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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF19_chr1_16192854_16217652 | 16207335 | AATTC | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0006a0002c0002others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 274 | 362 | 0.7569 | -4 | c.875 others(19): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 5/15 | chr1 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16213728 | TTTTA | T | upstream_gene_variant | MODIFIER | HG00423.hp2 HG00609.hp2 HG01069.hp1 others(21): Show |
a0001a0004a0012 | a0001c0001a0001c0006a0004c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 24 | 362 | 0.0663 | -4 | c.-12 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 1077 | chr1 | TogoVar | ||||||
ARHGEF19_chr1_16192854_16217652 | 16215419 | GTATT | G | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(43): Show |
a0001a0002a0008others(1): Show | a0001c0001a0002c0002a0008c0010others(1): Show | a0001c0001t0001a0001c0001t0008a0002c0002t0002others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 46 | 362 | 0.1271 | -4 | c.-29 others(15): Show |
ARHGEF19 | ENSG00000142632.17 | transcript | ENST00000270747.8 | protein_coding | 2768 | chr1 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41880391 | AAGAG | A | upstream_gene_variant | MODIFIER | HG00735.hp1 HG01243.hp1 HG02559.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0001g0105others(1): Show | 4 | 234 | 0.0171 | -4 | c.-29 others(15): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2792 | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41880451 | GGGAA | G | upstream_gene_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(43): Show | 51 | 234 | 0.2180 | -4 | c.-28 others(15): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2732 | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41900786 | GTTTT | G | intron_variant | MODIFIER | HG02027.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0038a0001c0002t0001g0076a0001c0002t0001g0130others(6): Show | 9 | 234 | 0.0385 | -4 | c.126 others(23): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41905426 | CATAT | C | intron_variant | MODIFIER | HG03195.hp2 NA19030.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | 234 | 0.0086 | -4 | c.233 others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154120421 | CATAA | C | upstream_gene_variant | MODIFIER | HG01243.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0005a0002c0002t0047 | a0002c0002t0005g0034a0002c0002t0005g0042a0002c0002t0005g0043others(1): Show | 4 | 283 | 0.0141 | -4 | c.-11 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 968 | chr3 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154149247 | AAATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0009a0001c0015others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(59): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | 283 | 0.9329 | -4 | c.127 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154154573 | TATAG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0009a0001c0015others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(142): Show | 148 | 283 | 0.5230 | -4 | c.148 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154163917 | GCTGT | G | intron_variant | MODIFIER | HG01884.hp2 HG02809.hp2 HG02818.hp1 |
a0001a0007 | a0001c0001a0007c0006 | a0001c0001t0017a0007c0006t0017 | a0001c0001t0017g0132a0007c0006t0017g0128a0007c0006t0017g0129 | 3 | 283 | 0.0106 | -4 | 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 | 154173447 | CAATT | C | intron_variant | MODIFIER | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0007 | a0001c0001t0037a0002c0002t0051a0002c0007t0018 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0007t0018g0090others(1): Show | 4 | 283 | 0.0141 | -4 | 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 | 154207024 | TTAAA | T | intron_variant | MODIFIER | HG01884.hp1 HG03453.hp2 |
a0002 | a0002c0003 | a0002c0003t0005a0002c0003t0026 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | 283 | 0.0071 | -4 | 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 | TACAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(175): Show | 181 | 283 | 0.6396 | -4 | 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 | 154230181 | TGTTA | T | intron_variant | MODIFIER | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0015a0001c0001t0030a0002c0003t0044 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | 283 | 0.0177 | -4 | 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 | 154232384 | ATGTT | A | intron_variant | MODIFIER | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
a0002 | a0002c0003 | a0002c0003t0018a0002c0003t0045a0002c0003t0046 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | 283 | 0.0106 | -4 | 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 | TCACA | T | intron_variant | MODIFIER | HG02602.hp2 HG03098.hp1 NA19030.hp1 others(1): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0003a0005c0008others(1): Show | a0001c0001t0014a0002c0003t0006a0005c0008t0014others(1): Show | a0001c0001t0014g0277a0002c0003t0006g0115a0005c0008t0014g0122others(1): Show | 4 | 283 | 0.0141 | -4 | 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 | 154239257 | AGAGG | A | intron_variant | MODIFIER | HG01099.hp1 HG01123.hp2 HG01934.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0021a0002c0002t0003a0002c0002t0028others(1): Show | a0001c0001t0021g0133a0002c0002t0003g0038a0002c0002t0003g0064others(5): Show | 8 | 283 | 0.0283 | -4 | 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 | 154247623 | CTCTA | C | intron_variant | MODIFIER | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0002c0003others(2): Show | a0001c0001t0007a0001c0001t0021a0001c0001t0036others(10): Show | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | 283 | 0.2262 | -4 | c.230 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154257634 | GTGTT | G | 3_prime_UTR_variant | MODIFIER | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0015a0001c0001t0030a0002c0003t0044 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | 283 | 0.0177 | -4 | c.*21 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 2168 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||
