SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6269762 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Rbm26 | Mm_Celera | 14:105124878 | TTCTGAGTTTAGAGT[A/T]TCAAAGTTTGAAATA | 74213 |
rs6270829 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Rbm26 | Mm_Celera | 14:105125082 | GAATGTATTTAAAAT[A/T]TAACAACTTTAAAAA | 74213 |
rs6285520 | snp | G/T | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105165562 | GACATGTTAATGGAA[G/T]TTTGATGGCTATTAT | 74213 |
rs6298955 | snp | G/T | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105165668 | TCTATTGTCTTTAAC[G/T]TATTCAATGTTTTAC | 74213 |
rs6299050 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rbm26 | Mm_Celera | 14:105138864 | aaaaaaGAATGGAGC[A/G]CACAGAAATAACAGA | 74213 |
rs6299457 | snp | A/G | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105165737 | AAAACTTATacaata[A/G]caacggtgcaaagct | 74213 |
rs6299911 | snp | A/G | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105165781 | aacccacttacagtg[A/G]cacttctctccaaca | 74213 |
rs6300072 | snp | A/G | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105139034 | aaaaaaaaaaaaTGA[A/G]GATGCCACCTGGAAA | 74213 |
rs6300458 | snp | A/T | 0.483471 | 0.0893938 | intron-variant | Rbm26 | Mm_Celera | 14:105165886 | TCCCAATTCACACAC[A/T]AAGAAGAGTGTTTCC | 74213 |
rs6319648 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Rbm26 | Mm_Celera | 14:105133857 | GCTACTTTACTACGT[A/C]ACAATTGCTAAGCTA | 74213 |
rs13468694 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Rbm26 | Mm_Celera | 14:105131984 | TACATCTACTGGTCT[A/G]ACAAAAACGGTGTAT | 74213 |
rs13468695 | snp | A/G/T | 0.465374 | 0.126941 | synonymous-codon | Rbm26 | GRCm38.p3 | 14:105140370 | GCTGGGTCCTGTACC[A/G/T]TCAGCTACAACAGAG | 74213 |
rs30122205 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105174318 | AAGGAAAAAAAAGAG[A/G]AAAAAAAAAAAAAAA | 74213 |
rs30141665 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Rbm26 | Mm_Celera | 14:105149298 | GTTGGACACTGATAC[A/G]TAACTCCAGAGTCTC | 74213 |
rs30144717 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Rbm26 | Mm_Celera | 14:105166768 | TTCAGCTCAAAAAAA[C/T]AGACTAAGGATATTA | 74213 |
rs30166676 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Rbm26 | Mm_Celera | 14:105147764 | TGAGGGCAAAAGGGT[C/G]ATTTATTAGCACTCC | 74213 |
rs30193705 | snp | C/T | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105156961 | ACAAGGATCTTACAA[C/T]AGTAATGACACTATC | 74213 |
rs30197926 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rbm26 | Mm_Celera | 14:105126523 | ACTTAAGTATGTGAG[A/G]TGATAAATAGATTAC | 74213 |
rs30200689 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rbm26 | Mm_Celera | 14:105126555 | CTGATAATTCATTCC[A/G]TGAGATACAGATGTA | 74213 |
rs30202037 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rbm26 | Mm_Celera | 14:105146662 | TAAAATGAATTATGG[A/G]AGCTGTGGCACAATG | 74213 |
rs30239391 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105168324 | CCTACTAGGATACAA[A/C]GCGAAACTTTGTCTC | 74213 |
rs30303034 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105177955 | AAATTACAATGTACT[A/G]AAGAAGAGCATTCAA | 74213 |
rs30345258 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105124237 | TTTCTGAGTTCGAGG[A/C]CAGCCTGGTCTATAG | 74213 |
rs30428422 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105154433 | TCTTTGTATATAAAC[A/G]ACATTCTCTATGATA | 74213 |
rs30456265 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105141978 | AAAATCTGGCTGTGC[A/G]CAAGCCAATAGGCAT | 74213 |
rs30461878 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105165542 | TGGGTTTTCTTCTTC[C/T]ACAAGACATGTTAAT | 74213 |
rs30491125 | snp | A/T | 0.455 | 0.143091 | intron-variant | Rbm26 | Mm_Celera | 14:105139409 | ACTTACAATGTCAAA[A/T]CAGTCCTCAAATAGG | 74213 |
rs30601113 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105118540 | GGGGAGGGTATGGGG[A/G]ACTTTCAGGATAACA | 74213 |
rs30604671 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rbm26 | Mm_Celera | 14:105127782 | TTAATATTTTCTTAT[A/G]TAAGATTTTTGCTAA | 74213 |
rs30683144 | snp | A/C/T | 0.345679 | 0.230967 | intron-variant | Rbm26 | GRCm38.p3 | 14:105121140 | GGCATTAGAAAATAA[A/C/T]CACAATCTAGAATTC | 74213 |
rs30698391 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105177614 | AAGACGGCCAGCAGT[A/G]TTTGCAGGGGTCCTG | 74213 |
rs30740620 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rbm26 | Mm_Celera | 14:105166911 | CAGGCTGGCCTCGAA[C/T]TCAGAAATCTGCCTG | 74213 |
rs30746686 | snp | A/G | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105122488 | ATAAAGAAGGAAGCT[A/G]GCTTTCTATCTCTCT | 74213 |
rs30775607 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105161440 | CCCCACCCCAAACTC[C/T]CTTCCCAAGTTCTCA | 74213 |
rs30791536 | snp | C/T | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105159492 | CTTAAAATACACACA[C/T]ACACACACACACACA | 74213 |
rs30805686 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rbm26 | Mm_Celera | 14:105146231 | TGTGCAAGCTGTGTC[C/T]GTGGTAGCAGAGCAC | 74213 |
rs30817637 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Rbm26 | Mm_Celera | 14:105149064 | TACCTTAGGGAGAAT[G/T]TAAAAGTCTACAGAA | 74213 |
rs30840620 | snp | C/T | 0.18 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105150596 | CTTCCAAAACATCCT[C/T]GTCCTTGGGTGATTT | 74213 |
rs30897430 | snp | A/G | 0.5 | 0 | intron-variant | Rbm26 | Mm_Celera | 14:105128349 | CACACACACACACAC[A/G]CACGAGAGAGAGAGA | 74213 |
rs30970796 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105177954 | GAAATTACAATGTAC[C/T]AAAGAAGAGCATTCA | 74213 |
rs31014745 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Rbm26 | GRCm38.p3 | 14:105128407 | AGACAGAGAGAGAGA[C/G/T]AGAGAGACAGAGAGA | 74213 |
rs31020579 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rbm26 | Mm_Celera | 14:105120242 | ATACTTTGTTATGGG[C/T]CAGATAAAATAGAGA | 74213 |
rs31020997 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105178020 | AAGTTTGGTTCTATT[A/C]TATTATTAGGAGACT | 74213 |
rs31023847 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105177766 | GATTAGTGTTCTTAT[C/T]CCAAAGTACAGGACT | 74213 |
rs31039600 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rbm26 | Mm_Celera | 14:105127399 | CTAACTCTCAGATAG[A/G]ATGGAGCCTAGGACA | 74213 |
rs31069610 | snp | C/T | 0.18 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105151816 | CTTTTGGCAAATATG[C/T]CTCATTATATAATAC | 74213 |
rs31104611 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105148758 | CTAATATAAACGCCT[C/G]TGGCTGACTGCTCGG | 74213 |
rs31116881 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rbm26 | Mm_Celera | 14:105127962 | ACAATGCTGATTTTT[A/G]GCAATTCAGCACAAC | 74213 |
rs31120501 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105118354 | ACAGATGGAACAATA[A/T]GAACTAACCAGTACC | 74213 |
rs31141669 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rbm26 | Mm_Celera | 14:105163180 | CAAATGAGCATAAAA[C/T]ATCTGATTTTTGGAG | 74213 |
rs31155721 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rbm26 | Mm_Celera | 14:105140110 | TCCACAAAGTAAAAA[A/G]GGTCTTTCTCATGAG | 74213 |
rs31156908 | snp | C/T | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105125679 | CCCAAACACCTACAA[C/T]GCAAAGTCATGACGC | 74213 |
rs31157052 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105164366 | ATTCAATTTAAAAAG[C/T]AAAAATATTTGTATA | 74213 |
rs31243512 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105172452 | GATAACCTTAGCCAT[C/G]AGAGAGAGGCAAGTT | 74213 |
rs31272319 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105166514 | GCAAAAAAAAAAAAA[A/G]GGTTTTAGGGCTAGA | 74213 |
rs31280437 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105154120 | GCCTAGACTGATCTG[C/T]AACTTGCTTTGTAGC | 74213 |
rs31319906 | snp | A/T | 0.188366 | 0.242283 | intron-variant | Rbm26 | Mm_Celera | 14:105144503 | TAAAATTCAATAAAT[A/T]TTTTGTGCTAAATTA | 74213 |
rs31324948 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105128403 | AGAGAGACAGAGAGA[C/G]AGACAGAGAGACAGA | 74213 |
rs31342655 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rbm26 | Mm_Celera | 14:105127482 | GACTTCTACTGTATT[A/G]TAAAGTAGGGGGGGA | 74213 |
rs31348116 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105166515 | CAAAAAAAAAAAAAG[A/G]GTTTTAGGGCTAGAA | 74213 |
rs31405014 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rbm26 | Mm_Celera | 14:105177877 | AAAAAAAAAAAAAAA[A/G]AAAAACAGTTTTGTT | 74213 |
rs31447932 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rbm26 | Mm_Celera | 14:105136441 | AACAAGCACATGAAG[A/G]CTCACAACTACAGTG | 74213 |
rs31489032 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rbm26 | Mm_Celera | 14:105167157 | TTAAATAAGCTTTTC[C/T]TTGGTCCAGAAATGA | 74213 |
rs32483044 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105144678 | CATAATTGAAATACA[A/T]TTTAAAAGAAATATT | 74213 |
rs32483045 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105144594 | AAAAATAAGTAAACC[C/T]GAGACTATCAAACTA | 74213 |
rs32483046 | snp | A/T | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105144558 | TTTAAAGATTAAAAA[A/T]TTCTATGCCACTCCT | 74213 |
rs32483047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105144542 | TAATGTAGGCTACTT[A/G]TTTAAAGATTAAAAA | 74213 |
rs32483048 | snp | C/T | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105144034 | GTGCCAAAGCAAACT[C/T]ATACATTTCTAGAAA | 74213 |
rs32483049 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105144016 | TAAGAACACAGCTTT[A/G]TAGTGCCAAAGCAAA | 74213 |
rs32483050 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105144009 | ACTTTTATAAGAACA[C/T]AGCTTTGTAGTGCCA | 74213 |
rs32483051 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105143273 | GTTATCAGTTTTGAG[A/T]TTCTTTTTTGTTTCT | 74213 |
rs32483052 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105143150 | CTACACTTAGCAAAA[A/G]TATACATACAAATCG | 74213 |
rs32483053 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105143137 | AAGGCACTACTATCT[A/G]CACTTAGCAAAAATA | 74213 |
rs32483564 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105124156 | TAGTTTAAGAATTAT[A/G]ACATTTCCTGGGCAG | 74213 |
rs32483565 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105124088 | CCTACTCTTGAGGTC[C/T]CTCTCTAAAACAATG | 74213 |
rs32483566 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105124072 | AAATTATCAACATAA[A/C]CCTACTCTTGAGGTC | 74213 |
rs32483567 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Rbm26 | Mm_Celera | 14:105123985 | AGAGTGTAATATTAA[A/C]AAAACTTTATTTTTA | 74213 |
rs32483568 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105123927 | GAACTTTTACACCAT[A/G]CATCAAAAGGAGACC | 74213 |
rs32483569 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105123851 | GATTAGGGGCTAGAA[C/T]CTGCTACTCTTCCAA | 74213 |
rs32483570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123778 | TGAGATGAAAGGGTC[C/T]GGTGCGTCTATCTCT | 74213 |
rs32483571 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123733 | TGCTCAGGAACCTAA[G/T]GTTAGGAAAACCCTA | 74213 |
rs32483572 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123702 | AAGGAGACCAGGACA[C/G]CCACGGTAATACTGA | 74213 |
rs32483573 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123582 | CTATAGCTTATTAAA[C/T]ACACAGCTCAGGGAT | 74213 |
rs32483894 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105143057 | TTTCATGGAAGCCAC[C/G]TGAGAAGGTTCACTA | 74213 |
rs32483895 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rbm26 | Mm_Celera | 14:105142628 | CAGATTTTCTATTTC[A/T]CTATGAATGTTTTCT | 74213 |
rs32483896 | snp | A/G | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105142455 | TATAGTAACAGATAC[A/G]ATGCTAACGCAATGT | 74213 |
rs32483897 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105142422 | CCAGTATAAGTTAGC[C/T]GTCTTCAGGGATTTC | 74213 |
rs32483898 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105141797 | ATCTGTGCCAGCAGT[C/G]CTAGTTAAATATTGT | 74213 |
rs32483899 | snp | A/G | 0.32 | 0.24 | intron-variant | Rbm26 | Mm_Celera | 14:105141392 | TGAGAACAGTTTACT[A/G]TTAAAGGAATGCATA | 74213 |
rs32483900 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105141192 | ACATACATTTCTCTC[C/T]TACCTTTGGTGAAGT | 74213 |
rs32483901 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rbm26 | Mm_Celera | 14:105140903 | GTAGAAGGGAGGGAA[A/G]GAAAAATGAATGTCT | 74213 |
rs32483902 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105140270 | AAGGAGAATTAACTG[A/G]TGGAGAAGCTACCTG | 74213 |
rs32483903 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105140065 | TAGTGTACTGAACTT[C/T]ACGCTCAGGCAAATT | 74213 |
rs32483970 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rbm26 | Mm_Celera | 14:105170892 | AAGCAACAGGCTATA[A/G]GTGGAAACTAGCAAG | 74213 |
rs32483971 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rbm26 | Mm_Celera | 14:105170687 | GAAGGAGTGCTACTA[A/C]ATGGCCCTAAGAGTC | 74213 |
rs32483972 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rbm26 | Mm_Celera | 14:105170562 | AAACATCTTTGGAGA[C/T]TGTCACCATCATTTA | 74213 |
rs32483973 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rbm26 | Mm_Celera | 14:105166126 | TTGTAGCCTGCTTGC[C/T]GGGCATGTAAGACAC | 74213 |
rs32484344 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123510 | CTAGTTCCCCATTTC[A/G]GGTTTACTCTCACTT | 74213 |
rs32484345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rbm26 | Mm_Celera | 14:105123392 | ACATCAATCATTTCT[C/T]TTATAACTTCCTTAT | 74213 |
rs32484346 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rbm26 | Mm_Celera | 14:105123278 | AGCTATCTCCAAGCA[C/T]CTAGCTAGTTCTCAC | 74213 |