view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 82 | 0.0122 | 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 |
a0001a0015 | a0001c0001a0015c0030 | a0001c0001t0001a0015c0030t0001 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0107 others(3): Show |
7 | 88 | 0.0795 | 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 | 82 | 0.0122 | 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 | 34 | 0.0294 | 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 | a0001c0001t0010 | a0001c0001t0010g0220 | 1 | 251 | 0.0040 | 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 | a0001c0003t0005g0015 a0001c0003t0005g0016 a0001c0003t0005g0017 others(11): Show |
17 | 168 | 0.1012 | 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 | a0001c0001t0003g0160 | 1 | 152 | 0.0066 | 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 | a0001c0004t0001g0058 | 1 | 424 | 0.0024 | 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 | a0001c0004t0001g0056 | 1 | 189 | 0.0053 | 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 | a0001c0001t0001g0011 | 1 | 168 | 0.0060 | 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 | a0001c0002t0010 | a0001c0002t0010g0041 | 1 | 277 | 0.0036 | 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 | a0001c0001t0001g0337 | 1 | 407 | 0.0025 | 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 | a0001c0001t0004g0300 | 1 | 359 | 0.0028 | 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 | 18 | 0.0556 | 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 | a0001c0001t0003g0081 | 1 | 224 | 0.0045 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
40 | 350 | 0.1143 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0154 a0001c0001t0001g0205 others(9): Show |
12 | 63 | 0.1905 | 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 |
a0001a0010 | a0001c0001a0010c0046 | a0001c0001t0001a0010c0046t0003 | a0001c0001t0001g0121 a0010c0046t0003g0029 |
2 | 53 | 0.0377 | 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 |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(17): Show | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | 144 | 0.0069 | 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 | a0001c0001t0002a0001c0001t0010a0001c0001t0023 | a0001c0001t0002g0022 a0001c0001t0010g0076 a0001c0001t0023g0112 |
3 | 50 | 0.0600 | 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 | 121 | 0.0083 | 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 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0003c0004t0001g0136 |
3 | 123 | 0.0244 | 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 | 121 | 0.0083 | 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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0016g0198 |
3 | 105 | 0.0286 | 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 | 24 | 0.0417 | 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 | a0001c0001t0022g0128 | 1 | 43 | 0.0233 | 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 | 130 | 0.0077 | 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 | 165 | 0.0061 | 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 | a0001c0003t0029g0168 | 1 | 316 | 0.0032 | 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 | a0001c0111t0013a0001c0112t0013a0006c0065t0013 | a0001c0111t0013g0138 a0001c0112t0013g0139 a0006c0065t0013g0140 |
3 | 358 | 0.0084 | 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 | a0002c0002t0002g0036 | 1 | 253 | 0.0040 | 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 | a0002c0002t0016g0253 a0003c0003t0003g0237 |
2 | 142 | 0.0141 | 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 |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(141): Show |
145 | 306 | 0.4739 | 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 | a0002c0003t0002g0081 | 1 | 72 | 0.0139 | 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 | a0001c0002t0003g0039 | 1 | 72 | 0.0139 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
45 | 231 | 0.1948 | 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 | a0001c0001t0001g0003 | 1 | 228 | 0.0044 | 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 | a0001c0002t0001g0128 | 1 | 215 | 0.0047 | 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 | a0001c0001t0001g0126 | 1 | 220 | 0.0045 | 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 | a0001c0001t0001g0215 | 1 | 245 | 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 | a0001c0001t0001g0045 | 1 | 15 | 0.0667 | 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 | a0001c0001t0004g0149 | 1 | 93 | 0.0108 | 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 | a0001c0001t0013g0050 | 1 | 273 | 0.0037 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0056 |
2 | 104 | 0.0192 | 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 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0002c0003t0001g0117 |
3 | 202 | 0.0149 | 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 | a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0103 | 1 | 200 | 0.0050 | 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 | a0001c0002t0001g0108 a0001c0002t0001g0113 a0002c0003t0001g0119 others(1): Show |
4 | 203 | 0.0197 | 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 | a0001c0002t0001g0016 a0001c0002t0001g0041 a0001c0002t0001g0063 others(1): Show |
4 | 194 | 0.0206 | 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 | 116 | 0.0086 | 38 | c.6+3 others(53): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 2/23 | chr1 | TogoVar |