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 | 143188613 | CATT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(52): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(52): Show |
55 | 88 | 0.6250 | -3 | c.166 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | CAAA | C | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01081.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0034 others(16): Show |
19 | 35 | 0.5429 | -3 | c.385 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143249112 | CAAT | C | intron_variant | MODIFIER | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | 160 | 0.0188 | -3 | c.385 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143254867 | TAAA | T | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(46): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(46): Show |
49 | 99 | 0.4949 | -3 | c.474 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143261325 | CTTT | C | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0029 others(32): Show |
35 | 98 | 0.3571 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTT | C | intron_variant | MODIFIER | HG02300.hp2 HG03927.hp2 NA18986.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0153 others(2): Show |
5 | 25 | 0.2000 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143282212 | TTAA | T | intron_variant | MODIFIER | HG00642.hp1 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0107 |
2 | 160 | 0.0125 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143298825 | TAAG | T | intron_variant | MODIFIER | HG01261.hp1 HG02280.hp2 HG02886.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0040 others(5): Show |
8 | 160 | 0.0500 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143308935 | CAAA | C | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(65): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
68 | 100 | 0.6800 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | CTTT | C | intron_variant | MODIFIER | HG02258.hp1 HG02280.hp1 HG03195.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | 74 | 0.0676 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143323894 | CAAA | C | intron_variant | MODIFIER | HG02129.hp1 HG02523.hp2 HG02698.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(5): Show |
8 | 51 | 0.1569 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143328754 | AACT | A | intron_variant | MODIFIER | HG00733.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0042 a0001c0002t0001g0043 a0001c0002t0001g0044 others(1): Show |
4 | 160 | 0.0250 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143330129 | AAAC | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0037 others(10): Show |
13 | 158 | 0.0823 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143335461 | CCTT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(30): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0019 others(30): Show |
33 | 160 | 0.2063 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143336006 | TTTA | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
14 | 160 | 0.0875 | -3 | c.474 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143371319 | GAGA | G | intron_variant | MODIFIER | HG02074.hp2 HG02523.hp2 HG02698.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | 160 | 0.0563 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143373629 | CAAA | C | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(63): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
66 | 121 | 0.5455 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143384565 | TAAA | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
44 | 88 | 0.5000 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143389106 | CATT | C | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(35): Show |
38 | 149 | 0.2550 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143393726 | TAAA | T | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(32): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | 71 | 0.4930 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397258 | AATG | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(135): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
138 | 160 | 0.8625 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397568 | CGAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(41): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(41): Show |
44 | 160 | 0.2750 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143421140 | TTTC | T | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(24): Show |
27 | 160 | 0.1688 | -3 | c.475 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143429220 | GTTT | G | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | 122 | 0.1639 | -3 | c.475 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143471008 | AAAG | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(56): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(56): Show |
59 | 160 | 0.3688 | -3 | c.704 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143471066 | TATG | T | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | 160 | 0.0250 | -3 | c.704 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143477394 | TATC | T | intron_variant | MODIFIER | HG01081.hp1 HG01256.hp2 HG01361.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 a0001c0001t0001g0108 a0001c0001t0001g0110 others(4): Show |
7 | 160 | 0.0438 | -3 | c.704 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143477426 | CATT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(28): Show |
31 | 159 | 0.1950 | -3 | c.704 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143542341 | TCGC | T | intron_variant | MODIFIER | NA18953.hp2 NA19062.hp2 NA19068.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | 160 | 0.0250 | -3 | c.926 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143622780 | TTAA | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0137 |
3 | 159 | 0.0189 | -3 | c.100 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143622781 | TAAA | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(55): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(55): Show |
58 | 83 | 0.6988 | -3 | c.100 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143635194 | CTTT | C | intron_variant | MODIFIER | HG00609.hp1 HG02074.hp2 HG02129.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0023 others(12): Show |
15 | 49 | 0.3061 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143639654 | CATT | C | intron_variant | MODIFIER | HG00609.hp1 HG02074.hp2 HG02129.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0023 others(13): Show |
16 | 160 | 0.1000 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143647359 | TAAA | T | intron_variant | MODIFIER | HG02280.hp1 HG02572.hp1 HG03195.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0106 others(4): Show |
7 | 96 | 0.0729 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656932 | CTGG | C | intron_variant | MODIFIER | HG04115.hp1 HG04115.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 a0001c0001t0001g0161 |
2 | 160 | 0.0125 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAA | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG02071.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0062 others(7): Show |
10 | 21 | 0.4762 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143692566 | TGAA | T | intron_variant | MODIFIER | HG02129.hp1 NA18947.hp1 NA19068.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0116 a0001c0001t0001g0144 a0001c0001t0001g0160 others(1): Show |
4 | 160 | 0.0250 | -3 | c.113 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143698519 | TACA | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(32): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(32): Show |
35 | 160 | 0.2188 | -3 | c.113 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143754133 | ATGT | A | intron_variant | MODIFIER | HG02145.hp2 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0127 |
2 | 160 | 0.0125 | -3 | c.124 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | CTTT | C | downstream_gene_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG01099.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0006a0001c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0049 others(26): Show |
29 | 74 | 0.3919 | -3 | c.*37 others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24945343 | AAAG | A | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(5): Show |
8 | 237 | 0.0338 | -3 | c.124 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24958697 | GAGA | G | intron_variant | MODIFIER | HG01243.hp1 HG02280.hp1 HG03516.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0003 | a0001c0001t0001g0109 a0001c0001t0002g0031 a0001c0003t0003g0210 |
3 | 238 | 0.0126 | -3 | c.724 others(18): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961213 | AAAC | A | intron_variant | MODIFIER | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(7): Show |
10 | 238 | 0.0420 | -3 | c.574 others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24978866 | TAAA | T | intron_variant | MODIFIER | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0001 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0001t0005g0004 others(3): Show |
7 | 120 | 0.0583 | -3 | c.93+ others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129578314 | CTAA | C | 3_prime_UTR_variant | MODIFIER | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(6): Show |
9 | 236 | 0.0381 | -3 | c.*19 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 196 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129581448 | AACT | A | intron_variant | MODIFIER | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(6): Show |
9 | 236 | 0.0381 | -3 | c.183 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129614748 | ATTT | A | intron_variant | MODIFIER | HG00597.hp2 HG02630.hp2 NA18612.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(1): Show | a0001c0001t0003g0224 a0001c0001t0005g0207 a0001c0001t0005g0212 others(3): Show |
6 | 124 | 0.0484 | -3 | c.104 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129623003 | AAAC | A | intron_variant | MODIFIER | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0017a0002c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0096 others(41): Show |
45 | 236 | 0.1907 | -3 | c.787 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625146 | ATAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0003a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(105): Show |
108 | 236 | 0.4576 | -3 | c.786 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625154 | TAGA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0003a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(105): Show |
108 | 230 | 0.4696 | -3 | c.786 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar |