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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARG2_chr14_67614920_67656708 | 67650556 | AGAG | A | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(70): Show | 79 | 438 | 0.1804 | -3 | c.860 others(18): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARG2_chr14_67614920_67656708 | 67651205 | CTGT | C | 3_prime_UTR_variant | MODIFIER | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0096a0001c0001t0004g0183a0001c0001t0004g0184others(16): Show | 19 | 438 | 0.0434 | -3 | c.*29 others(12): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 8/8 | 290 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||
ARG2_chr14_67614920_67656708 | 67652456 | CAGG | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(75): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0003c0004t0001 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0012others(64): Show | 78 | 438 | 0.1781 | -3 | c.*15 others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 749 | chr14 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121563368 | CATT | C | upstream_gene_variant | MODIFIER | HG01928.hp2 HG01934.hp1 HG01943.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0010others(3): Show | 6 | 410 | 0.0146 | -3 | c.-46 others(14): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 4580 | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121563903 | AAAT | A | upstream_gene_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(30): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0238others(30): Show | 33 | 410 | 0.0805 | -3 | c.-41 others(14): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 4045 | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121564244 | CTTT | C | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0265others(142): Show | 146 | 410 | 0.3561 | -3 | c.-37 others(14): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3704 | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121571730 | ATTT | A | intron_variant | MODIFIER | HG02027.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(5): Show | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(11): Show | 14 | 410 | 0.0342 | -3 | c.103 others(18): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121572236 | GTTT | G | intron_variant | MODIFIER | HG00323.hp2 HG02257.hp2 HG02809.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0007a0002c0002t0001g0032a0002c0002t0001g0164others(2): Show | 6 | 410 | 0.0146 | -3 | c.103 others(20): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121573848 | CAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(18): Show | a0001c0001t0002g0006a0001c0001t0002g0029a0001c0001t0002g0035others(137): Show | 143 | 410 | 0.3488 | -3 | c.104 others(20): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121578120 | CTTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0004others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(18): Show | a0001c0001t0002g0006a0001c0001t0002g0029a0001c0001t0002g0035others(140): Show | 146 | 410 | 0.3561 | -3 | c.220 others(20): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGLU1_chr13_106536673_106573137 | 106540918 | GCAC | G | downstream_gene_variant | MODIFIER | HG00280.hp1 HG01891.hp2 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0002g0022 | 3 | 376 | 0.0080 | -3 | c.*30 others(14): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 754 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106562495 | ACTC | A | intron_variant | MODIFIER | HG02809.hp1 HG02965.hp2 HG03471.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0019a0001c0001t0006g0058a0001c0001t0006g0059 | 5 | 376 | 0.0133 | -3 | c.348 others(20): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106566270 | ATAT | A | intron_variant | MODIFIER | HG01243.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0071a0001c0001t0008g0072a0001c0001t0008g0073others(1): Show | 4 | 376 | 0.0106 | -3 | c.347 others(20): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147743771 | CCTT | C | intron_variant | MODIFIER | HG02572.hp2 NA21309.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | 106 | 0.0189 | -3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147751190 | CAAA | C | intron_variant | MODIFIER | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | 106 | 0.0849 | -3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147751527 | CCAT | C | intron_variant | MODIFIER | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0001 | a0001c0001t0001g0077a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | 106 | 0.0283 | -3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784716 | TATA | T | intron_variant | MODIFIER | HG02109.hp1 HG03471.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0091a0001c0004t0001g0045 | 2 | 106 | 0.0189 | -3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147784773 | TATA | T | intron_variant | MODIFIER | HG01070.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0088others(4): Show | 7 | 106 | 0.0660 | -3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147784803 | TATA | T | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | 106 | 0.2642 | -3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147784908 | TATA | T | intron_variant | MODIFIER | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029others(1): Show | 4 | 106 | 0.0377 | -3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147820580 | GTTT | G | intron_variant | MODIFIER | HG00558.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(15): Show | 18 | 106 | 0.1698 | -3 | c.155 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147852728 | TTTA | T | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp2 HG01167.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0046others(10): Show | 13 | 106 | 0.1226 | -3 | c.385 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147857816 | CAAG | C | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | 106 | 0.0660 | -3 | c.486 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147867863 | CAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0007 | a0001c0001t0001a0002c0003t0001a0003c0007t0001 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | 106 | 0.0755 | -3 | c.702 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147870562 | CTTT | C | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(24): Show | 27 | 106 | 0.2547 | -3 | c.702 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147889667 | GTCT | G | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | 106 | 0.2736 | -3 | c.103 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147892187 | AGAG | A | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(7): Show | 10 | 106 | 0.0943 | -3 | c.103 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147912645 | CTTT | C | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(4): Show | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0034others(28): Show | 31 | 106 | 0.2925 | -3 | c.116 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147936317 | CTTT | C | intron_variant | MODIFIER | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | 106 | 0.0377 | -3 | c.122 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147950754 | AATG | A | intron_variant | MODIFIER | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0007 | a0001c0001t0001a0002c0003t0001a0003c0007t0001 | a0001c0001t0001g0083a0002c0003t0001g0096a0003c0007t0001g0079others(1): Show | 4 | 106 | 0.0377 | -3 | c.139 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147985963 | TCTC | T | intron_variant | MODIFIER | HG01884.hp2 HG01993.hp1 HG02109.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0037others(11): Show | 14 | 106 | 0.1321 | -3 | c.171 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148032327 | TCCC | T | intron_variant | MODIFIER | HG01169.hp2 HG01243.hp1 HG01261.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 22 | 106 | 0.2076 | -3 | c.186 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148050678 | ATCT | A | intron_variant | MODIFIER | HG02572.hp2 HG03225.hp1 |
a0001a0002 | a0001c0004a0002c0003 | a0001c0004t0001a0002c0003t0001 | a0001c0004t0001g0105a0002c0003t0001g0096 | 2 | 106 | 0.0189 | -3 | c.202 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32612829 | CAAA | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(120): Show | 192 | 335 | 0.5731 | -3 | c.-33 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2674 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32618758 | ACCC | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(107): Show | 180 | 335 | 0.5373 | -3 | c.130 others(20): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32619603 | ACTT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(53): Show |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0004a0001c0001t0021a0002c0005t0002 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(25): Show | 56 | 335 | 0.1672 | -3 | c.130 others(18): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32642568 | CAAA | C | downstream_gene_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG01891.hp1 others(6): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0002a0001c0002t0005a0007c0009t0005 | a0001c0001t0002g0123a0001c0001t0002g0138a0001c0002t0005g0020others(5): Show | 9 | 335 | 0.0269 | -3 | c.*47 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2628 | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30623960 | ATTG | A | upstream_gene_variant | MODIFIER | HG02280.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0034 | 2 | 247 | 0.0081 | -3 | c.-28 others(14): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2167 | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30624418 | CAAA | C | upstream_gene_variant | MODIFIER | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0062 | 5 | 247 | 0.0202 | -3 | c.-24 others(14): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1709 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31811542 | CTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
a0001 | a0001c0003a0001c0005 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | 322 | 0.0466 | -3 | c.195 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31835215 | AAAG | A | intron_variant | MODIFIER | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0023a0001c0001t0024others(1): Show | a0001c0001t0004g0034a0001c0001t0023g0040a0001c0001t0023g0069others(3): Show | 6 | 322 | 0.0186 | -3 | c.138 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31852729 | CTTT | C | intron_variant | MODIFIER | HG01516.hp1 NA18747.hp2 NA18940.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0007 | a0001c0001t0001g0099a0001c0001t0001g0101a0002c0002t0002g0243others(5): Show | 8 | 322 | 0.0248 | -3 | c.109 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | CAAA | C | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | 322 | 0.0497 | -3 | c.685 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31882392 | TAAG | T | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
a0001a0002a0003 | a0001c0007a0001c0010a0002c0002others(1): Show | a0001c0007t0028a0001c0010t0053a0002c0002t0002others(9): Show | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | 322 | 0.2609 | -3 | c.685 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31882820 | GAAA | G | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
a0001 | a0001c0001a0001c0006a0001c0008 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(7): Show | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | 322 | 0.1522 | -3 | c.685 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31889619 | GTTT | G | intron_variant | MODIFIER | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(5): Show | 8 | 322 | 0.0248 | -3 | c.684 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31922180 | CAAA | C | intron_variant | MODIFIER | HG00597.hp2 HG01192.hp1 HG01516.hp1 others(22): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(3): Show | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0099others(22): Show | 25 | 322 | 0.0776 | -3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31925889 | CATT | C | intron_variant | MODIFIER | HG01167.hp2 HG01175.hp1 HG04204.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | 322 | 0.0093 | -3 | c.-11 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143132927 | CACA | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | 162 | 0.0309 | -3 | c.-15 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143143564 | TTTC | T | intron_variant | MODIFIER | HG02074.hp1 HG02074.hp2 HG02523.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | 162 | 0.0679 | -3 | c.-14 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |