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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CYSLTR1_chrX_78266468_78332611 | 78269606 | A | AATACAGA others(1665): Show |
downstream_gene_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 240 | 0.0042 | 1672 | c.*31 others(1683): Show |
CYSLTR1 | ENSG00000173198.6 | transcript | ENST00000373304.4 | protein_coding | 1861 | chrX | TogoVar | |||||||
CYSLTR1_chrX_78266468_78332611 | 78269606 | A | AATACAGA others(1665): Show |
downstream_gene_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 240 | 0.0042 | 1672 | c.*31 others(1683): Show |
CYSLTR1 | ENSG00000173198.6 | transcript | ENST00000373304.4 | protein_coding | 1861 | chrX | TogoVar | |||||||
DCDC2C_chr2_3698575_3853008 | 3725423 | A | AGGTGGAT others(1665): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0256 a0001c0002t0004g0291 |
2 | 324 | 0.0062 | 1672 | c.340 others(1689): Show |
DCDC2C | ENSG00000214866.9 | transcript | ENST00000399143.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FHIT_chr3_59742277_61256452 | 60861252 | C | CATATCAT others(1665): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0021 | 1 | 46 | 0.0217 | 1672 | c.-11 others(1693): Show |
FHIT | ENSG00000189283.11 | transcript | ENST00000492590.6 | protein_coding | 3/9 | chr3 | TogoVar | |||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1665): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 404 | 0.0025 | 1672 | c.125 others(1689): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1665): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02559.hp1 |
a0001a0002 | a0001c0026a0002c0009 | a0001c0026t0001a0002c0009t0002 | a0001c0026t0001g0140 a0002c0009t0002g0116 |
2 | 404 | 0.0050 | 1672 | c.125 others(1689): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150668 | G | GCTCCTAC others(1665): Show |
intron_variant | MODIFIER | HG01071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0262 | 1 | 294 | 0.0034 | 1672 | c.902 others(1687): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132150747 | C | CGCCGCCT others(1665): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 294 | 0.0034 | 1672 | c.902 others(1687): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
PCCA_chr13_100084093_100535435 | 100451904 | C | CCTCTCTC others(1665): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 1 | 174 | 0.0058 | 1672 | c.189 others(1691): Show |
PCCA | ENSG00000175198.17 | transcript | ENST00000376285.6 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
SLC6A3_chr5_1387794_1450440 | 1414498 | G | GGAGAAGG others(1665): Show |
intron_variant | MODIFIER | NA19065.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 373 | 0.0027 | 1672 | c.115 others(1689): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | |||||||
SUPV3L1_chr10_69175234_69214093 | 69213563 | A | AAGGCCAC others(1665): Show |
downstream_gene_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0231 | 1 | 354 | 0.0028 | 1672 | c.*45 others(1683): Show |
SUPV3L1 | ENSG00000156502.14 | transcript | ENST00000359655.9 | protein_coding | 4471 | chr10 | TogoVar | |||||||
SUPV3L1_chr10_69175234_69214093 | 69213563 | A | AAGGCCAC others(1665): Show |
downstream_gene_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0230 | 1 | 354 | 0.0028 | 1672 | c.*45 others(1683): Show |
SUPV3L1 | ENSG00000156502.14 | transcript | ENST00000359655.9 | protein_coding | 4471 | chr10 | TogoVar | |||||||
SUPV3L1_chr10_69175234_69214093 | 69213563 | A | AAGGCCAC others(1665): Show |
downstream_gene_variant | MODIFIER | NA19084.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0050 | 1 | 354 | 0.0028 | 1672 | c.*45 others(1683): Show |
SUPV3L1 | ENSG00000156502.14 | transcript | ENST00000359655.9 | protein_coding | 4471 | chr10 | TogoVar | |||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 362 | 0.0028 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 362 | 0.0028 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0107 | 1 | 362 | 0.0028 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(12): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0002 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(12): Show |
15 | 362 | 0.0414 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | HG00558.hp1 HG02074.hp1 NA18945.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0125 a0001c0001t0001g0263 a0001c0001t0001g0264 others(8): Show |
11 | 362 | 0.0304 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02922.hp1 HG03453.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | 362 | 0.0083 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1665): Show |
intron_variant | MODIFIER | NA20905.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0327 | 1 | 362 | 0.0028 | 1672 | c.266 others(1687): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TMEM132D_chr12_129066726_129909025 | 129828762 | G | GGGAGGGA others(1665): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0081 | 1 | 94 | 0.0106 | 1672 | c.79+ others(1689): Show |
TMEM132D | ENSG00000151952.16 | transcript | ENST00000422113.7 | protein_coding | 1/8 | chr12 | TogoVar | |||||||
TMIGD1_chr17_30311333_30339057 | 30338426 | T | TCTTCTTT others(1665): Show |
upstream_gene_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0007 | 1 | 348 | 0.0029 | 1672 | c.-44 others(1683): Show |
TMIGD1 | ENSG00000182271.13 | transcript | ENST00000328886.5 | protein_coding | 4370 | chr17 | TogoVar | |||||||
CLEC17A_chr19_14578084_14617035 | 14595973 | A | ATGTTGTT others(1666): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 364 | 0.0028 | 1673 | c.445 others(1688): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
CLEC17A_chr19_14578084_14617035 | 14595973 | A | ATGTTGTT others(1666): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0222 | 1 | 364 | 0.0028 | 1673 | c.445 others(1688): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134657109 | C | CAGTTTAT others(1666): Show |
intron_variant | MODIFIER | HG00323.hp1 HG04115.hp1 |
a0001 | a0001c0002a0001c0008 | a0001c0002t0004a0001c0008t0001 | a0001c0002t0004g0150 a0001c0008t0001g0149 |
2 | 272 | 0.0074 | 1673 | c.109 others(1692): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 1/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
ENTREP2_chr15_29115252_29575979 | 29558678 | C | CCTCCCAC others(1666): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0011 | a0001c0011t0010 | a0001c0011t0010g0053 | 1 | 125 | 0.0080 | 1673 | c.219 others(1692): Show |
ENTREP2 | ENSG00000104059.5 | transcript | ENST00000261275.5 | protein_coding | 1/10 | chr15 | TogoVar | |||||||
FHOD3_chr18_36292713_36785220 | 36463416 | T | TAATATAT others(1666): Show |
intron_variant | MODIFIER | NA20905.hp2 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0041 | 1 | 168 | 0.0060 | 1673 | c.338 others(1692): Show |
FHOD3 | ENSG00000134775.16 | transcript | ENST00000590592.6 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
GTPBP6_chrX_299759_323796 | 323547 | C | CGTGTGTG others(1666): Show |
upstream_gene_variant | MODIFIER | HG00140.hp2 | a0004 | a0004c0006 | a0004c0006t0003 | a0004c0006t0003g0015 | 1 | 155 | 0.0065 | 1673 | c.-47 others(1684): Show |
GTPBP6 | ENSG00000178605.14 | transcript | ENST00000326153.10 | protein_coding | 4752 | chrX | TogoVar | |||||||
ITGA3_chr17_50051110_50095481 | 50086103 | G | GTATGTTA others(1666): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 402 | 0.0025 | 1673 | c.292 others(1692): Show |
ITGA3 | ENSG00000005884.18 | transcript | ENST00000320031.13 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ITGA3_chr17_50051110_50095481 | 50086103 | G | GTATGTTA others(1666): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0180 | 1 | 402 | 0.0025 | 1673 | c.292 others(1692): Show |
ITGA3 | ENSG00000005884.18 | transcript | ENST00000320031.13 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ITGA3_chr17_50051110_50095481 | 50086103 | G | GTATGTTA others(1666): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0178 | 1 | 402 | 0.0025 | 1673 | c.292 others(1692): Show |
ITGA3 | ENSG00000005884.18 | transcript | ENST00000320031.13 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
KCNQ2_chr20_63395208_63477655 | 63450548 | A | ACTGCTGG others(1666): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0005 | a0005c0025 | a0005c0025t0097 | a0005c0025t0097g0260 | 1 | 330 | 0.0030 | 1673 | c.297 others(1690): Show |
KCNQ2 | ENSG00000075043.21 | transcript | ENST00000359125.7 | protein_coding | 1/16 | chr20 | TogoVar | |||||||
KCNQ2_chr20_63395208_63477655 | 63450548 | A | ACTGCTGG others(1666): Show |
intron_variant | MODIFIER | HG02074.hp2 HG02080.hp1 HG02129.hp2 others(1): Show |
a0001 | a0001c0008 | a0001c0008t0027a0001c0008t0028 | a0001c0008t0027g0276 a0001c0008t0027g0310 a0001c0008t0027g0312 others(1): Show |
4 | 330 | 0.0121 | 1673 | c.297 others(1690): Show |
KCNQ2 | ENSG00000075043.21 | transcript | ENST00000359125.7 | protein_coding | 1/16 | chr20 | TogoVar | |||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG02027.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0217 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | NA19002.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0183 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG00673.hp1 NA19004.hp1 NA19055.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0142 |
5 | 404 | 0.0124 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0235 |
6 | 404 | 0.0149 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0018a0001c0023others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
153 | 404 | 0.3787 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0222 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | HG03492.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
MAN1B1_chr9_137081985_137114183 | 137102262 | T | TAGGTCGG others(1666): Show |
intron_variant | MODIFIER | NA18987.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190 | 1 | 404 | 0.0025 | 1673 | c.125 others(1690): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PNPLA7_chr9_137454952_137555402 | 137502737 | C | CGGGGGGG others(1666): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0015 | a0015c0014 | a0015c0014t0001 | a0015c0014t0001g0158 | 1 | 188 | 0.0053 | 1673 | c.147 others(1692): Show |
PNPLA7 | ENSG00000130653.16 | transcript | ENST00000406427.6 | protein_coding | 14/34 | chr9 | TogoVar | |||||||
SUPV3L1_chr10_69175234_69214093 | 69213563 | A | AAGGCCAC others(1666): Show |
downstream_gene_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0236 | 1 | 354 | 0.0028 | 1673 | c.*45 others(1684): Show |
SUPV3L1 | ENSG00000156502.14 | transcript | ENST00000359655.9 | protein_coding | 4471 | chr10 | TogoVar | |||||||
TAF11L8_chr5_17585364_17595960 | 17587287 | G | GTTGAAAT others(1666): Show |
downstream_gene_variant | MODIFIER | NA18959.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 102 | 0.0098 | 1673 | c.*30 others(1684): Show |
TAF11L8 | ENSG00000283967.1 | transcript | ENST00000640803.1 | protein_coding | 3076 | chr5 | TogoVar | |||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1666): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 362 | 0.0028 | 1673 | c.266 others(1688): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1666): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 362 | 0.0028 | 1673 | c.266 others(1688): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TAX1BP1_chr7_27735162_27834767 | 27765069 | G | GCAGTGGT others(1666): Show |
intron_variant | MODIFIER | NA18989.hp2 NA19063.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | 362 | 0.0055 | 1673 | c.266 others(1688): Show |
TAX1BP1 | ENSG00000106052.14 | transcript | ENST00000396319.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |