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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 147872099 | C | CAAA | intron_variant | MODIFIER | HG02572.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0001a0001c0004t0001a0001c0005t0001 | a0001c0001t0001g0081a0001c0004t0001g0045a0001c0004t0001g0105others(1): Show | 4 | 106 | 0.0377 | 3 | c.703 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147877819 | C | CTTT | intron_variant | MODIFIER | HG01261.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006a0001c0011 | a0001c0001t0001a0001c0006t0001a0001c0011t0001 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(2): Show | 5 | 106 | 0.0472 | 3 | c.833 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147882462 | C | CAAA | intron_variant | MODIFIER | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0034others(9): Show | 12 | 106 | 0.1132 | 3 | c.103 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147898187 | T | TTGA | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | 106 | 0.4528 | 3 | c.103 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147900819 | T | TCAA | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | 106 | 0.2547 | 3 | c.103 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147922687 | C | CAAA | intron_variant | MODIFIER | HG00558.hp1 HG02165.hp2 HG02258.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0002t0001a0001c0006t0001 | a0001c0001t0001g0025a0001c0002t0001g0021a0001c0006t0001g0040others(1): Show | 4 | 106 | 0.0377 | 3 | c.122 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148012924 | G | GTTT | intron_variant | MODIFIER | HG00558.hp2 HG01169.hp1 HG01261.hp1 others(13): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0003others(1): Show | a0001c0001t0001a0001c0011t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0052others(13): Show | 16 | 106 | 0.1509 | 3 | c.171 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148052392 | C | CTTT | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0010 | a0001c0001t0001a0001c0001t0003a0002c0003t0001others(1): Show | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(3): Show | 6 | 106 | 0.0566 | 3 | c.202 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAA | intron_variant | MODIFIER | HG02738.hp2 HG03239.hp1 HG03471.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0070a0001c0001t0002g0031a0001c0002t0001g0072others(2): Show | 5 | 106 | 0.0472 | 3 | c.227 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32613813 | C | CAAA | upstream_gene_variant | MODIFIER | HG00642.hp1 HG01169.hp2 HG01975.hp2 others(8): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0098others(6): Show | 11 | 335 | 0.0328 | 3 | c.-23 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1690 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32617471 | C | CTTT | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(7): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0004a0001c0002t0005a0007c0009t0005 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0002t0005g0020others(6): Show | 10 | 335 | 0.0299 | 3 | c.129 others(20): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32640121 | C | CTTT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00558.hp1 HG02451.hp2 others(14): Show |
a0001a0004a0008 | a0001c0001a0001c0006a0004c0007others(1): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0014others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0160others(9): Show | 17 | 335 | 0.0508 | 3 | c.*22 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 181 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32640123 | T | TTTC | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0001a0001c0002t0005a0007c0009t0005 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0044others(6): Show | 13 | 335 | 0.0388 | 3 | c.*22 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 183 | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30624418 | C | CAAA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(11): Show | 19 | 247 | 0.0769 | 3 | c.-24 others(14): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1709 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31804673 | C | CTTT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
a0001a0002 | a0001c0001a0001c0007a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(20): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(108): Show | 111 | 322 | 0.3447 | 3 | c.*29 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 724 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31823476 | C | CAAA | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
a0001 | a0001c0003a0001c0005 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | a0001c0003t0010g0005a0001c0003t0010g0009a0001c0003t0010g0010others(11): Show | 14 | 322 | 0.0435 | 3 | c.153 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31829154 | A | AAAC | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(101): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0003a0001c0001t0009a0001c0001t0017others(18): Show | a0001c0001t0003g0120a0001c0001t0003g0182a0001c0001t0009g0032others(101): Show | 104 | 322 | 0.3230 | 3 | c.144 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(36): Show |
a0002a0003 | a0002c0002a0003c0004 | a0002c0002t0002a0002c0002t0007a0002c0002t0014others(6): Show | a0002c0002t0002g0243a0002c0002t0002g0250a0002c0002t0002g0251others(36): Show | 39 | 322 | 0.1211 | 3 | c.685 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAA | intron_variant | MODIFIER | HG00639.hp2 HG00673.hp1 HG00738.hp2 others(70): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0008t0005others(10): Show | a0001c0001t0004g0068a0001c0001t0005g0043a0001c0008t0005g0074others(70): Show | 73 | 322 | 0.2267 | 3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAA | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
a0001a0002 | a0001c0001a0001c0008a0001c0010others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(8): Show | a0001c0001t0004g0034a0001c0001t0004g0037a0001c0001t0004g0038others(31): Show | 34 | 322 | 0.1056 | 3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31928535 | G | GCGC | intron_variant | MODIFIER | HG00673.hp2 HG01934.hp2 NA21309.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0007 | a0001c0001t0001g0236a0001c0001t0005g0235a0002c0002t0007g0320 | 3 | 322 | 0.0093 | 3 | c.-11 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31931501 | T | TTTG | upstream_gene_variant | MODIFIER | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | 322 | 0.0311 | 3 | c.-29 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2671 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153828 | T | TTCC | intron_variant | MODIFIER | HG00621.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | 162 | 0.0309 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153831 | T | TTCC | intron_variant | MODIFIER | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0061others(7): Show | 10 | 162 | 0.0617 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153834 | T | TTCC | intron_variant | MODIFIER | HG02074.hp1 HG02074.hp2 HG02129.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(6): Show | 9 | 162 | 0.0556 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153840 | T | TTCC | intron_variant | MODIFIER | HG02280.hp1 HG02602.hp1 HG02886.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0067a0001c0001t0001g0106a0001c0001t0001g0123others(3): Show | 6 | 162 | 0.0370 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153873 | T | TTCC | intron_variant | MODIFIER | NA18962.hp2 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0153 | 2 | 162 | 0.0124 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153876 | C | CTCT | intron_variant | MODIFIER | HG00738.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057a0001c0001t0001g0119a0001c0001t0001g0127others(1): Show | 4 | 162 | 0.0247 | 3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | C | CATT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0021others(23): Show | 26 | 162 | 0.1605 | 3 | c.166 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143218277 | C | CTTT | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0096a0001c0001t0001g0100others(3): Show | 6 | 162 | 0.0370 | 3 | c.296 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143235242 | G | GTTT | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0034others(20): Show | 23 | 162 | 0.1420 | 3 | c.384 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAA | intron_variant | MODIFIER | HG02698.hp1 HG02698.hp2 NA18970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0066a0001c0001t0001g0071others(2): Show | 5 | 162 | 0.0309 | 3 | c.385 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143270963 | C | CTGA | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(53): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(53): Show | 56 | 162 | 0.3457 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143291452 | G | GTTC | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(105): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | 162 | 0.6667 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143296776 | G | GTAT | intron_variant | MODIFIER | HG02109.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0055others(5): Show | 8 | 162 | 0.0494 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | C | CTTT | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | 162 | 0.0370 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143323894 | C | CAAA | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01261.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0106others(3): Show | 6 | 162 | 0.0370 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143330094 | C | CAAA | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG01358.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0112others(4): Show | 7 | 162 | 0.0432 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143330132 | C | CAAA | intron_variant | MODIFIER | HG02886.hp2 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003a0001c0002t0001g0105 | 2 | 162 | 0.0124 | 3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143345252 | A | AGAG | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(143): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 146 | 162 | 0.9012 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143389106 | C | CATT | intron_variant | MODIFIER | HG03139.hp1 HG06807.hp2 NA18947.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0048others(7): Show | 10 | 162 | 0.0617 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143390008 | T | TAAA | intron_variant | MODIFIER | HG02976.hp1 HG03491.hp2 NA18991.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0083others(2): Show | 5 | 162 | 0.0309 | 3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143428780 | G | GTAA | intron_variant | MODIFIER | HG00621.hp2 HG01496.hp1 HG02148.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0073others(4): Show | 7 | 162 | 0.0432 | 3 | c.475 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143433739 | A | ATGT | intron_variant | MODIFIER | HG01261.hp1 HG02071.hp1 HG02109.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0024others(13): Show | 16 | 162 | 0.0988 | 3 | c.475 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143445153 | A | ATTT | intron_variant | MODIFIER | HG00621.hp1 HG01243.hp1 HG02074.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0026a0001c0001t0001g0066a0001c0001t0001g0083others(7): Show | 10 | 162 | 0.0617 | 3 | c.703 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143461281 | C | CAAA | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0033others(14): Show | 17 | 162 | 0.1049 | 3 | c.703 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143465706 | A | AAAT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(142): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | 162 | 0.8951 | 3 | c.704 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143484365 | C | CAAA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(29): Show | 32 | 162 | 0.1975 | 3 | c.704 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143506460 | A | AATT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(59): Show | 62 | 162 | 0.3827 | 3 | c.827 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAA | intron_variant | MODIFIER | HG01261.hp1 HG02129.hp2 HG02258.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | 162 | 0.0741 | 3 | c.100 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |