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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 148038938 | G | GTTTTGAA others(12): Show |
intron_variant | MODIFIER | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0011others(2): Show | a0001c0001t0001a0001c0006t0001a0001c0011t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(27): Show | 30 | 106 | 0.2830 | 19 | c.186 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143320405 | C | CCCCCCCG others(12): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0137 | 1 | 162 | 0.0062 | 19 | c.474 others(38): 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(12): Show |
intron_variant | MODIFIER | HG02523.hp2 HG03927.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0038 | 2 | 162 | 0.0124 | 19 | c.474 others(38): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143439422 | C | CAAAAAAA others(12): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01515.hp2 HG02258.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0029others(3): Show | 6 | 162 | 0.0370 | 19 | c.703 others(36): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24950836 | C | CAAAAAAA others(12): Show |
intron_variant | MODIFIER | HG03130.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(1): Show | 4 | 240 | 0.0167 | 19 | c.104 others(38): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24976556 | A | AGGGAAAG others(12): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0147 | 1 | 240 | 0.0042 | 19 | c.198 others(34): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24625062 | G | GGGGGGGG others(12): Show |
intron_variant | MODIFIER | HG02148.hp2 NA19080.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0226a0003c0003t0001g0203 | 2 | 352 | 0.0057 | 19 | c.496 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(12): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01123.hp2 NA19066.hp1 others(1): Show |
a0001a0002a0020 | a0001c0001a0002c0002a0020c0019 | a0001c0001t0001a0002c0002t0001a0020c0019t0001 | a0001c0001t0001g0168a0001c0001t0001g0275a0002c0002t0001g0071others(1): Show | 4 | 352 | 0.0114 | 19 | c.495 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(12): Show |
intron_variant | MODIFIER | HG00733.hp2 NA19065.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0114a0002c0002t0001g0130 | 2 | 352 | 0.0057 | 19 | c.495 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATATA others(12): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264 | 1 | 352 | 0.0028 | 19 | c.495 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(12): Show |
upstream_gene_variant | MODIFIER | HG01074.hp2 HG01952.hp2 HG02165.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0134others(4): Show | 7 | 309 | 0.0227 | 19 | c.-19 others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | ATAATAAT others(12): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 309 | 0.0032 | 19 | c.344 others(38): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655810 | G | GAGAGAGA others(12): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0038 | 1 | 108 | 0.0093 | 19 | c.181 others(38): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85685643 | A | AAAAGAAA others(12): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01884.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0017 | a0001c0001t0001g0001a0001c0008t0017g0057 | 2 | 108 | 0.0185 | 19 | c.181 others(38): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(6): Show | 9 | 108 | 0.0833 | 19 | c.268 others(38): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142810424 | G | GAGACATA others(12): Show |
intron_variant | MODIFIER | HG00609.hp1 NA19090.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0002 | a0001c0001t0001g0153a0001c0003t0002g0157 | 2 | 198 | 0.0101 | 19 | c.154 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(12): Show |
intron_variant | MODIFIER | HG00438.hp2 HG02080.hp2 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0005 | a0001c0003t0001g0180a0001c0003t0005g0057 | 2 | 198 | 0.0101 | 19 | c.487 others(36): 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(12): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0066 | 1 | 198 | 0.0051 | 19 | c.487 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949176 | A | AGAGAGAG others(12): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0144 | 1 | 198 | 0.0051 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949178 | A | AGAGAGAG others(12): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01192.hp2 |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0003 | a0001c0002t0002g0189a0001c0002t0003g0124 | 2 | 198 | 0.0101 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949182 | A | AGAGAGAG others(12): Show |
intron_variant | MODIFIER | HG01167.hp2 HG02109.hp2 HG02735.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001a0001c0002t0003others(3): Show | a0001c0001t0002g0142a0001c0002t0001g0185a0001c0002t0003g0025others(5): Show | 8 | 198 | 0.0404 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949186 | A | AGAGAGAG others(12): Show |
intron_variant | MODIFIER | NA18939.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0059 | 1 | 198 | 0.0051 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949192 | A | AGAGAGAG others(12): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0010 | 1 | 198 | 0.0051 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(12): Show |
intron_variant | MODIFIER | HG02258.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0026 | a0001c0001t0005g0101a0001c0001t0026g0071 | 2 | 198 | 0.0101 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(12): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0003 | 1 | 198 | 0.0051 | 19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841125 | C | CTCTCTCT others(12): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00735.hp1 HG01099.hp2 others(4): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0016 | a0001c0001t0001a0002c0002t0002a0002c0002t0010others(1): Show | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0202others(4): Show | 7 | 248 | 0.0282 | 19 | c.543 others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841203 | C | CTCTCTCT others(12): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0067 | 1 | 248 | 0.0040 | 19 | c.543 others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909301 | T | TTTTCTTT others(12): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0171 | 1 | 248 | 0.0040 | 19 | c.209 others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(12): Show |
intron_variant | MODIFIER | HG03491.hp2 HG03492.hp1 NA19083.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0004t0064 | a0001c0001t0006g0065a0001c0001t0006g0066a0001c0004t0064g0061 | 3 | 310 | 0.0097 | 19 | c.100 others(38): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129193668 | A | ATATAATA others(12): Show |
upstream_gene_variant | MODIFIER | HG03492.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0172 | 1 | 398 | 0.0025 | 19 | c.-14 others(30): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1344 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193726 | A | ATATAATA others(12): Show |
upstream_gene_variant | MODIFIER | HG00438.hp2 HG01346.hp2 HG01943.hp1 others(14): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0005others(2): Show | a0001c0001t0002g0158a0001c0001t0004g0157a0001c0001t0004g0159others(14): Show | 17 | 398 | 0.0427 | 19 | c.-15 others(30): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1402 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193726 | A | ATATATTA others(12): Show |
upstream_gene_variant | MODIFIER | HG02257.hp1 HG02723.hp2 HG03209.hp2 others(2): Show |
a0002 | a0002c0007a0002c0008a0002c0033 | a0002c0007t0001a0002c0008t0001a0002c0033t0001 | a0002c0007t0001g0391a0002c0008t0001g0150a0002c0008t0001g0151others(2): Show | 5 | 398 | 0.0126 | 19 | c.-15 others(30): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1402 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(12): Show |
upstream_gene_variant | MODIFIER | HG01081.hp1 HG01106.hp1 HG01192.hp2 others(7): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001a0001c0002t0001g0017a0001c0002t0001g0030others(1): Show | 10 | 420 | 0.0238 | 19 | c.-36 others(30): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47008573 | G | GTATTGTC others(12): Show |
downstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(23): Show | a0001c0001t0001g0171a0001c0001t0001g0205a0001c0001t0004g0022others(88): Show | 91 | 298 | 0.3054 | 19 | c.*78 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3497 | chr19 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100751277 | G | GTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 |
a0001a0002 | a0001c0010a0002c0006 | a0001c0010t0001a0002c0006t0011 | a0001c0010t0001g0238a0002c0006t0011g0239 | 2 | 286 | 0.0070 | 19 | c.155 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0030 | 1 | 286 | 0.0035 | 19 | c.313 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTCT others(12): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 286 | 0.0035 | 19 | c.245 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(12): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0002 | a0002c0006 | a0002c0006t0012 | a0002c0006t0012g0176 | 1 | 286 | 0.0035 | 19 | c.245 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(12): Show |
intron_variant | MODIFIER | NA18966.hp2 NA18992.hp2 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135a0001c0001t0001g0190a0001c0001t0001g0210 | 3 | 286 | 0.0105 | 19 | c.245 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0190 | 1 | 230 | 0.0044 | 19 | c.54- others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(12): Show |
intron_variant | MODIFIER | NA18968.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0128 | 1 | 230 | 0.0044 | 19 | c.582 others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(12): Show |
intron_variant | MODIFIER | HG00673.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0112a0001c0001t0002g0105a0001c0001t0002g0122others(9): Show | 12 | 230 | 0.0522 | 19 | c.176 others(38): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076481 | G | GTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0004 | a0004c0005 | a0004c0005t0008 | a0004c0005t0008g0180 | 1 | 418 | 0.0024 | 19 | c.118 others(38): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | C | CTTTTTTT others(12): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0009 | a0009c0023 | a0009c0023t0002 | a0009c0023t0002g0240 | 1 | 418 | 0.0024 | 19 | c.118 others(38): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1085510 | T | TCCATCTC others(12): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
a0001a0002a0003others(6): Show | a0001c0004a0002c0001a0002c0021others(13): Show | a0001c0004t0005a0001c0004t0016a0002c0001t0003others(22): Show | a0001c0004t0005g0020a0001c0004t0005g0209a0001c0004t0005g0227others(68): Show | 93 | 418 | 0.2225 | 19 | c.306 others(36): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11484504 | G | GAGAAAAA others(12): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(15): Show | 18 | 144 | 0.1250 | 19 | c.588 others(40): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | T | TATATATA others(12): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0005 | 1 | 144 | 0.0069 | 19 | c.588 others(40): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590865 | A | AGAAAAGA others(12): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0137 | 1 | 144 | 0.0069 | 19 | c.588 others(38): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44752531 | C | CGGGGCTG others(12): Show |
upstream_gene_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0012 | 1 | 390 | 0.0026 | 19 | c.-16 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 43 | chr22 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17693136 | T | TAGCCATC others(12): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0018 | a0002c0018t0002 | a0002c0018t0002g0155 | 1 | 168 | 0.0060 | 19 | c.318 others(38): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |