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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143153777 | ATCT | A | intron_variant | MODIFIER | HG00621.hp2 HG01261.hp2 HG03209.hp1 others(8): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0001a0003c0005t0001 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0015others(8): Show | 11 | 162 | 0.0679 | -3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153873 | TTCC | T | intron_variant | MODIFIER | HG01081.hp2 HG02698.hp1 HG02965.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0130others(4): Show | 7 | 162 | 0.0432 | -3 | c.-14 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | CATT | C | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(52): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(52): Show | 55 | 162 | 0.3395 | -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 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0034others(16): Show | 19 | 162 | 0.1173 | -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 | a0001c0001t0001g0041a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | 162 | 0.0185 | -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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0021others(46): Show | 49 | 162 | 0.3025 | -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 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(32): Show | 35 | 162 | 0.2161 | -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 | a0001c0001t0001g0038a0001c0001t0001g0064a0001c0001t0001g0153others(2): Show | 5 | 162 | 0.0309 | -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 | a0001c0001t0001g0006a0001c0001t0001g0107 | 2 | 162 | 0.0124 | -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 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0039others(5): Show | 8 | 162 | 0.0494 | -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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | 162 | 0.4198 | -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 | a0001c0001t0001g0009a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | 162 | 0.0309 | -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 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | 162 | 0.0494 | -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 | a0001c0001t0001g0042a0001c0002t0001g0043a0001c0002t0001g0044others(1): Show | 4 | 162 | 0.0247 | -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 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0037others(10): Show | 13 | 162 | 0.0803 | -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 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(30): Show | 33 | 162 | 0.2037 | -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 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0037others(11): Show | 14 | 162 | 0.0864 | -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 | 143354031 | TTGG | T | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(158): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 161 | 162 | 0.9938 | -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 | 143371319 | GAGA | G | intron_variant | MODIFIER | HG02074.hp2 HG02523.hp2 HG02698.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | 162 | 0.0556 | -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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(63): Show | 66 | 162 | 0.4074 | -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 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | 162 | 0.2716 | -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 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(35): Show | 38 | 162 | 0.2346 | -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 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | 162 | 0.2161 | -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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(135): Show | 138 | 162 | 0.8519 | -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 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(41): Show | 44 | 162 | 0.2716 | -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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(24): Show | 27 | 162 | 0.1667 | -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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 20 | 162 | 0.1235 | -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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(56): Show | 59 | 162 | 0.3642 | -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 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | 162 | 0.0247 | -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 | a0001c0001t0001g0029a0001c0001t0001g0108a0001c0001t0001g0111others(4): Show | 7 | 162 | 0.0432 | -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 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(28): Show | 31 | 162 | 0.1914 | -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 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | 162 | 0.0247 | -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 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0137 | 3 | 162 | 0.0185 | -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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(55): Show | 58 | 162 | 0.3580 | -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(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0025others(13): Show | 16 | 162 | 0.0988 | -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(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0025others(14): Show | 17 | 162 | 0.1049 | -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 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0106others(4): Show | 7 | 162 | 0.0432 | -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 | a0001c0001t0001g0157a0001c0001t0001g0161 | 2 | 162 | 0.0124 | -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 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0062others(7): Show | 10 | 162 | 0.0617 | -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 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0160others(1): Show | 4 | 162 | 0.0247 | -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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | 162 | 0.2161 | -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 | a0001c0001t0001g0006a0001c0001t0001g0128 | 2 | 162 | 0.0124 | -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 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0048others(26): Show | 29 | 240 | 0.1208 | -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 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | 240 | 0.0333 | -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 | a0001c0001t0001g0109a0001c0001t0002g0031a0001c0003t0003g0212 | 3 | 240 | 0.0125 | -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 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | 240 | 0.0417 | -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 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0001t0005g0003others(3): Show | 7 | 240 | 0.0292 | -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 |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0008 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | 238 | 0.0378 | -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 |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0008 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | 238 | 0.0378 | -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 | a0001c0001t0003g0225a0001c0001t0005g0207a0001c0001t0005g0212others(3): Show | 6 | 238 | 0.0252 | -3 | c.104 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | TogoVar |