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 | 148023345 | C | T | missense_variant | MODERATE | NA18906.hp1 | a0004 | a0004c0010 | a0004c0010t0001 | a0004c0010t0001g0048 | 1 | 106 | 0.0094 | 0 | c.179 others(4): Show |
p.Ser others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2013/3270 | 1799/2361 | 600/786 | chr4 | TogoVar | ||
ARHGAP10_chr4_147727088_148077776 | 148023409 | A | C | missense_variant | MODERATE | NA18906.hp1 | a0004 | a0004c0010 | a0004c0010t0001 | a0004c0010t0001g0048 | 1 | 106 | 0.0094 | 0 | c.186 others(4): Show |
p.Glu others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2077/3270 | 1863/2361 | 621/786 | chr4 | TogoVar | ||
ARHGAP10_chr4_147727088_148077776 | 148063170 | A | G | missense_variant | MODERATE | HG01169.hp2 HG02165.hp1 HG03225.hp1 others(2): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0009a0002c0003t0001g0032a0002c0003t0001g0064others(2): Show | 5 | 106 | 0.0472 | 0 | c.205 others(4): Show |
p.Met others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/23 | 2264/3270 | 2050/2361 | 684/786 | chr4 | TogoVar | ||
ARHGAP10_chr4_147727088_148077776 | 148063227 | A | G | missense_variant | MODERATE | HG01891.hp2 HG03041.hp1 |
a0003 | a0003c0007 | a0003c0007t0001 | a0003c0007t0001g0079a0003c0007t0001g0082 | 2 | 106 | 0.0189 | 0 | c.210 others(4): Show |
p.Thr others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/23 | 2321/3270 | 2107/2361 | 703/786 | chr4 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32616234 | G | A | missense_variant | MODERATE | HG02451.hp2 | a0004 | a0004c0007 | a0004c0007t0001 | a0004c0007t0001g0195 | 1 | 335 | 0.0030 | 0 | c.23G others(2): Show |
p.Arg others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 731/5876 | 23/3072 | 8/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32629642 | A | G | missense_variant | MODERATE | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
a0002 | a0002c0005 | a0002c0005t0002 | a0002c0005t0002g0019 | 3 | 335 | 0.0090 | 0 | c.985 others(3): Show |
p.Thr others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/12 | 1693/5876 | 985/3072 | 329/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32636270 | C | G | missense_variant | MODERATE | HG00558.hp1 | a0008 | a0008c0013 | a0008c0013t0001 | a0008c0013t0001g0013 | 1 | 335 | 0.0030 | 0 | c.149 others(4): Show |
p.Ile others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2205/5876 | 1497/3072 | 499/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32636434 | T | C | missense_variant | MODERATE | HG02486.hp1 | a0007 | a0007c0009 | a0007c0009t0005 | a0007c0009t0005g0047 | 1 | 335 | 0.0030 | 0 | c.166 others(4): Show |
p.Ile others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2369/5876 | 1661/3072 | 554/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32636785 | A | G | missense_variant | MODERATE | HG02602.hp2 | a0006 | a0006c0011 | a0006c0011t0003 | a0006c0011t0003g0023 | 1 | 335 | 0.0030 | 0 | c.201 others(4): Show |
p.Glu others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2720/5876 | 2012/3072 | 671/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32637423 | A | G | missense_variant | MODERATE | HG00099.hp2 HG01516.hp1 HG06807.hp2 |
a0003 | a0003c0004 | a0003c0004t0007a0003c0004t0012 | a0003c0004t0007g0033a0003c0004t0007g0143a0003c0004t0012g0033 | 3 | 335 | 0.0090 | 0 | c.265 others(4): Show |
p.Ile others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3358/5876 | 2650/3072 | 884/1023 | chr15 | TogoVar | ||
ARHGAP11A_chr15_32610504_32644941 | 32637690 | C | G | missense_variant | MODERATE | HG01978.hp1 | a0005 | a0005c0010 | a0005c0010t0001 | a0005c0010t0001g0054 | 1 | 335 | 0.0030 | 0 | c.291 others(4): Show |
p.Pro others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3625/5876 | 2917/3072 | 973/1023 | chr15 | TogoVar | ||
ARHGAP11B_chr15_30621128_30643810 | 30626947 | G | C | missense_variant others(1): Show |
MODERATE | HG01081.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0009a0002c0002t0001g0058a0002c0002t0001g0083others(1): Show | 7 | 247 | 0.0283 | 0 | c.127 others(3): Show |
p.Gly others(5): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 820/1565 | 127/804 | 43/267 | chr15 | TogoVar | ||
ARHGAP11B_chr15_30621128_30643810 | 30633523 | A | C | missense_variant | MODERATE | HG01952.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0004 | 1 | 247 | 0.0041 | 0 | c.234 others(3): Show |
p.Glu others(5): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/7 | 927/1565 | 234/804 | 78/267 | chr15 | TogoVar | ||
ARHGAP11B_chr15_30621128_30643810 | 30635148 | G | A | missense_variant | MODERATE | HG00673.hp2 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0018 | 1 | 247 | 0.0041 | 0 | c.620 others(3): Show |
p.Ser others(6): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/7 | 1313/1565 | 620/804 | 207/267 | chr15 | TogoVar | ||
ARHGAP11B_chr15_30621128_30643810 | 30635624 | C | A | missense_variant | MODERATE | HG04204.hp1 | a0005 | a0005c0004 | a0005c0004t0001 | a0005c0004t0001g0007 | 1 | 247 | 0.0041 | 0 | c.798 others(3): Show |
p.Asn others(6): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/7 | 1491/1565 | 798/804 | 266/267 | chr15 | TogoVar | ||
ARHGAP12_chr10_31800398_31933831 | 31812781 | G | T | missense_variant | MODERATE | NA18960.hp1 | a0004 | a0004c0012 | a0004c0012t0003 | a0004c0012t0003g0192 | 1 | 322 | 0.0031 | 0 | c.187 others(4): Show |
p.Thr others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/20 | 2136/5060 | 1877/2541 | 626/846 | chr10 | TogoVar | ||
ARHGAP12_chr10_31800398_31933831 | 31839649 | C | A | missense_variant | MODERATE | HG01109.hp2 HG03130.hp1 NA18906.hp1 |
a0003 | a0003c0004 | a0003c0004t0007 | a0003c0004t0007g0309a0003c0004t0007g0310a0003c0004t0007g0311 | 3 | 322 | 0.0093 | 0 | c.135 others(4): Show |
p.Lys others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 8/20 | 1618/5060 | 1359/2541 | 453/846 | chr10 | TogoVar | ||
ARHGAP12_chr10_31800398_31933831 | 31839683 | A | G | missense_variant | MODERATE | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
a0002a0003 | a0002c0002a0003c0004 | a0002c0002t0002a0002c0002t0007a0002c0002t0014others(8): Show | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(79): Show | 82 | 322 | 0.2547 | 0 | c.132 others(4): Show |
p.Phe others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 8/20 | 1584/5060 | 1325/2541 | 442/846 | chr10 | TogoVar | ||
ARHGAP12_chr10_31800398_31933831 | 31908252 | C | T | missense_variant | MODERATE | HG01978.hp1 | a0005 | a0005c0009 | a0005c0009t0012 | a0005c0009t0012g0179 | 1 | 322 | 0.0031 | 0 | c.604 others(3): Show |
p.Ala others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | 863/5060 | 604/2541 | 202/846 | chr10 | TogoVar | ||
ARHGAP15_chr2_143124419_143773352 | 143202165 | A | G | missense_variant | MODERATE | NA18948.hp1 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0085 | 1 | 162 | 0.0062 | 0 | c.197 others(3): Show |
p.His others(5): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/14 | 259/1670 | 197/1428 | 66/475 | chr2 | TogoVar | ||
ARHGAP15_chr2_143124419_143773352 | 143435691 | G | C | missense_variant | MODERATE | HG01243.hp1 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0060 | 1 | 162 | 0.0062 | 0 | c.565 others(3): Show |
p.Asp others(6): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 7/14 | 627/1670 | 565/1428 | 189/475 | chr2 | TogoVar | ||
ARHGAP17_chr16_24914389_25020369 | 24939403 | G | A | missense_variant | MODERATE | HG04115.hp1 | a0002 | a0002c0006 | a0002c0006t0005 | a0002c0006t0005g0015 | 1 | 240 | 0.0042 | 0 | c.168 others(4): Show |
p.Ala others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/20 | 1793/3495 | 1685/2646 | 562/881 | chr16 | TogoVar | ||
ARHGAP17_chr16_24914389_25020369 | 24939563 | G | A | missense_variant | MODERATE | HG02486.hp1 | a0003 | a0003c0007 | a0003c0007t0001 | a0003c0007t0001g0224 | 1 | 240 | 0.0042 | 0 | c.152 others(4): Show |
p.Arg others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/20 | 1633/3495 | 1525/2646 | 509/881 | chr16 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129584076 | G | A | missense_variant | MODERATE | HG04115.hp1 | a0005 | a0005c0012 | a0005c0012t0002 | a0005c0012t0002g0095 | 1 | 238 | 0.0042 | 0 | c.175 others(4): Show |
p.Pro others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/15 | 1791/4414 | 1750/1992 | 584/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129599221 | T | C | missense_variant | MODERATE | NA19070.hp2 | a0009 | a0009c0007 | a0009c0007t0001 | a0009c0007t0001g0030 | 1 | 238 | 0.0042 | 0 | c.170 others(4): Show |
p.Asn others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/15 | 1749/4414 | 1708/1992 | 570/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129608031 | C | T | missense_variant | MODERATE | HG03704.hp2 | a0006 | a0006c0010 | a0006c0010t0001 | a0006c0010t0001g0197 | 1 | 238 | 0.0042 | 0 | c.114 others(4): Show |
p.Ala others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/15 | 1185/4414 | 1144/1992 | 382/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129629396 | T | C | missense_variant | MODERATE | HG03098.hp2 NA20300.hp1 |
a0003 | a0003c0004 | a0003c0004t0001a0003c0004t0005 | a0003c0004t0001g0151a0003c0004t0005g0088 | 2 | 238 | 0.0084 | 0 | c.743 others(3): Show |
p.Lys others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/15 | 784/4414 | 743/1992 | 248/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129634101 | G | A | missense_variant | MODERATE | HG04115.hp2 | a0004 | a0004c0013 | a0004c0013t0001 | a0004c0013t0001g0208 | 1 | 238 | 0.0042 | 0 | c.557 others(3): Show |
p.Pro others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/15 | 598/4414 | 557/1992 | 186/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129710043 | C | T | missense_variant | MODERATE | HG02615.hp2 | a0007 | a0007c0008 | a0007c0008t0004 | a0007c0008t0004g0055 | 1 | 238 | 0.0042 | 0 | c.94G others(2): Show |
p.Gly others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 135/4414 | 94/1992 | 32/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129710066 | A | G | missense_variant | MODERATE | HG02965.hp1 | a0008 | a0008c0005 | a0008c0005t0003 | a0008c0005t0003g0002 | 1 | 238 | 0.0042 | 0 | c.71T others(2): Show |
p.Val others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 112/4414 | 71/1992 | 24/663 | chr6 | TogoVar | ||
ARHGAP18_chr6_129571132_129715177 | 129710070 | T | C | missense_variant | MODERATE | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0003a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(181): Show | 185 | 238 | 0.7773 | 0 | c.67A others(2): Show |
p.Thr others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 108/4414 | 67/1992 | 23/663 | chr6 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97235242 | G | A | missense_variant | MODERATE | HG00639.hp2 | a0004 | a0004c0006 | a0004c0006t0001 | a0004c0006t0001g0196 | 1 | 242 | 0.0041 | 0 | c.125 others(4): Show |
p.Ser others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/12 | 1269/5438 | 1259/1485 | 420/494 | chr10 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97246304 | G | A | missense_variant | MODERATE | HG01123.hp1 | a0005 | a0005c0007 | a0005c0007t0006 | a0005c0007t0006g0007 | 1 | 242 | 0.0041 | 0 | c.961 others(3): Show |
p.His others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/12 | 971/5438 | 961/1485 | 321/494 | chr10 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97256331 | T | C | missense_variant | MODERATE | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0060a0002c0004t0002g0064a0002c0004t0002g0065others(17): Show | 20 | 242 | 0.0826 | 0 | c.914 others(3): Show |
p.Gln others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/12 | 924/5438 | 914/1485 | 305/494 | chr10 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97259530 | G | A | missense_variant | MODERATE | NA18962.hp2 | a0006 | a0006c0008 | a0006c0008t0001 | a0006c0008t0001g0186 | 1 | 242 | 0.0041 | 0 | c.712 others(3): Show |
p.Pro others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/12 | 722/5438 | 712/1485 | 238/494 | chr10 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97263446 | T | C | missense_variant | MODERATE | HG02257.hp2 | a0007 | a0007c0009 | a0007c0009t0001 | a0007c0009t0001g0210 | 1 | 242 | 0.0041 | 0 | c.587 others(3): Show |
p.His others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/12 | 597/5438 | 587/1485 | 196/494 | chr10 | TogoVar | ||
ARHGAP19_chr10_97217179_97297637 | 97265886 | C | T | missense_variant | MODERATE | HG00423.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0114 | 1 | 242 | 0.0041 | 0 | c.296 others(3): Show |
p.Arg others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/12 | 306/5438 | 296/1485 | 99/494 | chr10 | TogoVar | ||
ARHGAP1_chr11_46672080_46705619 | 46681351 | T | C | missense_variant | MODERATE | NA18961.hp2 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0120 | 1 | 344 | 0.0029 | 0 | c.478 others(3): Show |
p.Ile others(6): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/13 | 596/3395 | 478/1320 | 160/439 | chr11 | TogoVar | ||
ARHGAP1_chr11_46672080_46705619 | 46695734 | G | T | missense_variant | MODERATE | NA19007.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0049 | 1 | 344 | 0.0029 | 0 | c.155 others(3): Show |
p.Pro others(5): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/13 | 273/3395 | 155/1320 | 52/439 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110579620 | C | T | missense_variant | MODERATE | HG02970.hp2 | a0010 | a0010c0016 | a0010c0016t0002 | a0010c0016t0002g0060 | 1 | 226 | 0.0044 | 0 | c.332 others(4): Show |
p.Arg others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3532/6109 | 3326/3576 | 1109/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110579639 | G | C | missense_variant | MODERATE | NA19030.hp1 NA19240.hp2 |
a0009a0012 | a0009c0015a0012c0019 | a0009c0015t0004a0012c0019t0004 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | 226 | 0.0089 | 0 | c.330 others(4): Show |
p.Pro others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3513/6109 | 3307/3576 | 1103/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110579872 | G | A | missense_variant | MODERATE | NA19067.hp1 | a0008 | a0008c0017 | a0008c0017t0002 | a0008c0017t0002g0141 | 1 | 226 | 0.0044 | 0 | c.307 others(4): Show |
p.Ser others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3280/6109 | 3074/3576 | 1025/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110580287 | G | A | missense_variant | MODERATE | HG01981.hp1 NA18962.hp1 |
a0005 | a0005c0010 | a0005c0010t0001 | a0005c0010t0001g0161a0005c0010t0001g0180 | 2 | 226 | 0.0089 | 0 | c.265 others(4): Show |
p.Arg others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2865/6109 | 2659/3576 | 887/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110580781 | T | C | missense_variant | MODERATE | NA19075.hp2 NA19086.hp1 |
a0004 | a0004c0011 | a0004c0011t0002 | a0004c0011t0002g0028a0004c0011t0002g0128 | 2 | 226 | 0.0089 | 0 | c.216 others(4): Show |
p.Tyr others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2371/6109 | 2165/3576 | 722/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110580997 | T | G | missense_variant | MODERATE | HG02622.hp2 HG03491.hp1 HG03540.hp2 others(3): Show |
a0003a0006a0008 | a0003c0004a0006c0007a0008c0017 | a0003c0004t0002a0003c0004t0017a0006c0007t0010others(1): Show | a0003c0004t0002g0144a0003c0004t0002g0162a0003c0004t0017g0145others(3): Show | 6 | 226 | 0.0266 | 0 | c.194 others(4): Show |
p.Gln others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2155/6109 | 1949/3576 | 650/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110583589 | C | T | missense_variant | MODERATE | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
a0002a0006a0007 | a0002c0003a0002c0006a0002c0014others(2): Show | a0002c0003t0007a0002c0006t0012a0002c0014t0019others(2): Show | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(7): Show | 10 | 226 | 0.0443 | 0 | c.156 others(4): Show |
p.Ala others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1770/6109 | 1564/3576 | 522/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110606665 | G | C | missense_variant | MODERATE | HG02809.hp1 | a0011 | a0011c0018 | a0011c0018t0015 | a0011c0018t0015g0007 | 1 | 226 | 0.0044 | 0 | c.860 others(3): Show |
p.Pro others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/15 | 1066/6109 | 860/3576 | 287/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110624214 | T | C | missense_variant | MODERATE | NA19240.hp2 | a0012 | a0012c0019 | a0012c0019t0004 | a0012c0019t0004g0151 | 1 | 226 | 0.0044 | 0 | c.451 others(3): Show |
p.Met others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 657/6109 | 451/3576 | 151/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110690551 | T | C | missense_variant | MODERATE | HG06807.hp1 | a0007 | a0007c0020 | a0007c0020t0020 | a0007c0020t0020g0149 | 1 | 226 | 0.0044 | 0 | c.184 others(3): Show |
p.Thr others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/15 | 390/6109 | 184/3576 | 62/1191 | chr11 | TogoVar | ||
ARHGAP20_chr11_110572043_110717437 | 110712146 | C | A | missense_variant | MODERATE | HG03831.hp1 | a0013 | a0013c0021 | a0013c0021t0005 | a0013c0021t0005g0220 | 1 | 226 | 0.0044 | 0 | c.86G others(2): Show |
p.Gly others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 292/6109 | 86/3576 | 29/1191 | chr11 | TogoVar |