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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP12_chr10_31800398_31933831 | 31862701 | CACAG | C | intron_variant | MODIFIER | HG02135.hp1 NA18955.hp2 NA18974.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0041 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(4): Show | 7 | 322 | 0.0217 | -4 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | GACAC | G | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp2 HG01257.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0003g0169a0001c0001t0004g0021a0001c0001t0005g0046others(17): Show | 20 | 322 | 0.0621 | -4 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31869538 | AAAAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(105): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(11): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(105): Show | 108 | 322 | 0.3354 | -4 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31891614 | TTGAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0007others(4): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(19): Show | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(130): Show | 133 | 322 | 0.4130 | -4 | c.684 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | TCACA | T | intron_variant | MODIFIER | HG01071.hp1 HG01099.hp1 HG01167.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0013a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0019others(8): Show | a0001c0001t0003g0186a0001c0001t0006g0165a0001c0001t0019g0162others(15): Show | 18 | 322 | 0.0559 | -4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | CAAAA | C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(3): Show | 6 | 322 | 0.0186 | -4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31921763 | CAAAA | C | intron_variant | MODIFIER | HG02257.hp2 HG02451.hp1 HG02615.hp1 others(11): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(11): Show | 14 | 322 | 0.0435 | -4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31926023 | TTATA | T | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | 322 | 0.0497 | -4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31926752 | ATTCT | A | intron_variant | MODIFIER | HG02074.hp2 HG03834.hp1 NA18747.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0007a0002c0002t0020 | a0002c0002t0007g0313a0002c0002t0007g0314a0002c0002t0007g0316others(1): Show | 4 | 322 | 0.0124 | -4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31928174 | GCACA | G | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0001c0010others(2): Show | a0001c0001t0001a0001c0007t0028a0001c0010t0053others(10): Show | a0001c0001t0001g0083a0001c0007t0028g0239a0001c0007t0028g0240others(82): Show | 85 | 322 | 0.2640 | -4 | c.-11 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31931872 | CAAAT | C | upstream_gene_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | 322 | 0.0497 | -4 | c.-33 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3042 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | CATAT | C | upstream_gene_variant | MODIFIER | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0050others(5): Show | a0001c0001t0001g0164a0001c0001t0003g0201a0001c0001t0050g0028others(23): Show | 26 | 322 | 0.0808 | -4 | c.-46 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143129053 | GAGGA | G | upstream_gene_variant | MODIFIER | HG02258.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | 162 | 0.0124 | -4 | c.-42 others(13): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 365 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143134104 | AATCT | A | intron_variant | MODIFIER | HG02109.hp2 HG02148.hp1 HG02148.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0062others(14): Show | 17 | 162 | 0.1049 | -4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143134167 | CATCT | C | intron_variant | MODIFIER | HG02109.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | 162 | 0.0370 | -4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143134182 | CATCT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(55): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(55): Show | 58 | 162 | 0.3580 | -4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143134196 | CCTAT | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0103a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | 162 | 0.0370 | -4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143134632 | CTTTT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(100): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(100): Show | 103 | 162 | 0.6358 | -4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143145839 | GGTGT | G | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(73): Show | 76 | 162 | 0.4691 | -4 | c.-14 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143145880 | ATAAT | A | intron_variant | MODIFIER | HG00733.hp2 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | 162 | 0.0124 | -4 | c.-14 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165960 | GAGAA | G | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(21): Show | 24 | 162 | 0.1482 | -4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143166041 | AAAAG | A | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 29 | 162 | 0.1790 | -4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143207495 | AACAC | A | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(52): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(52): Show | 55 | 162 | 0.3395 | -4 | c.234 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143227879 | GATAT | G | intron_variant | MODIFIER | HG01361.hp1 HG01515.hp2 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029a0001c0001t0001g0126a0001c0001t0001g0143 | 3 | 162 | 0.0185 | -4 | c.297 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143261325 | CTTTT | C | intron_variant | MODIFIER | HG01081.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0092others(3): Show | 6 | 162 | 0.0370 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTTT | C | intron_variant | MODIFIER | HG02148.hp1 HG02602.hp2 HG03704.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 10 | 162 | 0.0617 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143302905 | GTAAA | G | intron_variant | MODIFIER | HG02523.hp1 HG02602.hp1 HG03490.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | 162 | 0.0617 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143308241 | TTCTG | T | intron_variant | MODIFIER | HG02809.hp2 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063a0001c0001t0001g0127 | 2 | 162 | 0.0124 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143308477 | AACAC | A | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(41): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 44 | 162 | 0.2716 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143308935 | CAAAA | C | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0100others(2): Show | 5 | 162 | 0.0309 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143309866 | TTGTG | T | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp1 HG01261.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0069others(8): Show | 11 | 162 | 0.0679 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143322079 | TTCTC | T | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0026others(29): Show | 32 | 162 | 0.1975 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143327917 | AAAAT | A | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(20): Show | 23 | 162 | 0.1420 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143341011 | GTATT | G | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp1 HG01261.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0080others(6): Show | 9 | 162 | 0.0556 | -4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143346172 | ACTCT | A | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(71): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | 162 | 0.4568 | -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 | 143346212 | ACTCT | A | intron_variant | MODIFIER | HG02280.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058a0001c0001t0001g0123 | 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 | 143346228 | ACTCT | A | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01255.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0021others(11): Show | 14 | 162 | 0.0864 | -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 | 143346250 | TCACA | T | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01256.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021a0001c0001t0001g0136a0001c0001t0001g0156 | 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 | 143372011 | GAAAT | G | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01243.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | 162 | 0.0617 | -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 | 143379485 | ATATG | A | intron_variant | MODIFIER | HG02523.hp1 HG02602.hp1 HG03490.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0068others(6): Show | 9 | 162 | 0.0556 | -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 | 143379487 | ATGTG | A | intron_variant | MODIFIER | HG00733.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0002t0001g0043others(2): Show | 5 | 162 | 0.0309 | -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 | 143387942 | TACAC | T | intron_variant | MODIFIER | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0099others(3): Show | 6 | 162 | 0.0370 | -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 | 143390731 | GCACA | G | intron_variant | MODIFIER | HG00733.hp2 HG01081.hp1 HG01256.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0040others(14): Show | 17 | 162 | 0.1049 | -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 | 143397316 | ATGTG | A | intron_variant | MODIFIER | HG02145.hp2 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0128a0001c0001t0001g0135 | 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 | 143397344 | GTGTA | G | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(21): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0031others(21): Show | 24 | 162 | 0.1482 | -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 | 143397903 | CAAAG | C | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | 162 | 0.0247 | -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 | 143405242 | CAAAT | C | intron_variant | MODIFIER | HG02559.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061a0001c0001t0001g0091 | 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 | 143407987 | GTATA | G | intron_variant | MODIFIER | HG01255.hp1 HG02071.hp1 HG02280.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0030others(5): Show | 8 | 162 | 0.0494 | -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 | 143411427 | AAAAC | A | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02602.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0012a0001c0002t0001g0036a0001c0002t0001g0065others(4): Show | 7 | 162 | 0.0432 | -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 | 143416263 | AAAAC | A | intron_variant | MODIFIER | HG00609.hp1 HG01358.hp2 HG02071.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0032others(19): Show | 22 | 162 | 0.1358 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |