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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF26_chr3_154116390_154262825 | 154239259 | AGG | A | intron_variant | MODIFIER | HG01255.hp1 HG01346.hp1 HG01516.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0002c0002t0003a0002c0002t0008others(1): Show | a0001c0001t0007g0206 a0001c0001t0007g0216 a0001c0001t0007g0220 others(7): Show |
10 | 283 | 0.0353 | -2 | c.209 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154243824 | AAT | A | intron_variant | MODIFIER | HG02280.hp1 HG02717.hp1 NA18522.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0009a0002c0003t0025 | a0001c0001t0009g0004 a0001c0001t0009g0261 a0002c0003t0025g0105 |
4 | 283 | 0.0141 | -2 | c.230 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154244736 | ACT | A | intron_variant | MODIFIER | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(67): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0007a0001c0001t0017a0001c0001t0021others(15): Show | a0001c0001t0007g0144 a0001c0001t0007g0160 a0001c0001t0007g0172 others(67): Show |
70 | 283 | 0.2474 | -2 | c.230 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154250962 | TAG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(49): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(201): Show |
206 | 283 | 0.7279 | -2 | c.230 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154252915 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(100): Show |
104 | 283 | 0.3675 | -2 | c.230 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154256574 | AAC | A | 3_prime_UTR_variant | MODIFIER | HG00738.hp2 HG01167.hp1 HG02280.hp1 others(6): Show |
a0001a0002a0006 | a0001c0001a0002c0003a0006c0013 | a0001c0001t0009a0002c0003t0025a0006c0013t0025 | a0001c0001t0009g0004 a0001c0001t0009g0227 a0001c0001t0009g0228 others(5): Show |
9 | 283 | 0.0318 | -2 | c.*11 others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1102 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154261142 | CTG | C | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0023a0001c0001t0043a0005c0008t0023 | a0001c0001t0023g0131 a0001c0001t0043g0134 a0005c0008t0023g0123 |
3 | 283 | 0.0106 | -2 | c.*56 others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3318 | chr3 | TogoVar | |||||||
ARHGEF26_chr3_154116390_154262825 | 154261653 | AAG | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(17): Show | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0150 others(101): Show |
106 | 283 | 0.3746 | -2 | c.*61 others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3829 | chr3 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73622433 | CAG | C | upstream_gene_variant | MODIFIER | HG02257.hp2 HG03490.hp2 |
a0003a0005 | a0003c0005a0005c0008 | a0003c0005t0002a0005c0008t0001 | a0003c0005t0002g0016 a0005c0008t0001g0017 |
2 | 188 | 0.0106 | -2 | c.-39 others(13): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 3762 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73636613 | TGG | T | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG02258.hp2 others(7): Show |
a0001a0002a0008others(3): Show | a0001c0025a0002c0002a0002c0003others(5): Show | a0001c0025t0005a0002c0002t0001a0002c0002t0003others(6): Show | a0001c0025t0005g0131 a0002c0002t0001g0130 a0002c0002t0001g0132 others(7): Show |
10 | 188 | 0.0532 | -2 | c.-12 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73657172 | CAA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0021a0001c0023others(27): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(35): Show | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(49): Show |
52 | 188 | 0.2766 | -2 | c.-11 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73658962 | TAC | T | intron_variant | MODIFIER | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
a0002a0004a0005others(4): Show | a0002c0002a0004c0004a0005c0008others(5): Show | a0002c0002t0001a0002c0002t0002a0004c0004t0001others(6): Show | a0002c0002t0001g0130 a0002c0002t0002g0133 a0004c0004t0001g0167 others(6): Show |
9 | 188 | 0.0479 | -2 | c.-11 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73681088 | ATT | A | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(19): Show |
a0001a0002a0004others(8): Show | a0001c0025a0002c0002a0002c0003others(11): Show | a0001c0025t0001a0002c0002t0001a0002c0002t0003others(14): Show | a0001c0025t0001g0156 a0002c0002t0001g0130 a0002c0002t0001g0132 others(19): Show |
22 | 188 | 0.1170 | -2 | c.-11 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73691296 | TAC | T | intron_variant | MODIFIER | HG00323.hp1 HG02809.hp2 HG03540.hp2 |
a0003a0006a0012 | a0003c0007a0006c0010a0012c0063 | a0003c0007t0001a0006c0010t0001a0012c0063t0001 | a0003c0007t0001g0140 a0006c0010t0001g0019 a0012c0063t0001g0152 |
3 | 188 | 0.0160 | -2 | c.33+ others(17): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73718591 | CTT | C | intron_variant | MODIFIER | HG02145.hp2 NA18906.hp1 |
a0005 | a0005c0022 | a0005c0022t0001a0005c0022t0005 | a0005c0022t0001g0120 a0005c0022t0005g0119 |
2 | 188 | 0.0106 | -2 | c.34- others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73722788 | ATC | A | intron_variant | MODIFIER | HG02965.hp1 HG03225.hp2 NA19030.hp1 |
a0001a0003a0039 | a0001c0021a0003c0007a0039c0051 | a0001c0021t0008a0003c0007t0005a0039c0051t0001 | a0001c0021t0008g0102 a0003c0007t0005g0151 a0039c0051t0001g0150 |
3 | 188 | 0.0160 | -2 | c.34- others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73738482 | CGT | C | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG02109.hp2 others(14): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0025a0002c0002others(9): Show | a0001c0001t0002a0001c0025t0001a0001c0025t0005others(10): Show | a0001c0001t0002g0099 a0001c0025t0001g0156 a0001c0025t0005g0131 others(14): Show |
17 | 188 | 0.0904 | -2 | c.34- others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73762455 | CAA | C | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
a0002a0003a0004others(6): Show | a0002c0002a0003c0058a0004c0004others(6): Show | a0002c0002t0001a0002c0002t0002a0003c0058t0001others(8): Show | a0002c0002t0001g0130 a0002c0002t0002g0158 a0002c0002t0002g0159 others(9): Show |
12 | 188 | 0.0638 | -2 | c.475 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73783345 | AGT | A | intron_variant | MODIFIER | HG01167.hp2 HG02109.hp2 HG02258.hp2 others(12): Show |
a0001a0002a0003others(4): Show | a0001c0025a0002c0002a0002c0003others(6): Show | a0001c0025t0001a0002c0002t0001a0002c0002t0002others(9): Show | a0001c0025t0001g0156 a0002c0002t0001g0130 a0002c0002t0001g0132 others(12): Show |
15 | 188 | 0.0798 | -2 | c.910 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73783384 | GTA | G | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp1 HG01175.hp2 others(9): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0028a0001c0077others(7): Show | a0001c0001t0001a0001c0028t0001a0001c0077t0002others(8): Show | a0001c0001t0001g0100 a0001c0028t0001g0146 a0001c0028t0001g0181 others(9): Show |
12 | 188 | 0.0638 | -2 | c.910 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73788919 | GGT | G | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG02055.hp1 others(15): Show |
a0002a0006a0007others(3): Show | a0002c0002a0002c0003a0006c0010others(5): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0005others(9): Show | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0182 others(15): Show |
18 | 188 | 0.0957 | -2 | c.911 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73793798 | CTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(48): Show |
a0001a0002a0006others(16): Show | a0001c0021a0002c0002a0002c0003others(24): Show | a0001c0021t0007a0002c0002t0001a0002c0002t0002others(36): Show | a0001c0021t0007g0178 a0002c0002t0001g0003 a0002c0002t0002g0086 others(48): Show |
51 | 188 | 0.2713 | -2 | c.911 others(17): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73794608 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
a0001a0002a0003others(30): Show | a0001c0021a0001c0028a0002c0002others(49): Show | a0001c0021t0007a0001c0021t0008a0001c0028t0001others(81): Show | a0001c0021t0007g0178 a0001c0021t0008g0102 a0001c0028t0001g0146 others(123): Show |
126 | 188 | 0.6702 | -2 | c.963 others(17): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73802870 | CTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
a0001a0002a0004others(18): Show | a0001c0001a0001c0021a0001c0023others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(36): Show | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0036 others(49): Show |
52 | 188 | 0.2766 | -2 | c.102 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806347 | TAG | T | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02602.hp1 others(4): Show |
a0002a0007a0013others(2): Show | a0002c0002a0002c0006a0007c0009others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(4): Show | a0002c0002t0001g0096 a0002c0002t0002g0086 a0002c0006t0002g0018 others(4): Show |
7 | 188 | 0.0372 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806431 | AGT | A | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
a0003a0004a0036others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140 a0004c0004t0001g0155 a0004c0004t0001g0167 others(4): Show |
7 | 188 | 0.0372 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73806434 | ATG | A | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02602.hp1 others(4): Show |
a0002a0007a0013others(2): Show | a0002c0002a0002c0006a0007c0009others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(4): Show | a0002c0002t0001g0096 a0002c0002t0002g0086 a0002c0006t0002g0018 others(4): Show |
7 | 188 | 0.0372 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806571 | AGT | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
a0003a0004a0037 | a0003c0007a0004c0004a0004c0018others(1): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(2): Show | a0003c0007t0001g0140 a0004c0004t0001g0155 a0004c0004t0001g0167 others(3): Show |
6 | 188 | 0.0319 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73806600 | CTA | C | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096 a0002c0002t0002g0086 a0002c0006t0002g0018 others(11): Show |
14 | 188 | 0.0745 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73807036 | GTT | G | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096 a0002c0002t0002g0086 a0002c0006t0002g0018 others(11): Show |
14 | 188 | 0.0745 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73811980 | CAA | C | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
a0001a0002a0003others(13): Show | a0001c0021a0002c0002a0002c0003others(20): Show | a0001c0021t0007a0001c0021t0008a0002c0002t0001others(28): Show | a0001c0021t0007g0178 a0001c0021t0008g0102 a0002c0002t0001g0003 others(36): Show |
39 | 188 | 0.2075 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73815190 | GTA | G | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(63): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0023a0001c0025others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(38): Show | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(63): Show |
66 | 188 | 0.3511 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73821806 | CAT | C | intron_variant | MODIFIER | HG00733.hp2 HG03139.hp2 |
a0002a0008 | a0002c0003a0008c0011 | a0002c0003t0001a0008c0011t0001 | a0002c0003t0001g0129 a0008c0011t0001g0128 |
2 | 188 | 0.0106 | -2 | c.102 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73834542 | CTG | C | intron_variant | MODIFIER | HG02109.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
a0001a0008a0012 | a0001c0025a0001c0071a0008c0011others(1): Show | a0001c0025t0001a0001c0071t0001a0008c0011t0002others(1): Show | a0001c0025t0001g0156 a0001c0071t0001g0073 a0008c0011t0002g0162 others(1): Show |
4 | 188 | 0.0213 | -2 | c.114 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73836303 | CTT | C | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
a0002a0007a0008others(1): Show | a0002c0002a0007c0009a0007c0013others(2): Show | a0002c0002t0001a0002c0002t0002a0007c0009t0001others(5): Show | a0002c0002t0001g0130 a0002c0002t0002g0158 a0002c0002t0002g0159 others(6): Show |
9 | 188 | 0.0479 | -2 | c.114 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73841712 | GAA | G | intron_variant | MODIFIER | HG00733.hp2 HG01517.hp1 HG02258.hp2 others(8): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(3): Show | a0001c0001t0002a0002c0002t0001a0002c0002t0002others(6): Show | a0001c0001t0002g0097 a0002c0002t0001g0130 a0002c0002t0002g0158 others(8): Show |
11 | 188 | 0.0585 | -2 | c.142 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73844640 | GTT | G | intron_variant | MODIFIER | HG02155.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
a0001a0004a0005 | a0001c0001a0001c0071a0004c0004others(2): Show | a0001c0001t0001a0001c0071t0001a0004c0004t0001others(2): Show | a0001c0001t0001g0036 a0001c0071t0001g0073 a0004c0004t0001g0187 others(3): Show |
6 | 188 | 0.0319 | -2 | c.142 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73845011 | ATT | A | intron_variant | MODIFIER | HG02258.hp2 HG02451.hp2 HG02922.hp1 others(2): Show |
a0002a0007a0008 | a0002c0002a0007c0009a0007c0013others(1): Show | a0002c0002t0001a0002c0002t0002a0007c0009t0001others(2): Show | a0002c0002t0001g0130 a0002c0002t0002g0159 a0007c0009t0001g0157 others(2): Show |
5 | 188 | 0.0266 | -2 | c.142 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73845986 | CAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(30): Show |
a0001a0003a0005others(15): Show | a0001c0071a0003c0007a0005c0070others(20): Show | a0001c0071t0001a0003c0007t0001a0005c0070t0001others(26): Show | a0001c0071t0001g0073 a0003c0007t0001g0140 a0005c0070t0001g0067 others(30): Show |
33 | 188 | 0.1755 | -2 | c.142 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73848606 | TAG | T | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(11): Show |
a0001a0002a0004others(6): Show | a0001c0025a0002c0002a0004c0004others(6): Show | a0001c0025t0005a0002c0002t0001a0002c0002t0002others(9): Show | a0001c0025t0005g0131 a0002c0002t0001g0096 a0002c0002t0002g0086 others(11): Show |
14 | 188 | 0.0745 | -2 | c.163 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73857564 | TAC | T | intron_variant | MODIFIER | HG02809.hp2 HG02976.hp1 NA18906.hp2 |
a0003a0006a0030 | a0003c0007a0006c0047a0030c0075 | a0003c0007t0001a0006c0047t0008a0030c0075t0010 | a0003c0007t0001g0140 a0006c0047t0008g0136 a0030c0075t0010g0138 |
3 | 188 | 0.0160 | -2 | c.179 others(17): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73881037 | GTT | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
a0001a0002a0003others(29): Show | a0001c0021a0001c0023a0001c0025others(48): Show | a0001c0021t0008a0001c0023t0002a0001c0025t0001others(69): Show | a0001c0021t0008g0102 a0001c0023t0002g0020 a0001c0025t0001g0156 others(93): Show |
96 | 188 | 0.5106 | -2 | c.281 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73883985 | TAA | T | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
a0003a0004a0007others(4): Show | a0003c0007a0004c0004a0007c0013others(4): Show | a0003c0007t0001a0003c0007t0005a0004c0004t0001others(6): Show | a0003c0007t0001g0045 a0003c0007t0001g0184 a0003c0007t0001g0186 others(8): Show |
11 | 188 | 0.0585 | -2 | c.305 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73905307 | TAA | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
a0001a0002a0003others(26): Show | a0001c0001a0001c0023a0001c0025others(50): Show | a0001c0001t0002a0001c0001t0006a0001c0023t0002others(73): Show | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0006g0169 others(99): Show |
102 | 188 | 0.5426 | -2 | c.416 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73929500 | TCA | T | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
a0001a0002a0003others(22): Show | a0001c0001a0001c0021a0001c0023others(41): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0008others(60): Show | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0063 others(83): Show |
86 | 188 | 0.4575 | -2 | c.494 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73931311 | CAT | C | intron_variant | MODIFIER | HG02145.hp1 HG02145.hp2 HG03486.hp1 |
a0001a0005a0036 | a0001c0028a0005c0022a0036c0055 | a0001c0028t0001a0005c0022t0001a0036c0055t0001 | a0001c0028t0001g0146 a0005c0022t0001g0120 a0036c0055t0001g0135 |
3 | 188 | 0.0160 | -2 | c.494 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73933932 | TTC | T | intron_variant | MODIFIER | HG01167.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
a0001a0002a0003others(7): Show | a0001c0021a0002c0002a0003c0005others(8): Show | a0001c0021t0008a0002c0002t0001a0002c0002t0002others(10): Show | a0001c0021t0008g0102 a0002c0002t0001g0130 a0002c0002t0001g0132 others(11): Show |
14 | 188 | 0.0745 | -2 | c.494 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | chr5 | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73934371 | TTG | T | intron_variant | MODIFIER | HG01243.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0025a0003c0007others(4): Show | a0001c0001t0001a0001c0025t0001a0003c0007t0001others(4): Show | a0001c0001t0001g0027 a0001c0025t0001g0156 a0003c0007t0001g0045 others(4): Show |
7 | 188 | 0.0372 | -2 | c.494 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73938160 | CCA | C | intron_variant | MODIFIER | HG01169.hp1 HG02615.hp2 HG02735.hp1 others(1): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0006others(1): Show | a0001c0001t0001a0002c0002t0005a0002c0006t0003others(1): Show | a0001c0001t0001g0038 a0002c0002t0005g0022 a0002c0006t0003g0111 others(1): Show |
4 | 188 | 0.0213 | -2 | c.494 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73942151 | GAA | G | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0023a0002c0002others(26): Show | a0001c0001t0002a0001c0023t0002a0002c0002t0002others(33): Show | a0001c0001t0002g0008 a0001c0001t0002g0050 a0001c0001t0002g0058 others(51): Show |
54 | 188 | 0.2872 | -2 | c.*11 others(13): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 162 | chr5 | TogoVar |