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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143330131 | ACC | A | intron_variant | MODIFIER | HG03704.hp2 HG03942.hp2 NA19240.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0046 others(1): Show |
4 | 162 | 0.0247 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143337242 | AAG | A | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp1 HG01069.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(31): Show |
34 | 162 | 0.2099 | -2 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346228 | ACT | A | intron_variant | MODIFIER | HG00642.hp1 HG02109.hp2 HG02486.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0033 others(14): Show |
17 | 162 | 0.1049 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143346250 | TCA | T | intron_variant | MODIFIER | HG01255.hp2 HG02300.hp2 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0109 |
3 | 162 | 0.0185 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143347814 | ATT | A | intron_variant | MODIFIER | HG02129.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0051 others(9): Show |
12 | 162 | 0.0741 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143350838 | CAA | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG01069.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0034 others(23): Show |
26 | 162 | 0.1605 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143372349 | TAA | T | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(94): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
97 | 162 | 0.5988 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143372984 | TAA | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01256.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0037 others(16): Show |
19 | 162 | 0.1173 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143373629 | CAA | C | intron_variant | MODIFIER | HG01243.hp2 HG01255.hp1 HG02074.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(19): Show |
22 | 162 | 0.1358 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379480 | CAT | C | intron_variant | MODIFIER | HG00609.hp2 HG01069.hp2 HG01243.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0055 others(5): Show |
8 | 162 | 0.0494 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | ATG | A | intron_variant | MODIFIER | HG00642.hp1 HG01071.hp2 HG01081.hp2 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(35): Show |
38 | 162 | 0.2346 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143384565 | TAA | T | intron_variant | MODIFIER | HG01261.hp1 HG01358.hp1 HG01358.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0046 others(11): Show |
14 | 162 | 0.0864 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143387841 | GCA | G | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0031 others(17): Show |
20 | 162 | 0.1235 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143387909 | GCA | G | intron_variant | MODIFIER | NA19043.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 a0001c0001t0001g0138 |
2 | 162 | 0.0124 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143390731 | GCA | G | intron_variant | MODIFIER | HG02258.hp1 HG02723.hp1 HG03486.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(3): Show |
6 | 162 | 0.0370 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143393726 | TAA | T | intron_variant | MODIFIER | HG00738.hp2 HG02258.hp1 HG02280.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
19 | 162 | 0.1173 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397026 | TAG | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0137 |
2 | 162 | 0.0124 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | ATG | A | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(23): Show |
26 | 162 | 0.1605 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397346 | GTA | G | intron_variant | MODIFIER | HG00609.hp2 HG01255.hp2 HG02145.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0041 others(5): Show |
8 | 162 | 0.0494 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143405096 | CAG | C | intron_variant | MODIFIER | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0099 others(3): Show |
6 | 162 | 0.0370 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | GTA | G | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02523.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0037 others(9): Show |
12 | 162 | 0.0741 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143416843 | ACG | A | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(53): Show |
56 | 162 | 0.3457 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143421766 | GTA | G | intron_variant | MODIFIER | HG02071.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0028 others(1): Show |
4 | 162 | 0.0247 | -2 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143467242 | CTT | C | intron_variant | MODIFIER | HG00741.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0099 others(6): Show |
9 | 162 | 0.0556 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143470669 | ATG | A | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0137 |
2 | 162 | 0.0124 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143470797 | CAT | C | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(59): Show |
62 | 162 | 0.3827 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143470987 | CAT | C | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | 162 | 0.0309 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143471046 | CAT | C | intron_variant | MODIFIER | HG02559.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0061 others(1): Show |
4 | 162 | 0.0247 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143477169 | TAC | T | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(29): Show |
32 | 162 | 0.1975 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143477212 | GCA | G | intron_variant | MODIFIER | HG00642.hp1 HG01261.hp1 HG02071.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0024 others(11): Show |
14 | 162 | 0.0864 | -2 | c.704 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143508731 | CAG | C | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(110): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
113 | 162 | 0.6975 | -2 | c.827 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143510018 | TAA | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(19): Show |
22 | 162 | 0.1358 | -2 | c.827 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143542735 | AAT | A | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(54): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(54): Show |
57 | 162 | 0.3519 | -2 | c.926 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143542804 | GTA | G | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0081 others(11): Show |
14 | 162 | 0.0864 | -2 | c.926 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143547568 | TAA | T | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(117): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
120 | 162 | 0.7407 | -2 | c.926 others(19): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143591937 | ACT | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(128): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
131 | 162 | 0.8086 | -2 | c.100 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143622000 | TTG | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0106 a0001c0001t0001g0135 others(1): Show |
4 | 162 | 0.0247 | -2 | c.100 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143626315 | GAA | G | intron_variant | MODIFIER | HG00609.hp1 HG02074.hp2 HG02129.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0025 others(15): Show |
18 | 162 | 0.1111 | -2 | c.113 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143643427 | ACC | A | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(57): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
60 | 162 | 0.3704 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143647359 | TAA | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0029 others(17): Show |
20 | 162 | 0.1235 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | GGT | G | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0049 others(18): Show |
21 | 162 | 0.1296 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143667582 | TAA | T | intron_variant | MODIFIER | HG00609.hp1 HG02071.hp1 HG02074.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0025 others(15): Show |
18 | 162 | 0.1111 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673722 | TTG | T | intron_variant | MODIFIER | HG03710.hp1 NA18966.hp2 NA18986.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 a0001c0001t0001g0132 a0001c0001t0001g0158 others(1): Show |
4 | 162 | 0.0247 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | GTA | G | intron_variant | MODIFIER | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0124 others(2): Show |
5 | 162 | 0.0309 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143679654 | CGT | C | intron_variant | MODIFIER | HG03098.hp2 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0103 |
2 | 162 | 0.0124 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143680021 | TAA | T | intron_variant | MODIFIER | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0106 others(4): Show |
7 | 162 | 0.0432 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAA | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00733.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(33): Show |
36 | 162 | 0.2222 | -2 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143709760 | AAT | A | intron_variant | MODIFIER | HG00609.hp1 HG00738.hp2 HG02071.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(10): Show |
13 | 162 | 0.0803 | -2 | c.124 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143722191 | TCA | T | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0108 a0002c0004t0001g0060 |
2 | 162 | 0.0124 | -2 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143724051 | ATG | A | intron_variant | MODIFIER | HG02572.hp1 HG03209.hp2 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0119 |
3 | 162 | 0.0185 | -2 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |