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 | 143153840 | T | TTCCTCCT others(11): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02976.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0099a0001c0002t0001g0110 | 2 | 162 | 0.0124 | 18 | c.-14 others(35): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153843 | T | TTCTTCCT others(11): Show |
intron_variant | MODIFIER | HG02148.hp1 HG04199.hp1 HG04228.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0079others(1): Show | 4 | 162 | 0.0247 | 18 | c.-14 others(35): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143320403 | T | TCCCCCCC others(11): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 | 1 | 162 | 0.0062 | 18 | c.474 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143320406 | C | CCCCCCGC others(11): Show |
intron_variant | MODIFIER | HG03491.hp2 NA18962.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0067 | 2 | 162 | 0.0124 | 18 | c.474 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143320406 | C | CCCCCCGC others(11): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 162 | 0.0062 | 18 | c.474 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGCGCG others(11): Show |
intron_variant | MODIFIER | HG02965.hp2 NA19006.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0155 | 2 | 162 | 0.0124 | 18 | c.475 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGCG others(11): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 162 | 0.0062 | 18 | c.475 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG02071.hp2 HG02523.hp1 HG02602.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0053a0001c0001t0001g0069others(3): Show | 6 | 162 | 0.0370 | 18 | c.475 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 162 | 0.0062 | 18 | c.475 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 162 | 0.0062 | 18 | c.100 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG02129.hp1 HG02698.hp1 HG02723.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0076others(3): Show | 6 | 162 | 0.0370 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673746 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG02074.hp1 HG03927.hp1 NA18948.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0026a0001c0002t0001g0121a0003c0005t0001g0085 | 3 | 162 | 0.0185 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673748 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01361.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0148 | 3 | 162 | 0.0185 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673750 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 162 | 0.0062 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673754 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 162 | 0.0062 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG00642.hp1 HG02723.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0107 | 3 | 162 | 0.0185 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG00741.hp1 HG02074.hp2 HG03942.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0079others(1): Show | 4 | 162 | 0.0247 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTATAT others(11): Show |
intron_variant | MODIFIER | HG02602.hp1 HG03704.hp1 NA18970.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0066a0001c0002t0001g0065a0001c0002t0002g0059 | 3 | 162 | 0.0185 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(11): Show |
intron_variant | MODIFIER | NA19085.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 162 | 0.0062 | 18 | c.113 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | T | TACACACA others(11): Show |
downstream_gene_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 | 1 | 240 | 0.0042 | 18 | c.*35 others(29): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24950836 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0232 | 2 | 240 | 0.0083 | 18 | c.104 others(37): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961911 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0007 | a0001c0001t0001a0001c0001t0002a0001c0004t0002others(1): Show | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0002g0031others(3): Show | 6 | 240 | 0.0250 | 18 | c.574 others(35): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129668362 | T | TCACACAC others(11): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0050 | 1 | 238 | 0.0042 | 18 | c.114 others(37): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129676915 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0070 | 1 | 238 | 0.0042 | 18 | c.113 others(37): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218631 | T | TTGTGTGT others(11): Show |
downstream_gene_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0081 | 1 | 242 | 0.0041 | 18 | c.*74 others(29): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3547 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218895 | A | ATGTGTGT others(11): Show |
downstream_gene_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0003 | a0001c0003t0015 | a0001c0003t0015g0061 | 1 | 242 | 0.0041 | 18 | c.*72 others(29): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3283 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110581295 | A | AAACTATG others(11): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
a0002a0006a0007 | a0002c0003a0002c0006a0002c0014others(2): Show | a0002c0003t0007a0002c0006t0012a0002c0014t0019others(2): Show | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(7): Show | 10 | 226 | 0.0443 | 18 | c.172 others(33): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110584971 | G | GTGAATAT others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
a0001a0005 | a0001c0001a0005c0010 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(76): Show | 82 | 226 | 0.3628 | 18 | c.141 others(37): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02015.hp1 HG02080.hp1 HG04199.hp1 others(2): Show |
a0001a0007 | a0001c0002a0007c0020 | a0001c0002t0005a0007c0020t0020 | a0001c0002t0005g0212a0001c0002t0005g0215a0001c0002t0005g0217others(2): Show | 5 | 226 | 0.0221 | 18 | c.188 others(35): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24592720 | A | AGTAAGAT others(11): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | 352 | 0.0085 | 18 | c.387 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24625062 | G | GGGGGGGG others(11): Show |
intron_variant | MODIFIER | HG00609.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0179 | 1 | 352 | 0.0028 | 18 | c.496 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628952 | C | CTATATAT others(11): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0256 | 1 | 352 | 0.0028 | 18 | c.495 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG01256.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0143a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | 352 | 0.0199 | 18 | c.495 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG01099.hp1 NA19081.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0115a0002c0002t0001g0123 | 2 | 352 | 0.0057 | 18 | c.495 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG02647.hp1 NA18953.hp2 NA18980.hp2 |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0001a0004c0004t0001 | a0002c0002t0001g0280a0002c0002t0001g0282a0004c0004t0001g0031 | 3 | 352 | 0.0085 | 18 | c.495 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG02630.hp2 HG03579.hp2 NA18995.hp1 |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0002c0002t0001a0004c0004t0001 | a0001c0001t0001g0253a0002c0002t0001g0113a0004c0004t0001g0067 | 3 | 352 | 0.0085 | 18 | c.495 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(11): Show |
upstream_gene_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG01070.hp1 others(23): Show |
a0001a0011 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(8): Show | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0078others(23): Show | 26 | 309 | 0.0841 | 18 | c.-19 others(29): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | AAATAATA others(11): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(47): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0012others(17): Show | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0125others(47): Show | 50 | 309 | 0.1618 | 18 | c.344 others(37): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38507300 | T | TAATAATA others(11): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0123 | 1 | 309 | 0.0032 | 18 | c.344 others(37): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(11): Show |
downstream_gene_variant | MODIFIER | HG01261.hp2 HG02896.hp1 |
a0001a0003 | a0001c0001a0003c0014 | a0001c0001t0008a0003c0014t0001 | a0001c0001t0008g0260a0003c0014t0001g0066 | 2 | 309 | 0.0065 | 18 | c.*21 others(29): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655766 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0044 | 1 | 108 | 0.0093 | 18 | c.181 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655788 | T | TAGAGAGA others(11): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0101 | 1 | 108 | 0.0093 | 18 | c.181 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655812 | G | GAGAGAGA others(11): Show |
intron_variant | MODIFIER | HG00323.hp2 HG02145.hp1 HG02809.hp1 |
a0001a0002 | a0001c0001a0001c0003a0002c0006 | a0001c0001t0001a0001c0003t0009a0002c0006t0006 | a0001c0001t0001g0082a0001c0003t0009g0047a0002c0006t0006g0031 | 3 | 108 | 0.0278 | 18 | c.181 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655814 | G | GAGAGAGA others(11): Show |
intron_variant | MODIFIER | HG01168.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 108 | 0.0093 | 18 | c.181 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85859212 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG01433.hp1 HG02155.hp1 HG02809.hp1 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0013a0001c0003t0001a0001c0003t0009others(1): Show | a0001c0002t0013g0029a0001c0003t0001g0007a0001c0003t0001g0091others(3): Show | 6 | 108 | 0.0556 | 18 | c.269 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 108 | 0.0093 | 18 | c.733 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142858061 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0189 | 1 | 198 | 0.0051 | 18 | c.155 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0003 | a0001c0003t0046 | a0001c0003t0046g0159 | 1 | 198 | 0.0051 | 18 | c.487 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(11): Show |
intron_variant | MODIFIER | NA19083.hp1 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0090 | 1 | 198 | 0.0051 | 18 | c.487 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142936108 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | NA19058.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 198 | 0.0051 | 18 | c.110 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |