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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP18_chr6_129571132_129715177 | 129582131 | G | GAAGGAAT others(8): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0008 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | 238 | 0.0378 | 15 | c.183 others(34): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625779 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0175 | 1 | 238 | 0.0042 | 15 | c.786 others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625908 | A | ATTATATA others(8): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0018 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | 238 | 0.0462 | 15 | c.786 others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97259828 | C | CTGTTTTG others(8): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0005a0004c0006others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(12): Show | a0001c0001t0001g0107a0001c0001t0001g0111a0001c0001t0001g0112others(124): Show | 127 | 242 | 0.5248 | 15 | c.614 others(30): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110658780 | A | ATTGTTTT others(8): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
a0001a0003a0008others(2): Show | a0001c0001a0001c0002a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0001g0210others(14): Show | 17 | 226 | 0.0752 | 15 | c.189 others(34): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110660054 | T | TAAAAAAC others(8): Show |
intron_variant | MODIFIER | NA19067.hp1 | a0008 | a0008c0017 | a0008c0017t0002 | a0008c0017t0002g0141 | 1 | 226 | 0.0044 | 15 | c.189 others(34): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24625062 | G | GGGGGGGG others(8): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01192.hp1 HG01993.hp1 others(7): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | 352 | 0.0284 | 15 | c.496 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 352 | 0.0028 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG01433.hp2 HG01884.hp1 NA18978.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0004 | a0001c0001t0001g0224a0002c0002t0001g0125a0002c0002t0004g0295 | 3 | 352 | 0.0085 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01978.hp1 HG02451.hp2 others(1): Show |
a0001a0003a0009 | a0001c0001a0003c0003a0009c0008 | a0001c0001t0001a0003c0003t0001a0009c0008t0004 | a0001c0001t0001g0142a0001c0001t0001g0260a0003c0003t0001g0202others(1): Show | 4 | 352 | 0.0114 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG02004.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0201 | 1 | 352 | 0.0028 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0236 | 1 | 352 | 0.0028 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATATA others(8): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0002 | a0002c0021 | a0002c0021t0001 | a0002c0021t0001g0084 | 1 | 352 | 0.0028 | 15 | c.495 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48558354 | T | TTTTTGTT others(8): Show |
intron_variant | MODIFIER | HG02717.hp1 HG03139.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0003 | a0001c0001t0002g0039a0001c0003t0003g0241 | 2 | 270 | 0.0074 | 15 | c.235 others(32): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 HG01109.hp1 HG01256.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0079a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | 309 | 0.0291 | 15 | c.-19 others(26): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | AAATAATA others(8): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(13): Show | a0001c0001t0001a0001c0001t0009a0001c0002t0002others(15): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(66): Show | 70 | 309 | 0.2265 | 15 | c.344 others(34): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85492137 | T | TTACCCTA others(8): Show |
intron_variant | MODIFIER | HG02630.hp1 HG02723.hp1 NA18522.hp1 |
a0001a0004 | a0001c0003a0001c0005a0004c0010 | a0001c0003t0001a0001c0005t0003a0004c0010t0001 | a0001c0003t0001g0086a0001c0005t0003g0085a0004c0010t0001g0088 | 3 | 108 | 0.0278 | 15 | c.-21 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85541142 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0087 | 1 | 108 | 0.0093 | 15 | c.-20 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | G | GTTTTTTT others(8): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0002 | a0002c0006 | a0002c0006t0006 | a0002c0006t0006g0095 | 1 | 108 | 0.0093 | 15 | c.180 others(34): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85982373 | T | TTTTTGTT others(8): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
a0001a0002 | a0001c0005a0001c0007a0002c0006 | a0001c0005t0003a0001c0005t0004a0001c0005t0019others(3): Show | a0001c0005t0003g0085a0001c0005t0003g0094a0001c0005t0004g0034others(7): Show | 10 | 108 | 0.0926 | 15 | c.928 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890136 | T | TAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00558.hp2 NA18612.hp2 NA18957.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0001 | a0001c0001t0001g0131a0001c0001t0002g0118a0001c0003t0001g0031others(1): Show | 4 | 198 | 0.0202 | 15 | c.487 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949194 | A | AGAGAGAG others(8): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0107 | 1 | 198 | 0.0051 | 15 | c.110 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(8): Show |
intron_variant | MODIFIER | HG01071.hp2 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0019 | a0001c0001t0006g0095a0001c0001t0019g0011 | 2 | 198 | 0.0101 | 15 | c.110 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTATTT others(8): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(17): Show |
a0001 | a0001c0001a0001c0003a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0002g0016others(17): Show | 20 | 198 | 0.1010 | 15 | c.110 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012576 | T | TATATATA others(8): Show |
