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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP12_chr10_31800398_31933831 | 31924702 | TCATAA | T | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(7): Show | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0096others(66): Show | 69 | 322 | 0.2143 | -5 | c.-11 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143209945 | CTAGAG | C | intron_variant | MODIFIER | HG01361.hp1 HG01515.hp2 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029a0001c0001t0001g0126a0001c0001t0001g0143 | 3 | 162 | 0.0185 | -5 | c.235 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143213514 | AAAAAT | A | intron_variant | MODIFIER | HG00642.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0107others(3): Show | 6 | 162 | 0.0370 | -5 | c.235 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143261325 | CTTTTT | C | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02886.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055a0001c0001t0001g0096a0001c0001t0001g0101others(3): Show | 6 | 162 | 0.0370 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTTTT | C | intron_variant | MODIFIER | HG00738.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0045others(13): Show | 16 | 162 | 0.0988 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143317930 | TTTTTG | T | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0037others(11): Show | 14 | 162 | 0.0864 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143318509 | CTTTTT | C | intron_variant | MODIFIER | HG01071.hp2 HG02698.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(3): Show | 6 | 162 | 0.0370 | -5 | c.474 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143364219 | ACATTC | A | intron_variant | MODIFIER | HG02074.hp2 HG02129.hp1 HG02523.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 10 | 162 | 0.0617 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143411425 | TCAAAA | T | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0101others(2): Show | 5 | 162 | 0.0309 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143419583 | ATATGT | A | intron_variant | MODIFIER | HG02258.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0106 | 2 | 162 | 0.0124 | -5 | c.475 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143439422 | CAAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(42): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(42): Show | 45 | 162 | 0.2778 | -5 | c.703 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143453075 | TTAATC | T | intron_variant | MODIFIER | HG01261.hp1 HG02071.hp1 HG02280.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0028others(7): Show | 10 | 162 | 0.0617 | -5 | c.703 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143457974 | GATAAA | G | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | 162 | 0.0247 | -5 | c.703 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143495705 | ATTGAG | A | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(22): Show | 25 | 162 | 0.1543 | -5 | c.826 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143555860 | AAGAAT | A | intron_variant | MODIFIER | HG01069.hp2 HG01358.hp1 HG01361.hp1 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0056others(16): Show | 19 | 162 | 0.1173 | -5 | c.926 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143601668 | TTTCTA | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0137 | 3 | 162 | 0.0185 | -5 | c.100 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143667629 | GTTAAT | G | intron_variant | MODIFIER | HG01071.hp2 HG02071.hp2 HG02698.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(3): Show | 6 | 162 | 0.0370 | -5 | c.113 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAA | C | intron_variant | MODIFIER | HG02129.hp1 NA18947.hp1 NA18962.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0115others(4): Show | 7 | 162 | 0.0432 | -5 | c.113 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143710154 | CTCTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(34): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0020others(34): Show | 37 | 162 | 0.2284 | -5 | 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 | 24982996 | ATTTTT | A | intron_variant | MODIFIER | HG00642.hp2 HG01261.hp1 HG01358.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0133others(2): Show | 5 | 240 | 0.0208 | -5 | c.54- others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129580322 | TTAAAA | T | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
a0001a0007 | a0001c0001a0007c0008 | a0001c0001t0004a0007c0008t0004 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | 238 | 0.0168 | -5 | c.183 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129585301 | AAAAAT | A | intron_variant | MODIFIER | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | 238 | 0.0126 | -5 | c.171 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129607593 | CTATTA | C | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | 238 | 0.0336 | -5 | c.128 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625091 | TATATG | T | intron_variant | MODIFIER | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0001g0189others(17): Show | 20 | 238 | 0.0840 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625311 | TATGTA | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | 238 | 0.0084 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625327 | TATATG | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | 238 | 0.0084 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625364 | TATTTA | T | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | 238 | 0.0084 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625729 | TATTTA | T | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | 238 | 0.2143 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625935 | ATATAT | A | intron_variant | MODIFIER | HG02451.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0010a0003c0004t0001others(1): Show | a0001c0001t0002g0145a0001c0001t0010g0137a0003c0004t0001g0151others(1): Show | 4 | 238 | 0.0168 | -5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129655337 | AAAAAG | A | intron_variant | MODIFIER | HG02004.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(1): Show | a0001c0001t0001g0063a0001c0001t0001g0084a0001c0001t0001g0091others(5): Show | 8 | 238 | 0.0336 | -5 | c.114 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129659456 | TTTTTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(110): Show | 114 | 238 | 0.4790 | -5 | c.114 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129683050 | TTTTTC | T | intron_variant | MODIFIER | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | 238 | 0.0252 | -5 | c.113 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129695821 | TAAAAG | T | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(63): Show | 67 | 238 | 0.2815 | -5 | c.113 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251753 | AGAAGG | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(28): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0025others(28): Show | 31 | 242 | 0.1281 | -5 | c.927 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97259828 | CTGTTT | C | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0002a0001c0001t0006a0005c0007t0006 | a0001c0001t0002g0011a0001c0001t0006g0008a0001c0001t0006g0009others(3): Show | 6 | 242 | 0.0248 | -5 | c.614 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110596975 | GTTCAT | G | intron_variant | MODIFIER | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
a0009a0011a0012 | a0009c0015a0011c0018a0012c0019 | a0009c0015t0004a0011c0018t0015a0012c0019t0004 | a0009c0015t0004g0153a0011c0018t0015g0007a0012c0019t0004g0151 | 3 | 226 | 0.0133 | -5 | c.965 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110628742 | AAAGTT | A | intron_variant | MODIFIER | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
a0001a0003a0008 | a0001c0001a0003c0004a0008c0017 | a0001c0001t0001a0003c0004t0002a0008c0017t0002 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | 226 | 0.0177 | -5 | c.353 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110689521 | ATAAAT | A | intron_variant | MODIFIER | HG02622.hp2 HG03540.hp2 |
a0006 | a0006c0007 | a0006c0007t0010 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | 226 | 0.0089 | -5 | c.188 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAA | C | downstream_gene_variant | MODIFIER | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0168others(3): Show | 6 | 352 | 0.0171 | -5 | c.*35 others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24587827 | TTACTC | T | intron_variant | MODIFIER | HG02145.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
a0001a0005 | a0001c0001a0001c0014a0005c0005 | a0001c0001t0001a0001c0014t0004a0005c0005t0004 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | 352 | 0.0171 | -5 | c.418 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24598528 | TAAGAG | T | intron_variant | MODIFIER | HG00642.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | 352 | 0.0171 | -5 | c.313 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24615771 | ATTATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
a0002a0005a0013others(4): Show | a0002c0002a0002c0015a0002c0017others(9): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(13): Show | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(132): Show | 135 | 352 | 0.3835 | -5 | c.242 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24649962 | AAACTT | A | intron_variant | MODIFIER | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
a0002a0019 | a0002c0002a0002c0017a0019c0020 | a0002c0002t0001a0002c0002t0014a0002c0017t0001others(1): Show | a0002c0002t0001g0019a0002c0002t0001g0106a0002c0002t0001g0107others(14): Show | 17 | 352 | 0.0483 | -5 | c.269 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24683095 | CAAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
a0001a0002a0004others(4): Show | a0001c0001a0002c0002a0002c0021others(5): Show | a0001c0001t0001a0001c0001t0013a0002c0002t0001others(8): Show | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(62): Show | 65 | 352 | 0.1847 | -5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAA | C | intron_variant | MODIFIER | HG01081.hp1 HG01258.hp2 HG01928.hp2 others(11): Show |
a0001a0006a0024 | a0001c0001a0006c0006a0024c0026 | a0001c0001t0002a0001c0001t0016a0006c0006t0002others(1): Show | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0322others(11): Show | 14 | 352 | 0.0398 | -5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24702127 | CTTTTT | C | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
a0002a0004a0014others(1): Show | a0002c0002a0004c0004a0014c0024others(1): Show | a0002c0002t0001a0004c0004t0001a0014c0024t0011others(1): Show | a0002c0002t0001g0071a0002c0002t0001g0088a0002c0002t0001g0136others(10): Show | 13 | 352 | 0.0369 | -5 | c.63+ others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48441421 | CAGAAG | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0055others(114): Show | 118 | 270 | 0.4370 | -5 | c.*49 others(16): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4614 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38446181 | ATTTTT | A | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
a0001a0003a0006 | a0001c0004a0001c0009a0001c0010others(3): Show | a0001c0004t0001a0001c0009t0003a0001c0010t0001others(3): Show | a0001c0004t0001g0057a0001c0004t0001g0069a0001c0004t0001g0170others(8): Show | 11 | 309 | 0.0356 | -5 | c.64- others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485377 | ATATAT | A | intron_variant | MODIFIER | HG00423.hp2 HG02080.hp1 HG02109.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0013 | a0001c0001t0001a0001c0003t0001a0001c0013t0001 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0097others(4): Show | 7 | 108 | 0.0648 | -5 | c.-21 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85586229 | TTTGGG | T | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(18): Show | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | 108 | 0.3611 | -5 | c.180 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |