SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023978 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Rimbp2 | Mm_Celera | 5:128888365 | AGAGCCACATGGCAG[C/G]CATTAACCCTCATGA | 231760 |
rs3023979 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128888392 | ATGATCACAAAGGAT[A/G]CTGGTCCAGGCATTC | 231760 |
rs3023980 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128888413 | CCAGGCATTCACCTT[A/G]GTTCCTCTGCAGATG | 231760 |
rs3657889 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128846043 | AGCACCAGGCAAAGA[A/G]AAAGGCATGCCCCCT | 231760 |
rs3674033 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rimbp2 | Mm_Celera | 5:128846405 | CACAACACACATGTG[A/G]TCCTGATGTGCGTCC | 231760 |
rs3678920 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Rimbp2 | Mm_Celera | 5:128840898 | CCCTTGGGCTACATA[C/G]AGACTAAATAATAAC | 231760 |
rs3679498 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rimbp2 | Mm_Celera | 5:128840969 | CTGCATGCTTGCCCC[A/G]TGAGGCAGACAAAGC | 231760 |
rs3679563 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rimbp2 | Mm_Celera | 5:128841000 | TCAATTGGCAGTGCC[A/G]GCCTCTGGGTACCTG | 231760 |
rs3680133 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Rimbp2 | Mm_Celera | 5:128841056 | GTTGTAGAGGGAGCC[C/G]AGAGGTGCCTGGCAG | 231760 |
rs3680160 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128841069 | CCGAGAGGTGCCTGG[C/T]AGAGAGCAGCTCACC | 231760 |
rs3680161 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128841070 | CGAGAGGTGCCTGGC[A/G]GAGAGCAGCTCACCA | 231760 |
rs3680761 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128841119 | CAAAGCAAACAAAGC[C/T]TCAAACCTCAACCTG | 231760 |
rs3680828 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rimbp2 | Mm_Celera | 5:128841145 | ACCTGCCGTGGAACA[G/T]CTGTCCTGCCTGGGG | 231760 |
rs3688355 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128805481 | GGGCTGTCCCATCCC[A/G]TCCATCTTGTTTCTC | 231760 |
rs3689007 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128805611 | ATGACACAGAACAAC[A/G]AGCATTGCCTAGTTT | 231760 |
rs3713177 | snp | A/C | 0.483471 | 0.0893938 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128903412 | CCACATACACAAACA[A/C]GAGCCACCTGCTCAG | 231760 |
rs3713908 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rimbp2 | Mm_Celera | 5:128903536 | ACTAACTACCCTCTG[C/T]TCTTGAACCCTGTCA | 231760 |
rs4138569 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Rimbp2 | Mm_Celera | 5:128846485 | AACTCTTGGACAGCA[A/C]GATGTACCCTAAAAG | 231760 |
rs4139279 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128789055 | AATGGGGTAGCGACA[G/T]CTGCAGTGATTTGAA | 231760 |
rs4139281 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128789056 | ATGGGGTAGCGACAT[C/T]TGCAGTGATTTGAAT | 231760 |
rs6177119 | snp | A/G | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128866362 | GAACACTAAGGTCCA[A/G]CATGAAAGCCCTGAG | 231760 |
rs6177210 | snp | C/T | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128866418 | TGTCATAATGACTGT[C/T]GCACCTTGGGTAGCA | 231760 |
rs6177593 | snp | A/T | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128866440 | TGGGTAGCAGGAGGG[A/T]CTGAGACATAGCGAG | 231760 |
rs6177640 | snp | C/T | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128866464 | TAGCGAGCCAGACTC[C/T]GCCATACCCTCTGCT | 231760 |
rs6194384 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128906551 | AAGTTGGCCAGTCTG[A/G]ACATATACAGCCATG | 231760 |
rs6207769 | snp | A/T | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128906684 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 231760 |
rs6211065 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128907319 | ATGTTATAAAGTGAC[A/G]ATTGGGCAGGTACAC | 231760 |
rs6211625 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rimbp2 | Mm_Celera | 5:128907443 | TGTCAGCTTGGGTCA[A/G]TGCTGCTTCGGAGCC | 231760 |
rs6212101 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rimbp2 | Mm_Celera | 5:128907513 | GTCAGATGTTCCTCA[A/G]TACTGTCCTGCTGGG | 231760 |
rs6220041 | snp | A/C | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128791841 | CACAGAGACAGGTCA[A/C]ANGTAGGGTGGCATT | 231760 |
rs6220042 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128791843 | CAGAGACAGGTCANA[A/G]GTAGGGTGGCATTCT | 231760 |
rs6220445 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128791864 | GTGGCATTCTCAGAG[A/G]CACGAATCATCCAGA | 231760 |
rs6220482 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128791881 | ACGAATCATCCAGAG[C/T]CCAATTGCATAAGAA | 231760 |
rs6221483 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128792062 | TGCATTAGGAAATAT[A/G]AAAGACCATTTTCTC | 231760 |
rs6221533 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128792093 | CAATTCCTCAAAGAA[C/T]GCATTATTTGAATAA | 231760 |
rs6221588 | snp | A/G | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128792119 | AATAAAGAGAAAAGC[A/G]ACGTATTAGGGAGCC | 231760 |
rs6388623 | snp | A/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786314 | CATACATGTACTTAT[A/T]TATGTACATAGGCAG | 231760 |
rs6389108 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786397 | tagacaaacagcaac[C/T]catacacacaccata | 231760 |
rs6389742 | snp | A/C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786549 | acatgagcacacaca[A/C/T]acccaGGGCAGGCNA | 231760 |
rs6389776 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786563 | anacccaGGGCAGGC[C/T]AGNCCAATGTCCCCA | 231760 |
rs6389780 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786566 | cccaGGGCAGGCNAG[A/G]CCAATGTCCCCATGC | 231760 |
rs6390197 | snp | C/T | 0.32 | 0.24 | intron-variant | Rimbp2 | Mm_Celera | 5:128786595 | GCCTCTCAACTCCTA[C/T]GCATCCTGCTAAAGC | 231760 |
rs6390273 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128786632 | CAGCCAAGGGCTAAT[A/G]CAGGGGTGCACACTC | 231760 |
rs6390732 | snp | C/T | 0.5 | 0 | synonymous-codon, intron-variant, nc-transcript-variant | Rimbp2 | GRCm38.p3 | 5:128786691 | GAGGAAGTCATCCAC[C/T]GAGGTGCCTCTCCTC | 231760 |
rs29500164 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128778605 | GATGACCTACCACTC[A/T]GATGATCTATTACAT | 231760 |
rs29500179 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rimbp2 | Mm_Celera | 5:128848729 | GGAGAGGTAAGCAGT[C/T]TTCCCAGTTTCCAAA | 231760 |
rs29505536 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rimbp2 | Mm_Celera | 5:128843141 | CTCCTGCTGTAGCTC[A/G]AGTTGGAATGGTCTC | 231760 |
rs29509015 | snp | A/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128928614 | GGCAGAGAGTGTGGC[A/T]CAGTTGTTAAGCACA | 231760 |
rs29509242 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rimbp2 | Mm_Celera | 5:128851359 | CATTCTTTCTGGGAA[A/G]AATTGGCAAGTGGTG | 231760 |
rs29511069 | snp | A/G | 0.265928 | 0.249492 | intron-variant, upstream-variant-2KB | Rimbp2 | GRCm38.p3 | 5:128879119 | AGAAAGGGAGCTGAT[A/G]ACATCATCTATGTAC | 231760 |
rs29511794 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128893421 | ACTGTCTCAGATGTG[A/G]ACACAGCCGCCCCAC | 231760 |
rs29512666 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128765043 | TGAAAGACAGCGCTG[C/T]CAAACCACACTCCTA | 231760 |
rs29513150 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rimbp2 | Mm_Celera | 5:128863396 | GCACTGATAAGCAGA[A/G]CCTTCTGCTATGAGC | 231760 |
rs29513340 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128940703 | AGGGAGAAGAAAGTG[A/G]AATAGGATTAGGGTT | 231760 |
rs29513965 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128907126 | CCATTCTCCCGGGTC[A/G]CCCTGTCTCTGCCTC | 231760 |
rs29516034 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128918642 | AACACTTACTAAAAG[C/T]CAATCTTATCTGCCC | 231760 |
rs29518911 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rimbp2 | Mm_Celera | 5:128784064 | CTGGGGCAGGTAGGA[A/G]TCTCAGATTCAGGAG | 231760 |
rs29520034 | snp | A/C | 0.32 | 0.24 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128804202 | GCCTATTGATACCCC[A/C]CACACACAGCCTGAT | 231760 |
rs29520243 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128827208 | GGATCTTAAAGCCCA[C/T]GTCCACAGTGACACA | 231760 |
rs29522271 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128942423 | GCACAGGGCTGCTAT[A/G]GGGATGCAGACTTGA | 231760 |
rs29524315 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128766883 | AAAGAAACTAGAAAA[A/G]CAAGCCCATTTAGTA | 231760 |
rs29525102 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128905912 | GCCAATCTTTAACAA[A/C]GGTCACCTAAGGCTC | 231760 |
rs29525375 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128891734 | CTTAACATTAGTGAC[A/G]TCACTGTGTTGGGAC | 231760 |
rs29525377 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128896786 | CCATGGAATATCATC[A/G]CCTCTTCTGACATCC | 231760 |
rs29525398 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128801114 | CACTAATGGTGTCAC[A/G]GCTTGTGCTAGCGAG | 231760 |
rs29526371 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128794883 | GGTCTGCATACCTTC[C/T]GTTGCATCCATCAAA | 231760 |
rs29526428 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128781151 | GCCTGTAGACAGTTG[A/G]GGGCGGGACAGATGT | 231760 |
rs29527060 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128948199 | CCCCTGCCTAGAATC[C/T]CCCAATGAGGGGCTG | 231760 |
rs29528321 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128777783 | AGCTCTGGTCCCTGC[A/G]TTAGTAGGGAGCTTG | 231760 |
rs29529187 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rimbp2 | Mm_Celera | 5:128831323 | AAATAAAACATTTTT[A/T]AAAACGTGTCCTTAT | 231760 |
rs29530907 | snp | A/G | 0.32 | 0.24 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128795740 | AATGGTGCCTCCTAC[A/G]GTGGGCTGGACACTC | 231760 |
rs29531989 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128905905 | CTCCACAGCCAATCT[C/T]TAACAACGGTCACCT | 231760 |
rs29532456 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rimbp2 | Mm_Celera | 5:128906381 | CCAGCATGGTGAGCA[A/G]TTACTAAACACTAAG | 231760 |
rs29534978 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128763374 | GGAACAGCAGGAACA[C/T]GAGGCTGCAGGGAAC | 231760 |
rs29540230 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128861669 | GGCCTCATAGGAGCA[A/G]GCCACAAGCTTAGCA | 231760 |
rs29543025 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128830010 | GGCCAAATTGGTACC[C/T]ATGGAATCTTGCCGA | 231760 |
rs29543644 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Rimbp2 | Mm_Celera | 5:128940013 | TCCATCAAGGGCTTA[A/C]AGGAGATTGCTATTG | 231760 |
rs29545160 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128802649 | TCTGGAGATGCGAGG[A/G]AGTGAGCCCCTGTGT | 231760 |
rs29547458 | snp | G/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128894388 | ATCCCCATGAAAGAC[G/T]GGGTTATATTTTTTC | 231760 |
rs29547597 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128789494 | GAGTGAAGGCCCAGT[G/T]GGATTTCATGAAGCC | 231760 |
rs29547609 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rimbp2 | GRCm38.p3 | 5:128878376 | CCCACATGGAGGCTC[A/G]CTACTTCCTCAGGCA | 231760 |
rs29548818 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128948166 | ATGAGGGACTGGGGG[C/T]GTGGCTCAGTGGTAG | 231760 |
rs29552444 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128823195 | ACACTGGGGCTGGGC[G/T]GGGTCATTTCTTCTG | 231760 |
rs29558276 | snp | C/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128893391 | AAGTCACAAACAATC[C/T]GCCTGGGGCCAAACA | 231760 |
rs29558960 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Rimbp2 | Mm_Celera | 5:128905223 | CAATAAAGTAATTCC[A/T]GAGTTCTAAAGACAC | 231760 |
rs29559416 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128783826 | CATGGGTGAGTGGCT[G/T]ATGCCCCTAGGATAC | 231760 |
rs29559448 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rimbp2 | Mm_Celera | 5:128842940 | AAGGAGGAGGCCACC[C/T]TTGGCAACCTGAGAA | 231760 |
rs29560453 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128892082 | AGTGACTGGGTGGGT[A/G]GGTAGGTGGGAGAGC | 231760 |
rs29560521 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128774522 | GAGATGGGACTGTGG[A/T]AGCGGGCAATTGCTT | 231760 |
rs29561870 | snp | A/G | 0.487535 | 0.077957 | downstream-variant-500B | Rimbp2 | Mm_Celera | 5:128757373 | CATCCCAGGAAAAAT[A/G]TGGCCAGTAGAACTG | 231760 |
rs29564322 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128794987 | CATGAGCCCAGGGGA[A/G]GTCTGGCACCCAAAC | 231760 |
rs29566515 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128891442 | ACAAGTGTGGAGACC[A/G]TGCAGTGATGGTATC | 231760 |
rs29568322 | snp | A/T | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128948376 | CTCACACACACACAC[A/T]CACACGCACACGCAC | 231760 |
rs29569167 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rimbp2 | Mm_Celera | 5:128856183 | GGTGGTTTTTTTTTT[A/T]AAAGAAAGTTACAGC | 231760 |
rs29569398 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rimbp2 | Mm_Celera | 5:128763529 | TATTTCTACCCTTGT[A/G]TATACACATGTGTGG | 231760 |
rs29577465 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rimbp2 | Mm_Celera | 5:128768920 | CTGGGCAGTGGTGGC[A/G]CATGCCTTTAATCCC | 231760 |
rs29578600 | snp | A/G | 0.5 | 0 | intron-variant | Rimbp2 | Mm_Celera | 5:128940322 | TTGAGAATCTGAGTG[A/G]AGAAAAAAAGTGTTT | 231760 |
rs29581102 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rimbp2 | Mm_Celera | 5:128815786 | TCTGCCTCTGGATGC[C/T]GCTCAGGAGTTCATT | 231760 |
rs29582321 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rimbp2 | Mm_Celera | 5:128921435 | CCGCCTCACTGGGTG[A/G]TGTGGACCCATCTCC | 231760 |
rs29583124 | snp | A/T | 0.32 | 0.24 | intron-variant | Rimbp2 | GRCm38.p3 | 5:128795849 | CTCCTCCAACATGGC[A/T]GTGGCTGTGTCAAGT | 231760 |