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 | 142949214 | A | AGAG | intron_variant | MODIFIER | HG00609.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0020a0001c0001t0002g0008a0001c0001t0004g0099others(2): Show | 5 | 198 | 0.0253 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142958922 | A | AAAG | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(157): Show | 160 | 198 | 0.8081 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143004017 | C | CAAA | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG02622.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0012a0001c0001t0033 | a0001c0001t0005g0101a0001c0001t0005g0108a0001c0001t0005g0109others(2): Show | 5 | 198 | 0.0253 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143006316 | C | CTGT | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG02698.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0005a0001c0001t0021others(4): Show | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0118others(9): Show | 12 | 198 | 0.0606 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143011303 | C | CTTT | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(46): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0141a0001c0001t0001g0196a0001c0001t0002g0005others(46): Show | 49 | 198 | 0.2475 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012578 | A | ATGG | intron_variant | MODIFIER | NA18612.hp1 NA18972.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0158a0001c0001t0002g0184 | 2 | 198 | 0.0101 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143028165 | G | GGAT | intron_variant | MODIFIER | HG00544.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0005a0001c0003t0038a0001c0003t0046 | a0001c0001t0005g0108a0001c0001t0005g0109a0001c0003t0038g0155others(1): Show | 4 | 198 | 0.0202 | 3 | c.114 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTT | intron_variant | MODIFIER | HG02155.hp2 HG03579.hp1 NA18944.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0153a0001c0001t0003g0019a0001c0001t0004g0056others(7): Show | 10 | 198 | 0.0505 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143097821 | C | CAAA | intron_variant | MODIFIER | HG01069.hp1 HG02074.hp2 HG02897.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0034a0001c0001t0001g0131a0001c0001t0002g0036others(7): Show | 10 | 198 | 0.0505 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143106466 | C | CTTT | intron_variant | MODIFIER | HG01071.hp1 HG01175.hp1 HG03017.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0007a0001c0001t0039a0001c0002t0001others(2): Show | a0001c0001t0007g0107a0001c0001t0039g0171a0001c0002t0001g0181others(3): Show | 6 | 198 | 0.0303 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143144398 | T | TTTA | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0116a0001c0001t0002g0007a0001c0001t0002g0016others(26): Show | 29 | 198 | 0.1465 | 3 | c.183 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143160474 | G | GTTT | intron_variant | MODIFIER | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022a0001c0001t0002g0043a0001c0001t0002g0046 | 3 | 198 | 0.0152 | 3 | c.198 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | C | CTTT | intron_variant | MODIFIER | HG00673.hp2 HG01361.hp2 HG02273.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(3): Show | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0002g0256others(11): Show | 14 | 347 | 0.0404 | 3 | c.658 others(20): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | A | ATTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0001a0001c0003t0003a0001c0012t0001others(4): Show | a0001c0001t0001g0042a0001c0001t0001g0129a0001c0001t0001g0189others(14): Show | 17 | 248 | 0.0686 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6802335 | C | CTTT | intron_variant | MODIFIER | HG01175.hp2 HG02109.hp2 HG02135.hp2 others(6): Show |
a0001a0007a0008 | a0001c0001a0001c0003a0007c0008others(1): Show | a0001c0001t0001a0001c0003t0003a0007c0008t0002others(1): Show | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0184others(6): Show | 9 | 248 | 0.0363 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6805479 | C | CTTT | intron_variant | MODIFIER | HG01891.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(2): Show | a0001c0001t0001g0209a0001c0001t0008g0074a0001c0001t0018g0111others(2): Show | 5 | 248 | 0.0202 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6811116 | T | TTAC | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(7): Show | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(20): Show | 23 | 248 | 0.0927 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841180 | C | CTCT | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp2 HG01106.hp1 others(4): Show |
a0001a0010 | a0001c0001a0001c0019a0010c0014 | a0001c0001t0001a0001c0019t0021a0010c0014t0001 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | 248 | 0.0282 | 3 | c.543 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841190 | T | TCTC | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp1 HG02818.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0018a0002c0002t0004 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0147 | 3 | 248 | 0.0121 | 3 | c.543 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841203 | C | CTCT | intron_variant | MODIFIER | HG01515.hp1 HG02523.hp2 HG03492.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0002c0002t0002 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0040others(4): Show | 7 | 248 | 0.0282 | 3 | c.543 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6871549 | C | CATT | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0012a0002c0005t0002 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0161others(8): Show | 11 | 248 | 0.0444 | 3 | c.954 others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6887430 | G | GTTT | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(3): Show |
a0001a0003 | a0001c0001a0001c0019a0003c0004 | a0001c0001t0001a0001c0001t0009a0001c0019t0021others(1): Show | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0009g0005others(3): Show | 6 | 248 | 0.0242 | 3 | c.153 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6900294 | C | CACA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0010a0001c0012others(12): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(22): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | 248 | 0.6169 | 3 | c.203 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94179592 | C | CAAA | intron_variant | MODIFIER | HG01928.hp1 HG02523.hp2 HG02559.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0004a0002c0003t0024 | a0001c0001t0004g0017a0001c0001t0004g0033a0001c0001t0004g0041others(5): Show | 9 | 356 | 0.0253 | 3 | c.248 others(20): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94211287 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(32): Show |
a0001a0008a0009 | a0001c0001a0001c0002a0008c0010others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(6): Show | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0040others(30): Show | 35 | 356 | 0.0983 | 3 | c.341 others(20): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94232263 | G | GATT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0007others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | 356 | 0.8315 | 3 | c.-32 others(18): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161066644 | C | CAAA | intron_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG01109.hp2 others(54): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(53): Show | 57 | 390 | 0.1462 | 3 | c.97+ others(18): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119392446 | T | TCAA | intron_variant | MODIFIER | HG01106.hp1 HG03491.hp2 HG03492.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0006a0002c0003t0002 | a0001c0001t0006g0065a0001c0001t0006g0066a0002c0003t0002g0145 | 3 | 310 | 0.0097 | 3 | c.882 others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | T | TTTA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(43): Show |
a0001a0006a0007others(1): Show | a0001c0001a0001c0003a0001c0010others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0002g0121others(43): Show | 46 | 398 | 0.1156 | 3 | c.212 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128992426 | T | TCAC | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
a0001 | a0001c0001a0001c0002a0001c0034 | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(3): Show | a0001c0001t0002g0002a0001c0001t0002g0041a0001c0001t0002g0094others(59): Show | 63 | 398 | 0.1583 | 3 | c.119 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129002805 | A | ATTT | intron_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG00735.hp1 others(83): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 86 | 398 | 0.2161 | 3 | c.104 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129029801 | C | CAAA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(30): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 165 | 398 | 0.4146 | 3 | c.104 others(24): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129036380 | C | CAAA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG02615.hp1 others(15): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103others(15): Show | 18 | 398 | 0.0452 | 3 | c.104 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129064138 | T | TAAA | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(91): Show |
a0001a0004 | a0001c0001a0001c0005a0001c0032others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 94 | 398 | 0.2362 | 3 | c.763 others(18): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 8/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129082882 | A | AAAC | intron_variant | MODIFIER | HG02572.hp1 HG03486.hp2 HG04199.hp1 others(2): Show |
a0001a0002 | a0001c0002a0002c0007 | a0001c0002t0001a0002c0007t0009 | a0001c0002t0001g0230a0001c0002t0001g0252a0001c0002t0001g0255others(2): Show | 5 | 398 | 0.0126 | 3 | c.531 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTT | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0005others(16): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(16): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 184 | 420 | 0.4381 | 3 | c.-36 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35773667 | T | TATA | upstream_gene_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(26): Show |
a0001a0002a0008 | a0001c0002a0001c0031a0002c0013others(1): Show | a0001c0002t0001a0001c0031t0001a0002c0013t0001others(1): Show | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 29 | 420 | 0.0691 | 3 | c.-19 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1896 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46857107 | A | ATTT | upstream_gene_variant | MODIFIER | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0004 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(14): Show | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0051others(23): Show | 26 | 298 | 0.0873 | 3 | c.-42 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3889 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46868893 | A | ATTT | intron_variant | MODIFIER | HG00438.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(3): Show | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(9): Show | 12 | 298 | 0.0403 | 3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46898775 | A | AGCT | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0192a0001c0001t0003g0001a0001c0001t0003g0002others(49): Show | 52 | 298 | 0.1745 | 3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46900222 | G | GTTT | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp2 HG02071.hp2 others(3): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0003a0001c0001t0013a0001c0001t0018others(2): Show | a0001c0001t0003g0065a0001c0001t0013g0049a0001c0001t0013g0226others(3): Show | 6 | 298 | 0.0201 | 3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46914446 | A | AAAT | intron_variant | MODIFIER | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0014a0001c0001t0017others(3): Show | a0001c0001t0005g0118a0001c0001t0014g0069a0001c0001t0014g0087others(9): Show | 12 | 298 | 0.0403 | 3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46929007 | T | TAAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(67): Show | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | 298 | 0.9966 | 3 | c.368 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46933137 | C | CTTT | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02155.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0004a0001c0001t0030a0001c0001t0040others(3): Show | a0001c0001t0004g0233a0001c0001t0030g0277a0001c0001t0040g0029others(4): Show | 7 | 298 | 0.0235 | 3 | c.368 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46941876 | T | TAAA | intron_variant | MODIFIER | HG00738.hp1 HG01071.hp1 HG01192.hp2 others(26): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | a0001c0001t0001g0189a0001c0001t0003g0021a0001c0001t0003g0044others(26): Show | 29 | 298 | 0.0973 | 3 | c.382 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46956956 | C | CCTT | intron_variant | MODIFIER | HG00597.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0017a0001c0001t0028 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(6): Show | 9 | 298 | 0.0302 | 3 | c.382 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46975631 | C | CAGA | intron_variant | MODIFIER | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(20): Show | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(63): Show | 66 | 298 | 0.2215 | 3 | c.382 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | C | CAAA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0172a0001c0001t0001g0185a0001c0001t0001g0186others(22): Show | 25 | 298 | 0.0839 | 3 | c.382 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46999228 | C | CCAT | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0007a0004c0008 | a0001c0001t0015a0001c0001t0023a0001c0001t0040others(3): Show | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | 298 | 0.0235 | 3 | c.403 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | C | CTTT | downstream_gene_variant | MODIFIER | HG00738.hp1 HG01069.hp2 HG01346.hp2 others(22): Show |
a0001a0006 | a0001c0001a0006c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0165others(22): Show | 25 | 298 | 0.0839 | 3 | c.*55 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar |