SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6368521 | snp | C/T | 0.5 | 0 | intron-variant | Znrf1 | Mm_Celera | 8:111548133 | caaacacaaacaCCA[C/T]GACCACCGCCagctc | 170737 |
rs31309526 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Znrf1 | Mm_Celera | 8:111541986 | ATTAAACAAAGACTC[C/G]TCTCCAACTATGTCA | 170737 |
rs31309529 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111542799 | AGGGGCTTCTCAGAC[A/G]TAGCTTCTGTCCTTC | 170737 |
rs31309532 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111543064 | AGTGCTGATTGGATA[A/G]CAGTGAAGACCAGTG | 170737 |
rs31310415 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Znrf1 | Mm_Celera | 8:111543079 | GCAGTGAAGACCAGT[A/G]GGCAGGTGGAGGTTT | 170737 |
rs31310418 | snp | C/T | 0.375 | 0.216506 | intron-variant | Znrf1 | GRCm38.p3 | 8:111543150 | GCTTCTAAACGGATG[C/T]GGCAGTTCACCTTGC | 170737 |
rs31310421 | snp | A/T | 0.375 | 0.216506 | intron-variant | Znrf1 | Mm_Celera | 8:111543309 | ATGAAACAGACACAA[A/T]CAGGAGCCTCTGATG | 170737 |
rs31311134 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Znrf1 | GRCm38.p3 | 8:111543374 | GGTGGTTTTTAGGGA[A/G]CCTCATAGCAATGCT | 170737 |
rs31311137 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Znrf1 | Mm_Celera | 8:111543445 | AGACTAAACAGATCC[C/T]GAGAGTACAGTTAGA | 170737 |
rs31311140 | snp | C/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111543719 | GTCTCCTACATAAAG[C/G]CCTAAGCCAGTGTGC | 170737 |
rs31311143 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Znrf1 | Mm_Celera | 8:111544402 | AGGCTGCTGTAAGGT[A/G]TTTCTTCTGAACTCT | 170737 |
rs31311475 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Znrf1 | GRCm38.p3 | 8:111557576 | TTGGCCTTGAAGACA[C/T]GGCAGTTCTCTTGCC | 170737 |
rs31311478 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111558296 | CTCTCCAAATTCAGG[C/T]CATTAGGTTTGGAGG | 170737 |
rs31311481 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Znrf1 | Mm_Celera | 8:111558357 | TAGCCTGGTGTTAGT[A/G]TTTTAGAGATGTTGC | 170737 |
rs31311864 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111577484 | TAAGAGTCTTCCCTC[G/T]GACCATTAGCTTCAA | 170737 |
rs31311867 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111577597 | TTCTTCGCTGAACAC[A/G]GGTTATAGTTATACA | 170737 |
rs31311870 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111577763 | AGATACATTGAGAAC[C/T]TCCTTTAGAAGCAAG | 170737 |
rs31311872 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111577790 | CAAGGCTTTGAGGCA[G/T]TTGACCTTGTAAAAG | 170737 |
rs31311916 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Znrf1 | Mm_Celera | 8:111545832 | ATGAAAAGGCAAAAA[A/C]TTCATTCTGAACTGC | 170737 |
rs31311919 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Znrf1 | GRCm38.p3 | 8:111546054 | TAAGGAAAACGACTC[C/T]CTTCTTACAAGCTGG | 170737 |
rs31311922 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Znrf1 | Mm_Celera | 8:111546078 | AAGCTGGAACTTTCT[A/G]TAAGCCCCCTAGACA | 170737 |
rs31312194 | snp | A/G | 0.375 | 0.216506 | intron-variant | Znrf1 | Mm_Celera | 8:111562225 | AATGCTGGTGTTTTA[A/G]TTGTACTTGGGTAAG | 170737 |
rs31312197 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Znrf1 | Mm_Celera | 8:111563223 | GAGAAGCCACAGAAC[C/T]TTTTGCTGACAGATA | 170737 |
rs31312200 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Znrf1 | Mm_Celera | 8:111570701 | AGTGTAGGGCATTTA[A/G]AACACAGGATTTTCT | 170737 |
rs31312203 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111571789 | CCCTTTGGGCCTATG[A/G]CAAGGCAGTGACTAA | 170737 |
rs31312665 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111591039 | CAGCCTGTTCCTCTC[C/T]GATTCCATCTTCATG | 170737 |
rs31312668 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111591065 | TCATGAAAACCACCA[A/G]CAGGTCTTGTCTGTC | 170737 |
rs31312671 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111591095 | CTTAAACCATAAAGA[G/T]GAATGCATCTGCTGA | 170737 |
rs31312716 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Znrf1 | Mm_Celera | 8:111583632 | ATGTAAAACCTACTA[A/T]GCTTTCTTCCCCGCA | 170737 |
rs31312719 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111583941 | AGTTTAGAGGGATAA[A/G]CTGGTATCCTCAGCT | 170737 |
rs31312722 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Znrf1 | Mm_Celera | 8:111584066 | ACAGGTGGGATTGGT[A/G]AGAGAGGGAGAGATA | 170737 |
rs31312745 | snp | C/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111546975 | CTGTGATGAGTGCTG[C/G]CTTGCAAGCTAGTGG | 170737 |
rs31312748 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Znrf1 | Mm_Celera | 8:111547662 | TCCGTGGATCACAAG[C/T]ACCTTCTTTCAGTGT | 170737 |
rs31312751 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Znrf1 | Mm_Celera | 8:111547899 | GATCCAACACCCTCT[C/T]ACAGGCAAAAACTCA | 170737 |
rs31312845 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111577925 | GGAACAAGAGGCCAT[C/G]GTTTTCTGTGACAGC | 170737 |
rs31312848 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Znrf1 | Mm_Celera | 8:111578121 | GTGGCCTGGCCTCAT[A/G]AGAAAGACTTCTGAT | 170737 |
rs31312851 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Znrf1 | Mm_Celera | 8:111578156 | CTGAGTTCCCTGGTG[A/C]TCCCAGCACTCTTGA | 170737 |
rs31313046 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Znrf1 | GRCm38.p3 | 8:111571840 | GAAAGGTATTCCTAT[C/T]ACAGCATCCAGAAAG | 170737 |
rs31313049 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Znrf1 | Mm_Celera | 8:111571998 | GCCTTTACCAGTGCA[A/C]TGAAACATTTCTCTG | 170737 |
rs31313052 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Znrf1 | GRCm38.p3 | 8:111572331 | CACAAGCCAGTCAGG[C/T]TACAAAGTGAAACCT | 170737 |
rs31313084 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | GRCm38.p3 | 8:111597063 | TCTCTTGAACAGAGA[A/G]AAAGCATCTGAGCAC | 170737 |
rs31313087 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111597627 | CCCTGGTAGAGATCA[C/T]GTGCTATTTTAGGGA | 170737 |
rs31313090 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Znrf1 | Mm_Celera | 8:111597658 | TCTTAGAATTGGAGG[C/T]TCTTTTTGTTTGTGC | 170737 |
rs31313092 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111597892 | CTGCCTCCATGTACT[C/T]CAGGGTGTAAGTGCA | 170737 |
rs31313426 | snp | A/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111602209 | TACTGTCTTCTGGTT[A/T]GTAGTATGCAGTGCC | 170737 |
rs31313429 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111602892 | GGCTTTGTCTTCCCA[A/G]TGCCCAGATGCTTTG | 170737 |
rs31313432 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111603808 | TTAAGTCGCTGGCGA[A/G]CTTTAGTATGCAGTC | 170737 |
rs31313584 | snp | G/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Znrf1 | Mm_Celera | 8:111578611 | ATGTTTTCTGCTATT[G/T]ATGCCAAGCAGATTT | 170737 |
rs31313587 | snp | C/G | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Znrf1 | Mm_Celera | 8:111578650 | AATGGCATCTAGTGA[C/G]GTTGCTCCAATACAT | 170737 |
rs31313590 | snp | G/T | 0.260355 | 0.249785 | intron-variant, downstream-variant-500B | Znrf1 | Mm_Celera | 8:111578716 | GAACTAAAGGTTTGA[G/T]AACTATACGGAGGCA | 170737 |
rs31313593 | snp | C/T | 0.35503 | 0.226867 | intron-variant, downstream-variant-500B | Znrf1 | Mm_Celera | 8:111578785 | TGATAAAGTCCTAAG[C/T]TTCAGGGTAAAGAGC | 170737 |
rs31313615 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111584171 | TATTCCCTGCCCATG[C/T]TATGTGAAAATATTG | 170737 |
rs31313618 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Znrf1 | Mm_Celera | 8:111584301 | CATTTCTGACCCCAC[A/G]TCTACAGTGTTTGCT | 170737 |
rs31313621 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | GRCm38.p3 | 8:111584842 | AGGGCAAGAGAGTCA[A/G]ACGTTCAAAGCCTGT | 170737 |
rs31313694 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Znrf1 | Mm_Celera | 8:111548984 | GTTGAGCACAGGAGA[C/T]GAGGTCGGTATGCTC | 170737 |
rs31313697 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Znrf1 | Mm_Celera | 8:111549763 | TTGAATAAGCCAGCA[C/T]ACCAGTATTCAAAAG | 170737 |
rs31313700 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Znrf1 | GRCm38.p3 | 8:111550649 | GGAGACTTGCTGGAT[A/G]CTTATCTTTGGATCC | 170737 |
rs31313703 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Znrf1 | Mm_Celera | 8:111550813 | TTAGGAAATCGGATA[A/G]TGCTGTGACTCTGAA | 170737 |
rs31313704 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111591307 | TAGATGCCAAAAAGC[A/G]CAGTAAGCAGGATAA | 170737 |
rs31313707 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111591455 | TTTCAGGGCAGTGAA[A/G]CCTGGTTCTTTCCAT | 170737 |
rs31313710 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111591483 | CATTTATACCAAACA[A/G]CAACCTGAATAGTAA | 170737 |
rs31313713 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111592423 | CCTTGTTTGTGGAGC[C/T]AGCGAGCATATTGCA | 170737 |
rs31313725 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111572368 | CAAACAAAAATGTAT[A/C]TTTGCTTTAGAGTTC | 170737 |
rs31313727 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Znrf1 | Mm_Celera | 8:111573097 | CCCCACCTGTCTTGG[C/T]TCAGCCACATTACTG | 170737 |
rs31313730 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111573234 | TATATTTGTCTCAGT[A/G]TTTTAATGTAGTGTT | 170737 |
rs31313733 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111573328 | CGTTTTGCTCTTAGC[C/T]CAACCCAAATCTCTC | 170737 |
rs31314064 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111597993 | TTCTTATGTGCTAGG[A/G]CCCAAGCTTCAGCTA | 170737 |
rs31314067 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111598030 | TCTGAGAAATGAACA[A/G]AGGAGTATGTGTTTT | 170737 |
rs31314069 | snp | C/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111598362 | AGTGCAAACAAATAG[C/T]TTTATTCTATATGAA | 170737 |
rs31314072 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111598443 | AATCAAGCATTTTCT[C/T]TCTTGTCATTGAAAA | 170737 |
rs31314335 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111609728 | AAGCCATCAAGAGGG[A/G]CCTAGACAGAATATC | 170737 |
rs31314338 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111610048 | CTAGCATGTTTCTGG[A/G]GATAAAGTTGAGTGG | 170737 |
rs31314341 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111610071 | TTGAGTGGCAGATCT[A/G]TTTGCTGTAGGTAAG | 170737 |
rs31314354 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111584939 | AGAGCTAGCTCGGTA[A/G]TAGAGCACATTCCTA | 170737 |
rs31314357 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Znrf1 | Mm_Celera | 8:111585037 | CCCCAAGACTGAGAT[C/G]GTCCATTCAACACTT | 170737 |
rs31314360 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Znrf1 | Mm_Celera | 8:111585078 | GGTGAAGGTAGAGAG[C/T]GTGCTGGTGGTTTTG | 170737 |
rs31314363 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111585220 | TGAGCACATTGCAAA[A/C]CTGCTCTGCTTCTTG | 170737 |
rs31314385 | snp | G/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111604790 | AAAGAGAATTAGAAG[G/T]CTGGGTCTTTCTATG | 170737 |
rs31314387 | snp | C/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111604820 | GCCCAGAATGTTCTT[C/T]AGGAGGCATACCTCA | 170737 |
rs31314390 | snp | C/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111604858 | GTTCATCGATTGATA[C/T]ACTGTGCATTGGGTT | 170737 |
rs31314393 | snp | A/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111604943 | AAACTATATAGAAAT[A/G]TTTGGAGCATCCCTC | 170737 |
rs31314466 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111592443 | AGCATATTGCAGTGT[G/T]GTGCTGACCTTTAGT | 170737 |
rs31314469 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Znrf1 | Mm_Celera | 8:111592474 | TAGTCCTGCAGTAAT[A/C]GTCTGCACTATGTGA | 170737 |
rs31314472 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111592507 | GAACTATATACGTTA[C/T]CCATTTGCTCTTACA | 170737 |
rs31314536 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Znrf1 | Mm_Celera | 8:111550872 | CTCAAACTATGAACT[A/T]TTTCAGGAATTCAAA | 170737 |
rs31314539 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Znrf1 | Mm_Celera | 8:111550898 | TCAAAAAAGATGATG[C/T]ATTTAACTCAATAAG | 170737 |
rs31314542 | snp | G/T | 0.375 | 0.216506 | intron-variant | Znrf1 | GRCm38.p3 | 8:111551461 | GGTTTACCTGTTAGC[G/T]CAGCAGATCACTTTC | 170737 |
rs31314586 | snp | C/T | 0.336735 | 0.234472 | intron-variant, downstream-variant-500B, missense | Znrf1 | Mm_Celera | 8:111578940 | GAGGACCTGAAGCAA[C/T]GTGAACAGGTGAAGG | 170737 |
rs31314589 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Znrf1 | Mm_Celera | 8:111579445 | TCAGCACAGTGCTTT[A/G]GGCAGAATGACCTGT | 170737 |
rs31314592 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Znrf1 | Mm_Celera | 8:111579507 | CAAAAGTCTGGGTGA[C/G]CAGAGGCTGCAGTGC | 170737 |
rs31314636 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Znrf1 | Mm_Celera | 8:111573448 | CCTTCTCTCCTGTCA[G/T]GAGTGCTTGCTGCTT | 170737 |
rs31314639 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Znrf1 | GRCm38.p3 | 8:111573464 | GAGTGCTTGCTGCTT[C/T]TTTCTTAGATGTGAG | 170737 |
rs31314641 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Znrf1 | Mm_Celera | 8:111573744 | CCTGTGAAAAGGAGA[G/T]TCTGAGGCTGCAGAC | 170737 |
rs31314643 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Znrf1 | Mm_Celera | 8:111573849 | GATTGGACCTGAGGG[A/T]GGAACCTCCTGAGGT | 170737 |
rs31314810 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Znrf1 | Mm_Celera | 8:111538955 | AGCTTTATTTCGAGA[C/T]GATTATGAGTACACT | 170737 |
rs31314813 | snp | C/G | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111539828 | AAGTCAAAGCTGTGG[C/G]CTTGTGCTGTGTTCC | 170737 |
rs31314875 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111598514 | CCAGAAATCAGTCCA[C/G]TATGAATTCTTGGTA | 170737 |
rs31314878 | snp | G/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111598960 | GAATATTGGGATCTT[G/T]AGCTATATGAATAAA | 170737 |
rs31314881 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Znrf1 | Mm_Celera | 8:111599034 | CAGTCAGTTTTCTTT[A/G]GGAAGTTTGCTGAGG | 170737 |
rs31314974 | snp | C/T | 0.32 | 0.24 | intron-variant | Znrf1 | Mm_Celera | 8:111618200 | GTGAGGGCATTACCG[C/T]GCCTGCCTGTGACTT | 170737 |