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 | 147798781 | C | CTATATAT others(3): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 106 | 0.0094 | 10 | c.155 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147798781 | C | CTCTCTAT others(3): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0066 | 1 | 106 | 0.0094 | 10 | c.155 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147798781 | C | CTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | 106 | 0.0189 | 10 | c.155 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147832646 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01261.hp1 HG01261.hp2 HG02109.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0026others(10): Show | 13 | 106 | 0.1226 | 10 | c.312 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147837643 | G | GTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG01261.hp1 HG03492.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | 106 | 0.0189 | 10 | c.313 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | T | TTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG02109.hp2 HG03130.hp1 HG03130.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0104 | 3 | 106 | 0.0283 | 10 | c.702 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | A | AACACACA others(3): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0003others(1): Show | a0001c0001t0001a0001c0004t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0036others(7): Show | 10 | 106 | 0.0943 | 10 | c.703 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147877819 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG01261.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0046others(4): Show | 7 | 106 | 0.0660 | 10 | c.833 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147911993 | A | ATATATGT others(3): Show |
intron_variant | MODIFIER | HG02165.hp2 HG03492.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021a0001c0002t0001g0072 | 2 | 106 | 0.0189 | 10 | c.116 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATATAT others(3): Show |
intron_variant | MODIFIER | HG01261.hp2 HG02572.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0018a0001c0004t0001g0105 | 2 | 106 | 0.0189 | 10 | c.171 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATATAT others(3): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 106 | 0.0094 | 10 | c.171 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATATATA others(3): Show |
intron_variant | MODIFIER | HG02572.hp1 HG03209.hp2 HG03239.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0002g0031 | 3 | 106 | 0.0283 | 10 | c.186 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00597.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0003a0001c0001t0011a0001c0012t0003 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0057others(14): Show | 32 | 335 | 0.0955 | 10 | c.110 others(27): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | A | AGTGTGTG others(3): Show |
downstream_gene_variant | MODIFIER | HG01891.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 2 | 247 | 0.0081 | 10 | c.*12 others(21): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31803794 | G | GCCCCCCC others(3): Show |
downstream_gene_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0043 | a0001c0001t0043g0025 | 1 | 322 | 0.0031 | 10 | c.*38 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1603 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACACAC others(3): Show |
3_prime_UTR_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0050 | a0001c0001t0050g0028 | 1 | 322 | 0.0031 | 10 | c.*20 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | |||||
ARHGAP12_chr10_31800398_31933831 | 31811665 | T | TTTTTATT others(3): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(212): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(35): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(212): Show | 215 | 322 | 0.6677 | 10 | c.195 others(27): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(42): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(10): Show | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0101others(42): Show | 45 | 322 | 0.1398 | 10 | c.173 others(29): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02257.hp2 HG03516.hp2 |
a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0005a0001c0003t0010g0017 | 2 | 322 | 0.0062 | 10 | c.-11 others(29): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31926564 | C | CCCATTTG others(3): Show |
intron_variant | MODIFIER | NA19057.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 322 | 0.0031 | 10 | c.-11 others(29): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | C | CATATATA others(3): Show |
upstream_gene_variant | MODIFIER | HG01123.hp1 NA18946.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0117a0001c0001t0006g0214 | 2 | 322 | 0.0062 | 10 | c.-46 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATATAT others(3): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG02602.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0004a0001c0006t0026 | a0001c0001t0004g0030a0001c0001t0004g0068a0001c0006t0026g0067 | 3 | 322 | 0.0093 | 10 | c.-46 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143225607 | A | AAAAACAA others(3): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 162 | 0.0062 | 10 | c.297 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143262535 | A | ATTTTTTT others(3): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01517.hp1 HG02300.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(10): Show | 13 | 162 | 0.0803 | 10 | c.474 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143330094 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02129.hp2 HG02965.hp1 NA18747.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0084others(1): Show | 4 | 162 | 0.0247 | 10 | c.474 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | A | ATGTGTGT others(3): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01517.hp1 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | 162 | 0.0185 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | A | ATGTGTGT others(3): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0133 | 1 | 162 | 0.0062 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTGTATAT others(3): Show |
intron_variant | MODIFIER | HG03486.hp2 NA18948.hp1 |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0001a0003c0005t0001 | a0001c0001t0001g0106a0003c0005t0001g0085 | 2 | 162 | 0.0124 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413927 | T | TTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 | 1 | 162 | 0.0062 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGCGCGCG others(3): Show |
intron_variant | MODIFIER | HG01515.hp2 HG04199.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029a0001c0001t0001g0130 | 2 | 162 | 0.0124 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGCGCG others(3): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 162 | 0.0062 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0101a0001c0001t0001g0133 | 2 | 162 | 0.0124 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143416821 | A | ACCCCCCC others(3): Show |
intron_variant | MODIFIER | HG03927.hp2 NA19006.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038a0001c0001t0001g0155 | 2 | 162 | 0.0124 | 10 | c.475 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143439422 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG03491.hp1 NA18747.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140a0001c0001t0001g0151 | 2 | 162 | 0.0124 | 10 | c.703 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143445153 | A | ACTTTTTT others(3): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02723.hp1 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0001g0133 | 3 | 162 | 0.0185 | 10 | c.703 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143486408 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG00609.hp1 HG02148.hp1 HG03927.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0073others(5): Show | 8 | 162 | 0.0494 | 10 | c.704 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143510018 | T | TAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01081.hp2 HG02602.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0065a0001c0002t0001g0125 | 2 | 162 | 0.0124 | 10 | c.827 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143555860 | A | AAGAATAG others(3): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01515.hp2 HG02258.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0082others(5): Show | 8 | 162 | 0.0494 | 10 | c.926 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02129.hp1 HG02615.hp1 HG02698.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0047others(3): Show | 6 | 162 | 0.0370 | 10 | c.100 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606060 | A | AAAAAAAA others(3): Show |
intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 162 | 0.0062 | 10 | c.100 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG01361.hp2 HG03490.hp1 HG03704.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0048others(9): Show | 12 | 162 | 0.0741 | 10 | c.113 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673746 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 162 | 0.0062 | 10 | c.113 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673750 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 | 1 | 162 | 0.0062 | 10 | c.113 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTATAT others(3): Show |
intron_variant | MODIFIER | HG02615.hp2 HG02965.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0040 | 2 | 162 | 0.0124 | 10 | c.113 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(3): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02280.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0123 | 3 | 162 | 0.0185 | 10 | c.113 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143721061 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01255.hp2 HG01256.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0088others(10): Show | 13 | 162 | 0.0803 | 10 | c.124 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | A | ATGTGTGT others(3): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0118 | 2 | 162 | 0.0124 | 10 | c.124 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916422 | C | CTTTTTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG02970.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0002 | a0001c0001t0002g0031a0001c0004t0002g0111a0001c0004t0002g0112others(1): Show | 4 | 240 | 0.0167 | 10 | c.*37 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2966 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | C | CTTTTTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG02723.hp1 HG03130.hp1 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012 | 3 | 240 | 0.0125 | 10 | c.*37 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | T | TACACACA others(3): Show |
downstream_gene_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0001c0001t0004a0003c0007t0001 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 10 | 240 | 0.0417 | 10 | c.*35 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar |