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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARGFX_chr3_121562949_121595622 | 121576707 | TTTTC | T | intron_variant | MODIFIER | HG00544.hp2 HG00735.hp1 HG01106.hp2 others(62): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0005others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(12): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0022others(61): Show | 65 | 410 | 0.1585 | -4 | c.104 others(17): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121577141 | CATAA | C | intron_variant | MODIFIER | NA18939.hp1 NA18954.hp2 NA18973.hp1 others(5): Show |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0001a0001c0001t0006a0006c0006t0006 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0280others(5): Show | 8 | 410 | 0.0195 | -4 | c.220 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121578120 | CTTTT | C | intron_variant | MODIFIER | NA18946.hp2 NA18962.hp1 NA18973.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0032 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0099others(3): Show | 6 | 410 | 0.0146 | -4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121579627 | AACAG | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0008 | a0001c0001t0001a0002c0002t0001a0002c0002t0006others(5): Show | a0001c0001t0001g0189a0002c0002t0001g0002a0002c0002t0001g0009others(44): Show | 49 | 410 | 0.1195 | -4 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121584204 | GAGGA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(65): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0011a0001c0001t0001g0237a0001c0001t0001g0239others(64): Show | 68 | 410 | 0.1659 | -4 | c.221 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGLU1_chr13_106536673_106573137 | 106539240 | CTATT | C | downstream_gene_variant | MODIFIER | HG04204.hp1 HG04228.hp2 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015a0001c0001t0001g0068 | 3 | 376 | 0.0080 | -4 | c.*47 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 2432 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106540792 | CTGGA | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 91 | 376 | 0.2420 | -4 | c.*32 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 880 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106546585 | TAATA | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0022a0001c0001t0002g0032a0001c0001t0002g0105others(3): Show | 9 | 376 | 0.0239 | -4 | c.658 others(21): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 3/3 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106561424 | TACAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(81): Show | 170 | 376 | 0.4521 | -4 | c.348 others(21): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106569333 | ATAAT | A | upstream_gene_variant | MODIFIER | HG01884.hp1 HG03130.hp2 NA20300.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0083 | 4 | 376 | 0.0106 | -4 | c.-14 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1197 | chr13 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147741788 | ACACG | A | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0007 | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(1): Show | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0050others(12): Show | 15 | 106 | 0.1415 | -4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147766799 | CATAT | C | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 NA18522.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0006t0001 | a0001c0001t0001g0081a0001c0001t0001g0094a0001c0005t0001g0074others(1): Show | 4 | 106 | 0.0377 | -4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147766836 | ATATT | A | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | 106 | 0.0377 | -4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147768587 | ATAAT | A | intron_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0001a0001c0005t0001a0002c0003t0001 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | 106 | 0.0283 | -4 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147783792 | TTATG | T | intron_variant | MODIFIER | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0047others(10): Show | 13 | 106 | 0.1226 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147783824 | TTGTG | T | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | 106 | 0.2547 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147783888 | TTGTG | T | intron_variant | MODIFIER | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | 106 | 0.0377 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147791569 | TTTTG | T | intron_variant | MODIFIER | HG02896.hp1 NA18522.hp1 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0002a0001c0009t0001g0007 | 2 | 106 | 0.0189 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147798722 | ACACT | A | intron_variant | MODIFIER | HG02895.hp1 HG02896.hp1 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0005 | 3 | 106 | 0.0283 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147820580 | GTTTT | G | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(19): Show | 22 | 106 | 0.2076 | -4 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839092 | GTATC | G | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(27): Show | 30 | 106 | 0.2830 | -4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839142 | ATCTG | A | intron_variant | MODIFIER | HG02145.hp2 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055a0001c0001t0001g0061 | 2 | 106 | 0.0189 | -4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | TTGTG | T | intron_variant | MODIFIER | HG02895.hp2 HG03209.hp1 NA19064.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | 106 | 0.0377 | -4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | CTGTG | C | intron_variant | MODIFIER | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0046others(7): Show | 10 | 106 | 0.0943 | -4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | AACAC | A | intron_variant | MODIFIER | HG02818.hp2 HG02896.hp1 NA18979.