SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6244643 | snp | C/T | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817107 | CGCTGACCTTGTACC[C/T]ACGTCTTANAAACCA | 67150 |
rs6244669 | snp | G/T | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817116 | TGTACCNACGTCTTA[G/T]AAACCACTGTGTACC | 67150 |
rs6245757 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110817283 | TACCTAGTTCCTTCA[C/T]CTTGNTTGCTACCAC | 67150 |
rs6245763 | snp | C/T | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817288 | AGTTCCTTCANCTTG[C/T]TTGCTACCACCAGCT | 67150 |
rs6246338 | snp | C/T | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817386 | AGGGAAGCTCCCTCT[C/T]ACCAGTGGGAGAGNT | 67150 |
rs6246355 | snp | C/T | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817400 | TNACCAGTGGGAGAG[C/T]TAGGGTAAAATGTGC | 67150 |
rs6246813 | snp | C/G | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817446 | ATTTTTAATTTAAGT[C/G]NAAACCACTGCACAT | 67150 |
rs6246814 | snp | A/G | 0.5 | 0 | intron-variant | Rnf141 | Mm_Celera | 7:110817447 | TTTTTAATTTAAGTN[A/G]AAACCACTGCACATT | 67150 |
rs6246907 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Rnf141 | Mm_Celera | 7:110817506 | CTGAGTAATTAAGGt[C/T]attttttaaaggtag | 67150 |
rs6321315 | snp | A/G | 0.415225 | 0.187619 | synonymous-codon, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110800822 | CCTCACGGTGGACTC[A/G]CTGGATGTTCATGCN | 67150 |
rs6321347 | snp | A/G | 0.415225 | 0.187619 | synonymous-codon, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110800837 | NCTGGATGTTCATGC[A/G]GTAAGCTAGCTCTGC | 67150 |
rs6322436 | snp | A/G | 0.5 | 0 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110801018 | AGTCAAAGGAAGACC[A/G]TGAAGTCGGATGGTT | 67150 |
rs6360194 | snp | C/T | 0.5 | 0 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110803391 | TTGAAGTATACATGG[C/T]GGGNGGACTACCCTC | 67150 |
rs6360211 | snp | C/G | 0.5 | 0 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110803395 | AGTATACATGGNGGG[C/G]GGACTACCCTCTCTT | 67150 |
rs13463902 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, intron-variant | Rnf141 | GRCm38.p3 | 7:110813775 | AACTTTGCAAGTGAA[C/T]ATTAGCTAACTAAAA | 67150 |
rs13463903 | snp | C/T | | | utr-variant-3-prime, intron-variant | Rnf141 | GRCm38.p3 | 7:110813730 | AATTTCACATTCTTA[C/T]ATACTAAATATTTAT | 67150 |
rs31109168 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rnf141 | Mm_Celera | 7:110819776 | GGACAGGGTGAGACT[A/G]GAGTGAAACAGACTT | 67150 |
rs31119414 | snp | G/T | 0.5 | 0 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110807532 | GTGGAGGGTGTAAGG[G/T]GTGGCCTCTTGCCCA | 67150 |
rs31122794 | snp | A/C | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Ampd3, Rnf141 | Mm_Celera | 7:110804506 | ATGGTAGTAGATGCC[A/C]GGCATATCAAGTAGC | 67150 |
rs31136437 | snp | A/C/G | 0.5 | 0 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808007 | CGGTGCTGGTTCACC[A/C/G]CCCCCCCCCCCCGTG | 67150 |
rs31138766 | snp | A/T | 0.33241 | 0.236027 | intron-variant, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110799477 | TCACATACACATGAA[A/T]AAAAATAATCTTTAA | 67150 |
rs31150256 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808950 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 67150 |
rs31294103 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808954 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCAC | 67150 |
rs31367892 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110802830 | GTTGCAGGCTGGCTT[C/T]AGGTAGAGACATGGC | 67150 |
rs31557311 | snp | A/G | 0.33241 | 0.236027 | intron-variant, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110799677 | CTGTGTTTCCATCAA[A/G]TGCAGGGGACCCACG | 67150 |
rs31641256 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110805469 | ACACAGCTACATTCC[C/T]TTCCCTGAGAGTCTA | 67150 |
rs31652166 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110809011 | CCCCAAAATAGTAAT[A/G]GAATCATTAAGTATT | 67150 |
rs31660865 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf141 | Mm_Celera | 7:110841845 | ATGAACAGCACGTAT[C/T]GTTCAATGAAGTCGC | 67150 |
rs31710444 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110804490 | CAGGGGACCTTGATG[A/G]ATGGTAGTAGATGCC | 67150 |
rs31863302 | snp | A/C | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110799626 | AAGGAAGCCAAGGTC[A/C]CACTGGGCTCCAGGC | 67150 |
rs32049620 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Ampd3, Rnf141 | Mm_Celera | 7:110804540 | ACCCCAGCATGGCAC[C/T]GCTGCCGTTGGCAGT | 67150 |
rs32165811 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808948 | CACTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 67150 |
rs32169469 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110801070 | TCACTTAGGAGTCAT[C/G]TACCCTTAGGTGAAT | 67150 |
rs32202799 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110801160 | GAAAGAGCATTTTCT[A/G]CTCTTGCAAGAAGAC | 67150 |
rs32235371 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110807223 | AGGATACAGCCTACC[C/G]TGGCAGGGATGCTGC | 67150 |
rs32282862 | snp | C/T | 0.32 | 0.24 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808779 | ACAATAGTAATGTAT[C/T]CGTTTGATGCCTAGA | 67150 |
rs32309775 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf141 | Mm_Celera | 7:110821896 | GGCTTGGAGCCAGCG[C/T]CACAGGAGCCCTGCT | 67150 |
rs32367988 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Ampd3, Rnf141 | Mm_Celera | 7:110804541 | CCCCAGCATGGCACT[A/G]CTGCCGTTGGCAGTG | 67150 |
rs32431937 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808952 | CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 67150 |
rs36251147 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Rnf141 | Mm_Celera | 7:110824348 | AGAAAAATCAGACCT[C/G]TGACAGGCCTAAGCA | 67150 |
rs36260198 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110839342 | TGTCTTTCTGAAAAT[A/T]ATGTTTATCTGGGTG | 67150 |
rs36263618 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110807705 | CAGACATCTCAGCCT[C/T]TGGATTCTGTTGGCA | 67150 |
rs36268028 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110802382 | CAGGAGAAACATATT[A/T]GGTAGCCGCATGGAA | 67150 |
rs36276148 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110843071 | TAAACAAACAGAGTA[A/C]TGAGTAAGTGCTGGA | 67150 |
rs36278627 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf141 | Mm_Celera | 7:110841800 | AACCGCTCTTCAGTC[A/G]CCAGCCTTTTCAGTG | 67150 |
rs36284925 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Ampd3, Rnf141 | Mm_Celera | 7:110811156 | GTCCCTGACTGTCCA[C/T]GTCTCCCGTGATTGC | 67150 |
rs36287784 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf141 | Mm_Celera | 7:110840413 | AGAAACAGAAACAAG[C/T]CAACTTACTGTGGCT | 67150 |
rs36294603 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rnf141 | Mm_Celera | 7:110839150 | TAAAAAATACAACGT[A/T]TAACATGAAAAGTAG | 67150 |
rs36299113 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110820881 | GCTTACTGAATGTCA[C/T]TATAAAGTCTCCTAG | 67150 |
rs36299854 | snp | C/T | 0.32 | 0.24 | synonymous-codon, intron-variant, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110807923 | TGTCTCTCTCTCTAC[C/T]GATGACCCCATGCAG | 67150 |
rs36305161 | snp | A/C/T | 0.244898 | 0.249948 | downstream-variant-500B, intron-variant | Rnf141 | Mm_Celera | 7:110813473 | TGAGCCGACAGACAA[A/C/T]GTAGGCTTCAGTCGA | 67150 |
rs36305209 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110836807 | CTCTTGTTACACAAC[A/G]GTTGAGCTGCAGTAC | 67150 |
rs36327333 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110811553 | TCCACTCCTGGGCTG[C/T]GGAAGGTACAAGGCG | 67150 |
rs36328726 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110833227 | AAACAACAGTGAGAG[C/T]CCAACAGCTCAAAGG | 67150 |
rs36328954 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf141 | Mm_Celera | 7:110822027 | TTTAAAAATTGCATA[C/T]AGCTGTTCCATGGTT | 67150 |
rs36356220 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf141 | Mm_Celera | 7:110816959 | ACAACATAGAAATGT[A/G]CAATGAAAAATTAAT | 67150 |
rs36359292 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110818901 | ATCCACCGAACACAG[A/G]AACGGAGGCTAACAC | 67150 |
rs36389836 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110803907 | GCAAGGGAGGGCACA[A/T]CTGCCCCACATGGGT | 67150 |
rs36390396 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf141 | Mm_Celera | 7:110821894 | CTGGCTTGGAGCCAG[C/T]GCCACAGGAGCCCTG | 67150 |
rs36393374 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf141 | Mm_Celera | 7:110838619 | TAAAAACAAAATTCT[C/T]CCATTACTATTTTGG | 67150 |
rs36398422 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110835590 | AATGCCTCTGGAACC[A/G]GTGCATACATATCAC | 67150 |
rs36408715 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf141 | Mm_Celera | 7:110822754 | TACCATTAAGGTCAG[A/G]TAACAGATTCATGTT | 67150 |
rs36409765 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Rnf141 | Mm_Celera | 7:110834680 | CCGCCTCAGTCAGTA[A/C]TGTCAGTCAAGGGAA | 67150 |
rs36413002 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B, intron-variant | Rnf141 | Mm_Celera | 7:110813529 | CTCCCAACACCTACG[A/G]ATGCAAGTTATTCAG | 67150 |
rs36428605 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808456 | TATGACTATGCTTTG[C/T]GTCTCTGGGAAGAGA | 67150 |
rs36449519 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110806376 | TTTGGCTCACTTTTA[A/G]CCATAAAATAACCAA | 67150 |
rs36451185 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Rnf141 | Mm_Celera | 7:110815988 | CCTCTGTGGAATCTG[A/G]AAATATAAAATGTGT | 67150 |
rs36455608 | snp | A/C | 0.336735 | 0.234472 | downstream-variant-500B, utr-variant-3-prime, intron-variant | Rnf141 | Mm_Celera | 7:110816377 | TGTCAACACTCTAAA[A/C]CTTAAACCTACTAAA | 67150 |
rs36456523 | snp | C/T | 0.489796 | 0.070696 | intron-variant, nc-transcript-variant | Ampd3, Rnf141 | Mm_Celera | 7:110800611 | ACTAGGGGAGGGGAC[C/T]GGCTCATTGACCAGT | 67150 |
rs36459920 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110806427 | AAAAAAACTAAAAAA[A/T]AATCTTACTTTCTTT | 67150 |
rs36465469 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110838799 | AGGAACAACCATTAA[G/T]ATTCCCAGCTTAGCA | 67150 |
rs36469007 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110833238 | AGAGTCCAACAGCTC[A/G]AAGGCAACATTATCA | 67150 |
rs36480979 | snp | A/C | 0.32 | 0.24 | utr-variant-5-prime, nc-transcript-variant | Rnf141 | GRCm38.p3 | 7:110837262 | AAAGAGTTTTGCTTC[A/C]CATAGTTTCTGTTAA | 67150 |
rs36492305 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110811564 | GCTGCGGAAGGTACA[A/G]GGCGAGGTTATGGGG | 67150 |
rs36498150 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110839858 | GAGATAGGTAGATCG[G/T]AGTACCTCTGAGGGA | 67150 |
rs36499454 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime, intron-variant | Rnf141 | Mm_Celera | 7:110815284 | GAGTAAGACTTTCTC[A/G]GGGTTGTGAAACCAT | 67150 |
rs36506138 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110804033 | TGAAAGGAACGGAGG[C/G]AGGCTTCTTCTCAGG | 67150 |
rs36506296 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Rnf141 | Mm_Celera | 7:110815300 | GGGTTGTGAAACCAT[C/T]TCAGCTAAGGTATGA | 67150 |
rs36508472 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110840992 | AAACTTCCAATTCTA[A/T]CTATATTACCTAACA | 67150 |
rs36511808 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110802633 | AGGGGCACATGTGAC[C/G]CTCTGTCCCTTCCTC | 67150 |
rs36523856 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110839713 | AAAGCATGGAAGAGA[A/G]TGAAAGACACTGGTC | 67150 |
rs36526112 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf141 | Mm_Celera | 7:110827274 | AGATATGAGAAGGCA[A/G]ACACACATATTTAAA | 67150 |
rs36527805 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110808506 | TGCACAGGGAACAGA[C/T]ATAACTGCTTCCAGA | 67150 |
rs36546600 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110833131 | CTCCACAGCAAGCTA[A/G]AGCTTCAGAAGACAG | 67150 |
rs36551044 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110801670 | AAAGACAGAGTAAAA[A/T]CTTAATTTTTTTTTC | 67150 |
rs36557992 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110834627 | ACACTGGCGGGACAG[C/T]TGCAAACAGTAAGTG | 67150 |
rs36560295 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110812602 | TCGGATGATGTCTTA[A/G]TCTGTTCACCAGGGT | 67150 |
rs36561179 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110810575 | TGAGTGGTCAGCGTC[A/T]CACGGAGGTCCAGGG | 67150 |
rs36564250 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf141 | Mm_Celera | 7:110822817 | AATTGAAATAGTGAA[A/C]TGGGTGAAAACCTAC | 67150 |
rs36565856 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110809528 | CATTTACCTAAGGAG[C/G]CTCCCTCTTAATAGG | 67150 |
rs36573551 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110810200 | GTTTCCCTTTTGAAA[A/G]GGAGTTGAGTGCAGA | 67150 |
rs36592699 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110812875 | CCATCTCTCCGCCTC[A/G]TGAATCCACACTTTA | 67150 |
rs36598643 | snp | C/T | 0.336735 | 0.234472 | downstream-variant-500B, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110812744 | TGCCTGTTTTACAGT[C/T]GGAAGCCAAGGCAAC | 67150 |
rs36600110 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime, intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110811504 | AGGACTCAACGAGTC[A/G]TCTCAAACCATATTC | 67150 |
rs36602637 | snp | G/T | 0.260355 | 0.249785 | utr-variant-3-prime, intron-variant | Rnf141 | Mm_Celera | 7:110815610 | AGGAAAACAGGGACA[G/T]TTGAAACTTGCCAAA | 67150 |
rs36611494 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf141 | Mm_Celera | 7:110832919 | GGTATTTTTAGCAGT[C/T]CTCTACAATACAAAA | 67150 |
rs36616900 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf141 | Mm_Celera | 7:110827072 | AGAAATCTTATGCGT[A/G]CATGAAAATAAATGA | 67150 |
rs36629014 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf141 | Mm_Celera | 7:110821776 | ATTGGAGAGAAATGG[C/T]AGGAGTGGCCTAAGT | 67150 |
rs36629156 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf141 | Mm_Celera | 7:110817020 | CTTCCAGGATCAACT[A/G]GTTGCCTACGTATTT | 67150 |
rs36629312 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ampd3, Rnf141 | Mm_Celera | 7:110810551 | TTCCACGACAATAGA[C/G]AGAATGACTGAGTGG | 67150 |