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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143330128 | AAAACCAA others(4): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG03491.hp2 NA19062.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0067 | 3 | 162 | 0.0185 | -11 | c.474 others(30): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143340271 | GACCAGTA others(4): Show |
G | intron_variant | MODIFIER | HG03491.hp1 HG04199.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069a0001c0001t0001g0151 | 2 | 162 | 0.0124 | -11 | c.474 others(30): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143605858 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(50): Show | 53 | 162 | 0.3272 | -11 | c.100 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606060 | AAAAAAAA others(4): Show |
A | intron_variant | MODIFIER | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0063others(6): Show | 9 | 162 | 0.0556 | -11 | c.100 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143680021 | TAAAAAAA others(4): Show |
T | intron_variant | MODIFIER | HG00609.hp1 HG02071.hp1 HG02074.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0025others(13): Show | 16 | 162 | 0.0988 | -11 | c.113 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00733.hp1 HG02486.hp2 HG03225.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0135others(1): Show | 4 | 162 | 0.0247 | -11 | c.113 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24961518 | ATTTTTTT others(4): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | 240 | 0.0958 | -11 | c.574 others(28): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129623006 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 238 | 0.0042 | -11 | c.787 others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129676912 | CCTCTTTT others(4): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0018 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(2): Show | 5 | 238 | 0.0210 | -11 | c.113 others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129686978 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG01175.hp2 HG01261.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | 238 | 0.0084 | -11 | c.113 others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97239547 | AGAGGGTG others(4): Show |
A | intron_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135 | 1 | 242 | 0.0041 | -11 | c.118 others(30): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97239548 | GAGGGTGT others(4): Show |
G | intron_variant | MODIFIER | NA19012.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 | 1 | 242 | 0.0041 | -11 | c.118 others(30): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97248786 | CGGCCAAA others(4): Show |
C | intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0161 | 1 | 242 | 0.0041 | -11 | c.928 others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251376 | TGGAAGGG others(4): Show |
T | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0002a0001c0001t0006a0001c0001t0014others(1): Show | a0001c0001t0002g0011a0001c0001t0006g0008a0001c0001t0006g0009others(4): Show | 7 | 242 | 0.0289 | -11 | c.927 others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251505 | TAAGGGGA others(4): Show |
T | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0062 | 1 | 242 | 0.0041 | -11 | c.927 others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110575534 | CTTCATTG others(4): Show |
C | downstream_gene_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 226 | 0.0044 | -11 | c.*38 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1508 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110619361 | ATAGCATA others(4): Show |
A | intron_variant | MODIFIER | HG06807.hp1 | a0007 | a0007c0020 | a0007c0020t0020 | a0007c0020t0020g0149 | 1 | 226 | 0.0044 | -11 | c.504 others(28): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAAAA others(4): Show |
C | downstream_gene_variant | MODIFIER | HG01069.hp1 HG01934.hp1 HG01981.hp1 others(8): Show |
a0001a0002a0007others(2): Show | a0001c0001a0002c0002a0007c0007others(2): Show | a0001c0001t0005a0002c0002t0001a0007c0007t0006others(3): Show | a0001c0001t0005g0005a0002c0002t0001g0038a0002c0002t0001g0049others(8): Show | 11 | 352 | 0.0313 | -11 | c.*35 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00621.hp1 HG01981.hp1 HG02055.hp2 others(11): Show |
a0001a0003a0008 | a0001c0001a0003c0003a0008c0009 | a0001c0001t0001a0001c0001t0005a0003c0003t0001others(1): Show | a0001c0001t0001g0174a0001c0001t0001g0220a0001c0001t0001g0222others(11): Show | 14 | 352 | 0.0398 | -11 | c.64- others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24717772 | TCAGCTGG others(4): Show |
T | intron_variant | MODIFIER | HG02818.hp2 HG03486.hp2 |
a0011 | a0011c0011 | a0011c0011t0001 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | 352 | 0.0057 | -11 | c.63+ others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG01256.hp1 HG02074.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0002t0002g0108others(1): Show | 4 | 309 | 0.0129 | -11 | c.344 others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485375 | AAATATAT others(4): Show |
A | intron_variant | MODIFIER | HG01071.hp1 HG01074.hp1 HG01433.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0108a0001c0002t0002g0098a0001c0003t0001g0091others(2): Show | 5 | 108 | 0.0463 | -11 | c.-21 others(28): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485377 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 108 | 0.0093 | -11 | c.-21 others(28): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | GTTTTTTT others(4): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(12): Show | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0026others(23): Show | 26 | 108 | 0.2407 | -11 | c.180 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85704662 | CTTAGTAA others(4): Show |
C | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0059 | 1 | 108 | 0.0093 | -11 | c.181 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85894978 | AAAAAAAA others(4): Show |
A | intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046 | 1 | 108 | 0.0093 | -11 | c.269 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85920948 | ACAATGTG others(4): Show |
A | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0007 | a0001c0007t0004 | a0001c0007t0004g0058 | 1 | 108 | 0.0093 | -11 | c.269 others(28): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68815443 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG02559.hp1 HG02976.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0003 | a0002c0002t0001g0268a0002c0002t0003g0136 | 2 | 368 | 0.0054 | -11 | c.808 others(26): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAAA others(4): Show |
G | intron_variant | MODIFIER | HG02132.hp1 NA18960.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0196a0001c0001t0002g0128 | 2 | 198 | 0.0101 | -11 | c.154 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142869179 | CTTTTCTT others(4): Show |
C | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0171 | 1 | 198 | 0.0051 | -11 | c.155 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890144 | AAAAAAAA others(4): Show |
A | intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0160 | 1 | 198 | 0.0051 | -11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890148 | AAAAATAT others(4): Show |
A | intron_variant | MODIFIER | HG03195.hp1 NA18945.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0003t0008 | a0001c0001t0003g0176a0001c0003t0008g0009 | 2 | 198 | 0.0101 | -11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890152 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0054 | a0001c0001t0054g0072 | 1 | 198 | 0.0051 | -11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTTTTT others(4): Show |
G | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0108a0001c0001t0005g0109 | 2 | 198 | 0.0101 | -11 | c.114 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143056316 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0105 | 1 | 198 | 0.0051 | -11 | c.143 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143167508 | AAAAAAAA others(4): Show |
A | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0041 | 1 | 198 | 0.0051 | -11 | c.198 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0053 | 1 | 198 | 0.0051 | -11 | c.198 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143177987 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG03098.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0001t0023a0001c0002t0049 | a0001c0001t0014g0038a0001c0001t0014g0041a0001c0001t0023g0055others(1): Show | 4 | 198 | 0.0202 | -11 | c.198 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143202473 | GAAAATAG others(4): Show |
G | intron_variant | MODIFIER | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0138others(51): Show | 54 | 198 | 0.2727 | -11 | c.198 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143222273 | ACACACAC others(4): Show |
A | intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0062 | 1 | 198 | 0.0051 | -11 | c.219 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | ATTTTTTT others(4): Show |
A | intron_variant | MODIFIER | HG01106.hp1 NA19043.hp1 NA19240.hp1 |
a0001a0010 | a0001c0003a0010c0014 | a0001c0003t0003a0010c0014t0001 | a0001c0003t0003g0085a0001c0003t0003g0104a0010c0014t0001g0142 | 3 | 248 | 0.0121 | -11 | c.123 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841169 | TCTCTCTC others(4): Show |
T | intron_variant | MODIFIER | HG00408.hp2 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0039 | 1 | 248 | 0.0040 | -11 | c.543 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841192 | TCTCTCTC others(4): Show |
T | intron_variant | MODIFIER | HG03239.hp1 HG03491.hp2 HG04204.hp2 |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0005t0002 | a0002c0002t0002g0046a0002c0002t0002g0047a0002c0005t0002g0057 | 3 | 248 | 0.0121 | -11 | c.543 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6873205 | TTTTGCTT others(4): Show |
T | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0154 | 1 | 248 | 0.0040 | -11 | c.955 others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6909290 | CTTTTCTT others(4): Show |
C | intron_variant | MODIFIER | HG01261.hp1 HG01515.hp2 HG02055.hp1 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0005a0003c0004 | a0001c0001t0001a0001c0001t0017a0001c0001t0019others(2): Show | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0161others(8): Show | 11 | 248 | 0.0444 | -11 | c.209 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6911170 | TTTCAAGC others(4): Show |
T | intron_variant | MODIFIER | NA19090.hp2 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0130 | 1 | 248 | 0.0040 | -11 | c.209 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94211287 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | NA19054.hp1 | a0004 | a0004c0006 | a0004c0006t0001 | a0004c0006t0001g0108 | 1 | 356 | 0.0028 | -11 | c.341 others(28): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94229684 | TCCATACA others(4): Show |
T | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0167 | 1 | 356 | 0.0028 | -11 | c.205 others(28): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055865 | TAAAATAA others(4): Show |
T | intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 390 | 0.0026 | -11 | c.345 others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055905 | TAAAATAA others(4): Show |
T | intron_variant | MODIFIER | HG00673.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0187others(4): Show | 7 | 390 | 0.0180 | -11 | c.345 others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar |