view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(27): Show |
30 | 104 | 0.2885 | 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 | 159 | 0.0063 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0038 |
2 | 154 | 0.0130 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0029 others(3): Show |
6 | 13 | 0.4615 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(1): Show |
4 | 174 | 0.0230 | 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 | 238 | 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 | a0001c0001t0001g0228 a0003c0003t0001g0202 |
2 | 276 | 0.0072 | 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 |
a0001a0002a0012 | a0001c0001a0002c0002a0012c0019 | a0001c0001t0001a0002c0002t0001a0012c0019t0001 | a0001c0001t0001g0169 a0001c0001t0001g0276 a0002c0002t0001g0071 others(1): Show |
4 | 143 | 0.0280 | 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 | a0002c0002t0001g0115 a0002c0002t0001g0131 |
2 | 141 | 0.0142 | 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 | a0001c0001t0001g0265 | 1 | 295 | 0.0034 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0136 others(4): Show |
7 | 134 | 0.0522 | 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 | a0001c0001t0001g0084 | 1 | 45 | 0.0222 | 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 | 98 | 0.0102 | 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 | a0001c0001t0001g0001 a0001c0008t0017g0058 |
2 | 97 | 0.0206 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(6): Show |
9 | 23 | 0.3913 | 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 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0153 a0001c0002t0002g0157 |
2 | 196 | 0.0102 | 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 | a0001c0002 | a0001c0002t0001a0001c0002t0005 | a0001c0002t0001g0180 a0001c0002t0005g0057 |
2 | 117 | 0.0171 | 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 | 116 | 0.0086 | 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 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0144 | 1 | 193 | 0.0052 | 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 | a0001c0003 | a0001c0003t0002a0001c0003t0003 | a0001c0003t0002g0189 a0001c0003t0003g0124 |
2 | 195 | 0.0103 | 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(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001a0001c0003t0003others(2): Show | a0001c0001t0002g0142 a0001c0003t0001g0185 a0001c0003t0003g0025 others(4): Show |
7 | 195 | 0.0359 | 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 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0059 | 1 | 194 | 0.0052 | 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 | a0001c0001t0018 | a0001c0001t0018g0010 | 1 | 193 | 0.0052 | 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 | a0001c0001t0005a0001c0001t0025 | a0001c0001t0005g0101 a0001c0001t0025g0071 |
2 | 77 | 0.0260 | 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 | a0001c0001t0030 | a0001c0001t0030g0003 | 1 | 100 | 0.0100 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0203 others(4): Show |
7 | 246 | 0.0285 | 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 | 160 | 0.0063 | 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 | 191 | 0.0052 | 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 | a0001c0001t0006a0001c0004t0063 | a0001c0001t0006g0066 a0001c0001t0006g0067 a0001c0004t0063g0062 |
3 | 10 | 0.3000 | 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 | 395 | 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(13): Show |
a0001a0011 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0005others(2): Show | a0001c0001t0002g0158 a0001c0001t0004g0157 a0001c0001t0004g0159 others(13): Show |
16 | 380 | 0.0421 | 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 | a0002c0007t0001g0391 a0002c0008t0001g0150 a0002c0008t0001g0151 others(2): Show |
5 | 369 | 0.0136 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0017 a0001c0002t0001g0030 others(1): Show |
10 | 11 | 0.9091 | 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(87): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | a0001c0001t0001g0077 a0001c0001t0001g0171 a0001c0001t0001g0205 others(87): Show |
90 | 296 | 0.3041 | 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 | a0001c0010t0001g0238 a0002c0006t0011g0239 |
2 | 268 | 0.0075 | 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 | 34 | 0.0294 | 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 | a0001c0001t0001g0080 | 1 | 24 | 0.0417 | 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 | a0001c0001t0001g0139 a0001c0001t0001g0191 a0001c0001t0001g0202 |
3 | 26 | 0.1154 | 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 | a0001c0003t0001g0182 | 1 | 109 | 0.0092 | 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 | a0001c0003t0001g0135 | 1 | 40 | 0.0250 | 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 | a0001c0001t0001g0113 a0001c0001t0002g0107 a0001c0001t0002g0114 others(9): Show |
12 | 142 | 0.0845 | 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 | a0004c0005t0008g0159 | 1 | 408 | 0.0025 | 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 | a0009c0023t0002g0208 | 1 | 123 | 0.0081 | 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(89): Show |
a0001a0002a0003others(5): Show | a0001c0004a0002c0001a0002c0021others(12): Show | a0001c0004t0005a0001c0004t0016a0002c0001t0003others(21): Show | a0001c0004t0005g0015 a0001c0004t0005g0044 a0001c0004t0005g0183 others(57): Show |
92 | 412 | 0.2233 | 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 | a0001c0001a0001c0006a0002c0002 | a0001c0001t0001a0001c0006t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0027 others(15): Show |
18 | 142 | 0.1268 | 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 | a0002c0002t0003g0009 | 1 | 29 | 0.0345 | 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 | 128 | 0.0078 | 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 | 382 | 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 | 166 | 0.0060 | 19 | c.318 others(38): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1824952 | T | TCCCCGCA others(12): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(26): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0004a0001c0009others(19): Show | a0001c0003t0001a0001c0003t0009a0001c0004t0004others(23): Show | a0001c0003t0001g0284 a0001c0003t0009g0282 a0001c0004t0004g0296 others(26): Show |
29 | 220 | 0.1318 | 19 | c.-48 others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |