SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4223150 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Stam2 | Mm_Celera | 2:52694847 | TGCTTACACACAGCC[A/G]GTGGGGATGTCTACA | 56324 |
rs4223151 | snp | A/G | 0.396694 | 0.202437 | synonymous-codon | Stam2 | Mm_Celera | 2:52694784 | TTTGCCTCAGCTGGC[A/G]GGCTTTCCAGTGGCA | 56324 |
rs4223152 | snp | C/T | 0.10314 | 0.202317 | utr-variant-3-prime | Stam2 | GRCm38.p3 | 2:52694669 | GCTTTGTGGGTGTGC[C/T]GTTTAATCTAGGGGA | 56324 |
rs4223153 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Stam2 | GRCm38.p3 | 2:52694534 | TTCCAGTCCAGTTGG[C/T]TTGAAGTTGACCTT | 56324 |
rs13474382 | snp | A/G | | | missense | Stam2 | Mm_Celera | 2:52716443 | AGAAGGGGTTACTTT[A/G]CCTTCCGCAGGCTCC | 56324 |
rs13474383 | snp | A/G | | | utr-variant-3-prime | Stam2 | Mm_Celera | 2:52692236 | TTGTACTGTATACTG[A/G]AGATGATAATAAAGT | 56324 |
rs13474384 | snp | A/G | | | utr-variant-3-prime | Stam2 | Mm_Celera | 2:52692555 | ATTTTCAGCCAAAGG[A/G]ATAGTTTACCTTCAG | 56324 |
rs13474385 | snp | A/G | | | utr-variant-3-prime | Stam2 | Mm_Celera | 2:52692604 | CCCATGATCCAGTTG[A/G]ACTGTACTTATTTTA | 56324 |
rs27912651 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52734645 | GTGCAGCGCATTAAA[C/T]GTAGGATGTGCCTGT | 56324 |
rs27912652 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52734597 | AGAAGCCTGGATCAG[C/T]ACTGCTTCCTTCAAG | 56324 |
rs27912653 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52734101 | TGGCCTGGGGCTAAC[C/T]CTGACTCATGGGTTG | 56324 |
rs27912654 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52733764 | CTAGTATTTCTAATA[C/T]TCCGGGTTTCATAAG | 56324 |
rs27912655 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52733673 | TGCCTACCTGAGCTC[A/C/G]GGCATGTATGCTTGG | 56324 |
rs27912656 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52733635 | CACCCAAGGGAATAA[A/G]GAAGAGAACAGGACA | 56324 |
rs27912657 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52733229 | AAACAATGAGATGGT[A/C]CTTGAACAGCTAAGA | 56324 |
rs27912658 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52732408 | CAGATTTTGCTATCT[C/T]GAGAGCCCACTGGTG | 56324 |
rs27912659 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Stam2 | GRCm38.p3 | 2:52732379 | GCAACTCTGCTATGT[A/G/T]CTGGGAACAGTAACA | 56324 |
rs27912660 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52732271 | GGCCCGGGTGCTCGA[A/G]GTCTGTGTGCTTAGA | 56324 |
rs27912661 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52732260 | AACTGTAACCGGGCC[C/T]GGGTGCTCGAGGTCT | 56324 |
rs27912662 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52732153 | AGAACAAATGAATTT[C/G]ATTGGCTGGGCAAAT | 56324 |
rs27912663 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52731429 | TTGCCAAGTAGGTTC[C/T]TCCCAAGTTATTTTT | 56324 |
rs27912664 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52731223 | ACATTTCTGTATGGT[A/G]GTGTACTCCAAGTGT | 56324 |
rs27912665 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52731211 | TTATACAGCAAAACA[G/T]TTCTGTATGGTGGTG | 56324 |
rs27912666 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52731152 | AAGAACATCTCCACT[C/T]TGTGAACGGAGAAAC | 56324 |
rs27912667 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52731069 | TAGCAGAGCTCCGAC[A/C]AGATGGTGACGATTC | 56324 |
rs27912668 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52731061 | GGTACATATAGCAGA[A/G]CTCCGACCAGATGGT | 56324 |
rs27912669 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52731051 | AAGATGAAGCGGTAC[A/G]TATAGCAGAGCTCCG | 56324 |
rs27912670 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52730142 | TCTCTCAGGCAGTGG[A/G]GCCCCTAACGAGATA | 56324 |
rs27912671 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52729686 | ACTGAACCTTTAAAG[A/C]GTTTTCCTTTTGTTA | 56324 |
rs27912672 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52729657 | GCATACTCCAGACTA[C/T]AGGCCCGTAAGCCAC | 56324 |
rs27912673 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52729590 | ACAGCTTTCAGTCAA[A/T]TCTGGAATCCCACTT | 56324 |
rs27912674 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52729587 | GTAACAGCTTTCAGT[A/C]AATTCTGGAATCCCA | 56324 |
rs27912675 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52729371 | GTGTGGGCATGTGAA[A/G]AGCACCTTCTTGTTG | 56324 |
rs27912676 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52727735 | AAAACACAATACACT[G/T]TACAATCTCCAATCA | 56324 |
rs27912677 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52726945 | ACAAACAAACAACAC[A/G]GCCCTCAGACTTAAA | 56324 |
rs27912678 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52726766 | GTAGAAGCCAGGGAC[A/G]ATAAAAAATGGAATT | 56324 |
rs27912679 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52726656 | CTAAAGTCAGTACAA[A/G]GAGATGCCAGCACAA | 56324 |
rs27912680 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Stam2 | Mm_Celera | 2:52726608 | CATAATATTAAAAAG[C/T]ACACCATCCACGATA | 56324 |
rs27912681 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Stam2 | Mm_Celera | 2:52726571 | ACTGCTCCACAGAAC[A/G]AAGAGTAAGCACAGT | 56324 |
rs27912682 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Stam2 | Mm_Celera | 2:52726477 | AAAAGTCCACATCTT[A/C]GAACACTCCTTTAGA | 56324 |
rs27912683 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52725971 | AGAGACAAGGCACCA[A/G]AAGAAAAGACTTGTG | 56324 |
rs27912684 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52725825 | TATGAGACAACTACT[A/G]TGGGAAGTGAGGAAC | 56324 |
rs27912685 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52725771 | AGTATCTGGCATTAA[C/T]TCGCTATTCTTCCAA | 56324 |
rs27912686 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52725598 | ACTGTGTTCACAGAA[C/G]GGCTTTGAAAAGCAT | 56324 |
rs27912687 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52725524 | AAAGTCTCTAACAAT[A/T]TCCTTAGACTCACTC | 56324 |
rs27912688 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52725445 | GGGTGTAAGTCGTAA[C/T]ACTTCATCACCAGGC | 56324 |
rs27912689 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52724491 | TATTAAGCAGCACAA[A/T]CATTTACAAGTCTGC | 56324 |
rs27912690 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Stam2 | Mm_Celera | 2:52723742 | TATCCTATGATGCTC[A/G]TGCAGCAGCTGCAAT | 56324 |
rs27912691 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Stam2 | Mm_Celera | 2:52723536 | GTAGGACTTCATACC[A/G]CGGCTATTCTGCAGC | 56324 |
rs27912692 | snp | A/C | 0.375 | 0.216506 | synonymous-codon | Stam2 | Mm_Celera | 2:52715749 | GTTTTTGGCAGCAGC[A/C]GCGACAGTCTGTAAG | 56324 |
rs27912693 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52714171 | GGTACATGCGCCACC[G/T]TTGTCATAGCAACAA | 56324 |
rs27912694 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52710815 | CACTGCCTCTTCCAC[A/G]GACTGACTTTTCTTT | 56324 |
rs27912695 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52710754 | GAAGGCGAGCCAGGC[A/G]TGCTTCAGCAAGCTC | 56324 |
rs27912696 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam2 | Mm_Celera | 2:52710083 | CACCTGTATGGAGAC[A/G]TGTTACCCGGGCAGA | 56324 |
rs27912697 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52709551 | AGGAAGATAACTTCA[A/G]TAGACTGGAGCTTCT | 56324 |
rs27912698 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52709318 | GAAAAGTTCCCAAGG[C/T]TCCTATCAACTAAGA | 56324 |
rs27912699 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52708962 | ACACAGAGATACAGT[G/T]AGAGTCAAGACACCT | 56324 |
rs27912700 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Stam2 | Mm_Celera | 2:52708853 | CTAATTTTAACTAAA[C/T]TTTGATGGAAACAAA | 56324 |
rs27912701 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52708821 | TACAAGTTCCCTGGA[A/G]CACTGTTAGAATGTA | 56324 |
rs27912702 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52708600 | GACTAAGCCAGTTTC[A/T]CTTATAACAGTGTTC | 56324 |
rs27912703 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Stam2 | Mm_Celera | 2:52708360 | TCAATATATTACACA[C/G]AGTCGTTCATTTACG | 56324 |
rs27912704 | snp | C/T | 0.32 | 0.24 | intron-variant | Stam2 | Mm_Celera | 2:52708044 | GAGAAGTCTGAAGAG[C/T]TAACCACGATGAATG | 56324 |
rs27912705 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52708020 | CCTAGGAAGAAAACA[C/G]GAGATGCTGAGAAGT | 56324 |
rs27912706 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52708013 | ATTTTACCCTAGGAA[A/G]AAAACAGGAGATGCT | 56324 |
rs27912707 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52707907 | AAGGTGAGTTCAACA[A/T]TAACTAATACCTTCC | 56324 |
rs27912708 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52707837 | AAAACACCATAAACA[A/G]GAAATCTATAAGTTA | 56324 |
rs27912709 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52707037 | CTTCATGTATTTCCA[A/C]ATGTAAACAAGTATA | 56324 |
rs27912710 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stam2 | Mm_Celera | 2:52706379 | GCCGTCAACCTGGTC[A/G]AAACAAGTAAGGCGC | 56324 |
rs27912711 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stam2 | Mm_Celera | 2:52706247 | ATACATATCACATTA[C/T]TGCCACTGATGAAAA | 56324 |
rs27912712 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52705899 | CAAACTTCTCCTTCC[A/G]AGTTCAGAGAGAGCT | 56324 |
rs27912713 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52705822 | TATACAGCAGTTCAA[C/T]CACTAGGGGCTGGAA | 56324 |
rs27912714 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52705817 | TGCTTTATACAGCAG[A/T]TCAACCACTAGGGGC | 56324 |
rs27912715 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52705377 | CACTAATCATTAGCA[A/G]CAGATGTATAAGTAG | 56324 |
rs27912716 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52704769 | AGCAAACTATTGCTG[A/G]TTTATTCGAGGAAAA | 56324 |
rs27912717 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Stam2 | Mm_Celera | 2:52704592 | CCAGAGTACCCAGAG[A/G]AAGAGTGAAAAGGCC | 56324 |
rs27912718 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52704565 | AGGCGAGGTGAAAAC[A/G]ACGAAGGACAACCAG | 56324 |
rs27912719 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52704479 | AATGGGGCGAGAACT[C/T]AGAGGTTAGAGTGAG | 56324 |
rs27912720 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52704438 | AGCAAATGAAGTAAC[A/C]TAGAGCCAAGTACAA | 56324 |
rs27912721 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stam2 | Mm_Celera | 2:52704397 | CTCTTTTCGGAAGAC[A/G]AGGTCAAGAGCACAA | 56324 |
rs27912722 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52704361 | CTCAGGACTACACTA[C/G]AACAAGGAGAACAGC | 56324 |
rs27912723 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam2 | Mm_Celera | 2:52704337 | AAAGGCAAGCCTTCA[C/T]GGATTACACTCAGGA | 56324 |
rs27912724 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Stam2 | Mm_Celera | 2:52703840 | CCATACTCACCCAGG[A/C]AACACACAGTAAAAA | 56324 |
rs27912725 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52703797 | ACCAGCCACCTTATT[C/G]TATAACAACAAATCC | 56324 |
rs27912726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam2 | Mm_Celera | 2:52703360 | ACAGGGAGCTGAGAG[A/G]AGAAACTGCTGAATT | 56324 |
rs27912727 | snp | C/T | 0.260355 | 0.249785 | missense | Stam2 | GRCm38.p3 | 2:52703250 | GACAGTTCTGAATGC[C/T]TCCTGATAGACAAGA | 56324 |
rs27912728 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam2 | Mm_Celera | 2:52702637 | AGTGAGTCCACGGCT[A/G]AACTGCTGTAAGAAG | 56324 |
rs27912729 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52701927 | GTGAATCTAACGCGT[G/T]CTCTGAGGATAAAAG | 56324 |
rs27912730 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stam2 | Mm_Celera | 2:52701760 | ATTTGAAAAATGCTT[C/T]GGAATGGGGATACTG | 56324 |
rs27912731 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam2 | Mm_Celera | 2:52701628 | TCATCTAATTTATGC[A/T]CCCACATTCTAGTTG | 56324 |
rs27912732 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam2 | GRCm38.p3 | 2:52701324 | CCTGGCCCAGGAATA[A/T]CAACCTCCCTTTACA | 56324 |
rs27912733 | snp | C/T | 0.32 | 0.24 | intron-variant | Stam2 | Mm_Celera | 2:52701101 | CAGTGACTGGCAATC[C/T]ACTGCCGAAAGGCTG | 56324 |
rs27912734 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stam2 | Mm_Celera | 2:52700786 | CTAAGACACCTGCCT[G/T]CAGAAGATGAGAAAG | 56324 |
rs27912735 | snp | C/G | 0.375 | 0.216506 | intron-variant | Stam2 | Mm_Celera | 2:52700784 | GACTAAGACACCTGC[C/G]TTCAGAAGATGAGAA | 56324 |
rs27912736 | snp | C/T | 0.5 | 0 | intron-variant | Stam2 | Mm_Celera | 2:52700593 | CTAAGCCCTCTCCTG[C/T]GGTGGAGTGGTACTA | 56324 |
rs27912737 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Stam2 | Mm_Celera | 2:52700548 | AACTCCCCGCTATTG[A/G]AGTGCAGGTTGAAAG | 56324 |
rs27912738 | snp | A/T | 0.5 | 0 | intron-variant | Stam2 | Mm_Celera | 2:52700403 | CGTGTTTGAAGAAAA[A/T]CAGTGGCAGCTGTAT | 56324 |
rs27912739 | snp | C/T | 0.5 | 0 | synonymous-codon | Stam2 | GRCm38.p3 | 2:52700040 | GGTGTGTGCTGTTAC[C/T]GAGTTCATATTTGGA | 56324 |
rs27912740 | snp | G/T | 0.5 | 0 | intron-variant | Stam2 | Mm_Celera | 2:52699951 | GCAAGGAGAAGAGTC[G/T]GTAGGTTCCTGGTCT | 56324 |
rs27912741 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Stam2 | GRCm38.p3 | 2:52696261 | ACTGAGGGTGCGAAG[C/G/T]GCACTTGCCTGTGAC | 56324 |
rs27912742 | snp | A/G | 0.5 | 0 | intron-variant | Stam2 | Mm_Celera | 2:52695890 | GTGAGTAAGAAATTG[A/G]CAAAAAGCAAGCTGT | 56324 |