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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP21_chr10_24578614_24728887 | 24584440 | C | G | missense_variant | MODERATE | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
a0002a0003a0004others(8): Show | a0002c0002a0002c0015a0002c0017others(13): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(18): Show | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(179): Show | 182 | 352 | 0.5171 | 0 | c.584 others(4): Show |
p.Ser others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24584440 | C | T | missense_variant | MODERATE | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(2): Show |
a0006 | a0006c0006 | a0006c0006t0002a0006c0006t0003 | a0006c0006t0002g0348a0006c0006t0002g0349a0006c0006t0002g0350others(2): Show | 5 | 352 | 0.0142 | 0 | c.584 others(4): Show |
p.Ser others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24584635 | G | A | missense_variant | MODERATE | HG02523.hp1 | a0018 | a0018c0013 | a0018c0013t0002 | a0018c0013t0002g0314 | 1 | 352 | 0.0028 | 0 | c.565 others(4): Show |
p.Thr others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6360/7381 | 5654/5877 | 1885/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24584959 | G | A | missense_variant | MODERATE | HG00642.hp2 | a0020 | a0020c0019 | a0020c0019t0001 | a0020c0019t0001g0066 | 1 | 352 | 0.0028 | 0 | c.533 others(4): Show |
p.Ala others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6036/7381 | 5330/5877 | 1777/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24585182 | G | A | missense_variant | MODERATE | HG01261.hp2 | a0019 | a0019c0020 | a0019c0020t0001 | a0019c0020t0001g0112 | 1 | 352 | 0.0028 | 0 | c.510 others(4): Show |
p.Leu others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5813/7381 | 5107/5877 | 1703/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24585335 | T | C | missense_variant | MODERATE | NA18989.hp1 | a0017 | a0017c0029 | a0017c0029t0006 | a0017c0029t0006g0290 | 1 | 352 | 0.0028 | 0 | c.495 others(4): Show |
p.Arg others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5660/7381 | 4954/5877 | 1652/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24596856 | C | T | missense_variant | MODERATE | HG02145.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
a0004a0014 | a0004c0004a0014c0024 | a0004c0004t0001a0014c0024t0011 | a0004c0004t0001g0031a0004c0004t0001g0032a0004c0004t0001g0067others(7): Show | 10 | 352 | 0.0284 | 0 | c.336 others(4): Show |
p.Gly others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/26 | 4067/7381 | 3361/5877 | 1121/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24600731 | C | G | missense_variant | MODERATE | HG02818.hp2 HG03486.hp2 |
a0011 | a0011c0011 | a0011c0011t0001 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | 352 | 0.0057 | 0 | c.304 others(4): Show |
p.Cys others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/26 | 3753/7381 | 3047/5877 | 1016/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24619599 | C | T | missense_variant | MODERATE | HG01433.hp1 homoSapiens_chm13v2.hp1 |
a0021a0023 | a0021c0016a0023c0025 | a0021c0016t0003a0023c0025t0003 | a0021c0016t0003g0028a0023c0025t0003g0029 | 2 | 352 | 0.0057 | 0 | c.229 others(4): Show |
p.Gly others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 3002/7381 | 2296/5877 | 766/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24619757 | T | C | missense_variant | MODERATE | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
a0002a0004a0005others(8): Show | a0002c0002a0002c0015a0002c0017others(13): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(18): Show | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | 352 | 0.4318 | 0 | c.213 others(4): Show |
p.Asn others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2844/7381 | 2138/5877 | 713/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24619844 | G | C | missense_variant | MODERATE | HG02723.hp1 HG02896.hp1 |
a0010 | a0010c0012 | a0010c0012t0010 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | 352 | 0.0057 | 0 | c.205 others(4): Show |
p.Ser others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2757/7381 | 2051/5877 | 684/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620069 | C | T | missense_variant | MODERATE | NA18941.hp2 NA18974.hp2 NA19066.hp2 |
a0009 | a0009c0008 | a0009c0008t0001a0009c0008t0004 | a0009c0008t0001g0261a0009c0008t0001g0262a0009c0008t0004g0347 | 3 | 352 | 0.0085 | 0 | c.182 others(4): Show |
p.Arg others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2532/7381 | 1826/5877 | 609/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620159 | G | T | missense_variant | MODERATE | NA19011.hp2 | a0022 | a0022c0028 | a0022c0028t0006 | a0022c0028t0006g0289 | 1 | 352 | 0.0028 | 0 | c.173 others(4): Show |
p.Ser others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2442/7381 | 1736/5877 | 579/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620286 | T | C | missense_variant | MODERATE | HG01109.hp1 | a0016 | a0016c0022 | a0016c0022t0002 | a0016c0022t0002g0339 | 1 | 352 | 0.0028 | 0 | c.160 others(4): Show |
p.Arg others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2315/7381 | 1609/5877 | 537/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620421 | T | C | missense_variant | MODERATE | HG02738.hp2 | a0015 | a0015c0023 | a0015c0023t0001 | a0015c0023t0001g0090 | 1 | 352 | 0.0028 | 0 | c.147 others(4): Show |
p.Arg others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2180/7381 | 1474/5877 | 492/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620630 | G | A | missense_variant | MODERATE | NA19030.hp2 | a0014 | a0014c0024 | a0014c0024t0011 | a0014c0024t0011g0033 | 1 | 352 | 0.0028 | 0 | c.126 others(4): Show |
p.Thr others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1971/7381 | 1265/5877 | 422/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620679 | G | A | missense_variant | MODERATE | homoSapiens_chm13v2.hp1 | a0023 | a0023c0025 | a0023c0025t0003 | a0023c0025t0003g0029 | 1 | 352 | 0.0028 | 0 | c.121 others(4): Show |
p.Arg others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1922/7381 | 1216/5877 | 406/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620709 | T | C | missense_variant | MODERATE | HG01081.hp1 | a0024 | a0024c0026 | a0024c0026t0003 | a0024c0026t0003g0156 | 1 | 352 | 0.0028 | 0 | c.118 others(4): Show |
p.Ile others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1892/7381 | 1186/5877 | 396/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24620916 | T | C | missense_variant | MODERATE | HG02647.hp2 | a0013 | a0013c0027 | a0013c0027t0001 | a0013c0027t0001g0065 | 1 | 352 | 0.0028 | 0 | c.979 others(3): Show |
p.Thr others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1685/7381 | 979/5877 | 327/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24621258 | C | T | missense_variant | MODERATE | HG02109.hp1 HG03195.hp1 |
a0012 | a0012c0010 | a0012c0010t0001 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | 352 | 0.0057 | 0 | c.637 others(3): Show |
p.Ala others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1343/7381 | 637/5877 | 213/1958 | chr10 | TogoVar | ||
ARHGAP21_chr10_24578614_24728887 | 24670388 | T | C | missense_variant | MODERATE | NA18995.hp2 NA19004.hp1 NA19011.hp1 |
a0008 | a0008c0009 | a0008c0009t0005 | a0008c0009t0005g0002a0008c0009t0005g0003a0008c0009t0005g0004 | 3 | 352 | 0.0085 | 0 | c.73A others(2): Show |
p.Asn others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/26 | 779/7381 | 73/5877 | 25/1958 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450405 | G | A | missense_variant | MODERATE | HG02698.hp1 HG03491.hp2 |
a0005 | a0005c0009 | a0005c0009t0001 | a0005c0009t0001g0056a0005c0009t0001g0140 | 2 | 270 | 0.0074 | 0 | c.172 others(4): Show |
p.Ala others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 2001/2729 | 1724/2097 | 575/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450540 | G | C | missense_variant | MODERATE | HG02056.hp1 | a0010 | a0010c0017 | a0010c0017t0002 | a0010c0017t0002g0052 | 1 | 270 | 0.0037 | 0 | c.158 others(4): Show |
p.Thr others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1866/2729 | 1589/2097 | 530/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450636 | G | A | missense_variant | MODERATE | HG02896.hp2 HG02897.hp1 |
a0004 | a0004c0008 | a0004c0008t0001 | a0004c0008t0001g0012a0004c0008t0001g0013 | 2 | 270 | 0.0074 | 0 | c.149 others(4): Show |
p.Pro others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1770/2729 | 1493/2097 | 498/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450675 | G | C | missense_variant | MODERATE | HG02976.hp2 | a0009 | a0009c0019 | a0009c0019t0003 | a0009c0019t0003g0244 | 1 | 270 | 0.0037 | 0 | c.145 others(4): Show |
p.Ser others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1731/2729 | 1454/2097 | 485/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450799 | C | A | missense_variant | MODERATE | HG02486.hp1 | a0011 | a0011c0020 | a0011c0020t0010 | a0011c0020t0010g0262 | 1 | 270 | 0.0037 | 0 | c.133 others(4): Show |
p.Gly others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1607/2729 | 1330/2097 | 444/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450900 | G | T | missense_variant | MODERATE | HG01361.hp2 HG02717.hp2 HG03579.hp1 others(1): Show |
a0003 | a0003c0007a0003c0012 | a0003c0007t0001a0003c0007t0003a0003c0007t0008others(1): Show | a0003c0007t0001g0010a0003c0007t0003g0225a0003c0007t0008g0243others(1): Show | 4 | 270 | 0.0148 | 0 | c.122 others(4): Show |
p.Thr others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1506/2729 | 1229/2097 | 410/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48450963 | G | A | missense_variant | MODERATE | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(2): Show |
a0002 | a0002c0006 | a0002c0006t0002 | a0002c0006t0002g0001a0002c0006t0002g0024a0002c0006t0002g0118others(1): Show | 5 | 270 | 0.0185 | 0 | c.116 others(4): Show |
p.Pro others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1443/2729 | 1166/2097 | 389/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48451080 | G | A | missense_variant | MODERATE | HG02258.hp2 | a0008 | a0008c0014 | a0008c0014t0009 | a0008c0014t0009g0162 | 1 | 270 | 0.0037 | 0 | c.104 others(4): Show |
p.Thr others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/10 | 1326/2729 | 1049/2097 | 350/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48453307 | C | T | missense_variant | MODERATE | HG02071.hp1 | a0012 | a0012c0015 | a0012c0015t0005 | a0012c0015t0005g0245 | 1 | 270 | 0.0037 | 0 | c.985 others(3): Show |
p.Glu others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 8/10 | 1262/2729 | 985/2097 | 329/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48459876 | C | T | missense_variant | MODERATE | HG02886.hp2 | a0007 | a0007c0011 | a0007c0011t0004 | a0007c0011t0004g0172 | 1 | 270 | 0.0037 | 0 | c.467 others(3): Show |
p.Arg others(6): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 5/10 | 744/2729 | 467/2097 | 156/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48583062 | C | T | missense_variant | MODERATE | HG03831.hp1 | a0006 | a0006c0010 | a0006c0010t0002 | a0006c0010t0002g0026 | 1 | 270 | 0.0037 | 0 | c.125 others(3): Show |
p.Gly others(5): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/10 | 402/2729 | 125/2097 | 42/698 | chr10 | TogoVar | ||
ARHGAP22_chr10_48441036_48610073 | 48583065 | G | A | missense_variant | MODERATE | NA18979.hp1 | a0013 | a0013c0021 | a0013c0021t0002 | a0013c0021t0002g0045 | 1 | 270 | 0.0037 | 0 | c.122 others(3): Show |
p.Ala others(5): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/10 | 399/2729 | 122/2097 | 41/698 | chr10 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38458241 | C | T | missense_variant | MODERATE | HG01099.hp2 | a0010 | a0010c0059 | a0010c0059t0001 | a0010c0059t0001g0021 | 1 | 309 | 0.0032 | 0 | c.203 others(3): Show |
p.Ser others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/24 | 225/5911 | 203/4476 | 68/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38462857 | C | T | missense_variant | MODERATE | HG03688.hp1 | a0019 | a0019c0058 | a0019c0058t0002 | a0019c0058t0002g0202 | 1 | 309 | 0.0032 | 0 | c.265 others(3): Show |
p.Arg others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 287/5911 | 265/4476 | 89/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38462864 | G | A | missense_variant | MODERATE | HG04199.hp1 | a0011 | a0011c0030 | a0011c0030t0001 | a0011c0030t0001g0167 | 1 | 309 | 0.0032 | 0 | c.272 others(3): Show |
p.Arg others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 294/5911 | 272/4476 | 91/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38466282 | G | A | missense_variant | MODERATE | HG02630.hp2 | a0012 | a0012c0034 | a0012c0034t0001 | a0012c0034t0001g0037 | 1 | 309 | 0.0032 | 0 | c.599 others(3): Show |
p.Arg others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 621/5911 | 599/4476 | 200/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38466480 | C | T | missense_variant | MODERATE | HG02145.hp1 HG02280.hp2 |
a0006 | a0006c0021 | a0006c0021t0003 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | 309 | 0.0065 | 0 | c.797 others(3): Show |
p.Thr others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 819/5911 | 797/4476 | 266/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38466804 | G | T | missense_variant | MODERATE | NA18940.hp1 NA18940.hp2 |
a0007 | a0007c0029 | a0007c0029t0001 | a0007c0029t0001g0181a0007c0029t0001g0289 | 2 | 309 | 0.0065 | 0 | c.112 others(4): Show |
p.Arg others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1143/5911 | 1121/4476 | 374/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38466879 | G | A | missense_variant | MODERATE | HG02135.hp1 | a0013 | a0013c0044 | a0013c0044t0001 | a0013c0044t0001g0192 | 1 | 309 | 0.0032 | 0 | c.119 others(4): Show |
p.Gly others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1218/5911 | 1196/4476 | 399/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38466942 | G | A | missense_variant | MODERATE | HG00733.hp2 | a0014 | a0014c0046 | a0014c0046t0003 | a0014c0046t0003g0027 | 1 | 309 | 0.0032 | 0 | c.125 others(4): Show |
p.Arg others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1281/5911 | 1259/4476 | 420/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38467128 | C | T | missense_variant | MODERATE | HG02145.hp1 HG02280.hp2 |
a0006 | a0006c0021 | a0006c0021t0003 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | 309 | 0.0065 | 0 | c.144 others(4): Show |
p.Ala others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1467/5911 | 1445/4476 | 482/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38467266 | G | A | missense_variant | MODERATE | HG01255.hp2 | a0015 | a0015c0039 | a0015c0039t0001 | a0015c0039t0001g0186 | 1 | 309 | 0.0032 | 0 | c.158 others(4): Show |
p.Arg others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1605/5911 | 1583/4476 | 528/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38471937 | T | G | missense_variant | MODERATE | HG01891.hp2 | a0018 | a0018c0047 | a0018c0047t0001 | a0018c0047t0001g0016 | 1 | 309 | 0.0032 | 0 | c.204 others(4): Show |
p.Asp others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/24 | 2071/5911 | 2049/4476 | 683/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38477679 | C | T | missense_variant | MODERATE | HG02165.hp2 | a0017 | a0017c0057 | a0017c0057t0001 | a0017c0057t0001g0282 | 1 | 309 | 0.0032 | 0 | c.221 others(4): Show |
p.Ala others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2241/5911 | 2219/4476 | 740/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38477718 | C | T | missense_variant | MODERATE | HG02109.hp2 | a0016 | a0016c0056 | a0016c0056t0001 | a0016c0056t0001g0011 | 1 | 309 | 0.0032 | 0 | c.225 others(4): Show |
p.Ala others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2280/5911 | 2258/4476 | 753/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38491417 | G | A | missense_variant | MODERATE | HG02109.hp1 NA18963.hp1 |
a0008 | a0008c0049a0008c0050 | a0008c0049t0001a0008c0050t0003 | a0008c0049t0001g0266a0008c0050t0003g0136 | 2 | 309 | 0.0065 | 0 | c.316 others(4): Show |
p.Arg others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/24 | 3183/5911 | 3161/4476 | 1054/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38510370 | G | C | missense_variant | MODERATE | HG02280.hp1 HG06807.hp2 NA19030.hp2 |
a0005 | a0005c0033a0005c0041a0005c0053 | a0005c0033t0001a0005c0041t0001a0005c0053t0001 | a0005c0033t0001g0073a0005c0041t0001g0030a0005c0053t0001g0126 | 3 | 309 | 0.0097 | 0 | c.387 others(4): Show |
p.Ala others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3896/5911 | 3874/4476 | 1292/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38510613 | C | T | missense_variant | MODERATE | NA18970.hp1 NA19065.hp1 |
a0009 | a0009c0026 | a0009c0026t0001 | a0009c0026t0001g0097a0009c0026t0001g0284 | 2 | 309 | 0.0065 | 0 | c.411 others(4): Show |
p.Arg others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4139/5911 | 4117/4476 | 1373/1491 | chr17 | TogoVar | ||
ARHGAP23_chr17_38423464_38517385 | 38510616 | C | G | missense_variant | MODERATE | HG01884.hp2 HG02145.hp2 HG02895.hp2 others(5): Show |
a0003 | a0003c0013a0003c0014a0003c0028others(1): Show | a0003c0013t0001a0003c0014t0001a0003c0028t0001others(1): Show | a0003c0013t0001g0127a0003c0013t0001g0128a0003c0013t0001g0130others(5): Show | 8 | 309 | 0.0259 | 0 | c.412 others(4): Show |
p.Leu others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4142/5911 | 4120/4476 | 1374/1491 | chr17 | TogoVar |