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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF1_chr19_41878184_41912452 | 41880451 | G | GGGAA | upstream_gene_variant | MODIFIER | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(31): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0008 | a0001c0001t0001a0001c0002t0001a0007c0008t0001 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | 34 | 234 | 0.1453 | 4 | c.-28 others(15): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2732 | chr19 | TogoVar | ||||||
ARHGEF1_chr19_41878184_41912452 | 41885454 | T | TTTTA | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(76): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(59): Show | 79 | 234 | 0.3376 | 4 | c.-20 others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41894135 | A | AGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
a0001a0003a0007 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(57): Show | 89 | 234 | 0.3803 | 4 | c.645 others(17): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41907905 | C | CACAA | downstream_gene_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(73): Show | 89 | 234 | 0.3803 | 4 | c.*81 others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 454 | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154124372 | C | CTTTT | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
a0002a0006a0010 | a0002c0002a0002c0003a0002c0014others(3): Show | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(23): Show | a0002c0002t0003g0031a0002c0002t0003g0037a0002c0002t0003g0038others(89): Show | 93 | 283 | 0.3286 | 4 | c.108 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154164456 | T | TTATC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0009a0001c0015others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(64): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | 283 | 0.9541 | 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 | 154186136 | G | GACAC | intron_variant | MODIFIER | HG02109.hp1 HG02257.hp1 HG02523.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0014a0001c0001t0036others(2): Show | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0014g0277others(3): Show | 6 | 283 | 0.0212 | 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 | 154186886 | C | CTTTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0004 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(5): Show | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0191others(24): Show | 28 | 283 | 0.0989 | 4 | c.148 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154202798 | C | CTGTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0009a0001c0015others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(66): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | 283 | 0.9611 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154211867 | A | ATGTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(24): Show | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(99): Show | 103 | 283 | 0.3640 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154213201 | T | TAGAG | intron_variant | MODIFIER | HG01433.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | 283 | 0.0283 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154213216 | A | AGAGT | intron_variant | MODIFIER | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0003others(2): Show | a0001c0001t0004a0001c0001t0023a0002c0002t0003others(7): Show | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0023g0131others(12): Show | 15 | 283 | 0.0530 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154213239 | G | GTATA | intron_variant | MODIFIER | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
a0002 | a0002c0003 | a0002c0003t0018a0002c0003t0045a0002c0003t0046 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | 283 | 0.0106 | 4 | c.184 others(23): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154226660 | T | TACAC | intron_variant | MODIFIER | HG00323.hp1 HG00741.hp2 HG01081.hp2 others(9): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0010a0001c0001t0011a0001c0001t0015others(6): Show | a0001c0001t0010g0138a0001c0001t0010g0140a0001c0001t0011g0141others(9): Show | 12 | 283 | 0.0424 | 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 | 154237538 | T | TCACA | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG01071.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0020others(8): Show | a0001c0001t0002g0240a0001c0001t0004g0139a0001c0001t0004g0219others(11): Show | 15 | 283 | 0.0530 | 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 | 154239289 | A | AGTGT | intron_variant | MODIFIER | HG02155.hp1 NA18947.hp1 NA18960.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0007a0002c0002t0003a0002c0003t0003 | a0001c0001t0007g0172a0002c0002t0003g0045a0002c0002t0003g0083others(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 | 154256886 | T | TTATC | 3_prime_UTR_variant | MODIFIER | HG03195.hp2 NA19043.hp1 |
a0003 | a0003c0004 | a0003c0004t0031a0003c0004t0032 | a0003c0004t0031g0010a0003c0004t0032g0008 | 2 | 283 | 0.0071 | 4 | c.*14 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1419 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||
ARHGEF28_chr5_73621196_73946990 | 73639228 | C | CATAT | intron_variant | MODIFIER | HG00733.hp2 HG01069.hp1 HG01167.hp2 others(9): Show |
a0001a0002a0006others(6): Show | a0001c0025a0002c0002a0002c0003others(8): Show | a0001c0025t0005a0002c0002t0001a0002c0003t0001others(8): Show | a0001c0025t0005g0131a0002c0002t0001g0130a0002c0002t0001g0132others(9): Show | 12 | 188 | 0.0638 | 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 | T | TACAC | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(16): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0028a0002c0002others(11): Show | a0001c0001t0002a0001c0028t0001a0002c0002t0002others(14): Show | a0001c0001t0002g0008a0001c0028t0001g0181a0002c0002t0002g0086others(16): Show | 19 | 188 | 0.1011 | 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 | 73687393 | C | CTCTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
a0001a0002a0003others(34): Show | a0001c0001a0001c0021a0001c0023others(60): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0007others(89): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(131): Show | 134 | 188 | 0.7128 | 4 | c.33+ others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73691296 | T | TACAC | intron_variant | MODIFIER | HG00323.hp2 HG01891.hp1 HG02451.hp2 others(4): Show |
a0002a0003a0004others(3): Show | a0002c0002a0003c0007a0004c0004others(3): Show | a0002c0002t0003a0003c0007t0011a0004c0004t0005others(4): Show | a0002c0002t0003g0124a0003c0007t0011g0148a0004c0004t0005g0183others(4): Show | 7 | 188 | 0.0372 | 4 | c.33+ others(19): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73703647 | T | TTGTG | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(14): Show |
a0003a0004a0005others(10): Show | a0003c0005a0003c0048a0004c0004others(13): Show | a0003c0005t0001a0003c0048t0006a0004c0004t0001others(14): Show | a0003c0005t0001g0043a0003c0048t0006g0176a0004c0004t0001g0170others(14): Show | 17 | 188 | 0.0904 | 4 | 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 | 73722211 | G | GGAGA | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
a0001a0002a0003others(16): Show | a0001c0021a0002c0002a0002c0003others(26): Show | a0001c0021t0008a0002c0002t0001a0002c0002t0002others(37): Show | a0001c0021t0008g0102a0002c0002t0001g0003a0002c0002t0001g0130others(50): Show | 53 | 188 | 0.2819 | 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 | 73731011 | T | TAAAA | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG01167.hp2 others(14): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0003a0003c0007others(11): Show | a0002c0002t0001a0002c0002t0005a0002c0003t0001others(14): Show | a0002c0002t0001g0132a0002c0002t0005g0022a0002c0003t0001g0129others(14): Show | 17 | 188 | 0.0904 | 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 | 73738482 | C | CGTGT | intron_variant | MODIFIER | HG00741.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
a0003a0005a0007others(3): Show | a0003c0007a0005c0008a0007c0009others(3): Show | a0003c0007t0001a0003c0007t0011a0005c0008t0001others(5): Show | a0003c0007t0001g0045a0003c0007t0001g0140a0003c0007t0011g0148others(6): Show | 9 | 188 | 0.0479 | 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 | A | AAAAT | intron_variant | MODIFIER | HG00733.hp2 HG01891.hp1 HG02145.hp2 others(16): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0003others(11): Show | a0001c0001t0002a0002c0002t0005a0002c0003t0001others(16): Show | a0001c0001t0002g0050a0002c0002t0005g0022a0002c0003t0001g0129others(16): Show | 19 | 188 | 0.1011 | 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 | 73783345 | A | AGTGT | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(33): Show |
a0001a0003a0004others(10): Show | a0001c0001a0001c0023a0003c0005others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0001others(21): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0038others(33): Show | 36 | 188 | 0.1915 | 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 | C | CTCTG | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(26): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0006a0003c0005others(14): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0001others(20): Show | a0002c0002t0001g0132a0002c0002t0001g0182a0002c0002t0002g0158others(26): Show | 29 | 188 | 0.1543 | 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 | 73804082 | C | CAAAA | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
a0003a0006a0007 | a0003c0058a0006c0047a0007c0013 | a0003c0058t0001a0006c0047t0008a0007c0013t0001others(2): Show | a0003c0058t0001g0139a0006c0047t0008g0136a0007c0013t0001g0137others(2): Show | 5 | 188 | 0.0266 | 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 | 73806341 | A | AGTAT | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
a0003a0004a0036others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140a0004c0004t0001g0155a0004c0004t0001g0167others(4): Show | 7 | 188 | 0.0372 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806356 | T | TATAC | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
a0003a0004a0036others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140a0004c0004t0001g0155a0004c0004t0001g0167others(4): Show | 7 | 188 | 0.0372 | 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 | 73807487 | C | CTTTT | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
a0003a0004a0013others(1): Show | a0003c0007a0004c0004a0004c0018others(2): Show | a0003c0007t0001a0004c0004t0001a0004c0004t0005others(3): Show | a0003c0007t0001g0140a0004c0004t0001g0155a0004c0004t0001g0167others(4): Show | 7 | 188 | 0.0372 | 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 | 73815190 | G | GTGTA | intron_variant | MODIFIER | HG02809.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
a0002a0003a0006others(2): Show | a0002c0002a0003c0007a0006c0010others(2): Show | a0002c0002t0001a0003c0007t0005a0006c0010t0001others(2): Show | a0002c0002t0001g0182a0003c0007t0005g0151a0006c0010t0001g0185others(2): Show | 5 | 188 | 0.0266 | 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 | 73815251 | A | AGCTC | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(21): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0003a0003c0049others(11): Show | a0002c0002t0001a0002c0002t0002a0002c0003t0001others(15): Show | a0002c0002t0001g0096a0002c0002t0001g0130a0002c0002t0001g0132others(21): Show | 24 | 188 | 0.1277 | 4 | c.102 others(25): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73837710 | T | TCTTC | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG04199.hp1 |
a0005a0007 | a0005c0024a0007c0009 | a0005c0024t0002a0007c0009t0001a0007c0009t0002 | a0005c0024t0002g0064a0007c0009t0001g0121a0007c0009t0002g0040 | 3 | 188 | 0.0160 | 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 | 73857564 | T | TACAC | intron_variant | MODIFIER | HG00733.hp1 NA18988.hp1 NA19065.hp2 others(1): Show |
a0001a0005 | a0001c0001a0001c0077a0005c0008 | a0001c0001t0002a0001c0077t0002a0005c0008t0002 | a0001c0001t0002g0058a0001c0001t0002g0099a0001c0077t0002g0028others(1): Show | 4 | 188 | 0.0213 | 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 | 73858425 | C | CCTCA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
a0001a0002a0003others(31): Show | a0001c0021a0001c0023a0001c0025others(53): Show | a0001c0021t0008a0001c0023t0001a0001c0025t0001others(81): Show | a0001c0021t0008g0102a0001c0023t0001g0034a0001c0025t0001g0156others(114): Show | 117 | 188 | 0.6223 | 4 | c.204 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73869222 | T | TGGGG | intron_variant | MODIFIER | HG01106.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0025a0002c0002a0003c0058others(5): Show | a0001c0025t0001a0002c0002t0001a0002c0002t0005others(6): Show | a0001c0025t0001g0156a0002c0002t0001g0182a0002c0002t0005g0022others(6): Show | 9 | 188 | 0.0479 | 4 | c.242 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73894845 | G | GGGAA | intron_variant | MODIFIER | HG02258.hp2 HG02965.hp2 HG03139.hp1 |
a0002a0012 | a0002c0002a0012c0073 | a0002c0002t0001a0002c0002t0003a0012c0073t0001 | a0002c0002t0001g0130a0002c0002t0003g0124a0012c0073t0001g0143 | 3 | 188 | 0.0160 | 4 | c.384 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73910381 | C | CAAAA | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0025a0001c0071others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(35): Show | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0002g0094others(49): Show | 52 | 188 | 0.2766 | 4 | c.464 others(21): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73913347 | A | ATGTT | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
a0001a0002a0003others(29): Show | a0001c0001a0001c0021a0001c0023others(59): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(93): Show | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0063others(129): Show | 132 | 188 | 0.7021 | 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 | 73938160 | C | CCACA | intron_variant | MODIFIER | HG00140.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0028a0002c0002others(6): Show | a0001c0001t0002a0001c0028t0001a0002c0002t0001others(6): Show | a0001c0001t0002g0032a0001c0028t0001g0146a0002c0002t0001g0182others(6): Show | 9 | 188 | 0.0479 | 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 | 73938931 | C | CTTTT | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp1 HG03704.hp2 others(5): Show |
a0017a0023a0026others(4): Show | a0017c0062a0017c0066a0023c0041others(5): Show | a0017c0062t0007a0017c0066t0001a0023c0041t0001others(5): Show | a0017c0062t0007g0171a0017c0066t0001g0015a0023c0041t0001g0079others(5): Show | 8 | 188 | 0.0426 | 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 | 73944548 | A | AACTT | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00621.hp1 HG03704.hp2 others(5): Show |
a0017a0023a0026others(4): Show | a0017c0062a0017c0066a0023c0041others(5): Show | a0017c0062t0007a0017c0066t0001a0023c0041t0001others(5): Show | a0017c0062t0007g0171a0017c0066t0001g0015a0023c0041t0001g0079others(5): Show | 8 | 188 | 0.0426 | 4 | c.*35 others(15): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2559 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73946071 | A | AAAAT | downstream_gene_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
a0001a0002a0003others(4): Show | a0001c0021a0001c0025a0002c0002others(7): Show | a0001c0021t0008a0001c0025t0005a0002c0002t0005others(7): Show | a0001c0021t0008g0102a0001c0025t0005g0131a0002c0002t0005g0022others(7): Show | 10 | 188 | 0.0532 | 4 | c.*50 others(15): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4082 | chr5 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155945280 | G | GGTGT | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(50): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0007a0003c0004t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(42): Show | 53 | 284 | 0.1866 | 4 | c.*26 others(15): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1573 | chr1 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155964167 | A | AATAT | intron_variant | MODIFIER | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 7 | 284 | 0.0247 | 4 | c.724 others(19): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | ||||||
ARHGEF2_chr1_155941854_155983547 | 155964174 | A | ATATG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(43): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(30): Show | 46 | 284 | 0.1620 | 4 | c.724 others(19): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38909975 | G | GTTAT | intron_variant | MODIFIER | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | 278 | 0.0108 | 4 | c.-85 others(21): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38929591 | C | CTCAT | intron_variant | MODIFIER | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0004a0001c0003t0004a0002c0002t0004 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | 278 | 0.0360 | 4 | c.241 others(17): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |