SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1128376 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190211 | GGAGGCTCTGGTTGT[C/T]TGAGCACCATGGGGG | 29882 |
rs1128395 | snp | A/G | 0.352504 | 0.228019 | utr-variant-3-prime, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190301 | GGGTTCTCCTTCACC[A/G]CAGAACCCAAACCTC | 29882 |
rs3087779 | snp | C/T | 0.306431 | 0.243548 | utr-variant-3-prime, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190033 | GGCACCTGCCCCTCT[C/T]GGCACCTGAGACAGT | 29882 |
rs3922734 | snp | A/G | 0.367913 | 0.220446 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137186047 | AGATGCGTCCTCGCT[A/G]TCACCAGGGCCCAGA | 29882 |
rs3922735 | snp | A/G | 0.384401 | 0.210799 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137186131 | CCCACCCAGGCCTCC[A/G]TGCTCTGGATGCTTC | 29882 |
rs4880219 | snp | C/T | 0.497881 | 0.0324789 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176186 | TAAGAAAAGGAAAGA[C/T]AGGAAGACACAGGCA | 29882 |
rs9696567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137189549 | GAGCCAGGTCTTGGG[C/T]AGAGCACCCAGCACG | 29882 |
rs9775861 | snp | C/G | 0.34659 | 0.230587 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182575 | CCACAAAGCACCAAA[C/G]GAGTCCAGGTAGGGG | 29882 |
rs9775873 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182861 | TCTCTCTGTGCTGGA[A/G]ATGGGGAGGCTGAGG | 29882 |
rs9776871 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182495 | gcctgggcgaaagag[A/T]gagactccatctcaa | 29882 |
rs10561545 | in-del | -/GCC | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178219 | ACCTCCACAAACGCC[-/GCC]ACTGGTCAGCCTGCC | 29882 |
rs10586196 | in-del | -/AG | 0.00716266 | 0.059414 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178258 | CACATGCAAGGGCTC[-/AG]GGGTGACGCTGTGGG | 29882 |
rs11271514 | in-del | -/GGGACCTGCCAA | 0.375399 | 0.216275 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177314 | GTTTGGACTCGCTGT[-/GGGACCTGCCAA]CCTTTTTCCTCCCAG | 29882 |
rs11549105 | snp | C/T | 0.316787 | 0.24093 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137183187 | CATCAAGGCGCTGCG[C/T]GTGCTGGACCCTTCC | 29882 |
rs11549106 | snp | C/T | 0.419307 | 0.183944 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137185070 | GATCGAGCGGGTGGT[C/T]GGCTGGCTCGGCAAG | 29882 |
rs11556579 | snp | C/G | 0.303438 | 0.244222 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137188868 | TGGACCCGCCTCGCT[C/G]CGGGCATCGCGCGGC | 29882 |
rs11556580 | snp | C/T | 0.358309 | 0.22533 | utr-variant-3-prime, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137189924 | GAGGCAGGCCCTGCC[C/T]GTGGTCTGGTCAGCT | 29882 |
rs11790251 | snp | C/G | 8.98642e-05 | 0.00670254 | upstream-variant-2KB, intron-variant | SSNA1, ANAPC2 | GRCh38.p7 | 9:137188145 | GGGGAACACAACATA[C/G]AGGTGGGGAGAGGCG | 29882 |
rs12002552 | snp | A/G | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190027 | TCCCTCACTGTCTCA[A/G]GTGCCGAGAGGGGCA | 29882 |
rs28369482 | snp | A/G | 0.351101 | 0.228645 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181906 | CAGTGTGGACACCCC[A/G]CGCGCACCTCCCACC | 29882 |
rs28393273 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185900 | GGGCAGCAAACAGGA[C/G/T]AAGGGGATCCATTCA | 29882 |
rs28393706 | snp | C/T | 0.371987 | 0.218218 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178842 | AGCCCCTTGGCCTCC[C/T]GCCCTGGGGGCCTCC | 29882 |
rs28416564 | snp | G/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137179501 | ACTGCTGGGATCTCA[G/T]CAGTGCTGCCAGGGG | 29882 |
rs28451678 | snp | C/T | 0.383824 | 0.211166 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181267 | CAGGCCTGGGCCCCA[C/T]AGCCCTCAGAGCCCT | 29882 |
rs28452292 | snp | C/G | 0.342134 | 0.232404 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185556 | GCACGGATGTTCACC[C/G]TCTCCACCCTACTAC | 29882 |
rs28490558 | snp | A/G | 0.345129 | 0.231194 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137183277 | CAGCAGTCATGCAGT[A/G]CCCGGGACCACAGCC | 29882 |
rs28491420 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SSNA1, ANAPC2 | GRCh38.p7 | 9:137187253 | CAGACACAAGCCACA[C/T]AGGGCCTTACCAGGG | 29882 |
rs28505406 | snp | G/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137179582 | TGCCAGTGACCTCCA[G/T]GCCAGGGCTCACTCC | 29882 |
rs28526257 | snp | A/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137180645 | GTGTGGGCACCCCAA[A/T]GGCTAGCACACCCCC | 29882 |
rs28544087 | snp | A/G | 0.387832 | 0.208572 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177231 | AGAGCCGCCGAGGCC[A/G]AGGCTGACGGAGCAG | 29882 |
rs28560209 | snp | C/T | 0.36606 | 0.221428 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178668 | CCAGAGCTCGAGGTG[C/T]GGGGATGGCCAGGGT | 29882 |
rs28571106 | snp | C/T | 0.451608 | 0.147832 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176160 | CCTAACCCAACTGAC[C/T]GGGGTCCTTCTAAGA | 29882 |
rs28617401 | snp | G/T | | | missense, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137175239 | CCTGCACGCGCACCA[G/T]CAGCTCCTCCTCCTT | 29882 |
rs28624882 | snp | A/G | 0.00307489 | 0.0390895 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137186399 | CCCAGAGCACACACC[A/G]GCCCCTCTAGCCCAG | 29882 |
rs28642244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185941 | TGGTGGGCCCAGCTT[C/T]GCCACACCTGCCTGA | 29882 |
rs28651923 | snp | C/G | 0.000100694 | 0.00709484 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181909 | TGTGGACACCCCGCG[C/G]GCACCTCCCACCACT | 29882 |
rs28652983 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137183866 | GTGCAGAGTGTGTGC[A/G]GTGTGGGAAAGGACA | 29882 |
rs28664164 | snp | C/T | 0.299916 | 0.244966 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178121 | TCCGGCAGCTTCTAA[C/T]GGAAACAAACCCCTC | 29882 |
rs28665875 | snp | C/T | 0.346147 | 0.230772 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181987 | TACACTCAGTGGTGA[C/T]GGGCTATGTACTAAA | 29882 |
rs28676711 | snp | C/G | 0.206947 | 0.246265 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176711 | TCCAGTGAGGTCTCA[C/G]ATGGAAATGACCGTG | 29882 |
rs28719036 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178305 | CGTGTCCAACAAGGT[A/C]GCTCGGCCAGGAGCT | 29882 |
rs28756048 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137179660 | GCCCCGGTCCTCAAG[A/T]ACCACTGGAGCCTGC | 29882 |
rs28758360 | snp | G/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137179572 | TGTCCCCATCTGCCA[G/T]TGACCTCCAGGCCAG | 29882 |
rs35045741 | snp | G/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175886 | GCTGCAGGGCGCTCA[G/T]GCCCGTGGGCTCTGC | 29882 |
rs35553050 | in-del | -/T | | | frameshift-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137189076 | CCAGGCATAGAGGAG[-/T]CTGTGCCAGAAGCGG | 29882 |
rs35790230 | in-del | -/C | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178296 | GCCAGCCACGTGTCC[-/C]AACAAGGTCGCTCGG | 29882 |
rs41307438 | snp | C/T | 0.138207 | 0.223612 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175945 | CAGAGCCACCTGCCC[C/T]ACCCCACCCTGGCAG | 29882 |
rs41317010 | snp | C/T | 0.00379723 | 0.0434073 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137175736 | ATACAGCAAGATCAC[C/T]GCCTGTACTGGGGTG | 29882 |
rs55642373 | snp | C/T | 0.34659 | 0.230587 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137180126 | GGCTGCTGGGAGCCC[C/T]GCAGTGCAGGGTAGG | 29882 |
rs55693304 | snp | C/T | | | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137189481 | GGGGCATCCTGGGTC[C/T]TGGTCTTTATCCGGT | 29882 |
rs55750716 | snp | G/T | 3.43749e-05 | 0.00414563 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SSNA1, ANAPC2 | GRCh38.p7 | 9:137188094 | CTGCACCGCTGGTCC[G/T]GGAAGACACCTGGGG | 29882 |
rs55956196 | snp | A/G | 0.358515 | 0.225221 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176959 | GGGGATCTGAAAAAT[A/G]CTCTATCCAGGCAGC | 29882 |
rs58268019 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182218 | AAAAAAAAGAAAAAG[A/G]AAAAGAAAAAAGGGC | 29882 |
rs58384967 | snp | C/T | 0.198084 | 0.24455 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181894 | TGCTGTGGCCCACAG[C/T]GTGGACACCCCGCGC | 29882 |
rs58461684 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177240 | GAGGCCAAGGCTGAC[A/G]GAGCAGGGGGCCAAA | 29882 |
rs58532611 | snp | C/T | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190411 | TCAACAGCATGGGGC[C/T]GCCAGACACCTGCAG | 29882 |
rs58821181 | in-del | -/A | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175921 | TGGTACCAGTGAGAA[-/A]GGGGCTCCCAGAGCC | 29882 |
rs59286481 | in-del | -/A | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176113 | GGCCATATTTGCAAA[-/A]CAGGGTTGATGCAGA | 29882 |
rs59462630 | in-del | -/GCACTCCAGCCTCACCTGTACCTTGTTTAGATCTATTTACGTAGAGGAATGGCGC | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177489 | GTAGAGGAATGGCGC[lengthTooLong]ACACTCCAGCCTCAC | 29882 |
rs59944646 | in-del | -/TGG/TGGGACCTGCC | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177312 | GGGTTTGGACTCGCT[-/TGG/TGGGACCTGCC]GTCCTTTTTCCTCCC | 29882 |
rs60118532 | in-del | -/TGGAAATGTGGCCATATTTGCAAACAGGGTTGATGCAGATGTAACTGAGGTG | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176141 | GATGTAACTGAGGTG[lengthTooLong]CATCCTAACCCAACT | 29882 |
rs60183962 | in-del | -/ACC/GGACCTGCCA/GT/TGGGACCTGCCAA | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177313 | GGTTTGGACTCGCTG[lengthTooLong]TCCTTTTTCCTCCCA | 29882 |
rs60245284 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137189619 | AAGTGTTTTGGGTCA[A/G]ATTCCGGAGGGAAGA | 29882 |
rs61298494 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137178085 | GCTCTGTGGGCCAAG[A/G]GCTCCTGAGTCCTTC | 29882 |
rs61319460 | snp | A/G | 0.336017 | 0.234736 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137190578 | CCAGCAGGGCCGCCG[A/G]TCCTCTTCCCCTGAC | 29882 |
rs61506971 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137183886 | GGGAAAGGACACGTG[A/C]TTGCCAGCCCCAGGA | 29882 |
rs61540427 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SSNA1, ANAPC2 | GRCh38.p7 | 9:137186838 | GCAGGGATGAGCCCA[A/G]CAGAAGCCCTTCACG | 29882 |
rs61758864 | snp | A/G | 0.00689238 | 0.0582982 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137186317 | CAGGGTGGTGGTCAC[A/G]GCCTCGGCACTGACC | 29882 |
rs71492149 | in-del | -/G | 0.5 | 0 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185248 | ACATCAAAACCTGCA[-/G]GGTGGGTGATGGCCC | 29882 |
rs71508900 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137186006 | TGCAGCCATGGGATT[C/T]TGCGCAGATCCGAAG | 29882 |
rs72240605 | in-del | -/AGAG | 0.0707826 | 0.174302 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177796 | ACGTCACCCTGGAAT[-/AGAG]AGAGTGTTCTTCTAA | 29882 |
rs72274261 | in-del | -/CGC | 0.36606 | 0.221428 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178215 | CATGACCTCCACAAA[-/CGC]CGCCACTGGTCAGCC | 29882 |
rs72619353 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175917 | CACCTGGTACCAGTG[A/G]GAAAGGGGCTCCCAG | 29882 |
rs72763283 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182012 | ACTAAACACAGGCCC[A/G]TCAGACTCCTTAAAA | 29882 |
rs72763284 | snp | A/G | 0.367503 | 0.220665 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137184315 | ACAAGGAGCCCAGAC[A/G]CAGACACAGAGCAGA | 29882 |
rs73563665 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | SSNA1, ANAPC2 | GRCh38.p7 | 9:137187139 | CAGGGCAAGGAATGT[C/T]GACGAGGGTGAGAAT | 29882 |
rs73563667 | snp | C/T | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | SSNA1, ANAPC2 | GRCh38.p7 | 9:137188893 | CGCGGCTGAGCAGAG[C/T]CCTCCGTGCCGGAGG | 29882 |
rs73571567 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137179375 | CCTCCCACCTGTGAC[A/G]ACCATCCTAACCCTT | 29882 |
rs73571568 | snp | C/G | 0.383824 | 0.211166 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137180729 | AGGGCCCTGTCCCGA[C/G]AGAGGCTGGGCAAAG | 29882 |
rs73571572 | snp | C/G | 0.0153678 | 0.0863002 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137181654 | GCCCCCCACACTGGT[C/G]AAAGGGACCATGTGG | 29882 |
rs73571576 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182283 | TTCAGGAGGCCGAGG[A/C]AGGCGGATCACGAGG | 29882 |
rs73571578 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185982 | TCGGGATCCTGGCCC[A/G]ATACCGCCTGCAGCC | 29882 |
rs73668401 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178581 | CGGAGCCGGGCCACA[C/T]GGATGATTTGTACCA | 29882 |
rs74312722 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176314 | GGCAACGGAGGTCTC[C/T]AAGAGGGTTCAGAGG | 29882 |
rs74758474 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137183952 | CCCCGACACTCTGGC[A/G/T]TGCTGATGCATTTGA | 29882 |
rs75514775 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178561 | AGGGGGAAAGGGACC[A/G]AGCACGGAGCCGGGC | 29882 |
rs75577902 | snp | C/T | 0.000666116 | 0.0182377 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137185022 | GCCGGCCTCGGGAGA[C/T]GCGGGCCTGGCGGGG | 29882 |
rs75838123 | snp | G/T | 0.444444 | 0.157135 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137183517 | CTGACGGGCACCTCA[G/T]ATCCCCTAAGGACCT | 29882 |
rs76044090 | snp | A/C | 0.225005 | 0.248747 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185523 | TGCCCCACAGACCTG[A/C]TACCCAGTGGCAAGA | 29882 |
rs76069568 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175906 | GTGGGCTCTGCCACC[C/T]GGTACCAGTGAGAAA | 29882 |
rs76292898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137178760 | CTGGACTCTTCCAGA[A/G]CCAAGCTGAGGCCTG | 29882 |
rs76321625 | snp | G/T | | | missense, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137180842 | GCCAGCAGCGAGCGG[G/T]ACTCATTGATGAAGA | 29882 |
rs77173745 | snp | C/T | 0.0275645 | 0.114116 | downstream-variant-500B | ANAPC2 | GRCh38.p7 | 9:137174470 | CTGAGCAGAGGGTGA[C/T]CCCAGGGCTCCTTCT | 29882 |
rs77950683 | snp | C/G | 0.5 | 0 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137175992 | AGCACAGGACTGGGT[C/G]GGGTCCCCACCTGCT | 29882 |
rs77975991 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137182963 | CGGCACGGGCAAGAG[A/G]AAAGGAAAGAGCCTC | 29882 |
rs78124115 | snp | C/T | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137185623 | TTTGAAAACCCAACA[C/T]CACAGCCAATCTGCA | 29882 |
rs78281530 | snp | A/G | | | intron-variant | ANAPC2 | GRCh38.p7 | 9:137177490 | GTAGAGGAATGGCGC[A/G]CACTCCAGCCTCACC | 29882 |
rs78332229 | in-del | -/AGG | 0.0490535 | 0.14873 | downstream-variant-500B | ANAPC2 | GRCh38.p7 | 9:137174641 | GCCCGGGATTCTCTC[-/AGG]AGGCTACATTCCCAG | 29882 |
rs78980797 | snp | C/T | 0.00535956 | 0.0514884 | synonymous-codon, nc-transcript-variant | ANAPC2 | GRCh38.p7 | 9:137175754 | CTGTACTGGGGTGAC[C/T]GCCACAGACAGCGTG | 29882 |
rs79138755 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ANAPC2 | GRCh38.p7 | 9:137176050 | AGCATCATAAGGTGT[A/G]TCCCGAAAAGGCTAC | 29882 |