ARHGEF28_chr5_73621196_73946990 | 73644979 | CTGTG | C | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG02486.hp1 others(4): Show |
a0002a0003a0004others(1): Show | a0002c0002a0003c0007a0004c0004others(1): Show | a0002c0002t0001a0003c0007t0001a0004c0004t0001others(2): Show | a0002c0002t0001g0182a0003c0007t0001g0184a0003c0007t0001g0186others(4): Show | 7 | 188 | 0.0372 | -4 | c.-12 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73650277 | CTTTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(44): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0021a0001c0025others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(39): Show | a0001c0001t0001g0063a0001c0001t0002g0050a0001c0001t0002g0058others(44): Show | 47 | 188 | 0.2500 | -4 | c.-12 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73658962 | TACAC | T | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG02622.hp1 others(4): Show |
a0002a0008a0011others(1): Show | a0002c0002a0002c0003a0008c0011others(3): Show | a0002c0002t0001a0002c0002t0003a0002c0003t0001others(4): Show | a0002c0002t0001g0132a0002c0002t0003g0124a0002c0003t0001g0129others(4): Show | 7 | 188 | 0.0372 | -4 | c.-11 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73669686 | CTTTA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
a0001a0002a0003others(36): Show | a0001c0001a0001c0021a0001c0023others(66): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(98): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(141): Show | 144 | 188 | 0.7660 | -4 | c.-11 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73681088 | ATTTT | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0021a0001c0023others(31): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(42): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(64): Show | 67 | 188 | 0.3564 | -4 | 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 | 73735216 | TATTA | T | intron_variant | MODIFIER | HG02145.hp2 NA18906.hp1 |
a0005 | a0005c0022 | a0005c0022t0001a0005c0022t0005 | a0005c0022t0001g0120a0005c0022t0005g0119 | 2 | 188 | 0.0106 | -4 | 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 | 73739828 | AAAAT | A | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(29): Show |
a0001a0002a0003others(10): Show | a0001c0025a0001c0071a0002c0002others(16): Show | a0001c0025t0001a0001c0025t0005a0001c0071t0001others(22): Show | a0001c0025t0001g0156a0001c0025t0005g0131a0001c0071t0001g0073others(29): Show | 32 | 188 | 0.1702 | -4 | 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 | 73741385 | GTATA | G | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp1 |
a0005a0015 | a0005c0008a0015c0037 | a0005c0008t0002a0015c0037t0003 | a0005c0008t0002g0083a0015c0037t0003g0110 | 2 | 188 | 0.0106 | -4 | 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 | 73754887 | TTTTA | T | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00733.hp2 others(54): Show |
a0001a0002a0003others(19): Show | a0001c0021a0001c0025a0001c0077others(36): Show | a0001c0021t0008a0001c0025t0001a0001c0025t0005others(48): Show | a0001c0021t0008g0102a0001c0025t0001g0156a0001c0025t0005g0131others(54): Show | 57 | 188 | 0.3032 | -4 | c.475 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73757395 | AATAG | A | intron_variant | MODIFIER | HG02965.hp1 NA19030.hp1 |
a0003a0039 | a0003c0007a0039c0051 | a0003c0007t0005a0039c0051t0001 | a0003c0007t0005g0151a0039c0051t0001g0150 | 2 | 188 | 0.0106 | -4 | c.475 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73783382 | GTGTA | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(43): Show |
a0001a0002a0006others(15): Show | a0001c0021a0002c0002a0002c0003others(22): Show | a0001c0021t0007a0002c0002t0001a0002c0002t0002others(33): Show | a0001c0021t0007g0178a0002c0002t0001g0003a0002c0002t0002g0086others(43): Show | 46 | 188 | 0.2447 | -4 | c.910 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73802870 | CTGTG | C | intron_variant | MODIFIER | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
a0001a0005a0006others(4): Show | a0001c0001a0005c0070a0006c0010others(4): Show | a0001c0001t0002a0005c0070t0001a0006c0010t0004others(5): Show | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0012others(8): Show | 11 | 188 | 0.0585 | -4 | 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 | GTATA | G | intron_variant | MODIFIER | HG01517.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
a0004a0025 | a0004c0004a0004c0018a0025c0033 | a0004c0004t0001a0004c0004t0005a0004c0018t0002others(1): Show | a0004c0004t0001g0167a0004c0004t0005g0183a0004c0018t0002g0154others(1): Show | 4 | 188 | 0.0213 | -4 | 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 | 73818374 | CTTAT | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0021a0001c0023others(41): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(62): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(97): Show | 100 | 188 | 0.5319 | -4 | 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 | 73834542 | CTGTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
