGT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(41): Show |
a0001a0005a0006others(1): Show | a0001c0001a0001c0002a0005c0009others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(3): Show | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0102others(35): Show | 44 | 234 | 0.1880 | 6 | c.645 others(19): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154186136 | G | GACACAC | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | a0001c0001t0001g0195a0001c0001t0001g0251a0001c0001t0002g0203others(65): Show | 68 | 283 | 0.2403 | 6 | c.148 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154211867 | A | ATGTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
a0001a0002a0012 | a0001c0001a0001c0015a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0204a0001c0001t0002g0152a0001c0001t0002g0161others(45): Show | 50 | 283 | 0.1767 | 6 | c.184 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | T | TACACAC | intron_variant | MODIFIER | HG00140.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0020others(1): Show | a0001c0001t0001g0204a0001c0001t0002g0225a0001c0001t0002g0229others(2): Show | 6 | 283 | 0.0212 | 6 | c.209 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154237538 | T | TCACACA | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(33): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0176a0001c0001t0001g0187a0001c0001t0001g0201others(32): Show | 36 | 283 | 0.1272 | 6 | c.209 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154239291 | A | AGTGTGT | intron_variant | MODIFIER | NA18978.hp2 NA18999.hp2 NA19060.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0008 | a0002c0002t0003g0049a0002c0002t0003g0071a0002c0002t0003g0075others(1): Show | 4 | 283 | 0.0141 | 6 | c.209 others(25): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73658962 | T | TACACAC | intron_variant | MODIFIER | HG01106.hp1 HG02602.hp2 HG03017.hp1 others(4): Show |
a0001a0002a0003others(4): Show | a0001c0028a0002c0003a0003c0005others(4): Show | a0001c0028t0001a0002c0003t0002a0003c0005t0002others(4): Show | a0001c0028t0001g0146a0002c0003t0002g0005a0003c0005t0002g0002others(4): Show | 7 | 188 | 0.0372 | 6 | c.-11 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73658987 | A | ACACACG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0023a0001c0077others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0001others(21): Show | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0038others(29): Show | 32 | 188 | 0.1702 | 6 | c.-11 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73691296 | T | TACACAC | intron_variant | MODIFIER | HG01243.hp2 HG03139.hp1 |
a0012 | a0012c0072a0012c0073 | a0012c0072t0005a0012c0073t0001 | a0012c0072t0005g0144a0012c0073t0001g0143 | 2 | 188 | 0.0106 | 6 | c.33+ others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73703647 | T | TTGTGTG | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp2 HG01167.hp2 others(13): Show |
a0002a0003a0004others(5): Show | a0002c0002a0002c0003a0003c0007others(7): Show | a0002c0002t0001a0002c0002t0005a0002c0003t0001others(10): Show | a0002c0002t0001g0132a0002c0002t0001g0182a0002c0002t0005g0022others(13): Show | 16 | 188 | 0.0851 | 6 | c.33+ others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73732800 | C | CTTTTAT | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
a0002a0003a0004others(21): Show | a0002c0002a0002c0003a0002c0006others(38): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0005others(53): Show | a0002c0002t0001g0003a0002c0002t0001g0130a0002c0002t0001g0132others(59): Show | 62 | 188 | 0.3298 | 6 | c.34- others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73738482 | C | CGTGTGT | intron_variant | MODIFIER | HG00438.hp1 HG00733.hp2 HG02145.hp1 others(4): Show |
a0001a0002a0004others(4): Show | a0001c0001a0002c0003a0004c0050others(4): Show | a0001c0001t0002a0002c0003t0001a0004c0050t0005others(4): Show | a0001c0001t0002g0008a0002c0003t0001g0129a0004c0050t0005g0046others(4): Show | 7 | 188 | 0.0372 | 6 | c.34- others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741385 | G | GTATATA | intron_variant | MODIFIER | HG02074.hp1 HG02074.hp2 |
a0001a0005 | a0001c0021a0005c0008 | a0001c0021t0007a0005c0008t0002 | a0001c0021t0007g0178a0005c0008t0002g0006 | 2 | 188 | 0.0106 | 6 | c.34- others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73783345 | A | AGTGTGT | intron_variant | MODIFIER | HG00408.hp1 HG00733.hp1 HG01069.hp2 others(6): Show |
a0001a0003a0005others(3): Show | a0001c0001a0001c0071a0003c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0071t0001others(5): Show | a0001c0001t0001g0036a0001c0001t0002g0011a0001c0001t0002g0012others(6): Show | 9 | 188 | 0.0479 | 6 | c.910 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73802870 | C | CTCTGTG | intron_variant | MODIFIER | HG02622.hp2 HG02698.hp1 HG02922.hp1 others(2): Show |
a0002a0004a0020 | a0002c0002a0004c0004a0004c0050others(1): Show | a0002c0002t0002a0004c0004t0004a0004c0050t0005others(1): Show | a0002c0002t0002g0133a0002c0002t0002g0159a0004c0004t0004g0112others(2): Show | 5 | 188 | 0.0266 | 6 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73802870 | C | CTGTGTG | intron_variant | MODIFIER | HG00733.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
a0004a0005 | a0004c0004a0005c0008 | a0004c0004t0001a0004c0004t0005a0005c0008t0002 | a0004c0004t0001g0155a0004c0004t0001g0167a0004c0004t0005g0183others(1): Show | 4 | 188 | 0.0213 | 6 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73806302 | G | GTATATC | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 6 | c.102 others(27): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73834542 | C | CTCTGTG | intron_variant | MODIFIER | HG02965.hp1 NA19030.hp1 |
a0003a0039 | a0003c0007a0039c0051 | a0003c0007t0005a0039c0051t0001 | a0003c0007t0005g0151a0039c0051t0001g0150 | 2 | 188 | 0.0106 | 6 | c.114 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |