SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3159862 | snp | G/T | | | intron-variant | Peli1 | Mm_Celera | 11:21115085 | ttgtgtgtatgccta[G/T]ggattaaattgttta | 67245 |
rs6182865 | snp | G/T | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21119574 | TGGCTTTTTAAGAAG[G/T]AGGATATTTTTCTTT | 67245 |
rs6183446 | snp | C/T | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21119668 | TACTTCCATTTCTTC[C/T]CTTTTGGGCCACATA | 67245 |
rs6184631 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Peli1 | Mm_Celera | 11:21119881 | TTTTATCCTCTGACC[A/G]AGGTGGTGTAGCGTG | 67245 |
rs6185181 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Peli1 | GRCm38.p3 | 11:21119989 | TGCAAGAGGGAATTA[A/G]CTGAAGCATAATCAG | 67245 |
rs6186206 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Peli1 | Mm_Celera | 11:21120166 | AAAAAAGCCTGAGAA[A/C]TATACTGACNGCAGG | 67245 |
rs6186223 | snp | C/T | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21120176 | GAGAANTATACTGAC[C/T]GCAGGTGTTATGGCC | 67245 |
rs6409632 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Peli1 | Mm_Celera | 11:21117883 | CAGAAAGATCAGAAA[C/G]AATGTTGTCAAGATT | 67245 |
rs6410722 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Peli1 | Mm_Celera | 11:21118090 | TGGGAGAGAAGGCCC[A/G]GATAAATTTAGGGCC | 67245 |
rs6411300 | snp | A/C | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21118178 | gaaggcagaggcagg[A/C]ggatttctgagttca | 67245 |
rs6411382 | snp | A/G | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21118227 | ctatacagagaaacc[A/G]tttctgtctcagggg | 67245 |
rs6411901 | snp | A/G | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21118311 | TTTGATACTAATTAA[A/G]ATTAATATGAGCACT | 67245 |
rs6412579 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Peli1 | Mm_Celera | 11:21118453 | ATGAGTACCAGCATC[A/G]ATTTTGGGGCAGGTA | 67245 |
rs13463189 | snp | C/T | | | utr-variant-3-prime | Peli1 | Mm_Celera | 11:21149272 | AACGTTTTATATGCT[C/T]CTTTGAATATGCAAT | 67245 |
rs26831732 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Peli1 | Mm_Celera | 11:21150595 | CTGAACTTTCTCTCC[A/G]ATCAGCTAAGAAAAG | 67245 |
rs26831733 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Peli1 | Mm_Celera | 11:21150191 | TTGAAGTTTTCTGGT[C/T]ACAAACTTTGTGACC | 67245 |
rs26831734 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Peli1 | Mm_Celera | 11:21150169 | TTTTCAAGGAAATTT[C/T]GTTGATTTGAAGTTT | 67245 |
rs26831735 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Peli1 | Mm_Celera | 11:21148581 | GATTGGGTTTGCTAA[C/T]CGACCCCTTGTCCAT | 67245 |
rs26831736 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Peli1 | Mm_Celera | 11:21148442 | TACGCACACTTTTCA[C/T]GCAGCCTGCCCCTTC | 67245 |
rs26831737 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon | Peli1 | Mm_Celera | 11:21148100 | GGAGATCAATGCAGC[G/T]CGGCCGCAGTGCCCT | 67245 |
rs26831738 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21147936 | AGTGGTAACTTCGGT[G/T]TTGATTCTTTTCTCC | 67245 |
rs26831739 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21147913 | TACTGAAGATAGAGT[A/G]TGAACACAGTGGTAA | 67245 |
rs26831740 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Peli1 | GRCm38.p3 | 11:21147881 | CAACCCTGGAGGTCT[C/T]CTGTCTTGTTAGGAC | 67245 |
rs26831741 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21147522 | ACAGTGTGTATGCAT[C/G]TTGCTTTTTTTTCAG | 67245 |
