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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(25): Show |
intron_variant | MODIFIER | HG02735.hp1 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0142 a0001c0001t0006g0084 |
2 | 49 | 0.0408 | 32 | c.110 others(51): 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(25): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0155 | 1 | 37 | 0.0270 | 32 | c.174 others(51): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(25): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0003 | a0003c0023 | a0003c0023t0001 | a0003c0023t0001g0120 | 1 | 121 | 0.0083 | 32 | c.122 others(47): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6736780 | A | ATTAAATG others(25): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0003t0003others(6): Show | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | 246 | 0.0488 | 32 | c.122 others(49): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(25): Show |
upstream_gene_variant | MODIFIER | HG00438.hp1 HG01975.hp2 HG02015.hp2 others(6): Show |
a0001a0010 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(6): Show | a0001c0001t0005g0023 a0001c0001t0017g0302 a0001c0001t0018g0208 others(6): Show |
9 | 209 | 0.0431 | 32 | c.-12 others(43): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(25): Show |
intron_variant | MODIFIER | HG02922.hp1 HG02970.hp1 HG03927.hp1 others(4): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0002a0001c0001t0004a0001c0014t0004 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0004g0173 others(4): Show |
7 | 109 | 0.0642 | 32 | c.226 others(51): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(25): Show |
intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 24 | 0.0417 | 32 | c.245 others(51): 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(25): Show |
intron_variant | MODIFIER | HG00099.hp1 HG01109.hp2 HG01243.hp1 others(15): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(6): Show | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0118 others(15): Show |
18 | 60 | 0.3000 | 32 | c.862 others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(25): Show |
intron_variant | MODIFIER | NA18984.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0105 | 1 | 131 | 0.0076 | 32 | c.176 others(51): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(25): Show |
intron_variant | MODIFIER | HG06807.hp1 NA19240.hp1 NA20905.hp1 |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0003a0002c0005t0006 | a0001c0001t0001g0045 a0002c0002t0003g0005 a0002c0005t0006g0018 |
3 | 54 | 0.0556 | 32 | c.589 others(51): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11567566 | A | AAAAAAAA others(25): Show |
intron_variant | MODIFIER | HG03098.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0006 | a0001c0001t0001g0024 a0002c0002t0006g0031 |
2 | 113 | 0.0177 | 32 | c.588 others(51): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44800566 | C | CCTCCCCA others(25): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0387 | 1 | 367 | 0.0027 | 32 | c.80- others(47): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44800566 | C | CCTCCCCG others(25): Show |
intron_variant | MODIFIER | HG02738.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0003a0002c0020others(2): Show | a0001c0001t0001a0002c0003t0004a0002c0020t0005others(2): Show | a0001c0001t0001g0042 a0002c0003t0004g0177 a0002c0020t0005g0073 others(2): Show |
5 | 371 | 0.0135 | 32 | c.80- others(47): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44800688 | G | GGGGGGCG others(25): Show |
intron_variant | MODIFIER | HG00639.hp2 HG01346.hp1 HG01928.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0050a0002c0051others(2): Show | a0001c0001t0003a0001c0050t0003a0002c0051t0004others(2): Show | a0001c0001t0003g0377 a0001c0050t0003g0217 a0002c0051t0004g0216 others(5): Show |
8 | 286 | 0.0280 | 32 | c.80- others(47): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839883 | T | AGTCTGGT others(25): Show |
intron_variant | MODIFIER | NA18980.hp2 | a0006 | a0006c0113 | a0006c0113t0004 | a0006c0113t0004g0300 | 1 | 336 | 0.0030 | 32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1840185 | A | ACTGTCTG others(25): Show |
intron_variant | MODIFIER | HG03834.hp2 NA21309.hp2 |
a0001 | a0001c0052a0001c0140 | a0001c0052t0045a0001c0140t0004 | a0001c0052t0045g0336 a0001c0140t0004g0294 |
2 | 360 | 0.0056 | 32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1860264 | C | CCGTAGAG others(25): Show |
intron_variant | MODIFIER | NA18957.hp1 | a0001 | a0001c0009 | a0001c0009t0005 | a0001c0009t0005g0141 | 1 | 289 | 0.0035 | 32 | c.481 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATATA others(25): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0002 | a0002c0004 | a0002c0004t0008 | a0002c0004t0008g0199 | 1 | 221 | 0.0045 | 32 | c.463 others(49): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAATATA others(25): Show |
intron_variant | MODIFIER | HG02145.hp2 HG03195.hp1 |
a0002 | a0002c0004 | a0002c0004t0013 | a0002c0004t0013g0185 a0002c0004t0013g0189 |
2 | 79 | 0.0253 | 32 | c.463 others(49): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(25): Show |
intron_variant | MODIFIER | NA19005.hp2 NA19010.hp1 |
a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0236 a0003c0003t0003g0256 |
2 | 142 | 0.0141 | 32 | c.33- others(49): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347179 | C | CCTTGCTT others(25): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0009 | a0009c0013 | a0009c0013t0001 | a0009c0013t0001g0293 | 1 | 79 | 0.0127 | 32 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(25): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0230 | 1 | 7 | 0.1429 | 32 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(25): Show |
intron_variant | MODIFIER | HG02257.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0216 a0001c0001t0001g0232 |
2 | 8 | 0.2500 | 32 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTTCTT others(25): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0018 | a0001c0018t0004 | a0001c0018t0004g0240 | 1 | 7 | 0.1429 | 32 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38934578 | T | TCCCCCCC others(25): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0246 | 1 | 272 | 0.0037 | 32 | c.506 others(49): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149598761 | T | TATATATA others(25): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0005 | a0005c0011 | a0005c0011t0003 | a0005c0011t0003g0316 | 1 | 260 | 0.0038 | 32 | c.186 others(47): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149599434 | C | CTTACTTA others(25): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0004 | a0004c0010 | a0004c0010t0014 | a0004c0010t0014g0319 | 1 | 45 | 0.0222 | 32 | c.186 others(49): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149599434 | C | CTTATTTA others(25): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
a0001a0003a0005others(1): Show | a0001c0002a0003c0003a0003c0029others(2): Show | a0001c0002t0005a0001c0002t0011a0003c0003t0002others(4): Show | a0001c0002t0005g0363 a0001c0002t0011g0356 a0003c0003t0002g0001 others(32): Show |
40 | 84 | 0.4762 | 32 | c.186 others(49): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561400 | T | TAGAATAG others(25): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0150 | 1 | 124 | 0.0081 | 32 | c.196 others(49): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105561400 | T | TAGAATAG others(25): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0039 | 1 | 124 | 0.0081 | 32 | c.196 others(49): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926048 | C | CTTTCTTT others(25): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02895.hp1 |
a0003a0007 | a0003c0003a0007c0017 | a0003c0003t0001a0007c0017t0001 | a0003c0003t0001g0030 a0007c0017t0001g0108 |
2 | 70 | 0.0286 | 32 | c.355 others(51): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926048 | C | CTTTCTTT others(25): Show |
intron_variant | MODIFIER | HG03516.hp1 NA18971.hp2 NA18990.hp1 others(1): Show |
a0003a0010a0013 | a0003c0003a0010c0048a0013c0019 | a0003c0003t0001a0010c0048t0001a0013c0019t0001 | a0003c0003t0001g0081 a0010c0048t0001g0110 a0013c0019t0001g0128 others(1): Show |
4 | 72 | 0.0556 | 32 | c.355 others(51): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130926048 | C | CTTTCTTT others(25): Show |
intron_variant | MODIFIER | HG04115.hp2 NA18970.hp2 |
a0005 | a0005c0004a0005c0046 | a0005c0004t0007a0005c0046t0001 | a0005c0004t0007g0006 a0005c0046t0001g0016 |
2 | 70 | 0.0286 | 32 | c.355 others(51): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARID1A_chr1_26691015_26787104 | 26710494 | T | TACACACA others(25): Show |
intron_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 15 | 0.0667 | 32 | c.113 others(53): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147439 | T | TCCCTCAC others(25): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 131 | 0.0076 | 32 | c.276 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147448 | C | CCCGCCTC others(25): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 148 | 0.0068 | 32 | c.276 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147554 | A | ACCCTGCC others(25): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0017 | a0001c0017t0020 | a0001c0017t0020g0049 | 1 | 100 | 0.0100 | 32 | c.276 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147642 | A | AGCCTCCG others(25): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
a0001a0004a0005others(3): Show | a0001c0002a0001c0008a0001c0021others(6): Show | a0001c0002t0001a0001c0008t0010a0001c0021t0007others(6): Show | a0001c0002t0001g0026 a0001c0008t0010g0133 a0001c0021t0007g0122 others(6): Show |
9 | 131 | 0.0687 | 32 | c.276 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147688 | C | CCCTCCGT others(25): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0001c0016others(9): Show | a0001c0001t0007a0001c0007t0001a0001c0007t0002others(10): Show | a0001c0001t0007g0030 a0001c0007t0001g0137 a0001c0007t0002g0006 others(10): Show |
13 | 146 | 0.0890 | 32 | c.276 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157147732 | C | CACCTCCG others(25): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02280.hp2 HG03453.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006 | a0001c0001t0004g0051 a0001c0001t0004g0060 a0001c0001t0004g0149 others(2): Show |
5 | 148 | 0.0338 | 32 | c.276 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157161431 | G | GTGTGTGT others(25): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0134 | 1 | 93 | 0.0108 | 32 | c.309 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID3A_chr19_921035_980939 | 973104 | A | ATTTTTTT others(25): Show |
3_prime_UTR_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0003 | a0001c0003t0172 | a0001c0003t0172g0039 | 1 | 22 | 0.0455 | 32 | c.*10 others(43): Show |
ARID3A | ENSG00000116017.11 | transcript | ENST00000263620.8 | protein_coding | 9/9 | 1061 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARID4A_chr14_58293555_58378876 | 58337242 | T | TTATATAT others(25): Show |
intron_variant | MODIFIER | HG02080.hp1 HG02559.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0002 | a0001c0001t0001g0084 a0001c0003t0002g0137 |
2 | 274 | 0.0073 | 32 | c.906 others(49): 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(25): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01891.hp1 HG02970.hp1 others(5): Show |
a0001a0002a0009 | a0001c0001a0001c0003a0002c0016others(1): Show | a0001c0001t0001a0001c0003t0002a0002c0016t0001others(1): Show | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | 110 | 0.0727 | 32 | c.906 others(49): Show |
ARID4A | ENSG00000032219.19 | transcript | ENST00000355431.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235236831 | A | AATATATA others(25): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0043 | 1 | 260 | 0.0038 | 32 | c.586 others(49): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | |||||||
ARID4B_chr1_235161902_235333179 | 235236862 | A | ATATATAT others(25): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 146 | 0.0068 | 32 | c.586 others(49): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 8/23 | chr1 | TogoVar | |||||||
ARID4B_chr1_235161902_235333179 | 235255265 | A | AGATAGAT others(25): Show |
intron_variant | MODIFIER | HG00438.hp2 HG03017.hp1 HG04199.hp2 |
a0001a0009 | a0001c0002a0009c0013 | a0001c0002t0001a0009c0013t0001 | a0001c0002t0001g0015 a0001c0002t0001g0078 a0009c0013t0001g0054 |
3 | 240 | 0.0125 | 32 | c.274 others(47): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 5/23 | chr1 | TogoVar | |||||||
ARID5B_chr10_61896699_62101944 | 62099312 | C | CAAAAAAA others(25): Show |
downstream_gene_variant | MODIFIER | HG01243.hp1 HG01884.hp1 NA19085.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0002g0085 |
3 | 102 | 0.0294 | 32 | c.*62 others(43): Show |
ARID5B | ENSG00000150347.17 | transcript | ENST00000279873.12 | protein_coding | 2369 | chr10 | TogoVar | |||||||
ARK2N_chr18_46169034_46271992 | 46190420 | T | TGAGGCAG others(25): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0002c0002others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0027 others(195): Show |
200 | 317 | 0.6309 | 32 | c.-71 others(51): Show |
ARK2N | ENSG00000152242.11 | transcript | ENST00000615052.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARK2N_chr18_46169034_46271992 | 46250491 | T | TACACACA others(25): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0276 | 1 | 117 | 0.0085 | 32 | c.899 others(49): Show |
ARK2N | ENSG00000152242.11 | transcript | ENST00000615052.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | TogoVar |