SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3656108 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnft2 | Mm_Celera | 5:118201680 | CCACTGCTAGCTGAT[C/T]ACAGTGAGCAAGATA | 269695 |
rs3661429 | snp | A/G | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194514 | GAGAGGATCCCTGGG[A/G]ACTGCGTTCACACGG | 269695 |
rs4136043 | snp | C/G | 0.489796 | 0.070696 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194166 | TGTGTGTGTTGGTTC[C/G]GCAGAACTGGAGTTA | 269695 |
rs6284287 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118213506 | GGCAGGTAGATAGCT[C/T]CACTGTCTGCATCTA | 269695 |
rs6284409 | snp | C/T | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213583 | TGAAAAATACTGTAG[C/T]CTTGAGGGCAGAGGG | 269695 |
rs6284823 | snp | A/T | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213625 | CCATTTCCTGTTTGC[A/T]TTTTTTTTTTTTCAA | 269695 |
rs6285375 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnft2 | Mm_Celera | 5:118213747 | CTCAGGACAAAACAG[C/T]GCCAGCGACCATCTG | 269695 |
rs6285426 | snp | C/T | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213780 | GGGCAAAGCCAGGGA[C/T]GGAGGGGCGCATCGG | 269695 |
rs6285955 | snp | A/G | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213858 | GAAGAAGCTGGAAAG[A/G]CTGCTGAGAGGAACA | 269695 |
rs6285994 | snp | C/T | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213874 | CTGCTGAGAGGAACA[C/T]AGGAAAAAAAAAAAA | 269695 |
rs6286408 | snp | A/G | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213904 | AGAGGCAGAGAGGAC[A/G]ATGGGGAAAAAGACT | 269695 |
rs6286532 | snp | G/T | 0.5 | 0 | intron-variant | Rnft2 | Mm_Celera | 5:118213989 | tgaacaggttggcca[G/T]gagtttataatcctc | 269695 |
rs6287023 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnft2 | Mm_Celera | 5:118214079 | TCCTTCTTTAGCACA[C/T]GTCAAGCAGGAACTA | 269695 |
rs29508208 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Rnft2 | Mm_Celera | 5:118190634 | GCTTCCTTCCTTCTC[A/G]GCTTCTCTAAGGAGA | 269695 |
rs29515305 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118218493 | GAAGGATTAGGAGGT[A/G]TGGCCTGGTTGGAGG | 269695 |
rs29523643 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118203971 | GGAAGCAGGAACAGG[G/T]GTCCCAGGCAAAGCT | 269695 |
rs29528946 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnft2 | Mm_Celera | 5:118197267 | GGTGACATCTGAACT[C/T]GTTCATTCATTGATG | 269695 |
rs29542395 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnft2 | Mm_Celera | 5:118234245 | CAGGTTGACATGGGG[A/G]ACACGCTGGCTTCCA | 269695 |
rs29545589 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Rnft2 | Mm_Celera | 5:118223908 | AGCCACGCTCCCATG[A/T]GATGATGTTGTGTTT | 269695 |
rs29581009 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118240317 | ACAAGCTGGCCTACA[C/T]ACGTGCCATGACACA | 269695 |
rs29630955 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | 2410131K14Rik, Rnft2 | Mm_Celera | 5:118243324 | CATGGTATTGCACTG[C/T]GTAATCCCAGCACTG | 269695 |
rs29817884 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118236538 | AACCTGGTCAGTGAG[C/T]TGCCGGCATTCTCCG | 269695 |
rs33047848 | snp | G/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118193888 | GCACCCTTTGTGGGA[G/T]GGTGGAGTGAGCTGT | 269695 |
rs33075933 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rnft2 | Mm_Celera | 5:118222959 | CCGCCATCTTTAACC[C/T]GAGGATCCTGACTTA | 269695 |
rs33103695 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118235376 | CTCAAGGACAACTTA[A/G]CTGCAAGGGCCAGGC | 269695 |
rs33127869 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rnft2 | Mm_Celera | 5:118210662 | TTTAAAGAAAAAAAC[A/G]ACTCGAGCCGGGTGT | 269695 |
rs33163468 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rnft2 | Mm_Celera | 5:118239782 | TACTGATGATATTAG[C/T]GGCGGCAACAACAAC | 269695 |
rs33189525 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118217153 | TATTCTTGCCCCTGT[C/T]TTTGTTTCTTGAGCA | 269695 |
rs33220352 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime, downstream-variant-500B | Rnft2 | Mm_Celera | 5:118193499 | TTTCCCAGGCATCCT[C/T]GGGGCTGGGCTCCCC | 269695 |
rs33260981 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | 2410131K14Rik, Rnft2 | Mm_Celera | 5:118243552 | CATATGCATGTGCAC[A/G]CTTATACACATACAC | 269695 |
rs33345410 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Rnft2 | Mm_Celera | 5:118239553 | ACTGTGGAAAGCCTA[C/T]TGCTGCTGTACAGGA | 269695 |
rs33351787 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118192181 | GCATGGGTCCTAAAT[C/T]TACAAAGGGGAGGAG | 269695 |
rs33385813 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118209200 | CAATGTAAACACCAT[A/G]TAAATAGACTCTGTT | 269695 |
rs33474203 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118196715 | TCCTGTATCTCGGTG[A/G]GTGGTAGGCCAGGAG | 269695 |
rs33509048 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | 2410131K14Rik, Rnft2 | Mm_Celera | 5:118247097 | TCTGTTCACAGCAGT[C/T]AAATGCTAACTAAGA | 269695 |
rs33533589 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118190824 | GCAGAGGACCTCAGG[C/T]CGCTGCCCACTTCCG | 269695 |
rs33594149 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnft2 | GRCm38.p3 | 5:118201045 | ACGGAGATTTGAACC[A/G/T]CGGTCTAGCTGCTTC | 269695 |
rs33601406 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Rnft2 | Mm_Celera | 5:118231669 | TTAAACAAAAAGCCA[A/G]CACAGCCACACACCT | 269695 |
rs33630302 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Rnft2 | Mm_Celera | 5:118203073 | GGCTCTAATGGGGAC[C/T]GATGGATGTAGCCAG | 269695 |
rs33647572 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft2 | Mm_Celera | 5:118196735 | AGGCCAGGAGCACAT[A/G]TGGGGAGGCTTCCTG | 269695 |
rs33651899 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118190849 | CTTCCGCTTCAGCAG[G/T]GGGGGATGGTCCCAA | 269695 |
rs36265719 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rnft2 | Mm_Celera | 5:118220779 | TCCTGGTCCGCCCTG[A/T]AGATGAAGCACTTCA | 269695 |
rs36289956 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnft2 | Mm_Celera | 5:118227286 | TATTCCTTGTCAAGG[C/T]GCATGGCCTCCAGGA | 269695 |
rs36301888 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnft2 | Mm_Celera | 5:118210010 | AAAGAGAGGTAGGGC[C/T]GGCCAGTAGTGGACC | 269695 |
rs36322814 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnft2 | Mm_Celera | 5:118214533 | GCGTTGCTTGGCAAC[A/G]GGCGCTGCGATGCCG | 269695 |
rs36326476 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118205453 | ACTGTTTGGCTGAGT[C/T]CCTGTGTATGTGTGT | 269695 |
rs36356895 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194420 | GAAGGATGGGATGAA[A/G]ACCTTCCCCGGCTGG | 269695 |
rs36361082 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118195956 | AGCAGTCAGGGTAAA[C/T]GCAGCCTGGATCCCG | 269695 |
rs36368371 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118207075 | GAACTGTGCATATCC[A/T]GGGAGAACACACGTC | 269695 |
rs36372851 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rnft2 | Mm_Celera | 5:118218822 | ATTTATCATTTGACT[A/T]ATACCATGGACCTTC | 269695 |
rs36381082 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118209316 | TGCTTGGTGTGGAAC[C/T]TGGAGACACAGCCAG | 269695 |
rs36384344 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118216324 | CCTTGTCCGAAGTAC[A/G]GATTGCCGGGCTTTT | 269695 |
rs36392289 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118208997 | GCAGTCTCTGGACCA[C/T]ACTACATCTCCTCAA | 269695 |
rs36402395 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Rnft2 | Mm_Celera | 5:118217205 | TTATGAGGCTGCCTC[C/G]GGCTCTGGAGTTAAG | 269695 |
rs36417154 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118210570 | TTCAAACAGCTAGGC[A/G/T]GATTCCTATGGCCAT | 269695 |
rs36426713 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Rnft2 | Mm_Celera | 5:118193227 | GTACTCTCTGAGCTC[A/G]TACTAGTTCGTAGCA | 269695 |
rs36434624 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118197077 | AGAGAGATCTTACAC[A/C]ACCATTTGTTCCATA | 269695 |
rs36470746 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118208968 | GAGTAGCAGCATTTC[A/G]GCAAGGGTACTCTGC | 269695 |
rs36473354 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Rnft2 | Mm_Celera | 5:118201706 | AGATAAGGCCTCAAG[G/T]CTGGTTCTACACTGA | 269695 |
rs36478435 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118192702 | GGCCTGAGCTGTCAG[C/T]GAGGGACAATGTAGA | 269695 |
rs36480863 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194081 | ACCATCTTATACTAA[C/T]GTGGACTTAATAGCC | 269695 |
rs36489848 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnft2 | Mm_Celera | 5:118223834 | GACAGATGGCTAAGT[A/G]AATGGTGGCCTGTCC | 269695 |
rs36524944 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rnft2 | Mm_Celera | 5:118204602 | GACACACACACGAGC[C/G]AACAGCCCTTCCTTG | 269695 |
rs36546576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118227186 | GATCACAAAGGTGAA[A/G]TGCTCTGTGTCTGCA | 269695 |
rs36551785 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnft2 | Mm_Celera | 5:118223391 | GCAAGGAGAGGCTGC[A/G]GACCTTTTCCCAGCC | 269695 |
rs36562047 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118195370 | GGTCCATTCTGTGCT[A/G]TGTGTATAGTGTGCA | 269695 |
rs36563822 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118204658 | GTGAGCTCTGTGCCT[C/G]TAACTCCTCTAACAA | 269695 |
rs36577084 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Rnft2 | Mm_Celera | 5:118213864 | GCTGGAAAGACTGCT[C/G]AGAGGAACACAGGAA | 269695 |
rs36582305 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Rnft2 | GRCm38.p3 | 5:118212103 | TGCTCTGTATTCCAG[A/C/T]GGTATTAACCCAGCT | 269695 |
rs36582612 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118211497 | AACTGGATCCTTCCC[A/G]GCATCTGTAAAGGGT | 269695 |
rs36620445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118201328 | AAGGGCTGCCGTGGG[C/T]TGCACCATTTGGTTC | 269695 |
rs36623479 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnft2 | Mm_Celera | 5:118214768 | CTTGCGGCTGTACTG[G/T]GTCCTTAGCAGGCTT | 269695 |
rs36646449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118206225 | TGACACTTCTCCCAG[C/T]GAGGCTGCACCTCTA | 269695 |
rs36693077 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118202055 | GTGGGTGAATCTCAA[A/G]AATGTCAATAAATCT | 269695 |
rs36721696 | snp | A/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194245 | ATGTCTGGGAAATTA[A/T]CGTGGGTCAGGACAG | 269695 |
rs36755718 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118203406 | TGTACAGTAAAGATA[A/C]TAAGCAGGAAGAGGA | 269695 |
rs36790046 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, downstream-variant-500B | Rnft2 | Mm_Celera | 5:118193533 | CACTCATGTTTAGCT[C/T]AATACACCTGCAAGT | 269695 |
rs36806478 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118206881 | TAGGGCAGAAGGCTC[C/G]ACCCTCATTACTCCT | 269695 |
rs36822059 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnft2 | Mm_Celera | 5:118221172 | CCCTGTGGTTTCTGA[C/T]TCTCTTGTGACTGTG | 269695 |
rs36830567 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Rnft2 | Mm_Celera | 5:118216489 | TCTGGCTTCCCACTG[A/T]CCAGTTCTGCCCCAA | 269695 |
rs36876132 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118198402 | GACAAGGGCAAGCAG[C/T]CTGTCACTAGCCTTT | 269695 |
rs36890127 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118214786 | CCTTAGCAGGCTTCG[A/C]ATTTAAGGCAGCCGG | 269695 |
rs36924809 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnft2 | Mm_Celera | 5:118194756 | ATGCTCTCTACCCAT[G/T]TGATCACATCCCAGC | 269695 |
rs36971855 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118215122 | CATCTTTCCAGTGCC[C/G]AAGATTTACTTTCAC | 269695 |
rs36975563 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118216080 | TTTCCTAACACCTTG[A/G]AGCCTTTGTGAACAG | 269695 |
rs36982164 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118192282 | CTTGGGCCAGCCTGT[C/T]GTGCGGATGCCGGCT | 269695 |
rs36991791 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118216132 | CCAGTGCGCTCCCAG[A/G]CCAGCTTCAGCTCTG | 269695 |
rs36995336 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118192792 | ACCCTTCTGAGACTG[A/T]CTGTCCCAGGTGGAT | 269695 |
rs37002122 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnft2 | Mm_Celera | 5:118214332 | TAATTCTGTGGGGTG[C/T]TTCAAGACATCCGTG | 269695 |
rs37009997 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnft2 | Mm_Celera | 5:118200552 | GAGTTACGTCTACCG[A/T]GGACATTTTTACAGA | 269695 |
rs37044643 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118192984 | CTGGAGACACATTGG[C/T]CCCTTACTAGCTGGG | 269695 |
rs37054993 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnft2 | Mm_Celera | 5:118224139 | CATGCCTGGCTATCC[C/T]GTGGTCAGGACCTCC | 269695 |
rs37065755 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Rnft2 | Mm_Celera | 5:118202407 | TAGCACACTGTGACA[G/T]CAAGTGCCATCGACT | 269695 |
rs37071420 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Rnft2 | Mm_Celera | 5:118193610 | AACCGAGCGGCAGAG[C/T]GGGCAGGTGCGTTCC | 269695 |
rs37087831 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Rnft2 | Mm_Celera | 5:118201160 | CACCTGGCACAGGAG[A/G]ATCATGGGATCTCGG | 269695 |
rs37090712 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118205401 | GCAGATACGTGTAAG[A/G]ACCAAGACTGGTCAT | 269695 |
rs37107824 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnft2 | Mm_Celera | 5:118198023 | GTGACAGCCATCTTC[A/G]CAGTAACAAGAGATG | 269695 |
rs37121206 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Rnft2 | Mm_Celera | 5:118220846 | TGCAGCTCGAATCCA[G/T]CCCTGCAGACATGCA | 269695 |
rs37132802 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnft2 | Mm_Celera | 5:118195906 | TGCTTGGTTATAGAG[C/T]TTAGGAAGTACACAT | 269695 |
rs37144598 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rnft2 | Mm_Celera | 5:118194246 | TGTCTGGGAAATTAA[C/T]GTGGGTCAGGACAGA | 269695 |