intron_variant | MODIFIER | NA18972.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 198 | 0.0051 | 15 | c.110 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG03471.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0006g0096others(3): Show | 6 | 198 | 0.0303 | 15 | c.153 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG04228.hp2 NA18945.hp2 NA19010.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(1): Show | a0001c0001t0003g0191a0001c0001t0005g0058a0001c0001t0007g0106others(1): Show | 4 | 198 | 0.0202 | 15 | c.198 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143232630 | C | CTTTTTTT others(8): Show |
downstream_gene_variant | MODIFIER | HG02132.hp2 HG02572.hp2 NA19081.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0011a0001c0003t0001 | a0001c0001t0002g0121a0001c0001t0011g0094a0001c0003t0001g0170 | 3 | 198 | 0.0152 | 15 | c.*10 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(8): Show |
intron_variant | MODIFIER | HG02004.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
a0001a0002a0003 | a0001c0009a0002c0002a0003c0007 | a0001c0009t0012a0002c0002t0001a0003c0007t0001 | a0001c0009t0012g0163a0001c0009t0012g0164a0002c0002t0001g0059others(1): Show | 4 | 347 | 0.0115 | 15 | c.174 others(34): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841144 | G | GTCTCTCT others(8): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01496.hp1 HG01515.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0003t0003g0077 | 3 | 248 | 0.0121 | 15 | c.543 others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6896899 | C | CTTTTATT others(8): Show |
intron_variant | MODIFIER | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
a0008 | a0008c0011 | a0008c0011t0005 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | 248 | 0.0121 | 15 | c.203 others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94182811 | T | TAAAACAA others(8): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0179 | 1 | 356 | 0.0028 | 15 | c.224 others(34): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055842 | T | TAAAATAA others(8): Show |
intron_variant | MODIFIER | HG02895.hp1 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 2 | 390 | 0.0051 | 15 | c.345 others(30): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | A | AAAGAAAG others(8): Show |
intron_variant | MODIFIER | NA18995.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 | 1 | 390 | 0.0026 | 15 | c.97+ others(30): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771985 | C | CTTTTTTT others(8): Show |
upstream_gene_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0044 | 1 | 420 | 0.0024 | 15 | c.-36 others(26): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3578 | chr19 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(8): Show |
upstream_gene_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0008 | 1 | 420 | 0.0024 | 15 | c.-36 others(26): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46981825 | G | GTGTTTTG others(8): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0005 | a0001c0005t0006 | a0001c0005t0006g0208 | 1 | 298 | 0.0034 | 15 | c.382 others(34): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | C | CTTTTTTT others(8): Show |
downstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0002 | a0001c0002t0053 | a0001c0002t0053g0127 | 1 | 298 | 0.0034 | 15 | c.*63 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144665463 | A | AGACCTTC others(8): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 | 1 | 246 | 0.0041 | 15 | c.-82 others(34): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02895.hp2 HG02896.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0076 | 3 | 246 | 0.0122 | 15 | c.-82 others(34): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100744840 | T | TACTCTGC others(8): Show |
intron_variant | MODIFIER | HG00597.hp1 NA18953.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0120a0001c0001t0013g0122 | 2 | 286 | 0.0070 | 15 | c.155 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0002 | a0002c0002 | a0002c0002t0039 | a0002c0002t0039g0195 | 1 | 286 | 0.0035 | 15 | c.251 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02572.hp2 HG03516.hp2 NA19030.hp2 others(1): Show |
a0001a0002 | a0001c0012a0002c0002a0002c0005 | a0001c0012t0001a0002c0002t0009a0002c0005t0010 | a0001c0012t0001g0131a0002c0002t0009g0043a0002c0005t0010g0255others(1): Show | 4 | 286 | 0.0140 | 15 | c.313 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(8): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01123.hp1 HG02055.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0002a0002c0002t0008others(4): Show | a0001c0001t0001g0093a0001c0001t0001g0095a0002c0002t0002g0045others(11): Show | 14 | 286 | 0.0490 | 15 | c.313 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0020 | 1 | 286 | 0.0035 | 15 | c.385 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02647.hp2 HG02886.hp1 others(7): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0007a0001c0001t0009a0001c0001t0012others(6): Show | a0001c0001t0007g0026a0001c0001t0007g0186a0001c0001t0009g0096others(7): Show | 10 | 230 | 0.0435 | 15 | c.54- others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(8): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0090 | 1 | 230 | 0.0044 | 15 | c.176 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02886.hp2 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0014 | a0001c0001t0001g0185a0001c0001t0014g0179 | 2 | 230 | 0.0087 | 15 | c.176 others(34): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCGAAAAA others(8): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0028a0001c0001t0003g0075 | 2 | 230 | 0.0087 | 15 | c.231 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1075058 | G | GCTCCAGC others(8): Show |
intron_variant | MODIFIER | NA18960.hp2 | a0001 | a0001c0002 | a0001c0002t0013 | a0001c0002t0013g0134 | 1 | 418 | 0.0024 | 15 | c.118 others(32): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |