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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
APOBEC3B_chr22_38977347_38997779 | 38988683 | C | CTCTCTTT others(31): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 | 1 | 354 | 0.0028 | 38 | c.570 others(53): Show |
APOBEC3B | ENSG00000179750.16 | transcript | ENST00000333467.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
APOBEC3B_chr22_38977347_38997779 | 38988683 | C | CTCTCTTT others(31): Show |
intron_variant | MODIFIER | HG01943.hp2 HG02622.hp1 NA18941.hp2 others(4): Show |
a0001a0014 | a0001c0001a0014c0030 | a0001c0001t0001a0014c0030t0001 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0107others(3): Show | 7 | 354 | 0.0198 | 38 | c.570 others(53): Show |
APOBEC3B | ENSG00000179750.16 | transcript | ENST00000333467.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
APOBEC3B_chr22_38977347_38997779 | 38988683 | C | CTCTCTTT others(31): Show |
intron_variant | MODIFIER | NA19083.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0183 | 1 | 354 | 0.0028 | 38 | c.570 others(53): Show |
APOBEC3B | ENSG00000179750.16 | transcript | ENST00000333467.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
APOL5_chr22_35712872_35734483 | 35717235 | A | AAAAAAAA others(31): Show |
upstream_gene_variant | MODIFIER | NA18976.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0001 | 1 | 401 | 0.0025 | 38 | c.-63 others(47): Show |
APOL5 | ENSG00000128313.2 | transcript | ENST00000249044.2 | protein_coding | 636 | chr22 | TogoVar | ||||||
APOOL_chrX_84998877_85098315 | 85067637 | C | CACACACA others(31): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0114 | a0001c0001t0114g0216 | 1 | 256 | 0.0039 | 38 | c.486 others(53): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
APPL2_chr12_105168300_105241174 | 105186622 | T | TATGATAT others(31): Show |
intron_variant | MODIFIER | HG01081.hp1 HG01943.hp1 HG01952.hp1 others(14): Show |
a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0015a0001c0003t0005g0016a0001c0003t0005g0017others(11): Show | 17 | 392 | 0.0434 | 38 | c.163 others(57): Show |
APPL2 | ENSG00000136044.12 | transcript | ENST00000258530.8 | protein_coding | 17/20 | chr12 | TogoVar | ||||||
APPL2_chr12_105168300_105241174 | 105186622 | T | TATGATAT others(31): Show |
intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0161 | 1 | 392 | 0.0026 | 38 | c.163 others(57): Show |
APPL2 | ENSG00000136044.12 | transcript | ENST00000258530.8 | protein_coding | 17/20 | chr12 | TogoVar | ||||||
AQP11_chr11_77584953_77615356 | 77596501 | T | TATATGTG others(31): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0063 | 1 | 432 | 0.0023 | 38 | c.619 others(55): Show |
AQP11 | ENSG00000178301.4 | transcript | ENST00000313578.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AQP11_chr11_77584953_77615356 | 77596537 | A | AATATATA others(31): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0061 | 1 | 432 | 0.0023 | 38 | c.619 others(55): Show |
AQP11 | ENSG00000178301.4 | transcript | ENST00000313578.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AQP12A_chr2_240686866_240703483 | 240693897 | G | GTCTCTCT others(31): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046 | 1 | 171 | 0.0059 | 38 | c.572 others(53): Show |
AQP12A | ENSG00000184945.15 | transcript | ENST00000337801.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARCN1_chr11_118567409_118608033 | 118581929 | G | GACACACA others(31): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0002 | a0001c0002t0014 | a0001c0002t0014g0034 | 1 | 368 | 0.0027 | 38 | c.267 others(53): Show |
ARCN1 | ENSG00000095139.15 | transcript | ENST00000264028.5 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121577240 | T | TATCTACA others(31): Show |
intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0358 | 1 | 410 | 0.0024 | 38 | c.220 others(53): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121577257 | A | ACATGTAC others(31): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0330 | 1 | 410 | 0.0024 | 38 | c.220 others(53): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | chr3 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(31): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 162 | 0.0062 | 38 | c.113 others(59): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP20_chr11_110572043_110717437 | 110648153 | T | TAATATAT others(31): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0076 | 1 | 226 | 0.0044 | 38 | c.189 others(57): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24588347 | C | CTAGGGTA others(31): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
a0001a0005 | a0001c0001a0001c0014a0005c0005 | a0001c0001t0001a0001c0014t0004a0005c0005t0004 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | 352 | 0.1136 | 38 | c.418 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(31): Show |
downstream_gene_variant | MODIFIER | HG00140.hp1 HG00544.hp1 HG01167.hp2 others(9): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0004a0001c0005others(4): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(4): Show | a0001c0001t0001g0056a0001c0001t0001g0151a0001c0001t0001g0205others(9): Show | 12 | 309 | 0.0388 | 38 | c.*21 others(49): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTATATAT others(31): Show |
downstream_gene_variant | MODIFIER | HG00733.hp2 HG02135.hp2 |
a0001a0014 | a0001c0001a0014c0046 | a0001c0001t0001a0014c0046t0003 | a0001c0001t0001g0119a0014c0046t0003g0027 | 2 | 309 | 0.0065 | 38 | c.*21 others(49): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85540973 | G | GGCTTAAT others(31): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(17): Show | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0030others(29): Show | 32 | 108 | 0.2963 | 38 | c.-20 others(57): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(31): Show |
intron_variant | MODIFIER | NA19082.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0126 | 1 | 198 | 0.0051 | 38 | c.110 others(59): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(31): Show |
intron_variant | MODIFIER | HG02523.hp1 HG02886.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010a0001c0001t0024 | a0001c0001t0002g0022a0001c0001t0010g0076a0001c0001t0024g0112 | 3 | 198 | 0.0152 | 38 | c.110 others(57): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(31): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 | 1 | 248 | 0.0040 | 38 | c.122 others(53): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(31): Show |
intron_variant | MODIFIER | HG02080.hp1 NA19010.hp2 NA19081.hp2 |
a0002a0003 | a0002c0002a0003c0004 | a0002c0002t0002a0003c0004t0001 | a0002c0002t0002g0137a0002c0002t0002g0138a0003c0004t0001g0136 | 3 | 248 | 0.0121 | 38 | c.122 others(53): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(31): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 248 | 0.0040 | 38 | c.122 others(53): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(31): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02886.hp1 HG04184.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0016 | a0001c0001t0002g0134a0001c0001t0002g0136a0001c0001t0016g0196 | 3 | 398 | 0.0075 | 38 | c.226 others(57): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(31): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0033 | 1 | 286 | 0.0035 | 38 | c.245 others(57): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(31): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0135 | 1 | 230 | 0.0044 | 38 | c.862 others(53): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11190464 | T | TATATTTA others(31): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 144 | 0.0069 | 38 | c.821 others(55): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17686108 | T | TTCTTTCT others(31): Show |
intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0017 | a0001c0017t0002 | a0001c0017t0002g0113 | 1 | 168 | 0.0060 | 38 | c.301 others(57): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1823999 | C | CGCGGGGG others(31): Show |
5_prime_UTR_variant | MODIFIER | HG01516.hp1 | a0001 | a0001c0003 | a0001c0003t0029 | a0001c0003t0029g0126 | 1 | 363 | 0.0028 | 38 | c.-15 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19390 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ARHGEF10_chr8_1818926_1963641 | 1825186 | C | CCGCACCC others(31): Show |
intron_variant | MODIFIER | NA18971.hp1 NA18983.hp2 NA19064.hp1 |
a0001a0006 | a0001c0111a0001c0112a0006c0065 | a0001c0111t0047a0001c0112t0017a0006c0065t0017 | a0001c0111t0047g0123a0001c0112t0017g0124a0006c0065t0017g0125 | 3 | 363 | 0.0083 | 38 | c.-48 others(55): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTTTCT others(31): Show |
downstream_gene_variant | MODIFIER | HG02647.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0029 | 1 | 362 | 0.0028 | 38 | c.*59 others(49): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(31): Show |
intron_variant | MODIFIER | NA18944.hp2 NA19064.hp1 |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0016a0003c0003t0003 | a0002c0002t0016g0256a0003c0003t0003g0240 | 2 | 362 | 0.0055 | 38 | c.33- others(55): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120341307 | C | CTCGGCCT others(31): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | 308 | 0.4708 | 38 | c.32+ others(53): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120367353 | C | CTTTTTTT others(31): Show |
intron_variant | MODIFIER | NA19005.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0080 | 1 | 308 | 0.0033 | 38 | c.32+ others(55): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAAA others(31): Show |
intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0030 | 1 | 308 | 0.0033 | 38 | c.33- others(53): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41893410 | C | CCTGGGTC others(31): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0004 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(38): Show | 45 | 234 | 0.1923 | 38 | c.644 others(53): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41893814 | G | GGGGGCTG others(31): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 234 | 0.0043 | 38 | c.645 others(53): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41896787 | T | TCCCCCTC others(31): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0130 | 1 | 234 | 0.0043 | 38 | c.112 others(55): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF1_chr19_41878184_41912452 | 41896830 | A | ATCCTCTC others(31): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 234 | 0.0043 | 38 | c.112 others(55): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF6_chrX_136660550_136785932 | 136663413 | A | ATATATAT others(31): Show |
downstream_gene_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0213 | 1 | 247 | 0.0041 | 38 | c.*46 others(49): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2136 | chrX | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26710494 | T | TACACACA others(31): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 146 | 0.0069 | 38 | c.113 others(59): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157161431 | G | GTGTGTGT others(31): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0150 | 1 | 150 | 0.0067 | 38 | c.309 others(57): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58337242 | T | TTATATAT others(31): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0067 | 1 | 294 | 0.0034 | 38 | c.906 others(55): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58337246 | T | TTATATAT others(31): Show |
intron_variant | MODIFIER | HG01169.hp2 HG01516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031a0001c0001t0001g0051 | 2 | 294 | 0.0068 | 38 | c.906 others(55): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARID4B_chr1_235161902_235333179 | 235255219 | C | CTATATAT others(31): Show |
intron_variant | MODIFIER | HG02027.hp2 HG02258.hp2 NA18978.hp2 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0098a0001c0002t0001g0099a0002c0003t0001g0117 | 3 | 272 | 0.0110 | 38 | c.274 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 5/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235255219 | C | CTATATAT others(31): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0007 | a0007c0016 | a0007c0016t0001 | a0007c0016t0001g0103 | 1 | 272 | 0.0037 | 38 | c.274 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 5/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235255219 | C | CTATATAT others(31): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02886.hp2 NA18943.hp1 others(1): Show |
a0001a0002a0003 | a0001c0002a0002c0003a0003c0005 | a0001c0002t0001a0002c0003t0001a0003c0005t0002 | a0001c0002t0001g0108a0001c0002t0001g0113a0002c0003t0001g0119others(1): Show | 4 | 272 | 0.0147 | 38 | c.274 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 5/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235255263 | A | ATAGATAG others(31): Show |
intron_variant | MODIFIER | HG00280.hp2 HG03704.hp2 NA18957.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0016a0001c0002t0001g0041a0001c0002t0001g0063others(1): Show | 4 | 272 | 0.0147 | 38 | c.274 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 5/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235296843 | A | AAGGGAGA others(31): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0092 | 1 | 272 | 0.0037 | 38 | c.6+3 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 2/23 | chr1 | TogoVar |