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0002t0001g0066 | 3 | 106 | 0.0283 | -4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147890293 | TTTGA | T | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | 106 | 0.3396 | -4 | c.103 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147911993 | ACGTG | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0003others(1): Show | a0001c0001t0001a0001c0011t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0083a0001c0011t0001g0092a0002c0003t0001g0096others(2): Show | 5 | 106 | 0.0472 | -4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911994 | CGTGT | C | intron_variant | MODIFIER | HG01993.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(4): Show | 7 | 106 | 0.0660 | -4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AATAT | A | intron_variant | MODIFIER | HG02818.hp2 HG02896.hp1 HG03209.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0053others(2): Show | 5 | 106 | 0.0472 | -4 | c.116 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147921558 | CAGAG | C | intron_variant | MODIFIER | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0001a0001c0005t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(6): Show | 9 | 106 | 0.0849 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147935343 | AAGAT | A | intron_variant | MODIFIER | HG02895.hp1 HG03516.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0006a0001c0005t0001g0003 | 2 | 106 | 0.0189 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147937236 | CCTCT | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(3): Show | 6 | 106 | 0.0566 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147948314 | AAGTC | A | intron_variant | MODIFIER | HG02451.hp2 HG02818.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0003a0001c0011t0001 | a0001c0001t0001g0093a0001c0001t0003g0087a0001c0011t0001g0092 | 3 | 106 | 0.0283 | -4 | c.139 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147955217 | TTAAG | T | intron_variant | MODIFIER | HG01884.hp2 HG02572.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0001 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | 106 | 0.0189 | -4 | c.139 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148005734 | TTCTC | T | intron_variant | MODIFIER | HG02056.hp2 HG02080.hp2 HG03098.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0001a0001c0004t0001 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(4): Show | 7 | 106 | 0.0660 | -4 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | CTATA | C | intron_variant | MODIFIER | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(11): Show |
a0001a0004 | a0001c0002a0001c0004a0001c0008others(2): Show | a0001c0002t0001a0001c0004t0001a0001c0008t0001others(2): Show | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(11): Show | 14 | 106 | 0.1321 | -4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148032327 | TCCCC | T | intron_variant | MODIFIER | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(10): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0030others(10): Show | 13 | 106 | 0.1226 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148039368 | ATTTT | A | intron_variant | MODIFIER | HG02922.hp1 HG03130.hp1 HG03239.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0104others(1): Show | 4 | 106 | 0.0377 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | AATAT | A | intron_variant | MODIFIER | HG02109.hp1 HG02451.hp1 NA18995.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0103 | 3 | 106 | 0.0283 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148049800 | TTTTG | T | intron_variant | MODIFIER | HG02109.hp1 HG02886.hp2 HG04184.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0010 | a0001c0001t0001a0004c0010t0001 | a0001c0001t0001g0058a0001c0001t0001g0080a0001c0001t0001g0091others(1): Show | 4 | 106 | 0.0377 | -4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148071638 | CAAAA | C | intron_variant | MODIFIER | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0007 | a0001c0001t0001a0001c0005t0001a0003c0007t0001 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0001g0076others(4): Show | 7 | 106 | 0.0660 | -4 | c.227 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32612829 | CAAAA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(47): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0104a0001c0001t0002g0003a0001c0001t0004g0006others(23): Show | 50 | 335 | 0.1493 | -4 | c.-33 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2674 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32640099 | AGTTT | A | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
a0001a0005 | a0001c0001a0005c0010 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(44): Show | 91 | 335 | 0.2716 | -4 | c.*22 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 159 | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30627147 | TGAGA | T | intron_variant | MODIFIER | HG01256.hp2 HG01258.hp2 HG01934.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 6 | 247 | 0.0243 | -4 | c.129 others(19): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30630401 | TACTG | T | intron_variant | MODIFIER | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0065 | 15 | 247 | 0.0607 | -4 | c.130 others(19): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | AGTGT | A | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(8): Show | 27 | 247 | 0.1093 | -4 | c.*12 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | TCACA | T | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG01081.hp2 others(22): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0014others(1): Show | a0001c0001t0004a0001c0006t0026a0001c0014t0004others(1): Show | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(22): Show | 25 | 322 | 0.0776 | -4 | c.*20 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2006 | chr10 | TogoVar | |||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | CGTGT | C | intron_variant | MODIFIER | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(3): Show | a0001c0001t0003g0026a0001c0001t0004g0044a0001c0001t0005g0045others(9): Show | 12 | 322 | 0.0373 | -4 | c.173 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31820712 | TTATA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(17): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(108): Show | 111 | 322 | 0.3447 | -4 | c.153 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31840925 | TTAAG | T | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0025 | a0001c0001t0001g0226a0001c0001t0008g0152a0001c0001t0025g0202 | 3 | 322 | 0.0093 | -4 | c.129 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | TogoVar |