SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6318068 | snp | A/T | 0.5 | 0 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195620 | tcattgtttgggtct[A/T]aataaaggtttgtac | 76863 |
rs6319116 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195797 | AGTTGAACTTAGATT[A/G]ACTATTTTATGTTTC | 76863 |
rs6319581 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195889 | GAGTTTAAAATTCAC[A/G]CTATATGGAATACTG | 76863 |
rs6333011 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195990 | ACAATTAGATTTTTG[A/G]ACTCAGGAATCACAC | 76863 |
rs13469812 | snp | C/T | | | utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7184756 | CGGAGCGCGATACCC[C/T]TCCCCGGCCGCCCTG | 76863 |
rs13469813 | snp | C/T | | | utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7184707 | CTCCGCTGCGGTCCC[C/T]GGCAGGCGGGAGCCG | 76863 |
rs29977414 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB | Dcun1d5 | Mm_Celera | 9:7182525 | AACCTTTAACCACTA[C/G]CACAGGATTCACTGT | 76863 |
rs45685018 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7204100 | TTATCCACTCAACTG[C/G]TTACCATACGTCATA | 76863 |
rs46043722 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7201831 | GTTCATATTGTTGTT[C/T]CACCTATAGGGTTGC | 76863 |
rs46067905 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196735 | CTGTGTACCACAGTG[C/T]ACTTACTGGGATTCA | 76863 |
rs46212536 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcun1d5 | Mm_Celera | 9:7197014 | AAGCTTCTAAGTTCT[A/G]AGATGACTGATAATT | 76863 |
rs46399524 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202511 | AGAGCAAGTTTGCTC[A/G]GGTCTTAATTTCTAG | 76863 |
rs46698294 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7189393 | AAAAATCAGTTTGGA[A/G]ACTTGAAAAATTATA | 76863 |
rs46850260 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7197050 | TACTGAGTTTATTTG[A/G]AAATTGTGTGGTTTT | 76863 |
rs47396232 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7203223 | AGTACTTTCATATAT[C/T]CACTCACTCTTAAAA | 76863 |
rs47541814 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7197509 | GCCTCAAAGGAGCAA[C/T]TTCACTTCCATATTC | 76863 |
rs47570819 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Dcun1d5 | Mm_Celera | 9:7201067 | CCCTCCTGTCATCAT[A/T]TAGACCCAAATCCAT | 76863 |
rs47765869 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196773 | GGAGTAGAGCCTCAC[G/T]TAAATCTCGCAAATG | 76863 |
rs47784331 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7205196 | AAAGGAAGAAATGTT[C/T]TAGAAAAGGCCAAAT | 76863 |
rs47820327 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202680 | GCGTTGTCTGCCTTC[C/T]TGTTAACAACATCAG | 76863 |
rs47834229 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7189470 | TAAGAAAAAATTCAA[A/G]CTGACTAAAATGTGT | 76863 |
rs48005048 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196387 | TAGTCAATTTCCTCC[C/T]AGAAGGGGCAGCGCT | 76863 |
rs48028882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7199782 | ATGTAACTGAATATG[A/G]AGGACCTAGTAAATA | 76863 |
rs48104242 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196813 | CTCTTTCTTGAAGTA[G/T]TTTCGTCCAAATCCT | 76863 |
rs48106083 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195978 | AGATATTGGGAAACA[A/G]TTAGATTTTTGGACT | 76863 |
rs48118891 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196669 | ATTCAAAATGCCTTC[C/T]TCAACATTCCAGTAC | 76863 |
rs48198586 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7204377 | AAATGAGTTTTGTAC[A/G]TATTGTTAAATCACT | 76863 |
rs48342495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196437 | TCTTGCTACCTGGAC[A/G]AAGATTAAAGGGAGA | 76863 |
rs48570652 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Dcun1d5 | Mm_Celera | 9:7207493 | TAGGAAAGCTTTAGA[A/G]CCAGTATTGAAGTTG | 76863 |
rs48663609 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7203709 | ATTGAGGTATACCTT[A/G]ATGATAGAATACAGA | 76863 |
rs48796277 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Dcun1d5 | Mm_Celera | 9:7197474 | ATAAGTGAGGCAAAT[G/T]AATTGATGTTTGTTT | 76863 |
rs48876524 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196988 | TAAGTATGTACAGGA[A/G]TGGTCTTTCTAAGCT | 76863 |
rs48961891 | snp | A/C | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7195999 | TTTTTGGACTCAGGA[A/C]TCACACAAGAGTTTT | 76863 |
rs48994949 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202866 | GAAGAGCTCAGTTAC[A/G]TTAATTCTGTGGTAT | 76863 |
rs49412461 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7189536 | TGAATAAGAAATGAT[C/T]AAAGCATTATTTGTT | 76863 |
rs49671270 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202914 | CACTTATGTCTGATC[A/C]TTTTCCCCAAGCTGA | 76863 |
rs49995379 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202587 | CCATGACTTTTGAGA[A/G]TGGTGAATGAAATGC | 76863 |
rs50117436 | snp | A/G | 0.497778 | 0.0332592 | downstream-variant-500B | Dcun1d5 | Mm_Celera | 9:7207171 | ATACTTGAGAGTATA[A/G]CTTGCCAACGGTGTG | 76863 |
rs50574325 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Dcun1d5 | Mm_Celera | 9:7190367 | TTTACAAAGCAGTGA[A/G]ATTATGTATTTGAAT | 76863 |
rs50583076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202967 | ATATGGAAATTGCCT[A/G]ATTATGATTTTCTGA | 76863 |
rs50629049 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196311 | TTGAAGGGACTGTAC[A/G]TGGTCATAATAGTGA | 76863 |
rs50707581 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7200660 | ACCACACTCGACTTG[C/T]TGTTGTCTGCAGCTT | 76863 |
rs50906303 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202913 | CCACTTATGTCTGAT[C/T]CTTTTCCCCAAGCTG | 76863 |
rs51068027 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196833 | GTCCAAATCCTCATA[C/T]TGAAATTGAAGCCAT | 76863 |
rs51141142 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Dcun1d5 | Mm_Celera | 9:7190589 | TCAGATGAACCAAAT[A/G]ATAATTGCTAGAATA | 76863 |
rs51262231 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Dcun1d5 | Mm_Celera | 9:7190045 | TTTTTAAGACATAAC[G/T]TTTTTTTTTTTAACT | 76863 |
rs51355658 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d5 | Mm_Celera | 9:7198103 | ATAGGCATACAAATC[A/G]AAACATGCTGAGATT | 76863 |
rs51462956 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcun1d5 | Mm_Celera | 9:7206434 | TGTGTCCCGTTTTTA[G/T]AATAAAGTCTTGTGT | 76863 |
rs51840445 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7202841 | CAAAACTGTGGGAAT[C/G]TGGATCTGTGAAGAG | 76863 |
rs51998778 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcun1d5 | Mm_Celera | 9:7196594 | ACTCCTATCCCTTTG[A/G]AGTTGATATCATCAA | 76863 |
rs52115555 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Dcun1d5 | Mm_Celera | 9:7204805 | GAGAGAGAGAGAGAG[A/C]GCAAACCTAGTTGTA | 76863 |
rs52125288 | snp | A/T | | | intron-variant | Dcun1d5 | GRCm38.p3 | 9:7204743 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 76863 |
rs52257755 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Dcun1d5 | Mm_Celera | 9:7200807 | TAGAATTCCTGTTTC[A/C]GCTTTTCAATGTAGG | 76863 |
rs52348662 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcun1d5 | Mm_Celera | 9:7204536 | AATCATTTAGCAGCT[A/G]AGGAAATGGAGACTA | 76863 |
rs211974675 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7206243 | ATGTTTTGAGAAAAA[C/T]AAGACAATCTTATCT | 76863 |
rs212410419 | snp | A/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7187210 | GGGCAACAACTTTGC[A/T]ATTGGGATCAGCAGA | 76863 |
rs212566289 | in-del | -/AAGA | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7190333 | TCTCCCTCAGTTCTT[-/AAGA]AAGGATGTGTATTTG | 76863 |
rs212623714 | snp | A/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7188084 | TTATGTCATATTTCA[A/T]ATCGTGACATTTGTT | 76863 |
rs212675946 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7204540 | ATTTAGCAGCTAAGG[A/G]AATGGAGACTAGGCT | 76863 |
rs212734826 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7183096 | AAAAGTTCTGTTTTC[C/T]ATTTCTTCATTCTAC | 76863 |
rs212769891 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7198083 | TAGTTTTACAGGTAA[A/G]TAAAATAGGCATACA | 76863 |
rs212933441 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7196128 | CATTGGGAGGCTGTG[A/G]ACTTTTATTTTCTTT | 76863 |
rs213094315 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7184295 | CCGAAAAAACTGGAG[A/C]GGTTGCACGTCAGGA | 76863 |
rs213242663 | snp | A/C | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7197356 | AAACATGCTAACATG[A/C]TTAACATGTTAATCT | 76863 |
rs213243448 | in-del | -/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7202362 | CTGACTTAAGATAGT[-/G]GAAAAACTTGGCTAA | 76863 |
rs213404091 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7203403 | CTTCAAATCCTAGTG[A/G]TTTCATTTTATGAGC | 76863 |
rs213428026 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7190692 | TGGTAAAGACCCATG[A/G]TTTCTTATGTCACAT | 76863 |
rs213438597 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7185860 | TCACTGGAAAGAGAG[A/G]CCCTTTGGTCTAACA | 76863 |
rs213439674 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7202762 | GAAATAATATGGACA[A/G]CTTGTTTGTAGCTTT | 76863 |
rs213845573 | snp | C/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7187008 | ACAACTTTTTTCTCT[C/G]TTACCTGCTTTCCTA | 76863 |
rs214159438 | in-del | -/TG | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7187452 | GATAGTCATTTTGTA[-/TG]TGTGTGTGTGTATAT | 76863 |
rs214514280 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7204581 | TTTGGGTTCTTTTGG[C/T]GATAGTGGTTGATGG | 76863 |
rs214779819 | snp | C/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7205499 | AACACAGTCTAGATT[C/G]AGGAGTGTTGTAAAA | 76863 |
rs214926277 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7198570 | CGCTGAAAAGTGATG[A/G]TAGGAAAATATTTTA | 76863 |
rs215173762 | snp | G/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7201219 | ACTTCTTTACAAAAT[G/T]TGTGATCATAAAGAA | 76863 |
rs215188277 | snp | G/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7188359 | ATTATACCAGTGGAA[G/T]AGGTTTTTTGTAATC | 76863 |
rs215590215 | snp | A/C | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7189630 | CAAATCTTAGGACCT[A/C]CTCACTCTGCTTTGT | 76863 |
rs215666829 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7187980 | ATATGGGTAATATGT[A/G]GAAGTACTAGAAATT | 76863 |
rs215671783 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7184425 | GAAAATCTCCGGAGA[C/T]TCAGGCTCCACCTGC | 76863 |
rs215705475 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7187125 | TGTACTAGCCATGTT[A/G]TAGTTTTAAGTGGTG | 76863 |
rs215855497 | snp | C/G | | | upstream-variant-2KB | Dcun1d5 | Mm_Celera | 9:7181717 | CTGATTACCTGCCTT[C/G]TAAGTTTCTCGTTAG | 76863 |
rs215906123 | in-del | -/ATATATATATATATATATATAT | | | upstream-variant-2KB | Dcun1d5 | Mm_Celera | 9:7182989 | CTATACTGAATATGA[-/ATATATATATATATATATATAT]ATATATATATATATA | 76863 |
rs216157058 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7183520 | TTCCACCTCAAGAGT[C/G]ACAAGATTGATGGAG | 76863 |
rs216236595 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7203603 | TGGACTGAGAATACA[C/T]TTTGAAGAAACAAAA | 76863 |
rs216276024 | snp | A/C | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7202802 | CCCTTAAGTCAGGTG[A/C]TTTGATGGTTGAACT | 76863 |
rs216327080 | in-del | -/ATTT | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7203422 | ATTTTATGAGCATAC[-/ATTT]ATTTATTTATTTATT | 76863 |
rs216502158 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7183614 | TATAAAACAAACAAA[-/C]AAAAAAAAAACCCTT | 76863 |
rs216613168 | snp | C/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7197099 | AATACTGGTTTTATA[C/G]TTTTGTTCACATGCT | 76863 |
rs216777991 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7189764 | CAGCCAGTTTATAGA[C/T]GTGTGTGTTCAGATT | 76863 |
rs217018035 | snp | A/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7190579 | AGTTCTTCTGTCAGA[A/T]GAACCAAATGATAAT | 76863 |
rs217133949 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Dcun1d5 | Mm_Celera | 9:7184485 | CGCTCCAGGCCCTGC[A/G]AGCTTCCTTTCTACG | 76863 |
rs217252421 | in-del | -/AAT | | | downstream-variant-500B | Dcun1d5 | Mm_Celera | 9:7207330 | GCCAACTTTATCTAA[-/AAT]AGAGTATAGGATTGG | 76863 |
rs217306406 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7185799 | CAGTACCCCCAGAAC[C/T]TATGTCTCTAACTGC | 76863 |
rs217556837 | snp | A/G | | | upstream-variant-2KB | Dcun1d5 | Mm_Celera | 9:7182734 | GTGCTGTCTTGAAAT[A/G]TCAAAAACAAAGTCC | 76863 |
rs217597770 | snp | C/G | | | upstream-variant-2KB | Dcun1d5 | Mm_Celera | 9:7182060 | TGAGGAAGAGTGAGA[C/G]TTACAAGCCCCAGGA | 76863 |
rs218116650 | in-del | -/AAATATTC | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7205425 | CATAAATCCCTATGA[-/AAATATTC]ATTCTGTAGCATTAA | 76863 |
rs218262866 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7185262 | AGTGTGAAAAAAGGA[A/G]CAGAGCTTGAAGAGT | 76863 |
rs218297688 | in-del | -/A | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7205892 | AGATTTTAATTTTTG[-/A]AAAAAATAATCGTTT | 76863 |
rs218303242 | snp | C/T | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7205850 | CAGACAACCTGTCTT[C/T]TGTATGTTCTTCCCT | 76863 |
rs218492435 | snp | A/G | | | intron-variant | Dcun1d5 | Mm_Celera | 9:7186246 | GCATACATTTTTCTT[A/G]ACTGTATTAGCTCTT | 76863 |