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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142936108 | AACACAC | A | intron_variant | MODIFIER | HG02258.hp1 HG02647.hp1 HG02818.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010a0001c0001t0026 | a0001c0001t0006g0086a0001c0001t0010g0080a0001c0001t0026g0071 | 3 | 198 | 0.0152 | -6 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142950994 | CCTTTCT | C | intron_variant | MODIFIER | HG00408.hp1 HG02056.hp1 HG02074.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0041 | a0001c0001t0002g0195a0001c0001t0007g0068a0001c0001t0041g0163 | 3 | 198 | 0.0152 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963217 | TGTGCGC | T | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01433.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0005a0001c0002t0028a0001c0003t0004others(1): Show | a0001c0001t0005g0101a0001c0001t0005g0108a0001c0001t0005g0109others(3): Show | 6 | 198 | 0.0303 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142997090 | TTTCCAA | T | intron_variant | MODIFIER | HG01071.hp1 HG01167.hp2 HG01433.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0003 | a0001c0002t0001g0149a0001c0002t0002g0183a0001c0002t0003g0050others(4): Show | 7 | 198 | 0.0354 | -6 | c.110 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTTTT | G | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0022a0001c0001t0025others(1): Show | a0001c0001t0006g0064a0001c0001t0006g0104a0001c0001t0022g0081others(2): Show | 5 | 198 | 0.0253 | -6 | c.114 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143085044 | CAAAAAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00597.hp2 HG02056.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0131a0001c0001t0001g0158a0001c0001t0002g0001others(30): Show | 33 | 198 | 0.1667 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143097360 | GAAAAAA | G | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(7): Show | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0003g0165others(9): Show | 12 | 198 | 0.0606 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143098854 | GGTTAGT | G | intron_variant | MODIFIER | HG01243.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0025a0001c0001t0054a0001c0002t0002others(1): Show | a0001c0001t0025g0103a0001c0001t0054g0072a0001c0002t0002g0044others(1): Show | 4 | 198 | 0.0202 | -6 | c.153 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATA | G | intron_variant | MODIFIER | HG01256.hp2 HG01358.hp2 HG01891.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0009a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0009t0012others(6): Show | a0001c0001t0001g0174a0001c0001t0001g0293a0001c0001t0006g0021others(12): Show | 16 | 347 | 0.0461 | -6 | c.657 others(25): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729481 | CACAGGT | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0016a0001c0003t0001others(13): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | 248 | 0.2581 | -6 | c.-34 others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 234 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841202 | TCCTCTC | T | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0002others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0179others(13): Show | 16 | 248 | 0.0645 | -6 | c.543 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6909295 | CTTTTCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(68): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0005others(3): Show | a0001c0001t0001a0001c0001t0009a0001c0003t0003others(5): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(68): Show | 71 | 248 | 0.2863 | -6 | c.209 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94209812 | TATATAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0002a0001c0005others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | 356 | 0.9298 | -6 | c.341 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94210606 | CAAAAAG | C | intron_variant | MODIFIER | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
a0001a0009 | a0001c0002a0009c0016 | a0001c0002t0016a0009c0016t0016 | a0001c0002t0016g0066a0001c0002t0016g0083a0001c0002t0016g0084others(1): Show | 4 | 356 | 0.0112 | -6 | c.341 others(23): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTC | T | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0007t0001a0002c0002t0001others(2): Show | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(26): Show | 29 | 390 | 0.0744 | -6 | c.537 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055890 | TAAAATA | T | intron_variant | MODIFIER | NA18960.hp1 NA18979.hp2 NA18982.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0234 | 3 | 390 | 0.0077 | -6 | c.345 others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055915 | TAAAATA | T | intron_variant | MODIFIER | HG01175.hp2 HG01433.hp2 HG01515.hp1 others(10): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0003a0001c0001t0001g0151a0001c0001t0001g0196others(9): Show | 13 | 390 | 0.0333 | -6 | c.345 others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064773 | GAAAGAA | G | intron_variant | MODIFIER | HG01099.hp2 HG01358.hp1 HG02717.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0106others(2): Show | 5 | 390 | 0.0128 | -6 | c.97+ others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064825 | AAGAAAG | A | intron_variant | MODIFIER | HG02559.hp2 HG02897.hp2 HG03471.hp1 others(4): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0003c0004t0001 | a0001c0001t0001g0163a0001c0001t0001g0190a0001c0001t0001g0228others(4): Show | 7 | 390 | 0.0180 | -6 | c.97+ others(21): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119321557 | TTATATA | T | intron_variant | MODIFIER | NA18960.hp2 NA18969.hp1 NA19003.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0006a0001c0002t0001a0001c0004t0003 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0002t0001g0105others(1): Show | 4 | 310 | 0.0129 | -6 | c.100 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332631 | TCTCTCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(7): Show | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | 310 | 0.0516 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119336632 | GTTTTAT | G | intron_variant | MODIFIER | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040 | 3 | 310 | 0.0097 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119354846 | CTATATT | C | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp1 HG02818.hp2 others(4): Show |
a0001a0003 | a0001c0004a0001c0005a0003c0006 | a0001c0004t0003a0001c0005t0001a0001c0005t0014others(2): Show | a0001c0004t0003g0007a0001c0004t0003g0147a0001c0005t0001g0012others(4): Show | 7 | 310 | 0.0226 | -6 | c.101 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | TTTTATA | T | intron_variant | MODIFIER | HG01099.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
a0001a0008 | a0001c0004a0001c0005a0008c0021 | a0001c0004t0059a0001c0005t0001a0008c0021t0001 | a0001c0004t0059g0015a0001c0005t0001g0067a0001c0005t0001g0069others(1): Show | 4 | 310 | 0.0129 | -6 | c.683 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | TTTATTA | T | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(119): Show | 123 | 398 | 0.3091 | -6 | c.212 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985831 | CGTGTGT | C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0200a0001c0003t0006g0201a0001c0003t0006g0202others(1): Show | 4 | 398 | 0.0101 | -6 | c.152 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129058188 | TACACAC | T | intron_variant | MODIFIER | HG02602.hp1 HG02735.hp2 HG03704.hp2 |
a0001a0002 | a0001c0003a0002c0004 | a0001c0003t0003a0002c0004t0001 | a0001c0003t0003g0319a0001c0003t0003g0320a0002c0004t0001g0204 | 3 | 398 | 0.0075 | -6 | c.963 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129058217 | ACACACT | A | intron_variant | MODIFIER | HG02280.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
a0001a0005 | a0001c0001a0001c0010a0005c0011 | a0001c0001t0016a0001c0001t0033a0001c0010t0014others(1): Show | a0001c0001t0016g0196a0001c0001t0033g0299a0001c0010t0014g0198others(1): Show | 4 | 398 | 0.0101 | -6 | c.963 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129082882 | AAACAAC | A | intron_variant | MODIFIER | HG01123.hp1 HG02602.hp2 HG02683.hp2 others(1): Show |
a0001 | a0001c0003a0001c0010 | a0001c0003t0005a0001c0010t0008 | a0001c0003t0005g0384a0001c0003t0005g0385a0001c0010t0008g0191others(1): Show | 4 | 398 | 0.0101 | -6 | c.531 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129183766 | ACCCACC | A | intron_variant | MODIFIER | HG00642.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
a0001a0002a0011 | a0001c0001a0001c0002a0002c0008others(1): Show | a0001c0001t0002a0001c0002t0001a0002c0008t0001others(1): Show | a0001c0001t0002g0188a0001c0002t0001g0224a0001c0002t0001g0225others(3): Show | 6 | 398 | 0.0151 | -6 | c.116 others(23): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTT | C | upstream_gene_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(21): Show |
a0001a0002a0008 | a0001c0002a0001c0031a0002c0013others(1): Show | a0001c0002t0001a0001c0031t0001a0002c0013t0001others(1): Show | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 24 | 420 | 0.0571 | -6 | c.-16 others(17): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46877569 | AAATAAC | A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0019a0001c0001t0029a0001c0001t0042 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | 298 | 0.0134 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATAT | A | intron_variant | MODIFIER | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(30): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0171others(30): Show | 33 | 298 | 0.1107 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46898775 | AGCTGCT | A | intron_variant | MODIFIER | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0289 | 3 | 298 | 0.0101 | -6 | c.-18 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131065041 | TTGTGTG | T | intron_variant | MODIFIER | HG02109.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(1): Show | 4 | 302 | 0.0133 | -6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATAT | C | intron_variant | MODIFIER | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0003g0219others(1): Show | 4 | 302 | 0.0133 | -6 | c.-14 others(25): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144603896 | ACAGGAT | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(5): Show | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | 246 | 0.0529 | -6 | c.80+ others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144619394 | CCATGTG | C | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0001t0002a0001c0018t0001 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | 246 | 0.0488 | -6 | c.-81 others(25): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38617577 | CCACCTA | C | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
a0001a0007a0019 | a0001c0008a0001c0021a0001c0038others(2): Show | a0001c0008t0004a0001c0008t0006a0001c0021t0002others(3): Show | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(5): Show | 9 | 350 | 0.0257 | -6 | c.138 others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100691921 | AATATAT | A | intron_variant | MODIFIER | HG02280.hp2 HG02723.hp2 HG02809.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0008t0001a0002c0002t0002others(4): Show | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0008t0001g0004others(9): Show | 12 | 286 | 0.0420 | -6 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100704644 | GATGTCA | G | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002others(1): Show | a0001c0001t0001a0001c0010t0001a0002c0002t0028others(3): Show | a0001c0001t0001g0002a0001c0010t0001g0238a0002c0002t0028g0001others(6): Show | 9 | 286 | 0.0315 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(93): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(22): Show | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0184others(93): Show | 96 | 286 | 0.3357 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATAT | C | intron_variant | MODIFIER | HG00639.hp1 HG00673.hp2 HG01257.hp2 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(10): Show | a0001c0001t0001g0076a0001c0001t0001g0086a0001c0001t0001g0179others(27): Show | 30 | 286 | 0.1049 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATA | G | intron_variant | MODIFIER | HG00642.hp1 HG01109.hp1 HG01192.hp2 others(20): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0032others(6): Show | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0100others(20): Show | 23 | 286 | 0.0804 | -6 | c.154 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100739148 | TTTTTTG | T | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(3): Show | a0001c0001t0001g0011a0001c0003t0014g0234a0001c0003t0014g0235others(5): Show | 8 | 286 | 0.0280 | -6 | c.155 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0015others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(68): Show | 71 | 286 | 0.2483 | -6 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAA | C | intron_variant | MODIFIER | HG01358.hp1 HG02080.hp2 HG02809.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0002c0002t0002others(2): Show | a0001c0001t0001g0087a0001c0001t0001g0276a0001c0003t0003g0258others(7): Show | 10 | 286 | 0.0350 | -6 | c.251 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100830736 | TATAATA | T | intron_variant | MODIFIER | HG00735.hp2 HG01975.hp1 HG02145.hp2 others(4): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0004others(1): Show | a0001c0003t0014a0002c0002t0012a0002c0002t0021others(2): Show | a0001c0003t0014g0234a0001c0003t0014g0235a0002c0002t0012g0024others(4): Show | 7 | 286 | 0.0245 | -6 | c.313 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100863050 | AAAACAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(6): Show | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0266others(34): Show | 37 | 286 | 0.1294 | -6 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100863059 | AACACAC | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(32): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(162): Show | 165 | 286 | 0.5769 | -6 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |