view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 148039368 | ATTTT | A | intron_variant | MODIFIER | HG02922.hp1 HG03130.hp1 HG03239.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0104 others(1): Show |
4 | 106 | 0.0377 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | AATAT | A | intron_variant | MODIFIER | HG02109.hp1 HG02451.hp1 NA18995.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 a0001c0001t0001g0091 a0001c0001t0001g0103 |
3 | 106 | 0.0283 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148049800 | TTTTG | T | intron_variant | MODIFIER | HG02109.hp1 HG02886.hp2 HG04184.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0010 | a0001c0001t0001a0004c0010t0001 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0091 others(1): Show |
4 | 106 | 0.0377 | -4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148071638 | CAAAA | C | intron_variant | MODIFIER | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0007 | a0001c0001t0001a0001c0005t0001a0003c0007t0001 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0076 others(4): Show |
7 | 106 | 0.0660 | -4 | c.227 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32612829 | CAAAA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(47): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0104 a0001c0001t0002g0003 a0001c0001t0004g0006 others(23): Show |
50 | 335 | 0.1493 | -4 | c.-33 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2674 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32640099 | AGTTT | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
a0001a0005a0009 | a0001c0001a0005c0011a0009c0007 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(45): Show |
91 | 335 | 0.2716 | -4 | c.*22 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 159 | chr15 | TogoVar | |||||||
ARHGAP11B_chr15_30621128_30643810 | 30627147 | TGAGA | T | intron_variant | MODIFIER | HG01256.hp2 HG01258.hp2 HG01934.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0001a0005c0004t0001 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
6 | 247 | 0.0243 | -4 | c.129 others(19): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30630401 | TACTG | T | intron_variant | MODIFIER | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0065 |
15 | 247 | 0.0607 | -4 | c.130 others(19): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | AGTGT | A | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(8): Show |
27 | 247 | 0.1093 | -4 | c.*12 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | TCACA | T | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG01081.hp2 others(22): Show |
a0001a0002a0004 | a0001c0001a0001c0006a0001c0017others(2): Show | a0001c0001t0004a0001c0006t0026a0001c0017t0004others(2): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(22): Show |
25 | 322 | 0.0776 | -4 | c.*20 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2006 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | CGTGT | C | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(3): Show | a0001c0001t0003g0026 a0001c0001t0004g0044 a0001c0001t0005g0045 others(9): Show |
12 | 322 | 0.0373 | -4 | c.173 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31820712 | TTATA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0007others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(18): Show | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0088 others(108): Show |
111 | 322 | 0.3447 | -4 | c.153 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31840925 | TTAAG | T | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0025 | a0001c0001t0001g0226 a0001c0001t0008g0152 a0001c0001t0025g0202 |
3 | 322 | 0.0093 | -4 | c.129 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862701 | CACAG | C | intron_variant | MODIFIER | HG02135.hp1 NA18955.hp2 NA18974.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0041 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0111 others(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 | a0001c0001t0003g0169 a0001c0001t0004g0021 a0001c0001t0005g0046 others(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 |
a0001a0009 | a0001c0001a0001c0012a0009c0014 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(12): Show | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 |
a0001a0002a0003others(3): Show | a0001c0001a0001c0006a0001c0007others(7): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(21): Show | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(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 | a0001c0001a0001c0015a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0019others(8): Show | a0001c0001t0003g0186 a0001c0001t0006g0165 a0001c0001t0019g0162 others(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 | a0001c0001t0011g0055 a0001c0001t0011g0056 a0001c0001t0011g0057 others(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 | a0001c0003a0001c0005a0001c0017 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | a0001c0003t0010g0005 a0001c0003t0010g0006 a0001c0003t0010g0009 others(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 | a0001c0003a0001c0005a0001c0017 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005 a0001c0003t0010g0006 a0001c0003t0010g0009 others(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 | a0002c0002t0007g0313 a0002c0002t0007g0314 a0002c0002t0007g0316 others(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 |
a0001a0002a0003others(3): Show | a0001c0001a0001c0007a0001c0010others(5): Show | a0001c0001t0001a0001c0007t0028a0001c0010t0053others(12): Show | a0001c0001t0001g0083 a0001c0007t0028g0239 a0001c0007t0028g0240 others(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 | a0001c0003a0001c0005a0001c0017 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005 a0001c0003t0010g0006 a0001c0003t0010g0009 others(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 |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0050others(6): Show | a0001c0001t0001g0164 a0001c0001t0003g0201 a0001c0001t0050g0028 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0126 a0001c0001t0001g0143 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0127 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 |