SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13480664 | snp | C/T | 0.15879 | 0.232768 | intron-variant | Btbd2 | GRCm38.p3 | 10:80649503 | AGAGCCATATCAGAA[C/T]CCCCTGCACAAGGTG | 208198 |
rs29375331 | snp | C/T | 0.375 | 0.216506 | intron-variant | Btbd2 | Mm_Celera | 10:80654666 | ACCTGAAGGGTCTTT[C/T]TGGTGCCTTCCAACA | 208198 |
rs46111488 | snp | A/G | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80657850 | GATCACAAATTCAAA[A/G]GTGGACAAAGCTACT | 208198 |
rs46711657 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658827 | CTGATTCTGTGACCC[C/T]GGAACATTCCTTTTA | 208198 |
rs46824884 | snp | A/G | 0.165289 | 0.235211 | downstream-variant-500B | Btbd2 | Mm_Celera | 10:80642606 | ATGTAACACTCAGAC[A/G]ACATAGCACTCGATG | 208198 |
rs46838461 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btbd2 | Mm_Celera | 10:80645084 | TTCACAGCCAGTCTC[A/G]TCGCGCCGCAGCTTC | 208198 |
rs47160795 | snp | A/G | 0.375 | 0.216506 | missense | Btbd2 | GRCm38.p3 | 10:80645402 | AGGGCCTTGCCCAGC[A/G]CCTTCCTCTTGTTCT | 208198 |
rs47174020 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658687 | ACAGACAGACCTGAC[A/G]TTAGGACAAGTAACC | 208198 |
rs47567295 | snp | A/G | 0.32 | 0.24 | intron-variant | Btbd2 | Mm_Celera | 10:80645019 | TTTATACTGGGTAGA[A/G]CTTGTACCCTGCCTG | 208198 |
rs47958946 | snp | A/G | 0.260355 | 0.249785 | downstream-variant-500B | Btbd2 | Mm_Celera | 10:80642475 | CTTCTTGGGGCCTAA[A/G]ATGGCAGACCACATC | 208198 |
rs47965208 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658715 | ACCTTCTTAAGACAG[C/T]ATTCAAAGAGAAAAA | 208198 |
rs48492813 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Btbd2 | Mm_Celera | 10:80645087 | ACAGCCAGTCTCATC[A/G]CGCCGCAGCTTCCTA | 208198 |
rs49632751 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Btbd2 | Mm_Celera | 10:80644481 | TCATCTAACGCATGC[G/T]CAGTTCCTGCTGCCC | 208198 |
rs50094647 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80649978 | TCTACAGAGTGAGTT[C/T]TAGGACAGTCAGGGC | 208198 |
rs50100861 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btbd2 | Mm_Celera | 10:80644000 | GCTGCTCAGATGCCA[A/G]GGTCTGTGCTGGGCA | 208198 |
rs50107310 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658021 | AAAGAATCCTAGCAC[A/G]AGGATAAACCATCCA | 208198 |
rs50302030 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btbd2 | Mm_Celera | 10:80644399 | CCCATAAAGTTGAGC[A/G]GCTACAATGGCCATG | 208198 |
rs50734606 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Btbd2 | Mm_Celera | 10:80644111 | AAAAAAGCCTGATGG[C/G]ACACGTGTGGGACCA | 208198 |
rs50933271 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80649942 | GAGGCAGGCGGATTT[C/T]TGAGTTCGAGGCCAC | 208198 |
rs51018209 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Btbd2 | Mm_Celera | 10:80644182 | ATGCAGGGGATGGGA[C/T]GGCACCAGGCTGTGG | 208198 |
rs51059957 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Btbd2 | Mm_Celera | 10:80642433 | CCACCACTGCCCAGC[C/T]AGGTGTCATGTACCC | 208198 |
rs51345263 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Btbd2 | Mm_Celera | 10:80643101 | GGGGGCAGCAGTGCA[C/G]GCAGGTCAGGACCTG | 208198 |
rs51797505 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Btbd2 | Mm_Celera | 10:80644437 | CTGGAGCTGTGGGGA[C/G]GTCACATTGCCCATT | 208198 |
rs211899766 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80652092 | GCCCAAGGCAGAGAA[C/T]TGTGGTTAGCTGGAG | 208198 |
rs211908211 | snp | A/G | | | downstream-variant-500B | Btbd2 | Mm_Celera | 10:80642369 | CTGGCCTCAAACTCA[A/G]GAGATCTGCCTGCCT | 208198 |
rs212062230 | snp | A/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80653123 | TCACTATGTAGCCAA[A/T]GATAAATCTTTGCTC | 208198 |
rs212346733 | in-del | -/CA | | | intron-variant | Btbd2 | Mm_Celera | 10:80654794 | GAAGCCCCCCCCCCC[-/CA]ACTCTCCACAAGCTG | 208198 |
rs212388345 | in-del | -/GACA | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658670 | GAAACTGAACAATTG[-/GACA]GACAGACAGACCTGA | 208198 |
rs212601849 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80656078 | GTGGGGTTCAGGGTC[C/T]GGGGATGCAGGGTCT | 208198 |
rs212869340 | snp | G/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80644106 | ATGGCAAAAAAGCCT[G/T]ATGGGACACGTGTGG | 208198 |
rs212912741 | snp | C/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80654767 | TCCTCCACTGCCCAC[C/G]GTACCACCTGTGAAG | 208198 |
rs212966559 | in-del | -/AA | | | utr-variant-3-prime | Btbd2 | Mm_Celera | 10:80642648 | TGTTTTCCTTTATTT[-/AA]AAAAAAAAAATCATT | 208198 |
rs213028270 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80654085 | TAAATATTTTTATTA[C/T]TACGTATTTTCCTCA | 208198 |
rs213306101 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80651036 | CACTCTGCAAAGAAC[A/G]CAGCATAGCTCACAG | 208198 |
rs213435317 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80650168 | ATCCCCCAGTGAGGG[A/G]CTGGGGGCGTGGTTC | 208198 |
rs213754882 | in-del | -/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80654075 | ATTTTTTTTTAAATA[-/T]TTTTTATTACTACGT | 208198 |
rs213832077 | in-del | -/CGCCCC | | | intron-variant | Btbd2 | Mm_Celera | 10:80643810 | TGGGTTGCAGTGCAG[-/CGCCCC]CCCCCCCCACCTTCA | 208198 |
rs213920990 | in-del | -/A | | | intron-variant | Btbd2 | Mm_Celera | 10:80654069 | TCTTTAATTTTTTTT[-/A]TAAATATTTTTATTA | 208198 |
rs213973576 | snp | C/G | | | utr-variant-5-prime | Btbd2 | GRCm38.p3 | 10:80657015 | CCATGGAGGCGCAGG[C/G]CATCCCTGGATTCGA | 208198 |
rs214017446 | in-del | -/GGGACAGC | | | intron-variant | Btbd2 | Mm_Celera | 10:80649118 | GGTGCTAAAGCTTGG[-/GGGACAGC]GGGACAGCGGGGCCT | 208198 |
rs214144302 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80648830 | GTCCTTCTAGGAGGG[A/G]ACCGGAAAGAAGGCT | 208198 |
rs214301079 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80643819 | GTGCAGCGCCCCCCC[A/C]CCCCACCTTCAGCGT | 208198 |
rs214376110 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80653279 | AAAGTAGGGGCCTGG[C/T]ACCCCTCTGCCCTGA | 208198 |
rs214410549 | snp | C/T | | | downstream-variant-500B | Btbd2 | Mm_Celera | 10:80642427 | CGTGAGCCACCACTG[C/T]CCAGCCAGGTGTCAT | 208198 |
rs214412527 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80653951 | AATCTTACTTTTCAG[C/T]GCTGGACATTGAACC | 208198 |
rs214484265 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80647682 | AGTCTGGAAGCTGCT[A/G]TATCCTCCCAGAGCA | 208198 |
rs214487010 | snp | G/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80652235 | CCAGCCTCAGCTCAG[G/T]TAGACAGGACAGACA | 208198 |
rs215007322 | in-del | -/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80650114 | AGAATCCCCCAATGA[-/G]GGGGCTGGGGGCGTG | 208198 |
rs215137172 | in-del | -/A | | | intron-variant | Btbd2 | Mm_Celera | 10:80646888 | GAGGACTCCAATGGT[-/A]AGGGACAGAACTTCA | 208198 |
rs215309952 | snp | C/G | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80657879 | CTCAGGGAGGCAGAA[C/G]GGGAAGAGAGGAAGG | 208198 |
rs215349639 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80655887 | TGGTTCATGGGGTGC[A/G]GGGTCCAGGTGAAGT | 208198 |
rs215351311 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80645203 | TGGCTGATAAGACAC[A/G]GCCTGCCCATCCCCC | 208198 |
rs215387991 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80646089 | TGCCTATAAAGCCAT[C/T]AGCAAGAGCCACAAG | 208198 |
rs215455842 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80654991 | ATCAAGCTGGACAAG[C/T]TACCCCACATGGTCA | 208198 |
rs215730337 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Btbd2 | GRCm38.p3 | 10:80657082 | AAGGCATGGAGAGGT[A/G]AAGGACAGACAGAGG | 208198 |
rs216273254 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80648902 | TGCGTCTCCCTCCTA[A/C]CCCTCCCTCAGCCCT | 208198 |
rs216306999 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80649880 | GAAAAGAAAAGCAGC[A/G]CCCGGCCGTGGTAGC | 208198 |
rs216540982 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80651131 | AGGCCTGAACACAAG[C/T]GCATATATACACACA | 208198 |
rs216681297 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80644890 | AGGACCTGGCTAAGT[A/G]GAGGGGTGCCTCCTT | 208198 |
rs216898596 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80651763 | ATACTGTGTAGCCCT[A/G]GTTAGTCTGGAACTT | 208198 |
rs217019612 | in-del | -/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80644572 | CCCCCCCCCCCCCGC[-/G]CCCGCCCCCACCAAA | 208198 |
rs218080693 | snp | C/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80653431 | GTCAGAAACCACAGG[C/G]ATCCAGAGACTCCGG | 208198 |
rs218125723 | snp | G/T | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658742 | AAAACACAAACGTAA[G/T]AGGCCACAGAAAGCA | 208198 |
rs218202755 | snp | G/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80653968 | CTGGACATTGAACCA[G/T]ATTGGCATGTGTCCG | 208198 |
rs218335148 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80655345 | ATGTTGGGGTGACTA[A/G]TGGATTCAGAGAGCA | 208198 |
rs218388477 | in-del | -/CCC | | | intron-variant | Btbd2 | Mm_Celera | 10:80654783 | GTACCACCTGTGAAG[-/CCC]CCCCCCCCCAACTCT | 208198 |
rs218453907 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80654513 | GCTACCTTCTGACTC[A/G]TCTGTGTTGAACCCT | 208198 |
rs218484565 | in-del | -/CA | | | intron-variant | Btbd2 | Mm_Celera | 10:80643817 | AGTGCAGCGCCCCCC[-/CA]CCCCCCACCTTCAGC | 208198 |
rs218651389 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80649093 | AGGTCAGAGGCCACA[A/G]GCTCAGGGAGGGTGC | 208198 |
rs218730828 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80649957 | CTGAGTTCGAGGCCA[A/C]CCTGGTCTACAGAGT | 208198 |
rs218791810 | snp | A/C | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658108 | CTTTTGTCCTGACAG[A/C]TAATAAATGTCTTTA | 208198 |
rs219140352 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80653537 | TCAGCGTGAGGCATG[C/T]ATAGGTCCTGCAGGC | 208198 |
rs219399078 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80656004 | GCATGGTCTGTGATG[A/C]ACGGTCCCGGGTAGG | 208198 |
rs219433167 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80648385 | GGCCTGAGTGCTGGG[A/G]CACTGCCATCTCTCC | 208198 |
rs219434611 | snp | G/T | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80658309 | AGTTAGCAGTGGACA[G/T]GAAAGGATTGTAAAC | 208198 |
rs219439655 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80646327 | ACCTGACCCAAGCCC[C/T]GCCCTTTCCCATCCT | 208198 |
rs219458537 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80647320 | GCAAAGGCCCAGGGC[A/G]TGAGAGTGGCGTGGT | 208198 |
rs219466382 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80649429 | CAGGGTGGTTCTGAG[C/T]AGCCTCTCCAGCTGG | 208198 |
rs219533244 | snp | A/G | | | upstream-variant-2KB | Btbd2 | Mm_Celera | 10:80657484 | ACTAGCTGGGCAGTG[A/G]TGGCGCGCTCCTTTA | 208198 |
rs219622919 | snp | A/G | | | utr-variant-5-prime | Btbd2 | GRCm38.p3 | 10:80656863 | GGAAACAGAGGAAAA[A/G]GGGACCGAGAGAAAT | 208198 |
rs219847672 | in-del | -/ATTGACTAGAG | | | intron-variant | Btbd2 | Mm_Celera | 10:80649845 | ATGAGACCTTATCTC[-/ATTGACTAGAG]AAACCCTGAGAAAAG | 208198 |
rs220053933 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80651289 | TGCCTCTGCCTTCTA[A/C]GAGTGTCGTGATCAC | 208198 |
rs220067368 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80651364 | GTTGCTCCAGGCCTG[C/T]GTCCCCATCACGAGT | 208198 |
rs220176532 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80650613 | GCAGACGCCTAGCCA[C/T]GCAGCGGCTCTCAAC | 208198 |
rs220321643 | in-del | -/GA | | | intron-variant | Btbd2 | Mm_Celera | 10:80651928 | TGGTTTTGGTTTTTC[-/GA]GACAGGGTTTCTCTG | 208198 |
rs220431948 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80646837 | CGACATAGCACAGTG[A/G]GTAAAGGTGCTTGCC | 208198 |
rs220464914 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80648053 | GCGCAGGCCGCCCTG[A/G]GCTAACAAAGGCTGA | 208198 |
rs220537958 | snp | C/G | | | synonymous-codon | Btbd2 | Mm_Celera | 10:80645521 | GGTATCCCGCTCCAG[C/G]ACTGCCACCAGCGTG | 208198 |
rs220556367 | snp | A/C | | | intron-variant | Btbd2 | Mm_Celera | 10:80650544 | TGCCTCTTTCTGGTT[A/C]GGGAGCACCTAGTCC | 208198 |
rs220725073 | snp | C/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80645333 | GGCCGCCATTCAAGT[C/T]TGTTACCTGCGGCAA | 208198 |
rs220796833 | in-del | -/ACA | | | intron-variant | Btbd2 | Mm_Celera | 10:80651103 | CATGAACACATACCC[-/ACA]ACATGAGCACAGGCC | 208198 |
rs221227789 | snp | A/G | | | utr-variant-3-prime | Btbd2 | GRCm38.p3 | 10:80643036 | TGTCACCTACCCTGG[A/G]GCAGAGCTCCCAGTG | 208198 |
rs221231278 | snp | G/T | | | intron-variant | Btbd2 | Mm_Celera | 10:80654300 | ACACCTGAGTCTTTA[G/T]AGTTTCTCTGACAGA | 208198 |
rs221269893 | snp | A/G | | | utr-variant-3-prime | Btbd2 | Mm_Celera | 10:80642800 | TCACTGGATGGGGTG[A/G]TGTGGTGGCCTAGAG | 208198 |
rs221356271 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80653665 | TGGGAATTGAACTCA[A/G]GACCTCAGGAAGAGA | 208198 |
rs221407854 | in-del | -/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80650164 | AGAATCCCCCAGTGA[-/G]GGGGCTGGGGGCGTG | 208198 |
rs221661809 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80650474 | CTGATTGTTCGGCAC[A/G]GCATCTCCCAGGCCC | 208198 |
rs221790249 | snp | C/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80649588 | GAGGTTCCTCCTGCC[C/G]AGAGGCCGGCCACTA | 208198 |
rs221901286 | snp | A/G | | | intron-variant | Btbd2 | Mm_Celera | 10:80652468 | GCCATCTTGGAAAAT[A/G]CTGGTGGGTGGGCGG | 208198 |
rs221932003 | in-del | -/CAGA | | | intron-variant | Btbd2 | Mm_Celera | 10:80650769 | TTCCTCGAATGTGGT[-/CAGA]CACAGTGTGTTCCAC | 208198 |