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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143606052 | AAAAAAAA others(12): Show |
A | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG06807.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0121 |
3 | 160 | 0.0188 | -19 | c.100 others(40): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | chr2 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | NA18986.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 | 1 | 12 | 0.0833 | -19 | c.113 others(40): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24982982 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | 220 | 0.0409 | -19 | c.54- others(34): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982984 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 1 | 235 | 0.0043 | -19 | c.54- others(34): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24982986 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 1 | 220 | 0.0045 | -19 | c.54- others(34): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP1_chr11_46672080_46705619 | 46703278 | TTCCCCAC others(12): Show |
T | upstream_gene_variant | MODIFIER | NA19057.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 342 | 0.0029 | -19 | c.-27 others(30): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 2660 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110600700 | ATAACAGT others(12): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0021 | a0001c0001t0001a0001c0001t0003a0001c0002t0005others(1): Show | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | 224 | 0.0446 | -19 | c.964 others(36): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628972 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02129.hp2 NA18747.hp1 NA19011.hp2 others(1): Show |
a0006a0020 | a0006c0007a0020c0028 | a0006c0007t0006a0006c0007t0015a0020c0028t0006 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0015g0289 others(1): Show |
4 | 350 | 0.0114 | -19 | c.495 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628974 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | NA18989.hp1 | a0006 | a0006c0029 | a0006c0029t0006 | a0006c0029t0006g0291 | 1 | 349 | 0.0029 | -19 | c.495 others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24629043 | TGGAGTGC others(12): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(6): Show |
9 | 350 | 0.0257 | -19 | c.495 others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | NA18964.hp2 NA19074.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0336 a0001c0001t0002g0337 |
2 | 4 | 0.5000 | -19 | c.64- others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(12): Show |
C | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0027 | a0001c0027t0005 | a0001c0027t0005g0155 | 1 | 14 | 0.0714 | -19 | c.344 others(38): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | HG02486.hp1 HG02630.hp2 |
a0001 | a0001c0007 | a0001c0007t0003a0001c0007t0004 | a0001c0007t0003g0043 a0001c0007t0004g0057 |
2 | 8 | 0.2500 | -19 | c.268 others(38): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85965572 | CTCCCTCC others(12): Show |
C | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0008 | a0001c0008t0014 | a0001c0008t0014g0065 | 1 | 108 | 0.0093 | -19 | c.600 others(36): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAAA others(12): Show |
G | intron_variant | MODIFIER | HG03139.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0049 | a0001c0001t0002g0117 a0001c0001t0049g0047 |
2 | 4 | 0.5000 | -19 | c.154 others(38): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142876571 | TTCAAGAC others(12): Show |
T | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0131 others(33): Show |
36 | 196 | 0.1837 | -19 | c.312 others(36): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142890146 | AAAAAAAT others(12): Show |
A | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0024 | 1 | 193 | 0.0052 | -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 | 142890148 | AAAAATAT others(12): Show |
A | intron_variant | MODIFIER | HG01071.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0011 | 1 | 192 | 0.0052 | -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 | 142948958 | AGCCAGGC others(12): Show |
A | intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0172 | 1 | 196 | 0.0051 | -19 | c.110 others(40): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45431246 | CAGGGATG others(12): Show |
C | intron_variant | MODIFIER | HG03710.hp2 | a0004 | a0004c0004 | a0004c0004t0014 | a0004c0004t0014g0167 | 1 | 346 | 0.0029 | -19 | c.-19 others(34): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | ATTTTTTT others(12): Show |
A | intron_variant | MODIFIER | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(2): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0006c0008others(1): Show | a0001c0001t0001a0001c0001t0006a0002c0002t0002others(2): Show | a0001c0001t0001g0161 a0001c0001t0006g0164 a0002c0002t0002g0163 others(2): Show |
5 | 17 | 0.2941 | -19 | c.123 others(38): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841167 | CCTCTCTC others(12): Show |
C | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0005 | 1 | 243 | 0.0041 | -19 | c.543 others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064777 | GAAAAAGA others(12): Show |
G | intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0197 | 1 | 372 | 0.0027 | -19 | c.97+ others(34): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144604010 | GCGAACAA others(12): Show |
G | intron_variant | MODIFIER | NA19009.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 244 | 0.0041 | -19 | c.80+ others(34): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100699496 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG01123.hp1 HG02965.hp2 NA18906.hp1 |
a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0035 a0002c0002t0009g0036 a0002c0002t0009g0037 |
3 | 281 | 0.0107 | -19 | c.154 others(38): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | NA19072.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021 | 1 | 14 | 0.0714 | -19 | c.251 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921229 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG01109.hp2 HG02572.hp1 HG02622.hp1 |
a0002 | a0002c0006 | a0002c0006t0011 | a0002c0006t0011g0239 a0002c0006t0011g0241 a0002c0006t0011g0242 |
3 | 249 | 0.0120 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921231 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02615.hp1 HG03239.hp2 |
a0002 | a0002c0002a0002c0004 | a0002c0002t0009a0002c0004t0007 | a0002c0002t0009g0042 a0002c0004t0007g0085 |
2 | 239 | 0.0084 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG03130.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0034 a0002c0002t0002g0251 |
2 | 271 | 0.0074 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921237 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02145.hp2 HG03688.hp2 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0003a0002c0002t0021 | a0001c0003t0003g0214 a0002c0002t0021g0144 |
2 | 269 | 0.0074 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02300.hp1 NA18989.hp1 |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0033 | a0001c0003t0003g0107 a0001c0003t0033g0284 |
2 | 267 | 0.0075 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(12): Show |
A | intron_variant | MODIFIER | HG02523.hp2 NA18943.hp2 |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0153 a0001c0003t0003g0257 |
2 | 275 | 0.0073 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(12): Show |
A | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0283 | 1 | 278 | 0.0036 | -19 | c.487 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802946 | TATATATA others(12): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG02280.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0040 a0001c0001t0008g0041 a0001c0001t0008g0042 |
3 | 224 | 0.0134 | -19 | c.53+ others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802948 | TATATATA others(12): Show |
T | intron_variant | MODIFIER | HG00738.hp1 HG01106.hp2 HG02698.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0017 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0017g0043 |
3 | 214 | 0.0140 | -19 | c.53+ others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802950 | TATATATA others(12): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG02258.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0009 | a0001c0001t0002g0167 a0001c0001t0006g0168 a0001c0001t0009g0151 |
3 | 217 | 0.0138 | -19 | c.53+ others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12802951 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02809.hp2 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | 228 | 0.0088 | -19 | c.53+ others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802953 | ATATATAT others(12): Show |
A | intron_variant | MODIFIER | HG02109.hp2 HG02809.hp1 NA19043.hp1 |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0009a0001c0003t0001a0001c0005t0032 | a0001c0001t0009g0183 a0001c0003t0001g0182 a0001c0005t0032g0184 |
3 | 228 | 0.0132 | -19 | c.53+ others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12880669 | CACTAGTG others(12): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
a0001a0005a0006 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(96): Show |
99 | 228 | 0.4342 | -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 | 12903125 | AGGAGAGA others(12): Show |
A | intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0005 | a0001c0005t0005 | a0001c0005t0005g0088 | 1 | 131 | 0.0076 | -19 | c.199 others(36): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1085510 | TCCATCTC others(12): Show |
T | intron_variant | MODIFIER | HG02559.hp2 HG02818.hp2 HG03471.hp1 others(1): Show |
a0001a0004a0015 | a0001c0004a0004c0005a0004c0048others(1): Show | a0001c0004t0006a0004c0005t0008a0004c0048t0021others(1): Show | a0001c0004t0006g0209 a0004c0005t0008g0162 a0004c0048t0021g0158 others(1): Show |
4 | 324 | 0.0123 | -19 | c.306 others(36): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
a0003 | a0003c0003 | a0003c0003t0001a0003c0003t0019 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | 25 | 0.1200 | -19 | c.418 others(36): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590850 | AGAAAAGA others(12): Show |
A | intron_variant | MODIFIER | HG02083.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 | 1 | 141 | 0.0071 | -19 | c.588 others(38): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(12): Show |
C | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0142 | 1 | 5 | 0.2000 | -19 | c.588 others(36): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44756088 | TGAAGGCC others(12): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0004a0001c0007others(50): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(63): Show | a0001c0001t0001g0024 a0001c0001t0001g0192 a0001c0001t0001g0200 others(190): Show |
193 | 388 | 0.4974 | -19 | c.-72 others(36): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44839384 | ATGCAGAA others(12): Show |
A | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
a0001a0002a0007others(3): Show | a0001c0007a0002c0011a0002c0019others(6): Show | a0001c0007t0001a0002c0011t0005a0002c0019t0008others(6): Show | a0001c0007t0001g0202 a0001c0007t0001g0324 a0002c0011t0005g0319 others(9): Show |
12 | 388 | 0.0309 | -19 | c.597 others(36): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17556279 | GGGGCCTG others(12): Show |
G | intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 151 | 0.0066 | -19 | c.-44 others(38): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1845908 | GCTGGGGC others(12): Show |
G | intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0002 | a0001c0002t0020 | a0001c0002t0020g0264 | 1 | 362 | 0.0028 | -19 | c.37+ others(34): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1919249 | GGAGCTGT others(12): Show |
G | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0003 | a0001c0003t0058 | a0001c0003t0058g0338 | 1 | 362 | 0.0028 | -19 | c.214 others(38): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1919739 | GGTGATAA others(12): Show |
G | intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0140 | a0001c0140t0004 | a0001c0140t0004g0294 | 1 | 362 | 0.0028 | -19 | c.214 others(38): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |