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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143421766 | GTATA | G | intron_variant | MODIFIER | HG03139.hp1 HG06807.hp2 NA18955.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0124 | 3 | 162 | 0.0185 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143425341 | TTATA | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041a0001c0001t0001g0137 | 2 | 162 | 0.0124 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143433766 | GTTTA | G | intron_variant | MODIFIER | HG02486.hp1 HG02809.hp1 HG02976.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0088others(1): Show | 4 | 162 | 0.0247 | -4 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143468633 | TGAGA | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(59): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(59): Show | 62 | 162 | 0.3827 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143471007 | TAAAG | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(19): Show | 22 | 162 | 0.1358 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143477190 | GCACA | G | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(29): Show | 32 | 162 | 0.1975 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143535380 | TTTAA | T | intron_variant | MODIFIER | HG02071.hp1 NA18747.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024a0001c0001t0001g0028 | 2 | 162 | 0.0124 | -4 | c.925 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143573462 | TAAAG | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(45): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0013others(45): Show | 48 | 162 | 0.2963 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143610719 | GTATT | G | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 62 | 162 | 0.3827 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143613154 | TTAAG | T | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(50): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | 162 | 0.3272 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143621380 | GGTTA | G | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0068others(17): Show | 20 | 162 | 0.1235 | -4 | c.100 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143622781 | TAAAA | T | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(64): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(64): Show | 67 | 162 | 0.4136 | -4 | c.100 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143638657 | AAAAT | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 57 | 162 | 0.3519 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143643045 | TTAAC | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0068others(14): Show | 17 | 162 | 0.1049 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | GGTGT | G | intron_variant | MODIFIER | HG00621.hp1 HG01243.hp1 HG02145.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | 162 | 0.1235 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143679646 | CGTGT | C | intron_variant | MODIFIER | HG02109.hp1 HG03139.hp2 HG03831.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0100others(2): Show | 5 | 162 | 0.0309 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01255.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(16): Show | 19 | 162 | 0.1173 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143696179 | GAAGA | G | intron_variant | MODIFIER | HG01261.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0049others(4): Show | 7 | 162 | 0.0432 | -4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143701800 | CTCTT | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01071.hp2 others(25): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | 162 | 0.1728 | -4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143727455 | TTTTG | T | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0081others(10): Show | 13 | 162 | 0.0803 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143730400 | ATTTC | A | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(30): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(30): Show | 33 | 162 | 0.2037 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143737726 | TTTTA | T | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp2 HG01081.hp1 others(36): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(36): Show | 39 | 162 | 0.2407 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143761513 | AAAAG | A | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0109others(9): Show | 12 | 162 | 0.0741 | -4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | ATGTG | A | intron_variant | MODIFIER | HG00738.hp2 HG01243.hp2 HG02145.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(14): Show | 17 | 162 | 0.1049 | -4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | CTTTT | C | downstream_gene_variant | MODIFIER | HG00323.hp2 HG01069.hp2 HG01074.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 25 | 240 | 0.1042 | -4 | c.*37 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | TACAC | T | downstream_gene_variant | MODIFIER | HG00323.hp2 HG01099.hp1 HG01243.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0076others(7): Show | 10 | 240 | 0.0417 | -4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916626 | CACAT | C | downstream_gene_variant | MODIFIER | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0214others(4): Show | 7 | 240 | 0.0292 | -4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2762 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916816 | GCGCA | G | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0008 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | 240 | 0.0333 | -4 | c.*33 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2572 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916818 | GCACA | G | downstream_gene_variant | MODIFIER | HG01978.hp2 HG02523.hp2 HG04199.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050a0001c0001t0001g0164a0001c0001t0001g0184others(3): Show | 6 | 240 | 0.0250 | -4 | c.*33 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2570 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24917332 | CCTCT | C | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0002a0001c0004t0008 | a0001c0001t0002g0031a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | 240 | 0.0375 | -4 | c.*27 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2056 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24926118 | AAAAG | A | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0003c0007t0001 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | 240 | 0.0500 | -4 | c.251 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24933254 | TCTGA | T | intron_variant | MODIFIER | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(29): Show | 33 | 240 | 0.1375 | -4 | c.189 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24938937 | GAATC | G | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(20): Show | 24 | 240 | 0.1000 | -4 | c.172 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961911 | TTATA | T | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0005a0001c0003t0003a0001c0005t0001 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | 240 | 0.0583 | -4 | c.574 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24985188 | CCACA | C | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(120): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(115): Show | 123 | 240 | 0.5125 | -4 | c.54- others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25009364 | CAAAA | C | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0001c0001t0004a0003c0007t0001 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | 240 | 0.0958 | -4 | c.53+ others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | GAAGA | G | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0126others(18): Show | 21 | 240 | 0.0875 | -4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129608966 | TAGAG | T | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0018 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | 238 | 0.0462 | -4 | c.112 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625208 | GTAAT | G | intron_variant | MODIFIER | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0003 | a0001c0001t0001g0155a0001c0001t0001g0216a0001c0001t0001g0218others(2): Show | 5 | 238 | 0.0210 | -4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625739 | ATATT | A | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | 238 | 0.2101 | -4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129626065 | TACAC | T | intron_variant | MODIFIER | HG01192.hp2 HG02451.hp2 HG02895.hp1 others(13): Show |
a0001a0002a0008 | a0001c0001a0002c0002a0008c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0142a0001c0001t0001g0218a0001c0001t0002g0125others(13): Show | 16 | 238 | 0.0672 | -4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129626672 | TACAC | T | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(43): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0011a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(43): Show | 46 | 238 | 0.1933 | -4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129640042 | CAAAA | C | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(46): Show | 50 | 238 | 0.2101 | -4 | c.317 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129655338 | AAAAG | A | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0199others(6): Show | 9 | 238 | 0.0378 | -4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129655353 | AAAAG | A | intron_variant | MODIFIER | HG01192.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0007c0008others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0019others(4): Show | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(5): Show | 8 | 238 | 0.0336 | -4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129667469 | ATGTG | A | intron_variant | MODIFIER | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 25 | 238 | 0.1050 | -4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129668362 | TCACA | T | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 HG03669.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0007a0001c0003t0002 | a0001c0001t0001g0079a0001c0001t0001g0216a0001c0001t0007g0077others(2): Show | 5 | 238 | 0.0210 | -4 | c.114 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129676912 | CCTCT | C | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
a0001a0008 | a0001c0001a0008c0005 | a0001c0001t0001a0001c0001t0003a0008c0005t0003 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | 238 | 0.0168 | -4 | c.113 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129679170 | TACTA | T | intron_variant | MODIFIER | HG00597.hp2 HG03669.hp2 HG04115.hp2 others(7): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0082others(7): Show | 10 | 238 | 0.0420 | -4 | c.113 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129686974 | TTTTC | T | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(23): Show |
a0001 | a0001c0001a0001c0003a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 26 | 238 | 0.1092 | -4 | c.113 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar |