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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0277 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02647.hp1 |
a0001 | a0001c0002 | a0001c0002t0013 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | 289 | 0.0069 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0101 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0239 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG00323.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0014 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | 289 | 0.0242 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0258 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG02965.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0085a0004c0005t0001g0086a0004c0005t0001g0087others(1): Show | 4 | 289 | 0.0138 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170399756 | G | GAAGGTAG others(3140): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0084 | 1 | 289 | 0.0035 | 3147 | c.269 others(3166): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
LAMA5_chr20_62304065_62372312 | 62318235 | A | AGAGAGCA others(3140): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0024 | a0024c0017 | a0024c0017t0001 | a0024c0017t0001g0157 | 1 | 186 | 0.0054 | 3147 | c.723 others(3164): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | ||||||
MEGF6_chr1_3482951_3616508 | 3502044 | C | CCCCCCAC others(3140): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0208 | 1 | 292 | 0.0034 | 3147 | c.218 others(3164): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3140): Show |
intron_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 | 1 | 434 | 0.0023 | 3147 | c.33- others(3160): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3140): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0277 | 1 | 434 | 0.0023 | 3147 | c.33- others(3160): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3140): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 434 | 0.0023 | 3147 | c.33- others(3160): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3140): Show |
intron_variant | MODIFIER | HG02896.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203a0001c0001t0001g0267 | 2 | 434 | 0.0046 | 3147 | c.33- others(3160): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3140): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03130.hp2 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0204a0001c0003t0001g0234 | 2 | 434 | 0.0046 | 3147 | c.33- others(3160): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3140): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0188 | 1 | 188 | 0.0053 | 3147 | c.103 others(3164): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3140): Show |
intron_variant | MODIFIER | NA19081.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0173 | 1 | 188 | 0.0053 | 3147 | c.103 others(3164): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3141): Show |
intron_variant | MODIFIER | NA20805.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0242 | 1 | 264 | 0.0038 | 3148 | c.400 others(3167): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3141): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0018 | a0001c0018t0001 | a0001c0018t0001g0053 | 1 | 264 | 0.0038 | 3148 | c.400 others(3167): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3141): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0037 | 1 | 264 | 0.0038 | 3148 | c.400 others(3167): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3141): Show |
intron_variant | MODIFIER | HG02027.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0207 | 1 | 264 | 0.0038 | 3148 | c.400 others(3167): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NBPF10_chr1_146059711_146149804 | 146084423 | C | CTGAAAAC others(3141): Show |
intron_variant | MODIFIER | HG02040.hp1 | a0214 | a0214c0229 | a0214c0229t0003 | a0214c0229t0003g0275 | 1 | 283 | 0.0035 | 3148 | c.844 others(3163): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 67/89 | chr1 | TogoVar | ||||||
OSBPL5_chr11_3082107_3170310 | 3097061 | A | AAGGGGGA others(3141): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0068 | 1 | 326 | 0.0031 | 3148 | c.162 others(3167): Show |
OSBPL5 | ENSG00000021762.20 | transcript | ENST00000263650.12 | protein_coding | 14/21 | chr11 | TogoVar | ||||||
PTGR1_chr9_111557567_111604647 | 111578316 | T | TTATTTCT others(3141): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0050 | 1 | 408 | 0.0025 | 3148 | c.651 others(3163): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | TogoVar | ||||||
RAB3B_chr1_51902956_51995700 | 51906876 | G | GGAAGGAA others(3141): Show |
downstream_gene_variant | MODIFIER | HG01071.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0032 | 1 | 62 | 0.0161 | 3148 | c.*13 others(3161): Show |
RAB3B | ENSG00000169213.7 | transcript | ENST00000371655.4 | protein_coding | 1079 | chr1 | TogoVar | ||||||
RRAS2_chr11_14272922_14364183 | 14276623 | A | AGGGAGGG others(3141): Show |
downstream_gene_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208 | 1 | 279 | 0.0036 | 3148 | c.*27 others(3159): Show |
RRAS2 | ENSG00000133818.14 | transcript | ENST00000256196.9 | protein_coding | 1298 | chr11 | TogoVar | ||||||
TUBGCP5_chr15_22994177_23044569 | 23043111 | C | AATAACCC others(3141): Show |
upstream_gene_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 351 | 0.0029 | 3148 | c.-35 others(3159): Show |
TUBGCP5 | ENSG00000275835.5 | transcript | ENST00000615383.5 | protein_coding | 3542 | chr15 | TogoVar | ||||||
DIP2B_chr12_50499985_50753657 | 50604179 | A | ACTCTGAA others(3142): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0019 | 1 | 284 | 0.0035 | 3149 | c.101 others(3168): Show |
DIP2B | ENSG00000066084.13 | transcript | ENST00000301180.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3142): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0002 | a0002c0008 | a0002c0008t0022 | a0002c0008t0022g0102 | 1 | 264 | 0.0038 | 3149 | c.400 others(3168): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MORN1_chr1_2316253_2396554 | 2325121 | C | CCTTCCCT others(3142): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 | 1 | 80 | 0.0125 | 3149 | c.125 others(3166): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | ||||||
MORN1_chr1_2316253_2396554 | 2325121 | C | CCTTCCCT others(3142): Show |
intron_variant | MODIFIER | HG01517.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 80 | 0.0125 | 3149 | c.125 others(3166): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3142): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0003 | a0003c0010 | a0003c0010t0001 | a0003c0010t0001g0074 | 1 | 434 | 0.0023 | 3149 | c.33- others(3162): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3142): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0275 | 1 | 434 | 0.0023 | 3149 | c.33- others(3162): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3142): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0223 | 1 | 434 | 0.0023 | 3149 | c.33- others(3162): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3142): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02922.hp1 HG03225.hp2 others(5): Show |
a0001 | a0001c0001a0001c0007a0001c0012 | a0001c0001t0001a0001c0007t0001a0001c0007t0003others(1): Show | a0001c0001t0001g0231a0001c0007t0001g0040a0001c0007t0001g0140others(5): Show | 8 | 434 | 0.0184 | 3149 | c.33- others(3162): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236714265 | T | TGTGTGTT others(3143): Show |
intron_variant | MODIFIER | HG01516.hp1 | a0001 | a0001c0027 | a0001c0027t0001 | a0001c0027t0001g0311 | 1 | 344 | 0.0029 | 3150 | c.127 others(3167): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236714265 | T | TGTGTGTT others(3143): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0341 | 1 | 344 | 0.0029 | 3150 | c.127 others(3167): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236714265 | T | TGTGTGTT others(3143): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0271 | 1 | 344 | 0.0029 | 3150 | c.127 others(3167): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACTN2_chr1_236681499_236769631 | 236714265 | T | TGTGTGTT others(3143): Show |
intron_variant | MODIFIER | HG01258.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0287 | 1 | 344 | 0.0029 | 3150 | c.127 others(3167): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ADGRA1_chr10_133082924_133136675 | 133111331 | C | CACCTGCC others(3143): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0286 | 1 | 368 | 0.0027 | 3150 | c.401 others(3167): Show |
ADGRA1 | ENSG00000197177.16 | transcript | ENST00000392607.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
CHL1_chr3_191763_414417 | 262424 | C | CAGATCTA others(3143): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0039 | 1 | 290 | 0.0035 | 3150 | c.-95 others(3169): Show |
CHL1 | ENSG00000134121.10 | transcript | ENST00000256509.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
DOCK2_chr5_169632275_170088382 | 169949675 | T | TCAATGTG others(3143): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0003 | a0003c0050 | a0003c0050t0002 | a0003c0050t0002g0174 | 1 | 184 | 0.0054 | 3150 | c.280 others(3171): Show |
DOCK2 | ENSG00000134516.20 | transcript | ENST00000520908.7 | protein_coding | 27/51 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3143): Show |
intron_variant | MODIFIER | HG01978.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0167 | 1 | 264 | 0.0038 | 3150 | c.400 others(3169): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
HPCAL1_chr2_10297904_10432604 | 10399271 | C | CCACCACC others(3143): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0236 | 1 | 314 | 0.0032 | 3150 | c.-25 others(3167): Show |
HPCAL1 | ENSG00000115756.13 | transcript | ENST00000307845.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
INSYN2B_chr5_169856303_169985495 | 169949675 | T | TCAATGTG others(3143): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0242 | 1 | 318 | 0.0031 | 3150 | c.-91 others(3171): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | TogoVar | ||||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(3143): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0085 | a0085c0055 | a0085c0055t0005 | a0085c0055t0005g0239 | 1 | 292 | 0.0034 | 3150 | c.218 others(3165): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3143): Show |
intron_variant | MODIFIER | NA18972.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0143 | 1 | 434 | 0.0023 | 3150 | c.33- others(3163): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3143): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02258.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 2 | 434 | 0.0046 | 3150 | c.33- others(3163): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NKX1-1_chr4_1397932_1411442 | 1398178 | G | GGGCATCT others(3143): Show |
downstream_gene_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0003 | 1 | 382 | 0.0026 | 3150 | c.*47 others(3161): Show |
NKX1-1 | ENSG00000235608.2 | transcript | ENST00000422806.2 | protein_coding | 4753 | chr4 | TogoVar |