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 | 147798724 | ACTCTCTC others(5): Show |
A | intron_variant | MODIFIER | HG01261.hp1 HG02109.hp1 HG02818.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0003a0002c0003t0001 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0003g0087 others(1): Show |
4 | 69 | 0.0580 | -12 | c.155 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147833703 | TGCTAAGT others(5): Show |
T | intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072 | 1 | 104 | 0.0096 | -12 | 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 | 147834988 | GGTACTTA others(5): Show |
G | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0090 | 1 | 104 | 0.0096 | -12 | 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 | 147839092 | GTATCTAT others(5): Show |
G | intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 | 1 | 57 | 0.0175 | -12 | c.313 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839138 | ATCTATCT others(5): Show |
A | intron_variant | MODIFIER | HG01261.hp1 HG03492.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0052 a0001c0002t0001g0072 |
2 | 88 | 0.0227 | -12 | c.313 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911994 | CGTGTGTG others(5): Show |
C | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(9): Show |
12 | 23 | 0.5217 | -12 | c.116 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
36 | 38 | 0.9474 | -12 | c.116 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0045 | 1 | 10 | 0.1000 | -12 | c.186 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043752 | ATGTATAT others(5): Show |
A | intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 104 | 0.0096 | -12 | c.186 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30624418 | CAAAAAAA others(5): Show |
C | upstream_gene_variant | MODIFIER | HG00544.hp1 HG00609.hp2 NA19074.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0098 |
4 | 77 | 0.0519 | -12 | c.-24 others(23): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1709 | chr15 | TogoVar | |||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | AGTGTGTG others(5): Show |
A | downstream_gene_variant | MODIFIER | HG01257.hp2 HG02976.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0059 |
2 | 68 | 0.0294 | -12 | c.*12 others(23): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31829154 | AAACAACA others(5): Show |
A | intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0166 | 1 | 216 | 0.0046 | -12 | c.144 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862696 | GCACACAC others(5): Show |
G | intron_variant | MODIFIER | HG01106.hp1 HG01258.hp1 HG01515.hp1 others(7): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(2): Show | a0001c0001t0001g0082 a0001c0001t0001g0099 a0001c0001t0001g0107 others(7): Show |
10 | 260 | 0.0385 | -12 | c.685 others(29): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | GACACACA others(5): Show |
G | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0012a0002c0002t0002a0002c0002t0007others(1): Show | a0001c0001t0012g0028 a0002c0002t0002g0266 a0002c0002t0002g0268 others(3): Show |
6 | 135 | 0.0444 | -12 | c.685 others(29): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | TCACACAC others(5): Show |
T | intron_variant | MODIFIER | HG01123.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0023a0001c0001t0024others(1): Show | a0001c0001t0006g0213 a0001c0001t0023g0038 a0001c0001t0023g0068 others(3): Show |
6 | 65 | 0.0923 | -12 | c.-11 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31920665 | AGTTTTTG others(5): Show |
A | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0017others(1): Show | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(15): Show |
18 | 319 | 0.0564 | -12 | c.-11 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31921763 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0232 | 1 | 126 | 0.0079 | -12 | c.-11 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | CATATATA others(5): Show |
C | upstream_gene_variant | MODIFIER | HG02074.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0009a0001c0001t0044others(3): Show | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0133 others(15): Show |
18 | 112 | 0.1607 | -12 | c.-46 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143134104 | AATCTATC others(5): Show |
A | intron_variant | MODIFIER | HG02071.hp2 HG02109.hp1 HG02523.hp1 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
13 | 89 | 0.1461 | -12 | c.-15 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143134142 | TCTATCTA others(5): Show |
T | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 | 1 | 160 | 0.0063 | -12 | c.-15 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143145839 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0065 | 1 | 25 | 0.0400 | -12 | c.-14 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153777 | ATCTTCTT others(5): Show |
A | intron_variant | MODIFIER | HG02559.hp1 HG02698.hp1 HG02965.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0121 others(4): Show |
7 | 129 | 0.0543 | -12 | c.-14 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153834 | TTCTTCTT others(5): Show |
T | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 1 | 122 | 0.0082 | -12 | c.-14 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165960 | GAGAAAGA others(5): Show |
G | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 26 | 0.0385 | -12 | c.165 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | CATTATTA others(5): Show |
C | intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 34 | 0.0294 | -12 | c.166 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143197967 | TACACACA others(5): Show |
T | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(26): Show |
29 | 127 | 0.2283 | -12 | c.166 others(29): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143330127 | AAAAACCA others(5): Show |
A | intron_variant | MODIFIER | HG02809.hp2 NA18962.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 a0001c0001t0001g0128 |
2 | 157 | 0.0127 | -12 | c.474 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143372011 | GAAATAAA others(5): Show |
G | intron_variant | MODIFIER | HG00733.hp2 HG01361.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | 47 | 0.0638 | -12 | c.475 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143390731 | GCACACAC others(5): Show |
G | intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 5 | 0.2000 | -12 | c.475 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143416817 | CACCACCC others(5): Show |
C | intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 160 | 0.0063 | -12 | c.475 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143421766 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | 121 | 0.0331 | -12 | c.475 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143468657 | AGAGAGAG others(5): Show |
A | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0121 |
3 | 156 | 0.0192 | -12 | c.704 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143606059 | AAAAAAAA others(5): Show |
A | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp1 HG00738.hp1 others(32): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0025 others(32): Show |
35 | 160 | 0.2188 | -12 | c.100 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143609144 | GAAATCCA others(5): Show |
G | intron_variant | MODIFIER | HG02723.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 a0001c0001t0001g0119 |
2 | 160 | 0.0125 | -12 | c.100 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0095 others(2): Show |
5 | 14 | 0.3571 | -12 | c.113 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | GTGTATAT others(5): Show |
G | intron_variant | MODIFIER | NA18947.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 87 | 0.0115 | -12 | c.113 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143680021 | TAAAAAAA others(5): Show |
T | intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 19 | 0.0526 | -12 | c.113 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(41): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0029 others(41): Show |
44 | 55 | 0.8000 | -12 | c.113 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143737726 | TTTTATTT others(5): Show |
T | intron_variant | MODIFIER | HG00609.hp1 HG02071.hp1 HG02572.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0028 others(11): Show |
14 | 60 | 0.2333 | -12 | c.124 others(33): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143763694 | GTATGTGT others(5): Show |
G | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0025 others(11): Show |
14 | 160 | 0.0875 | -12 | 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 | ATGTGTGT others(5): Show |
A | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0030 others(24): Show |
27 | 52 | 0.5192 | -12 | c.124 others(31): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | TACACACA others(5): Show |
T | downstream_gene_variant | MODIFIER | HG02040.hp1 HG02074.hp2 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0130 |
3 | 122 | 0.0246 | -12 | c.*35 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916818 | GCACACAC others(5): Show |
G | downstream_gene_variant | MODIFIER | HG02258.hp1 HG02486.hp1 NA18522.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0001a0002c0007t0001 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0223 others(1): Show |
4 | 91 | 0.0440 | -12 | c.*33 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2570 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961518 | ATTTTTTT others(5): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 a0001c0001t0001g0118 |
2 | 100 | 0.0200 | -12 | c.574 others(29): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982990 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | NA18969.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 237 | 0.0042 | -12 | c.54- others(27): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25003230 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(26): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(24): Show |
29 | 144 | 0.2014 | -12 | c.53+ others(29): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020190 | CGGAAGGA others(5): Show |
C | upstream_gene_variant | MODIFIER | NA18978.hp2 NA19007.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 a0001c0002t0001g0039 |
2 | 96 | 0.0208 | -12 | c.-49 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4822 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020224 | GAAGGAAG others(5): Show |
G | upstream_gene_variant | MODIFIER | HG01261.hp2 HG03491.hp2 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 a0001c0001t0001g0168 a0001c0001t0001g0196 |
3 | 236 | 0.0127 | -12 | c.-49 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4856 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129601535 | GAAGAAAA others(5): Show |
G | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0004a0001c0001t0006a0004c0008t0004 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(2): Show |
5 | 236 | 0.0212 | -12 | c.136 others(29): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129606493 | ATTATCAT others(5): Show |
A | intron_variant | MODIFIER | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | 236 | 0.0127 | -12 | c.128 others(29): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | TogoVar |