rs26831742 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Peli1 | GRCm38.p3 | 11:21147082 | GATTTATGCTGCAGG[A/G]TTTGATTCATCAAAA | 67245 |
rs26831743 | snp | A/G | 0.231111 | 0.249285 | missense, intron-variant | Peli1 | Mm_Celera | 11:21147048 | TCATATGTGAGCGCA[A/G]TCCCCCCTTTACAGC | 67245 |
rs26831744 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant | Peli1 | Mm_Celera | 11:21146953 | TATTGATTTTGTAGT[A/G]ACTGACACCGTTCCT | 67245 |
rs26831745 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Peli1 | Mm_Celera | 11:21146881 | ACTGTGTTCGTTGAA[A/T]CAAATTTATATTCTT | 67245 |
rs26831746 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21146479 | TGAAGATGCAGGTAA[C/T]TTACTCATGGGCTAA | 67245 |
rs26831747 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Peli1 | GRCm38.p3 | 11:21146438 | CATGTGACATCCATT[C/T]ATTTCCTTTTTTTCC | 67245 |
rs26831748 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Peli1 | GRCm38.p3 | 11:21146262 | CTAGGTTATCCTGTG[G/T]AGCTAGGGACTACAG | 67245 |
rs26831749 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21146077 | AGAAGGCTGTCAGAT[A/G]AACTGTATGAAGTGT | 67245 |
rs26831750 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon | Peli1 | Mm_Celera | 11:21136168 | CCCAGTAAAATATGG[C/T]GAACTCATTGTCTTA | 67245 |
rs26831751 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21135245 | CCTTCCCAAGCCTGC[A/C]TGACACCATCCTACT | 67245 |
rs26831752 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21123851 | CCAGAATCTGTGGCT[C/T]TAAGTTATTAGTAAG | 67245 |
rs26831753 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21123347 | TGAATCAGCACTATG[G/T]AACTCATTCCTGGAA | 67245 |
rs26831754 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21122576 | GCAGTAGTAGAGGGG[A/C]AATGTTATTGTTAGA | 67245 |
rs26831755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21121687 | ACTCATCCAACTTTA[C/T]GTATGTACACTCACT | 67245 |
rs26831756 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21121638 | TCATGTTTTTCCTAT[C/T]GCCTAGCTCTTCCCA | 67245 |
rs26831757 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21121435 | TGAGAAATGGTTAGG[C/T]CGTAAGTGATGAGGC | 67245 |
rs26831758 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21120974 | CAAAGAAGGAAAGAA[A/G]CTACAGGATTAAACT | 67245 |
rs26831759 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Peli1 | GRCm38.p3 | 11:21120466 | AATCGATTTTTAACC[A/G]CAGGGAAGCTTTCCA | 67245 |
rs26831760 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21120212 | ATTATACACCAGCAG[A/G]AAATGGAAAGCTGTT | 67245 |
rs26831761 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21117487 | AAGAAAAATGTATGG[C/T]CCAGGATACATAGCC | 67245 |
rs26831762 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21117130 | CTCTCATAGTCTAGG[C/T]GTTTGGAACAGAAGA | 67245 |
rs26831763 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21116808 | CACCTGCTTAGGGTG[C/T]GGCTAGAAGCACAGG | 67245 |
rs26831764 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21116765 | ATCACCACCAGGAAG[A/G]TGGAACTAAAGGAAG | 67245 |
rs26831765 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Peli1 | GRCm38.p3 | 11:21116726 | CCATCTAAATGAATT[G/T]TATTGTGGCTAGTTG | 67245 |
rs26831766 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21115838 | ATAGAGGAAGATATC[C/T]GACATTGATCCCTAC | 67245 |
rs26831767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Peli1 | GRCm38.p3 | 11:21115025 | ATTTGAGGCAATGCT[A/G]TAAACATTGATGCAG | 67245 |
rs26831768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21114977 | ATAACCGTTTGGTCT[A/G]TTTCCACTGTGGGGC | 67245 |
rs26831769 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Peli1 | GRCm38.p3 | 11:21114917 | TTTTCATGGGCCACT[A/G]ACGTATTGCTTCATT | 67245 |
rs26831770 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21114601 | AGGAATAGAGAAAGA[C/G]ACTGAAGGAGCGATG | 67245 |
rs26831771 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Peli1 | GRCm38.p3 | 11:21114386 | GACCTGATATTCTCA[C/T]AGCTGTATGGAGGTC | 67245 |
rs26831772 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21114122 | GCAAAGGAGCCCCTC[C/T]GTTTATATCCAGTAG | 67245 |
rs26831773 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Peli1 | GRCm38.p3 | 11:21113903 | TAAATGCCTGTACTT[A/G]CATTTGACTGTCTAT | 67245 |
rs26831774 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21113605 | GATACTATGGCTATA[A/G]AATGCTACAAGTATG | 67245 |
rs26831775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21113253 | TCCAGTGGTAGAGAA[C/T]AGTCAACTGGCAACC | 67245 |
rs26831776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21112608 | GCAGTGTTTCTTCCA[C/T]TTGAAAGTGCTTTCT | 67245 |
rs26831777 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Peli1 | Mm_Celera | 11:21112418 | TCTCATTCATTTACA[A/C]GTCTTAAGAGTGTGT | 67245 |
rs26831778 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Peli1 | Mm_Celera | 11:21111566 | ATCATGCATTCTGTC[A/T]AAATGCACATGCTTT | 67245 |
rs26831779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | Mm_Celera | 11:21111148 | ATTAAAAGCCTGAGT[C/T]ATAGTTGGTTATAAA | 67245 |
rs26831780 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Peli1 | Mm_Celera | 11:21111058 | GGCATATGCTATCAT[A/G]CCAGGTTTAAGGGAT | 67245 |
rs26831781 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1 | GRCm38.p3 | 11:21111011 | GGGATTCACTTAACT[C/T]GCCCTCTGTGCCTTG | 67245 |
rs26831782 | snp | C/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Peli1, LOC105245353 | Mm_Celera | 11:21110660 | GAAAGCTCAATTTCA[C/T]TTTCAAATGTTACTT | 67245 |
rs26831783 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Peli1, LOC105245353 | Mm_Celera | 11:21110358 | GGGCTTTTAATAGCA[C/T]TGCCCATCTCCTTGT | 67245 |
rs26831784 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Peli1, LOC105245353 | Mm_Celera | 11:21109660 | CCTTGTAGATACTTG[A/G]CTCAGTCGTTACAGA | 67245 |
rs26831785 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Peli1, LOC105245353 | Mm_Celera | 11:21108133 | TCTCTTCAGACAGGC[A/G]CAAGAATTTATGAGC | 67245 |
rs26831786 | snp | C/T | 0.124444 | 0.216185 | intron-variant, missense | Peli1, LOC105245353 | Mm_Celera | 11:21107174 | GTTGCCCAGGTGAGG[C/T]ACAAGGCCTGTTCTC | 67245 |
rs26831787 | snp | A/C/T | 0.32 | 0.24 | intron-variant, synonymous-codon | Peli1, LOC105245353 | GRCm38.p3 | 11:21107121 | CCACCTCAGGGCTGG[A/C/T]TTGCCTGGACCTTTG | 67245 |
rs26831788 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21106500 | TGGCTAACTCAATGA[C/T]TGAGCACTCCTAAAC | 67245 |
rs26831789 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21106409 | GAGTTTTTTGCTATA[C/T]TGTGCTCCTGGTAGG | 67245 |
rs26831790 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21104944 | TTGTTCAGACTTAGA[A/G]TATGGCTTGAGCAAA | 67245 |
rs26831791 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21104475 | TCAACACCTTTCTAC[C/T]GGCACGGAAAGGGAT | 67245 |
rs26831792 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21103983 | TCATTCTTGGTAAAT[G/T]CGTCTGAGTAGAGCT | 67245 |
rs26831793 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21103314 | CCCCTCATGAAAGCT[A/G]TAAGTAATTGTTGAT | 67245 |
rs26831794 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21102134 | CTTAGTGTTTCAGTT[C/T]CTGTGGGGTTATCCC | 67245 |
rs26831795 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21101496 | AGAGCCAAGAAGTAA[A/G]GATACACATATGGCA | 67245 |
rs26831796 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Peli1, LOC105245353 | GRCm38.p3 | 11:21090305 | GTGGTCTGTGGGCAT[C/T]CAGGGTTTTTGATCC | 67245 |
rs26831797 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21089724 | AGCCTCTGTGTCCTC[A/G]AGCTCCCTGCTCCTT | 67245 |
rs26831798 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21089695 | CTTCTGCCACCGCCA[G/T]CAAATGTGCCATTAG | 67245 |
rs29412564 | snp | G/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Peli1, LOC105245353 | Mm_Celera | 11:21110489 | AGGGAATTTCATTTA[G/T]ATTTTATTTATTTAT | 67245 |
rs29413390 | snp | A/G | 0.32 | 0.24 | intron-variant | Peli1 | Mm_Celera | 11:21140133 | AACATAGTTGGAATA[A/G]AACTCAGTTGGATAG | 67245 |
rs29459366 | snp | A/G | 0.5 | 0 | intron-variant | Peli1 | Mm_Celera | 11:21132155 | AGGGCAGGCGTTGGG[A/G]ACAAATGGTGTTGGT | 67245 |
rs47167773 | snp | C/T | | | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21093755 | GCCTCAGAGGGTTCC[C/T]ATTTGCCTTAGTTTC | 67245 |
rs47909878 | snp | C/T | | | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21098401 | CAGTCCAACTTGCTG[C/T]CCATCTATTCCTGGG | 67245 |
rs48917895 | snp | A/T | | | intron-variant | Peli1 | Mm_Celera | 11:21143200 | AACAAAAATTACAGA[A/T]AATTTTCTAACTATT | 67245 |
rs49017343 | snp | A/C | | | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21106696 | CTCTTAAGCCCCCCC[A/C]CCCCCAGTCTCCCCT | 67245 |
rs49637111 | snp | A/T | | | intron-variant, utr-variant-3-prime | Peli1, LOC105245353 | Mm_Celera | 11:21109146 | TAAATAAATCTTTTT[A/T]AAAAAAAAAATTCAA | 67245 |
rs50519264 | snp | A/G | | | intron-variant | Peli1, LOC105245353 | Mm_Celera | 11:21093667 | CTTCCTGAGTTCTTT[A/G]GGATGCTTTAAAACA | 67245 |
rs51200954 | snp | G/T | | | intron-variant | Peli1 | Mm_Celera | 11:21145978 | ACAGAAGTTCCACGG[G/T]CCTCTTTGTCATCTG | 67245 |
rs108216990 | snp | C/T | | | intron-variant | Peli1 | Mm_Celera | 11:21121146 | TGAAGTTGATTAAGA[C/T]ATTTTGAAAATACCA | 67245 |
rs108291416 | snp | C/T | | | intron-variant | Peli1 | Mm_Celera | 11:21121270 | ATGTATACACACACA[C/T]ATGTGTGTATATATA | 67245 |
rs108418340 | snp | C/T | | | intron-variant | Peli1 | Mm_Celera | 11:21121199 | TAGTAAAAACATGTC[C/T]AAACTCATCTGATTT | 67245 |
rs108489003 | snp | C/T | | | intron-variant | Peli1 | Mm_Celera | 11:21121264 | ATATATATGTATACA[C/T]ACACATATGTGTGTA | 67245 |
rs108741918 | snp | A/G | | | intron-variant | Peli1 | Mm_Celera | 11:21121273 | TATACACACACATAT[A/G]TGTGTATATATATAT | 67245 |
rs211697418 | snp | A/G | | | upstream-variant-2KB, intron-variant | Peli1, LOC105245353 | GRCm38.p3 | 11:21090111 | ATGAGGCCAGAAGAT[A/G]GTGTTGGATTCCCTG | 67245 |
rs211701480 | in-del | -/TTTT | | | intron-variant | Peli1 | Mm_Celera | 11:21111810 | AGTTACAGCATATGC[-/TTTT]TTTTTTTTTTTTTCC | 67245 |
rs211701760 | snp | A/G | | | intron-variant | Peli1 | Mm_Celera | 11:21139446 | TCTACTTAATTTTCT[A/G]TTGCTGTAGTCATAT | 67245 |
rs211762166 | snp | C/T | | | intron-variant | Peli1 | Mm_Celera | 11:21140374 | AATACTTCTATGTGG[C/T]TCAAAACATAGCCAG | 67245 |