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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF18_chr19_7343937_7477478 | 7385443 | CATT | C | intron_variant | MODIFIER | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0013others(26): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(33): Show | a0001c0001t0001g0056a0001c0001t0002g0074a0001c0001t0004g0004others(51): Show | 54 | 298 | 0.1812 | -3 | c.967 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385886 | CCCT | C | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp2 HG02922.hp1 others(1): Show |
a0002a0007a0026 | a0002c0006a0007c0014a0026c0029 | a0002c0006t0007a0007c0014t0004a0026c0029t0020 | a0002c0006t0007g0274a0002c0006t0007g0276a0007c0014t0004g0051others(1): Show | 4 | 298 | 0.0134 | -3 | c.967 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7387139 | TTTG | T | intron_variant | MODIFIER | HG00408.hp1 HG02040.hp2 HG02129.hp2 others(7): Show |
a0006a0008 | a0006c0008a0008c0010 | a0006c0008t0002a0006c0008t0032a0008c0010t0001others(1): Show | a0006c0008t0002g0281a0006c0008t0002g0282a0006c0008t0002g0283others(7): Show | 10 | 298 | 0.0336 | -3 | c.967 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7387949 | GCCA | G | intron_variant | MODIFIER | HG00544.hp1 HG00639.hp2 HG01070.hp2 others(45): Show |
a0001a0003a0013others(1): Show | a0001c0001a0001c0002a0001c0016others(5): Show | a0001c0001t0002a0001c0001t0008a0001c0002t0036others(11): Show | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(45): Show | 48 | 298 | 0.1611 | -3 | c.967 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7390534 | AAAG | A | intron_variant | MODIFIER | HG01106.hp2 HG03834.hp1 NA18942.hp1 others(2): Show |
a0001a0018 | a0001c0019a0001c0021a0018c0053 | a0001c0019t0006a0001c0021t0006a0018c0053t0001 | a0001c0019t0006g0057a0001c0019t0006g0063a0001c0019t0006g0078others(2): Show | 5 | 298 | 0.0168 | -3 | c.967 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7403546 | TTTC | T | intron_variant | MODIFIER | HG01099.hp2 HG01891.hp1 HG01891.hp2 others(39): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0013others(17): Show | a0001c0001t0030a0001c0002t0003a0001c0013t0001others(18): Show | a0001c0001t0030g0008a0001c0002t0003g0280a0001c0013t0001g0010others(39): Show | 42 | 298 | 0.1409 | -3 | c.967 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7429128 | TCCC | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
a0001a0002a0003others(26): Show | a0001c0001a0001c0002a0001c0013others(47): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(67): Show | a0001c0001t0001g0056a0001c0001t0002g0012a0001c0001t0002g0028others(211): Show | 214 | 298 | 0.7181 | -3 | c.968 others(22): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7434035 | AAAG | A | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
a0001a0002a0004others(19): Show | a0001c0001a0001c0013a0001c0016others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(44): Show | a0001c0001t0001g0056a0001c0001t0002g0012a0001c0001t0002g0028others(123): Show | 126 | 298 | 0.4228 | -3 | c.968 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7456031 | GTGT | G | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01169.hp2 others(14): Show |
a0001a0002a0015others(3): Show | a0001c0013a0001c0048a0002c0007others(4): Show | a0001c0013t0001a0001c0048t0001a0002c0007t0001others(4): Show | a0001c0013t0001g0010a0001c0013t0001g0195a0001c0013t0001g0204others(14): Show | 17 | 298 | 0.0571 | -3 | c.210 others(20): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7472806 | TCTC | T | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0047others(9): Show | a0001c0001t0002a0001c0001t0011a0001c0001t0016others(18): Show | a0001c0001t0002g0012a0001c0001t0002g0028a0001c0001t0002g0032others(86): Show | 89 | 298 | 0.2987 | -3 | c.*25 others(14): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 329 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7473808 | CAAA | C | downstream_gene_variant | MODIFIER | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0016a0001c0021others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(13): Show | a0001c0001t0001g0053a0001c0001t0002g0012a0001c0001t0002g0070others(20): Show | 23 | 298 | 0.0772 | -3 | c.*35 others(14): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1331 | chr19 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16194459 | CAAA | C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(16): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0002a0003c0003t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0066others(6): Show | 19 | 362 | 0.0525 | -3 | c.*41 others(14): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 3394 | chr1 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16203188 | AGGG | A | intron_variant | MODIFIER | HG00544.hp2 HG00741.hp1 HG01069.hp1 others(83): Show |
a0002a0004 | a0002c0002a0002c0009a0004c0004 | a0002c0002t0001a0002c0002t0002a0002c0002t0010others(3): Show | a0002c0002t0001g0010a0002c0002t0001g0076a0002c0002t0002g0002others(12): Show | 86 | 362 | 0.2376 | -3 | c.190 others(20): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 12/15 | chr1 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16211601 | GGAA | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0003a0004c0004others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(22): Show | 104 | 362 | 0.2873 | -3 | c.-30 others(18): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1/15 | chr1 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41880456 | GGAA | G | upstream_gene_variant | MODIFIER | HG00597.hp2 HG02055.hp1 HG02155.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(4): Show | 8 | 234 | 0.0342 | -3 | c.-28 others(14): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2727 | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41900786 | GTTT | G | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0013others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(48): Show | 64 | 234 | 0.2735 | -3 | c.126 others(22): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154120967 | GACC | G | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0009a0001c0015others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(33): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(160): Show | 166 | 283 | 0.5866 | -3 | c.-60 others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 422 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154127600 | ATTT | A | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(6): Show | a0001c0001t0009a0002c0002t0003a0002c0002t0005others(30): Show | a0001c0001t0009g0267a0002c0002t0003g0022a0002c0002t0003g0023others(105): Show | 109 | 283 | 0.3852 | -3 | c.112 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154161099 | TTTG | T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0041a0001c0009t0022 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | 283 | 0.0106 | -3 | c.148 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154186370 | TATA | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
a0001a0002a0012 | a0001c0001a0001c0009a0001c0015others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(12): Show | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | 283 | 0.1767 | -3 | c.148 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154216506 | TTTA | T | intron_variant | MODIFIER | HG01069.hp1 HG02109.hp2 HG03041.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(7): Show | a0001c0001t0001g0223a0001c0001t0004g0215a0001c0001t0007g0175others(7): Show | 10 | 283 | 0.0353 | -3 | c.184 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154239257 | AGAG | A | intron_variant | MODIFIER | HG00408.hp1 HG02809.hp1 NA18906.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0005a0002c0003t0006 | a0001c0001t0001g0156a0002c0003t0005g0113a0002c0003t0006g0088 | 3 | 283 | 0.0106 | -3 | c.209 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154257054 | AACT | A | 3_prime_UTR_variant | MODIFIER | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0014a0005c0008t0014 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | 283 | 0.0106 | -3 | c.*15 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1585 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||
ARHGEF26_chr3_154116390_154262825 | 154259309 | TCAG | T | downstream_gene_variant | MODIFIER | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0037a0002c0007t0018 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | 283 | 0.0106 | -3 | c.*38 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1485 | chr3 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73650277 | CTTT | C | intron_variant | MODIFIER | HG00741.hp2 HG01074.hp2 HG01243.hp1 others(25): Show |
a0001a0002a0003others(8): Show | a0001c0021a0001c0025a0002c0002others(17): Show | a0001c0021t0008a0001c0025t0001a0002c0002t0002others(20): Show | a0001c0021t0008g0102a0001c0025t0001g0156a0002c0002t0002g0133others(25): Show | 28 | 188 | 0.1489 | -3 | c.-12 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73668946 | AAGG | A | intron_variant | MODIFIER | HG00735.hp2 HG01261.hp2 |
a0002 | a0002c0003a0002c0029 | a0002c0003t0002a0002c0029t0001 | a0002c0003t0002g0092a0002c0029t0001g0091 | 2 | 188 | 0.0106 | -3 | c.-11 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671731 | TATA | T | intron_variant | MODIFIER | HG02809.hp2 HG03017.hp2 |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0006a0003c0007t0001 | a0001c0001t0006g0169a0003c0007t0001g0140 | 2 | 188 | 0.0106 | -3 | c.-11 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671821 | TCTC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0021a0001c0023others(26): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(35): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(49): Show | 52 | 188 | 0.2766 | -3 | c.-11 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73681088 | ATTT | A | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG02615.hp1 others(12): Show |
a0001a0002a0003others(6): Show | a0001c0025a0002c0002a0003c0005others(7): Show | a0001c0025t0005a0002c0002t0002a0003c0005t0004others(8): Show | a0001c0025t0005g0131a0002c0002t0002g0133a0002c0002t0002g0158others(12): Show | 15 | 188 | 0.0798 | -3 | c.-11 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73725502 | TAAG | T | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG01071.hp1 others(23): Show |
a0002a0004a0005others(9): Show | a0002c0002a0002c0006a0004c0004others(15): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0003others(19): Show | a0002c0002t0001g0003a0002c0002t0001g0130a0002c0002t0002g0158others(23): Show | 26 | 188 | 0.1383 | -3 | c.34- others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737658 | CACG | C | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG01243.hp2 others(19): Show |
a0001a0002a0003others(10): Show | a0001c0025a0002c0002a0002c0003others(13): Show | a0001c0025t0001a0002c0002t0001a0002c0002t0002others(16): Show | a0001c0025t0001g0156a0002c0002t0001g0130a0002c0002t0001g0132others(19): Show | 22 | 188 | 0.1170 | -3 | c.34- others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73762455 | CAAA | C | intron_variant | MODIFIER | HG00741.hp2 HG01891.hp2 HG02723.hp2 others(2): Show |
a0003a0004a0007others(2): Show | a0003c0007a0004c0018a0007c0009others(2): Show | a0003c0007t0001a0004c0018t0002a0007c0009t0009others(2): Show | a0003c0007t0001g0045a0004c0018t0002g0154a0007c0009t0009g0164others(2): Show | 5 | 188 | 0.0266 | -3 | c.475 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73765015 | TTCA | T | intron_variant | MODIFIER | HG02145.hp2 NA18906.hp1 |
a0005 | a0005c0022 | a0005c0022t0001a0005c0022t0005 | a0005c0022t0001g0120a0005c0022t0005g0119 | 2 | 188 | 0.0106 | -3 | c.476 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73781037 | TCTC | T | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(25): Show |
a0003a0004a0013others(3): Show | a0003c0005a0003c0007a0003c0048others(8): Show | a0003c0005t0001a0003c0005t0002a0003c0005t0006others(16): Show | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0075others(25): Show | 28 | 188 | 0.1489 | -3 | c.910 others(18): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73789109 | AAAC | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
a0003a0004a0037 | a0003c0005a0003c0007a0004c0004others(2): Show | a0003c0005t0004a0003c0007t0001a0004c0004t0001others(3): Show | a0003c0005t0004g0103a0003c0007t0001g0140a0004c0004t0001g0155others(4): Show | 7 | 188 | 0.0372 | -3 | c.911 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73802245 | TAAG | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
a0001a0002a0003others(29): Show | a0001c0021a0001c0025a0001c0028others(55): Show | a0001c0021t0007a0001c0021t0008a0001c0025t0005others(85): Show | a0001c0021t0007g0178a0001c0021t0008g0102a0001c0025t0005g0131others(116): Show | 119 | 188 | 0.6330 | -3 | c.102 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73806277 | ATAC | A | 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 | -3 | c.102 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806328 | AGAG | A | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02602.hp1 others(4): Show |
a0002a0007a0013others(2): Show | a0002c0002a0002c0006a0007c0009others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(4): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(4): Show | 7 | 188 | 0.0372 | -3 | c.102 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73810044 | CAAG | C | intron_variant | MODIFIER | HG02630.hp1 NA21309.hp1 |
a0004a0028 | a0004c0017a0028c0031 | a0004c0017t0005a0028c0031t0004 | a0004c0017t0005g0078a0028c0031t0004g0113 | 2 | 188 | 0.0106 | -3 | c.102 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73837237 | TGTA | T | intron_variant | MODIFIER | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
a0002a0007a0008 | a0002c0002a0007c0009a0008c0011 | a0002c0002t0001a0002c0002t0002a0007c0009t0001others(2): Show | a0002c0002t0001g0130a0002c0002t0002g0158a0002c0002t0002g0159others(3): Show | 6 | 188 | 0.0319 | -3 | c.114 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73838919 | AGTT | A | intron_variant | MODIFIER | HG00741.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
a0002a0003a0004others(3): Show | a0002c0002a0003c0007a0004c0004others(3): Show | a0002c0002t0001a0003c0007t0005a0004c0004t0001others(3): Show | a0002c0002t0001g0182a0003c0007t0005g0151a0004c0004t0001g0187others(4): Show | 7 | 188 | 0.0372 | -3 | c.114 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73845986 | CAAA | C | intron_variant | MODIFIER | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(5): Show |
a0002a0003a0007others(2): Show | a0002c0002a0003c0058a0007c0013others(3): Show | a0002c0002t0001a0003c0058t0001a0007c0013t0001others(4): Show | a0002c0002t0001g0130a0002c0002t0001g0132a0003c0058t0001g0139others(5): Show | 8 | 188 | 0.0426 | -3 | c.142 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73854852 | AAAC | A | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG01106.hp1 others(28): Show |
a0001a0002a0003others(9): Show | a0001c0021a0001c0028a0002c0002others(15): Show | a0001c0021t0008a0001c0028t0001a0002c0002t0002others(22): Show | a0001c0021t0008g0102a0001c0028t0001g0146a0001c0028t0001g0181others(28): Show | 31 | 188 | 0.1649 | -3 | c.179 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73885488 | TTTC | T | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(9): Show |
a0003a0004a0005others(4): Show | a0003c0007a0004c0004a0004c0060others(5): Show | a0003c0007t0001a0003c0007t0005a0004c0004t0001others(7): Show | a0003c0007t0001g0045a0003c0007t0001g0184a0003c0007t0001g0186others(9): Show | 12 | 188 | 0.0638 | -3 | c.305 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73914391 | CTTT | C | intron_variant | MODIFIER | HG00741.hp2 HG01167.hp2 HG01891.hp2 others(9): Show |
a0002a0004a0005others(4): Show | a0002c0002a0004c0004a0004c0017others(6): Show | a0002c0002t0001a0002c0002t0002a0004c0004t0001others(9): Show | a0002c0002t0001g0132a0002c0002t0002g0158a0004c0004t0001g0155others(9): Show | 12 | 188 | 0.0638 | -3 | c.494 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38920398 | CTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(170): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(167): Show | 173 | 278 | 0.6223 | -3 | c.25+ others(16): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38942005 | ATTT | A | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(203): Show | 209 | 278 | 0.7518 | -3 | c.791 others(20): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38946429 | CCTT | C | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(1): Show | a0001c0001t0001g0120a0001c0001t0002g0025a0001c0001t0002g0027others(21): Show | 24 | 278 | 0.0863 | -3 | c.920 others(20): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38975530 | TCAC | T | downstream_gene_variant | MODIFIER | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(2): Show | a0001c0001t0002g0223a0001c0001t0003g0209a0001c0001t0003g0220others(33): Show | 36 | 278 | 0.1295 | -3 | c.*16 others(14): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 77 | chr2 | TogoVar | ||||||
ARHGEF35_chr7_144181083_144200833 | 144188504 | ATTC | A | intron_variant | MODIFIER | HG02818.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
a0002a0005a0008 | a0002c0009a0002c0012a0005c0006others(1): Show | a0002c0009t0009a0002c0012t0016a0005c0006t0005others(2): Show | a0002c0009t0009g0070a0002c0012t0016g0061a0005c0006t0005g0035others(3): Show | 7 | 383 | 0.0183 | -3 | c.-12 others(18): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 1/1 | chr7 | TogoVar |