a0001a0002a0003others(29): Show | a0001c0001a0001c0021a0001c0023others(54): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(78): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(117): Show | 120 | 188 | 0.6383 | -4 | c.114 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73837745 | GTTTT | G | 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 | -4 | c.114 others(23): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73845986 | CAAAA | C | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
a0001a0002a0003others(7): Show | a0001c0028a0002c0002a0003c0005others(10): Show | a0001c0028t0001a0002c0002t0001a0002c0002t0002others(18): Show | a0001c0028t0001g0146a0001c0028t0001g0181a0002c0002t0001g0182others(24): Show | 27 | 188 | 0.1436 | -4 | 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 | 73857564 | TACAC | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
a0001a0002a0006others(17): Show | a0001c0021a0001c0025a0002c0002others(22): Show | a0001c0021t0008a0001c0025t0001a0002c0002t0001others(31): Show | a0001c0021t0008g0102a0001c0025t0001g0156a0002c0002t0001g0096others(37): Show | 40 | 188 | 0.2128 | -4 | c.179 others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73882359 | ATATT | A | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(9): Show |
a0002a0003a0004others(5): Show | a0002c0003a0003c0007a0004c0004others(5): Show | a0002c0003t0001a0003c0007t0001a0003c0007t0005others(7): Show | a0002c0003t0001g0129a0003c0007t0001g0045a0003c0007t0001g0184others(9): Show | 12 | 188 | 0.0638 | -4 | 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 | 73885040 | ATTGT | A | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
a0003a0004a0005others(4): Show | a0003c0007a0004c0004a0005c0070others(4): Show | a0003c0007t0001a0003c0007t0005a0004c0004t0001others(6): Show | a0003c0007t0001g0045a0003c0007t0001g0184a0003c0007t0001g0186others(8): Show | 11 | 188 | 0.0585 | -4 | c.305 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73914391 | CTTTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0025a0001c0028others(34): Show | a0001c0001t0001a0001c0001t0002a0001c0025t0005others(46): Show | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0002g0011others(58): Show | 61 | 188 | 0.3245 | -4 | 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 | 73920433 | CTTTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(28): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0021a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0002g0008others(28): Show | 31 | 188 | 0.1649 | -4 | 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 | 73928929 | TTTTA | T | intron_variant | MODIFIER | HG00733.hp1 HG01167.hp2 HG02055.hp1 others(21): Show |
a0001a0002a0003others(8): Show | a0001c0021a0002c0002a0003c0005others(13): Show | a0001c0021t0008a0002c0002t0001a0002c0002t0002others(17): Show | a0001c0021t0008g0102a0002c0002t0001g0003a0002c0002t0001g0130others(21): Show | 24 | 188 | 0.1277 | -4 | c.494 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF2_chr1_155941854_155983547 | 155943811 | CTTGT | C | downstream_gene_variant | MODIFIER | HG02559.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | 284 | 0.0141 | -4 | c.*41 others(15): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 3042 | chr1 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155945280 | GGTGT | G | downstream_gene_variant | MODIFIER | HG03239.hp2 HG04199.hp1 NA19067.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0084a0001c0001t0001g0169a0001c0001t0001g0172others(1): Show | 4 | 284 | 0.0141 | -4 | c.*26 others(15): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1573 | chr1 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38894487 | AAAAC | A | intron_variant | MODIFIER | HG01516.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0002g0222a0001c0001t0004g0259a0001c0001t0004g0260others(4): Show | 7 | 278 | 0.0252 | -4 | c.-15 others(23): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38920398 | CTTTT | C | intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 HG02280.hp1 others(7): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(4): Show | a0001c0001t0001g0140a0001c0001t0001g0156a0001c0001t0002g0269others(6): Show | 10 | 278 | 0.0360 | -4 | c.25+ others(17): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38925080 | AAGAG | A | intron_variant | MODIFIER | NA18953.hp1 NA18955.hp1 NA18979.hp1 others(3): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0013 | a0001c0001t0001a0002c0002t0001a0009c0013t0001 | a0001c0001t0001g0195a0002c0002t0001g0096a0002c0002t0001g0187others(3): Show | 6 | 278 | 0.0216 | -4 | c.75+ others(19): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF35_chr7_144181083_144200833 | 144192230 | TACAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0017others(7): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(14): Show | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0026others(44): Show | 101 | 383 | 0.2637 | -4 | c.-13 others(21): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 1/1 | chr7 | TogoVar | ||||||
ARHGEF35_chr7_144181083_144200833 | 144196747 | CTGTG | C | upstream_gene_variant | MODIFIER | HG00642.hp2 HG01433.hp2 NA18980.hp2 |
a0001a0002a0007 | a0001c0003a0002c0002a0007c0008 | a0001c0003t0001a0002c0002t0002a0007c0008t0002 | a0001c0003t0001g0140a0002c0002t0002g0004a0007c0008t0002g0055 | 3 | 383 | 0.0078 | -4 | c.-12 others(15): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 915 | chr7 | TogoVar |