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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0072 | 1 | 108 | 0.0093 | 25 | c.268 others(44): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85982373 | T | TTTTTGTT others(18): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01516.hp2 HG02055.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0010 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0039others(4): Show | 7 | 108 | 0.0648 | 25 | c.928 others(42): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949174 | A | AGAGAGAG others(18): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0048 | 1 | 198 | 0.0051 | 25 | c.110 others(46): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949176 | A | AGAGAGAG others(18): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0183 | 1 | 198 | 0.0051 | 25 | c.110 others(46): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949186 | A | AGAGAGAG others(18): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0096 | 1 | 198 | 0.0051 | 25 | c.110 others(46): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(18): Show |
intron_variant | MODIFIER | HG02818.hp1 NA18971.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0002t0003 | a0001c0001t0006g0086a0001c0002t0003g0173 | 2 | 198 | 0.0101 | 25 | c.110 others(46): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTATTT others(18): Show |
intron_variant | MODIFIER | HG02572.hp2 HG03490.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0011 | a0001c0001t0001g0034a0001c0001t0003g0033a0001c0001t0011g0094 | 3 | 198 | 0.0152 | 25 | c.110 others(46): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012578 | A | ATATATAT others(18): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0052 | a0001c0001t0052g0078 | 1 | 198 | 0.0051 | 25 | c.110 others(44): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(18): Show |
intron_variant | MODIFIER | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(41): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(10): Show | a0001c0001t0001g0259a0001c0001t0005g0209a0001c0001t0021g0171others(40): Show | 44 | 347 | 0.1268 | 25 | c.174 others(44): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(18): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01496.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0006a0002c0003t0031 | a0001c0001t0006g0100a0002c0003t0031g0089 | 2 | 310 | 0.0065 | 25 | c.100 others(44): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47007643 | C | CTTTTTTT others(18): Show |
downstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0002 | a0001c0002t0053 | a0001c0002t0053g0127 | 1 | 298 | 0.0034 | 25 | c.*69 others(36): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2567 | chr19 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(18): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01243.hp2 HG01515.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0037a0002c0002t0002others(5): Show | a0001c0001t0001g0099a0001c0001t0001g0148a0001c0001t0037g0041others(9): Show | 12 | 286 | 0.0420 | 25 | c.313 others(44): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTCT others(18): Show |
intron_variant | MODIFIER | HG01934.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 286 | 0.0035 | 25 | c.245 others(44): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(18): Show |
intron_variant | MODIFIER | HG03579.hp1 NA19057.hp2 |
a0001 | a0001c0003a0001c0008 | a0001c0003t0003a0001c0008t0001 | a0001c0003t0003g0269a0001c0008t0001g0004 | 2 | 286 | 0.0070 | 25 | c.245 others(44): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | HG00597.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0220others(2): Show | 5 | 286 | 0.0175 | 25 | c.245 others(44): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948751 | C | CACACACA others(18): Show |
intron_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0220 | 1 | 230 | 0.0044 | 25 | c.862 others(40): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | chr17 | TogoVar | ||||||
ARHGAP9_chr12_57467269_57484866 | 57483097 | T | TCAAAAAA others(18): Show |
upstream_gene_variant | MODIFIER | HG01496.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 406 | 0.0025 | 25 | c.-33 others(36): Show |
ARHGAP9 | ENSG00000123329.20 | transcript | ENST00000393791.8 | protein_coding | 3232 | chr12 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 286148 | C | CCTCCCTG others(18): Show |
downstream_gene_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 442 | 0.0023 | 25 | c.*33 others(36): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3139 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1830262 | T | TCAGGCGG others(18): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(66): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(94): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(133): Show | 136 | 363 | 0.3747 | 25 | c.-48 others(42): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 157013300 | C | CACACACA others(18): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0147 | 1 | 362 | 0.0028 | 25 | c.33- others(42): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120367353 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | HG03453.hp2 NA19083.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0031a0002c0003t0002 | a0001c0001t0031g0090a0002c0003t0002g0069 | 2 | 308 | 0.0065 | 25 | c.32+ others(42): 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(18): Show |
intron_variant | MODIFIER | NA20905.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0037 | 1 | 308 | 0.0033 | 25 | c.33- others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3467795 | C | CCCGGCAT others(18): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0186 | 1 | 334 | 0.0030 | 25 | c.804 others(40): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7367844 | A | ATATATAT others(18): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
a0005 | a0005c0009a0005c0039 | a0005c0009t0009a0005c0039t0001 | a0005c0009t0009g0061a0005c0009t0009g0067a0005c0009t0009g0068others(2): Show | 5 | 298 | 0.0168 | 25 | c.15+ others(40): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | C | CTTCTTTT others(18): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(5): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0003a0005c0022others(3): Show | a0001c0001t0002a0002c0003t0002a0005c0022t0001others(3): Show | a0001c0001t0002g0008a0001c0001t0002g0032a0001c0001t0002g0062others(5): Show | 8 | 188 | 0.0426 | 25 | c.34- others(42): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737501 | T | TCTTTTCT others(18): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0024 | a0024c0040 | a0024c0040t0004 | a0024c0040t0004g0116 | 1 | 188 | 0.0053 | 25 | c.34- others(42): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | G | GGAATGGA others(18): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0016 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561434 | A | AGAATGGA others(18): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0004 | a0001c0004t0009 | a0001c0004t0009g0103 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561439 | A | AGAATGGA others(18): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0172 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561444 | A | AGAATAGA others(18): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0083 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561444 | A | AGAATAGA others(18): Show |
intron_variant | MODIFIER | HG01074.hp1 | a0004 | a0004c0006 | a0004c0006t0001 | a0004c0006t0001g0093 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561444 | A | AGAATGGA others(18): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01346.hp2 |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0036a0001c0004t0005g0039 | 2 | 186 | 0.0108 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561454 | A | AGAATAGA others(18): Show |
intron_variant | MODIFIER | HG02027.hp1 | a0002 | a0002c0027 | a0002c0027t0001 | a0002c0027t0001g0055 | 1 | 186 | 0.0054 | 25 | c.196 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105643140 | T | TTTTTCAG others(18): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0009 | a0009c0021 | a0009c0021t0001 | a0009c0021t0001g0023 | 1 | 186 | 0.0054 | 25 | c.675 others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARID1A_chr1_26691015_26787104 | 26708266 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0133 | 1 | 146 | 0.0069 | 25 | c.113 others(46): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156856802 | T | TTGCCTTT others(18): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(99): Show |
a0001a0002a0003others(22): Show | a0001c0001a0001c0002a0001c0007others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(45): Show | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 102 | 150 | 0.6800 | 25 | c.198 others(46): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156893045 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0136 | 1 | 150 | 0.0067 | 25 | c.198 others(44): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156932419 | C | CTTTTAAA others(18): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01109.hp1 HG01109.hp2 others(54): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0002a0001c0007others(25): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0034others(54): Show | 57 | 150 | 0.3800 | 25 | c.213 others(44): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039322 | C | CTTTTTTT others(18): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 | 1 | 150 | 0.0067 | 25 | c.224 others(46): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID3A_chr19_921035_980939 | 973104 | A | ATTTTTTT others(18): Show |
3_prime_UTR_variant | MODIFIER | HG00733.hp2 HG01109.hp2 HG02027.hp2 others(6): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0146a0001c0003t0033a0001c0003t0112others(4): Show | a0001c0001t0146g0247a0001c0003t0033g0328a0001c0003t0033g0340others(6): Show | 9 | 364 | 0.0247 | 25 | c.*10 others(36): Show |
ARID3A | ENSG00000116017.11 | transcript | ENST00000263620.8 | protein_coding | 9/9 | 1061 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||
ARID3B_chr15_74536220_74603131 | 74560031 | T | TAAAAAAA others(18): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0002g0021a0001c0001t0002g0057a0001c0001t0002g0153others(16): Show | 20 | 338 | 0.0592 | 25 | c.553 others(44): Show |
ARID3B | ENSG00000179361.18 | transcript | ENST00000346246.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58337246 | T | TATATATA others(18): Show |
intron_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 294 | 0.0034 | 25 | c.906 others(42): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 11/23 | chr14 | TogoVar | ||||||
ARID4A_chr14_58293555_58378876 | 58337249 | T | TATATATA others(18): Show |
intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 294 | 0.0034 | 25 | c.906 others(42): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARID4B_chr1_235161902_235333179 | 235236833 | A | AAAAAAAA others(18): Show |
intron_variant | MODIFIER | HG01346.hp2 NA18956.hp2 NA19082.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208a0001c0001t0001g0224a0001c0001t0001g0237 | 3 | 272 | 0.0110 | 25 | c.586 others(42): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235236862 | A | ATATATAT others(18): Show |
intron_variant | MODIFIER | HG01109.hp2 HG03041.hp2 |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0001a0003c0006t0001 | a0001c0001t0001g0261a0003c0006t0001g0153 | 2 | 272 | 0.0074 | 25 | c.586 others(42): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235236862 | A | ATATATAT others(18): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0155 | 1 | 272 | 0.0037 | 25 | c.586 others(42): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235236862 | A | ATATATAT others(18): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0154 | 1 | 272 | 0.0037 | 25 | c.586 others(42): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235238153 | A | AAAAAAAA others(18): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01891.hp2 HG02622.hp1 others(6): Show |
a0002a0009 | a0002c0003a0009c0018 | a0002c0003t0001a0009c0018t0001 | a0002c0003t0001g0097a0002c0003t0001g0102a0002c0003t0001g0109others(6): Show | 9 | 272 | 0.0331 | 25 | c.585 others(42): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | ||||||
ARID5B_chr10_61896699_62101944 | 62099312 | C | CAAAAAAA others(18): Show |
downstream_gene_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0223 | 1 | 242 | 0.0041 | 25 | c.*62 others(36): Show |
ARID5B | ENSG00000150347.17 | transcript | ENST00000279873.12 | protein_coding | 2369 | chr10 | TogoVar | ||||||
ARL13B_chr3_93975155_94060678 | 94041500 | T | TTCAAAGC others(18): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0253 | 1 | 264 | 0.0038 | 25 | c.798 others(42): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |