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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFGEF2_chr20_48916711_49041693 | 48963175 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0005 | 1 | 207 | 0.0048 | 14 | c.839 others(29): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARFGEF2_chr20_48916711_49041693 | 48975800 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01243.hp1 HG04184.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001 | a0001c0001t0002g0259 a0001c0003t0001g0035 a0001c0003t0001g0053 others(6): Show |
9 | 146 | 0.0616 | 14 | c.177 others(31): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARFGEF3_chr6_138156939_138349663 | 138194989 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0002 | a0002c0007 | a0002c0007t0025 | a0002c0007t0025g0088 | 1 | 63 | 0.0159 | 14 | c.138 others(33): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARFGEF3_chr6_138156939_138349663 | 138266848 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0051 | 1 | 30 | 0.0333 | 14 | c.212 others(33): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARFGEF3_chr6_138156939_138349663 | 138270427 | G | GACACACA others(7): Show |
intron_variant | MODIFIER | HG00597.hp2 HG01433.hp2 HG02132.hp2 others(2): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0025 | a0001c0001t0001a0001c0001t0003a0001c0001t0018others(2): Show | a0001c0001t0001g0129 a0001c0001t0003g0156 a0001c0001t0018g0132 others(2): Show |
5 | 37 | 0.1351 | 14 | c.212 others(33): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152795820 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00609.hp2 HG02027.hp1 HG03239.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0137 others(2): Show |
5 | 19 | 0.2632 | 14 | c.-10 others(33): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152808283 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG01106.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0075 others(15): Show |
18 | 22 | 0.8182 | 14 | c.-9- others(31): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152847124 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01169.hp1 HG02135.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0002 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0098 others(5): Show |
8 | 94 | 0.0851 | 14 | c.94- others(31): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152905545 | G | GTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02056.hp1 HG02074.hp1 HG02132.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0069 a0001c0001t0001g0097 a0001c0001t0001g0116 others(8): Show |
11 | 110 | 0.1000 | 14 | c.967 others(31): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152908891 | A | AGTGTGTG others(7): Show |
intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0297 | 1 | 33 | 0.0303 | 14 | c.967 others(31): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFRP1_chr20_63693647_63712976 | 63694153 | T | TGGGGGGG others(7): Show |
downstream_gene_variant | MODIFIER | NA19001.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0001 | 1 | 294 | 0.0034 | 14 | c.*62 others(25): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4493 | chr20 | TogoVar | |||||||
ARG1_chr6_131568226_131589329 | 131584816 | T | TACACACA others(7): Show |
downstream_gene_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 184 | 0.0054 | 14 | c.*90 others(23): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 488 | chr6 | TogoVar | |||||||
ARG2_chr14_67614920_67656708 | 67627256 | G | GATATATA others(7): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0185 a0001c0001t0003g0057 a0001c0001t0003g0059 others(13): Show |
16 | 49 | 0.3265 | 14 | c.184 others(31): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67642793 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02622.hp2 HG02818.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0004g0181 others(1): Show |
4 | 35 | 0.1143 | 14 | c.362 others(29): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121576707 | T | TTCTTTCT others(7): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG03041.hp1 |
a0003 | a0003c0003 | a0003c0003t0008a0003c0003t0023a0003c0003t0040 | a0003c0003t0008g0329 a0003c0003t0023g0367 a0003c0003t0040g0327 |
3 | 131 | 0.0229 | 14 | c.104 others(27): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577259 | A | ATATATAT others(7): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0061 | 1 | 188 | 0.0053 | 14 | c.220 others(29): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106540314 | C | CGGGGGGG others(7): Show |
downstream_gene_variant | MODIFIER | HG02451.hp2 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0043 a0001c0001t0002g0016 |
2 | 166 | 0.0120 | 14 | c.*36 others(25): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1358 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147798722 | A | ACTCTCTC others(7): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0074 | 1 | 92 | 0.0109 | 14 | c.155 others(33): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147798765 | C | CTATATAT others(7): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 94 | 0.0106 | 14 | c.155 others(33): 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(7): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072 | 1 | 24 | 0.0417 | 14 | c.312 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0049 others(3): Show |
6 | 25 | 0.2400 | 14 | c.703 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATATAT others(7): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | 68 | 0.0441 | 14 | c.171 others(33): 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(7): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 10 | 0.1000 | 14 | c.186 others(33): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGAGTGTG others(7): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0196 | 1 | 121 | 0.0083 | 14 | c.110 others(31): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0153 |
5 | 125 | 0.0400 | 14 | c.110 others(31): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30621572 | A | ATGTGTGC others(7): Show |
upstream_gene_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 246 | 0.0041 | 14 | c.-52 others(25): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4555 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACACAC others(7): Show |
3_prime_UTR_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0042a0001c0003t0010 | a0001c0001t0042g0083 a0001c0003t0010g0006 a0001c0003t0010g0007 others(6): Show |
9 | 38 | 0.2368 | 14 | c.*19 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00741.hp2 HG02300.hp1 HG02818.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0007others(1): Show | a0001c0001t0001g0128 a0001c0001t0001g0219 a0002c0002t0002g0265 others(2): Show |
5 | 46 | 0.1087 | 14 | c.173 others(33): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31927229 | A | AATTTTAA others(7): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(172): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(38): Show | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(171): Show |
175 | 319 | 0.5486 | 14 | c.-11 others(33): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATATAT others(7): Show |
upstream_gene_variant | MODIFIER | HG01175.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0024 | a0001c0001t0004g0001 a0001c0001t0004g0023 a0001c0001t0004g0032 others(1): Show |
4 | 276 | 0.0145 | 14 | c.-46 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143231069 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 | 1 | 120 | 0.0083 | 14 | c.384 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143262535 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0092 a0001c0001t0001g0123 |
2 | 67 | 0.0299 | 14 | c.474 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143309866 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 96 | 0.0104 | 14 | c.474 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143320409 | C | CCCGCCCC others(7): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01358.hp2 HG02071.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0091 others(5): Show |
8 | 148 | 0.0541 | 14 | c.474 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143320410 | C | CCGCCCCC others(7): Show |
intron_variant | MODIFIER | HG00609.hp2 HG02615.hp1 HG03942.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0077 others(3): Show |
6 | 144 | 0.0417 | 14 | c.474 others(33): 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(7): Show |
intron_variant | MODIFIER | HG01255.hp2 NA19085.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 a0001c0001t0001g0111 |
2 | 89 | 0.0225 | 14 | c.474 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTATGTAT others(7): Show |
intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129 | 1 | 57 | 0.0175 | 14 | c.475 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02572.hp2 NA18966.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 a0001c0001t0001g0087 |
2 | 58 | 0.0345 | 14 | c.475 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00609.hp1 HG01256.hp2 HG01496.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0110 |
3 | 24 | 0.1250 | 14 | c.475 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGCG others(7): Show |
intron_variant | MODIFIER | HG01358.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0080 others(2): Show |
5 | 26 | 0.1923 | 14 | c.475 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03098.hp1 HG04228.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 a0001c0001t0001g0089 a0001c0001t0001g0123 |
3 | 24 | 0.1250 | 14 | c.475 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02965.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0055 |
2 | 23 | 0.0870 | 14 | c.475 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00609.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
17 | 24 | 0.7083 | 14 | c.703 others(31): 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(7): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 7 | 0.1429 | 14 | c.703 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143605858 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0035 | 1 | 19 | 0.0526 | 14 | c.100 others(35): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01243.hp1 HG03927.hp1 NA18953.hp2 |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0052 a0001c0002t0001g0118 a0002c0004t0001g0060 |
3 | 92 | 0.0326 | 14 | c.100 others(35): 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(7): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00621.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 a0001c0001t0001g0077 |
2 | 11 | 0.1818 | 14 | c.113 others(35): 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(7): Show |
intron_variant | MODIFIER | HG04115.hp2 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083 a0001c0001t0001g0161 |
2 | 136 | 0.0147 | 14 | c.113 others(35): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673748 | G | GTATATAT others(7): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01256.hp2 HG02300.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074 a0001c0001t0001g0110 a0001c0001t0001g0126 others(1): Show |
4 | 120 | 0.0333 | 14 | c.113 others(35): 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(7): Show |
intron_variant | MODIFIER | NA18747.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140 | 1 | 110 | 0.0091 | 14 | c.113 others(35): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |