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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG02015.hp1 HG02647.hp1 NA19086.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0002g0129 | 3 | 144 | 0.0208 | -15 | c.588 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44772223 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG01243.hp2 HG01943.hp2 others(22): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0001c0008others(14): Show | a0001c0001t0003a0001c0007t0001a0001c0008t0001others(14): Show | a0001c0001t0003g0063a0001c0001t0003g0074a0001c0007t0001g0069others(22): Show | 25 | 390 | 0.0641 | -15 | c.-71 others(34): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787321 | CTTTGTTT others(8): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0004a0001c0007others(54): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(65): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0042others(164): Show | 167 | 390 | 0.4282 | -15 | c.79+ others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG03927.hp1 | a0003 | a0003c0002 | a0003c0002t0002 | a0003c0002t0002g0144 | 1 | 390 | 0.0026 | -15 | c.877 others(32): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG02155.hp2 HG02257.hp2 others(7): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0001c0008others(5): Show | a0001c0001t0003a0001c0004t0003a0001c0008t0003others(5): Show | a0001c0001t0003g0080a0001c0001t0003g0153a0001c0001t0003g0293others(7): Show | 10 | 390 | 0.0256 | -15 | c.878 others(32): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17594728 | GCCTGCCT others(8): Show |
G | intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0101 | 1 | 168 | 0.0060 | -15 | c.257 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1826400 | TTGTGTGT others(8): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0001c0003others(74): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(106): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(148): Show | 151 | 363 | 0.4160 | -15 | c.-48 others(32): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1839893 | GGGGACTG others(8): Show |
G | intron_variant | MODIFIER | NA19082.hp1 | a0002 | a0002c0030 | a0002c0030t0002 | a0002c0030t0002g0077 | 1 | 363 | 0.0028 | -15 | c.-47 others(32): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1841943 | GACCGGAA others(8): Show |
G | intron_variant | MODIFIER | HG02083.hp2 HG02132.hp1 HG02630.hp2 others(1): Show |
a0001a0014a0016others(1): Show | a0001c0005a0014c0107a0016c0146others(1): Show | a0001c0005t0031a0014c0107t0004a0016c0146t0006others(1): Show | a0001c0005t0031g0351a0014c0107t0004g0135a0016c0146t0006g0111others(1): Show | 4 | 363 | 0.0110 | -15 | c.-47 others(32): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1859208 | TGGCCATA others(8): Show |
T | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0012 | a0001c0012t0074 | a0001c0012t0074g0191 | 1 | 363 | 0.0028 | -15 | c.194 others(30): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 3/28 | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(24): Show |
a0002a0010 | a0002c0004a0010c0014 | a0002c0004t0005a0002c0004t0009a0002c0004t0014others(3): Show | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(23): Show | 27 | 362 | 0.0746 | -15 | c.179 others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347145 | TTCCTTCC others(8): Show |
T | intron_variant | MODIFIER | HG01123.hp1 NA18942.hp2 NA19086.hp2 |
a0001a0002 | a0001c0006a0002c0003 | a0001c0006t0002a0002c0003t0002 | a0001c0006t0002g0306a0002c0003t0002g0017a0002c0003t0002g0084 | 3 | 308 | 0.0097 | -15 | c.32+ others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0018 | 1 | 308 | 0.0033 | -15 | c.33- others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120446198 | AAATAATA others(8): Show |
A | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0102 | 1 | 308 | 0.0033 | -15 | c.134 others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF15_chr17_8305241_8327511 | 8327407 | CACTCTCG others(8): Show |
C | downstream_gene_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0027 | 1 | 428 | 0.0023 | -15 | c.*64 others(26): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 4897 | chr17 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73305885 | CCACCCCT others(8): Show |
C | upstream_gene_variant | MODIFIER | HG02109.hp1 HG02615.hp2 |
a0002 | a0002c0016 | a0002c0016t0003 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | 228 | 0.0088 | -15 | c.-27 others(26): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2390 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73305910 | ACAACTCA others(8): Show |
A | upstream_gene_variant | MODIFIER | HG03490.hp1 | a0019 | a0019c0041 | a0019c0041t0016 | a0019c0041t0016g0154 | 1 | 228 | 0.0044 | -15 | c.-27 others(26): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2365 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329354 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG03139.hp1 | a0003 | a0003c0003 | a0003c0003t0011 | a0003c0003t0011g0136 | 1 | 228 | 0.0044 | -15 | c.319 others(36): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329356 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG02083.hp1 HG02132.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0119 | 3 | 228 | 0.0132 | -15 | c.319 others(36): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329358 | TATATATA others(8): Show |
T | intron_variant | MODIFIER | HG02630.hp2 NA18612.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116a0001c0001t0001g0171 | 2 | 228 | 0.0088 | -15 | c.319 others(36): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7362131 | GAGAAGGA others(8): Show |
G | intron_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0078 | 1 | 298 | 0.0034 | -15 | c.-11 others(32): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7380623 | GCAGTGAG others(8): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
a0001a0002a0027others(4): Show | a0001c0001a0001c0002a0001c0021others(9): Show | a0001c0001t0002a0001c0002t0003a0001c0021t0006others(12): Show | a0001c0001t0002g0144a0001c0001t0002g0202a0001c0002t0003g0060others(25): Show | 28 | 298 | 0.0940 | -15 | c.645 others(30): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 7/28 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7385443 | CATTATTA others(8): Show |
C | intron_variant | MODIFIER | HG03225.hp2 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0251 | 1 | 298 | 0.0034 | -15 | c.967 others(32): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41903765 | CTATGCTG others(8): Show |
C | disruptive_inframe_deletion | MODERATE | HG00738.hp2 | a0006 | a0006c0005 | a0006c0005t0001 | a0006c0005t0001g0089 | 1 | 234 | 0.0043 | -15 | c.189 others(24): Show |
p.Met others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/29 | 2024/3229 | 1899/2739 | 633/912 | chr19 | TogoVar | ||
ARHGEF26_chr3_154116390_154262825 | 154161099 | TTTGTGTG others(8): Show |
T | intron_variant | MODIFIER | HG02055.hp1 HG03195.hp1 HG03453.hp1 others(5): Show |
a0002a0006 | a0002c0002a0002c0003a0002c0007others(1): Show | a0002c0002t0019a0002c0003t0018a0002c0003t0044others(4): Show | a0002c0002t0019g0056a0002c0003t0018g0092a0002c0003t0044g0094others(5): Show | 8 | 283 | 0.0283 | -15 | c.148 others(34): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154186886 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(67): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(5): Show | a0001c0001t0007a0002c0002t0003a0002c0002t0005others(16): Show | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(67): Show | 70 | 283 | 0.2474 | -15 | c.148 others(32): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | CTTCTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01169.hp1 HG03453.hp2 NA19030.hp2 |
a0002a0005a0007 | a0002c0006a0005c0061a0007c0009 | a0002c0006t0003a0005c0061t0002a0007c0009t0009 | a0002c0006t0003g0111a0005c0061t0002g0001a0007c0009t0009g0164 | 3 | 188 | 0.0160 | -15 | c.34- others(32): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73769105 | CTCAGGTA others(8): Show |
C | intron_variant | MODIFIER | HG01123.hp1 | a0016 | a0016c0027 | a0016c0027t0001 | a0016c0027t0001g0080 | 1 | 188 | 0.0053 | -15 | c.476 others(32): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598263 | CTCTTCTT others(8): Show |
C | intron_variant | MODIFIER | HG02615.hp2 NA19012.hp1 NA19012.hp2 |
a0005a0007 | a0005c0007a0005c0011a0007c0008 | a0005c0007t0003a0005c0011t0003a0007c0008t0001 | a0005c0007t0003g0163a0005c0011t0003g0372a0007c0008t0001g0102 | 3 | 394 | 0.0076 | -15 | c.186 others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598348 | TTCTTCTT others(8): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(67): Show |
a0001a0003a0004others(6): Show | a0001c0002a0003c0003a0003c0029others(8): Show | a0001c0002t0005a0003c0003t0002a0003c0029t0002others(12): Show | a0001c0002t0005g0374a0003c0003t0002g0007a0003c0003t0002g0010others(62): Show | 70 | 394 | 0.1777 | -15 | c.186 others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561398 | AATAATAG others(8): Show |
A | intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0075 | 1 | 186 | 0.0054 | -15 | c.196 others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF3_chr3_56722420_56806949 | 56789020 | ATGCTGCT others(8): Show |
A | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp2 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0001a0001c0005t0001 | a0001c0003t0001g0103a0001c0005t0001g0308 | 2 | 358 | 0.0056 | -15 | c.96+ others(32): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833372 | AAGGAAGG others(8): Show |
A | upstream_gene_variant | MODIFIER | HG02723.hp2 | a0010 | a0010c0009 | a0010c0009t0001 | a0010c0009t0001g0068 | 1 | 144 | 0.0069 | -15 | c.-35 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3541 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833387 | GAAAGAAA others(8): Show |
G | upstream_gene_variant | MODIFIER | HG01884.hp2 HG01975.hp2 HG04204.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0011a0002c0042 | a0001c0001t0001a0002c0011t0001a0002c0042t0001 | a0001c0001t0001g0017a0001c0001t0001g0115a0001c0001t0001g0123others(2): Show | 5 | 144 | 0.0347 | -15 | c.-35 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3526 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926810 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
a0007a0013 | a0007c0013a0013c0016 | a0007c0013t0001a0007c0013t0003a0013c0016t0003 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | 144 | 0.0278 | -15 | c.355 others(34): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF5_chr7_144350402_144385632 | 144354843 | ACAACAAC others(8): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
a0001a0002a0003others(25): Show | a0001c0010a0002c0001a0002c0016others(31): Show | a0001c0010t0002a0002c0001t0001a0002c0016t0001others(31): Show | a0001c0010t0002g0032a0001c0010t0002g0130a0001c0010t0002g0131others(85): Show | 109 | 288 | 0.3785 | -15 | c.-67 others(24): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 558 | chr7 | TogoVar | ||||||
ARHGEF5_chr7_144350402_144385632 | 144361232 | AAAAAAAA others(8): Show |
A | intron_variant | MODIFIER | HG02015.hp2 | a0006 | a0006c0005 | a0006c0005t0001 | a0006c0005t0001g0084 | 1 | 288 | 0.0035 | -15 | c.-12 others(32): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111271056 | CGGCAGTG others(8): Show |
C | intron_variant | MODIFIER | HG03471.hp1 HG03486.hp2 |
a0001a0007 | a0001c0001a0007c0010 | a0001c0001t0012a0007c0010t0001 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | 274 | 0.0073 | -15 | c.107 others(34): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARID1A_chr1_26691015_26787104 | 26694709 | TTCTGCAT others(8): Show |
T | upstream_gene_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 146 | 0.0069 | -15 | c.-16 others(26): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1305 | chr1 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26740593 | ATCACAGG others(8): Show |
A | intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 146 | 0.0069 | -15 | c.192 others(34): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156897218 | GCTTCTTC others(8): Show |
G | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 150 | 0.0067 | -15 | c.198 others(34): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156897264 | CTTATTAT others(8): Show |
C | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 150 | 0.0067 | -15 | c.198 others(34): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45729665 | GCGCCGCC others(8): Show |
G | upstream_gene_variant | MODIFIER | NA19001.hp2 | a0005 | a0005c0008 | a0005c0008t0001 | a0005c0008t0001g0080 | 1 | 318 | 0.0031 | -15 | c.-17 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 40 | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45899270 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0303 | 1 | 318 | 0.0031 | -15 | c.536 others(34): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45901150 | CTTAATTT others(8): Show |
C | intron_variant | MODIFIER | HG03704.hp1 HG04115.hp2 HG04204.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(1): Show | 4 | 318 | 0.0126 | -15 | c.536 others(34): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45901154 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG00673.hp1 HG01981.hp2 HG02148.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | 318 | 0.0094 | -15 | c.536 others(34): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID3A_chr19_921035_980939 | 928099 | TTGTCTGC others(8): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG02735.hp1 HG03942.hp2 |
a0001a0002 | a0001c0003a0002c0004 | a0001c0003t0166a0002c0004t0002a0002c0004t0071 | a0001c0003t0166g0002a0002c0004t0002g0304a0002c0004t0071g0001 | 3 | 364 | 0.0082 | -15 | c.-26 others(34): Show |
ARID3A | ENSG00000116017.11 | transcript | ENST00000263620.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARID3B_chr15_74536220_74603131 | 74570462 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0003a0002c0004others(2): Show | a0001c0002t0001a0001c0002t0006a0001c0002t0009others(6): Show | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0181others(44): Show | 49 | 338 | 0.1450 | -15 | c.553 others(32): Show |
ARID3B | ENSG00000179361.18 | transcript | ENST00000346246.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58319521 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 NA20300.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015 | 3 | 294 | 0.0102 | -15 | c.449 others(30): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58346927 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | NA18962.hp2 NA19006.hp2 NA19012.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0039a0001c0001t0001g0075a0002c0002t0001g0248 | 3 | 294 | 0.0102 | -15 | c.107 others(30): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |