SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3713507 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp46 | GRCm38.p3 | 5:74020285 | ATCATAGGCAACGCT[C/T]TACCAAGAGAGAATG | 69727 |
rs3714654 | snp | A/G | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020448 | TAATTTGCTACCCAG[A/G]ATCAAGAACAGATTA | 69727 |
rs3714684 | snp | C/G | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020457 | ACCCAGGATCAAGAA[C/G]AGATTAATCCACTGT | 69727 |
rs3714685 | snp | A/C | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020460 | CAGGATCAAGAACAG[A/C]TTAATCCACTGTGAC | 69727 |
rs3715915 | snp | A/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020614 | AACCCAGTCCTGCAC[A/T]TTCAACAAGCAGGAG | 69727 |
rs3715916 | snp | G/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020615 | ACCCAGTCCTGCACT[G/T]TCAACAAGCAGGAGA | 69727 |
rs3716031 | snp | A/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020681 | GGCTTTCTAACAATT[A/T]GAGCTGGCTAAAAAT | 69727 |
rs4136423 | snp | A/G | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020377 | GAGGAACAAGAAGAG[A/G]TTGAAGGGGGCCGTG | 69727 |
rs4139076 | snp | C/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74020776 | AACTGGCTGGGACAC[C/T]ATGGAGCATACCCGG | 69727 |
rs6372503 | snp | A/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74022419 | CTATATGCTCTCATG[A/T]ATGTACCCCAGTACT | 69727 |
rs29506683 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Usp46 | GRCm38.p3 | 5:74067012 | CATGGCTCCTTAATG[C/T]GCTGTGCCATGTGTT | 69727 |
rs29506785 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74032809 | CCTGATGATGTGGTG[G/T]CACCCCCCCCCCAAC | 69727 |
rs29509810 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74052080 | AATCACCAATGGGCA[C/T]GCCCCGCCCCCACCT | 69727 |
rs29515316 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74025261 | AATACACACTACACA[C/T]ACACACACACATATC | 69727 |
rs29528662 | snp | G/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74048538 | AATCCTCTTAACTCG[G/T]AACATTTTATATGGA | 69727 |
rs29529534 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74034405 | ATATGGTATTACACA[A/T]GTCCCTGGTCCCTCT | 69727 |
rs29531523 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Usp46 | Mm_Celera | 5:74067677 | CCAGAACAAATTGCC[A/G]TGCTTTTCCGATACC | 69727 |
rs29540396 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74023621 | CACCATGTGAGAACC[A/T]ACTGGCTTTACCTGG | 69727 |
rs29543993 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74039644 | TGAAGCAGACTGGGA[G/T]CCAGTCCAAGTGGTC | 69727 |
rs29545646 | snp | A/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74027122 | CTCGCAGGTAAGTAT[A/T]AGATCAGTATATGAC | 69727 |
rs29546720 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74062096 | CAAAAAAGTAAACCC[C/T]GTGATTATTAATAAA | 69727 |
rs29562918 | snp | C/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74018676 | ACTACATGAATTGCT[C/T]AACTGAAGATGAACT | 69727 |
rs29563169 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74054257 | GAATCTAAAATTTAA[A/T]AAAAAATTAATAAAA | 69727 |
rs29563538 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74061899 | CCCCTCCCCCAACCA[C/T]GCTGGCTAGAACACA | 69727 |
rs29568546 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74017198 | CTGTGCTAATTCCCA[C/T]TGAGCTGTCCTTCCA | 69727 |
rs29568665 | snp | A/G | 0.5 | 0 | intron-variant | Usp46 | Mm_Celera | 5:74048405 | TCCTAGAACTGAAGT[A/G]ACAGATGGCTGGAAA | 69727 |
rs29578954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74031097 | ATGTTGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 69727 |
rs29579764 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74042925 | GAGAGTGAAGAGGCT[C/T]GGGAGACTCAGGGGC | 69727 |
rs29582256 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74054256 | TGAATCTAAAATTTA[A/T]AAAAAAATTAATAAA | 69727 |
rs29585216 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74061984 | CCCTTTCCCTTTGAC[A/G]CAGTAATCCCCTTCT | 69727 |
rs29585507 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp46 | GRCm38.p3 | 5:74003692 | AGCAGAAGGAATCGT[C/T]TGGCACACCTGGGCA | 69727 |
rs29585781 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74034977 | GAACTATTCACAGTT[A/G]CTAAAATAAGCTTTC | 69727 |
rs29622732 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp46 | GRCm38.p3 | 5:74017200 | GTGCTAATTCCCATT[A/G]AGCTGTCCTTCCAGA | 69727 |
rs29629950 | snp | C/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74034448 | GGGCCCACACAGCAA[C/T]ACTCAATCCCTCTCC | 69727 |
rs29633207 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Usp46 | GRCm38.p3 | 5:74003664 | GCAGACAGAACTTCC[A/G]GTGCTAAAGACTAGC | 69727 |
rs29679071 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Usp46 | GRCm38.p3 | 5:74003640 | TGGGAAAAGGAGCAG[G/T]CAAATGATGCAGACA | 69727 |
rs29681665 | snp | C/T | 0.5 | 0 | intron-variant | Usp46 | Mm_Celera | 5:74043634 | TATAATCTTATTAAT[C/T]ACTATGGTAAATGTG | 69727 |
rs29682646 | snp | C/G | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Usp46 | Mm_Celera | 5:73999565 | ACAGCCACTGTCATC[C/G]CCTGCTTAATGCTAG | 69727 |
rs29683054 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74023365 | ATTCCCGGCAGATAT[G/T]CAGAGAATGGAGAGA | 69727 |
rs29684402 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74018165 | TCCTGCTCCGCACCC[A/G]CACTACACTTGCCCC | 69727 |
rs29684718 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74033076 | ACATTAAGTGGAAAT[G/T]TACAGAATAAGTTAC | 69727 |
rs29727203 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Usp46 | Mm_Celera | 5:73999546 | GATTGGTCTCACGTG[C/T]CTCACAGCCACTGTC | 69727 |
rs29731260 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74061749 | AACACAATATACACA[G/T]GAGATGTTCAGCCTC | 69727 |
rs29732041 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74034563 | GGAGGCCCTAGCTGA[A/G]ACCTGTACTTTAAGG | 69727 |
rs29733495 | snp | C/T | 0.33241 | 0.236027 | downstream-variant-500B, utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:73999702 | ACTACCAGATAGTTC[C/T]ATACTGGATAAACTG | 69727 |
rs29734805 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74023668 | CATGTTCTATGACCA[A/G]CAATTCTGTGCCTGA | 69727 |
rs29770403 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Usp46 | Mm_Celera | 5:74067965 | TCCCTCGGGACTTCG[C/G]TGTGCAGCCACCTCG | 69727 |
rs29774587 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp46 | GRCm38.p3 | 5:74052014 | ACGCAAACACCACCA[C/T]AGCGCTTCAGGGCTC | 69727 |
rs29774649 | snp | C/G/T | 0.415225 | 0.187619 | intron-variant | Usp46 | GRCm38.p3 | 5:74053411 | AGCCAAGCACGGAAA[C/G/T]GAGACTGAGTGTCTT | 69727 |
rs29776833 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74030739 | GGCAGAGAATGAGAG[A/G]AGAACTAGGAACCAG | 69727 |
rs29777851 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74033045 | TCAGTTATGGGGAGT[C/T]AACCACAGTCTGTGA | 69727 |
rs29777884 | snp | C/T | 0.42 | 0.183303 | utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:74000419 | GAACAAATGAAGCGT[C/T]GGCATGCTGAAGTTC | 69727 |
rs29778439 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74035266 | TCTGTCTCTGTCTCT[C/G]TCTGTCTCTCTCTGT | 69727 |
rs29780221 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:73999130 | GGACAGGAAACCGTG[C/T]GGGAAATGGCTTCCT | 69727 |
rs29781083 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74023787 | AGATGTGTGTGAAAG[A/G]GTTTCCAGCACTGGC | 69727 |
rs29821750 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Usp46 | Mm_Celera | 5:74069546 | GGGTGAGGGTGGGGG[A/G]CGGGTCACATGGATA | 69727 |
rs29822986 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:73999621 | TGACTTCTCTGTGGG[A/G]AAAAAAAAGGATGGG | 69727 |
rs33054305 | snp | A/C/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74030524 | ACATGTTTCTATCAC[A/C/T]GTTTCCCTCCAAAAA | 69727 |
rs33059166 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp46 | GRCm38.p3 | 5:74052400 | AAGCCCAGCGTCTAC[C/T]CCTGGGACATCTGAC | 69727 |
rs33059168 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Usp46 | Mm_Celera | 5:74036614 | ACATCACTATGAAAG[C/T]GACACAGACAAAGGA | 69727 |
rs33062247 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74032266 | GCAGAACCTCTGCCG[A/T]TCCTCTTACCGGAGC | 69727 |
rs33067551 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74052103 | CCCCACCTCCCAGGC[A/G]AAGGAGGGCTGTGTA | 69727 |
rs33075000 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74053029 | ACCTCTGCATTGTCC[C/T]CCCTCATGGCAAAGA | 69727 |
rs33093448 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp46 | GRCm38.p3 | 5:74017299 | GCCACTATCAGCTAA[A/G]CCTGCTCACTGCTTC | 69727 |
rs33111129 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp46 | GRCm38.p3 | 5:74061459 | GGATTTTCACCAAGG[C/T]CAATTTCATTCAAAC | 69727 |
rs33113573 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:74000224 | GAATGAAGGTTCACC[A/G]TCCATGTAAGTGATT | 69727 |
rs33137673 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74035014 | ACTTTGAAAACTGAG[C/T]TTTGCCAATACAATA | 69727 |
rs33145176 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74018140 | CTCCAGGTCTGTGCC[C/G]TGTCCCATATCCTGC | 69727 |
rs33171867 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp46 | GRCm38.p3 | 5:74053659 | ACAAACAAAAACCAA[A/C]CAAACAAACAAAAAC | 69727 |
rs33181236 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74061958 | CTGGCAATATGTTAC[A/C]GCGGAAGATGCCCTT | 69727 |
rs33219450 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp46 | GRCm38.p3 | 5:74018701 | TGAACTGAACGAAGA[C/T]TAAGATACCTAAGTC | 69727 |
rs33220979 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74054178 | TCCAAATGTGCCAGG[A/C]ATGCACATGGTGCAC | 69727 |
rs33221509 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74061353 | TTTAGAATAAGACCA[G/T]TTTCTCAAAGACCTT | 69727 |
rs33230697 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Usp46 | GRCm38.p3 | 5:74060554 | GAAGCAAAGAGAAAG[A/G]GTGTTGAAAGCTGGT | 69727 |
rs33243515 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp46 | GRCm38.p3 | 5:74062348 | AAATTCGGAACAATG[A/G]CCCCTGTGTCCTAGG | 69727 |
rs33244110 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Usp46 | GRCm38.p3 | 5:74018678 | TACATGAATTGCTCA[A/G]CTGAAGATGAACTGA | 69727 |
rs33245466 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74034938 | ATTTCCAGGAATTGA[A/G]AACTCTTCAGAGAGT | 69727 |
rs33249066 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Usp46 | GRCm38.p3 | 5:74052521 | GAGCATAGGAGAAAC[A/G]GCAGAGTCTATGTCT | 69727 |
rs33275340 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74055734 | ACATGCAGTCACATA[C/T]GCACACATACACACA | 69727 |
rs33311511 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp46 | GRCm38.p3 | 5:74062369 | GTGTCCTAGGAGCCT[C/T]CCAGGGGAGGTTTGA | 69727 |
rs33314755 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Usp46 | GRCm38.p3 | 5:74032583 | CTGCCGGACAGGAGC[A/C/T]GGGAGAGAGGTGCCA | 69727 |
rs33340734 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Usp46 | Mm_Celera | 5:73999376 | AAAAAAAATGTTAAA[A/G]TCTCTTGAAAGACAC | 69727 |
rs33350347 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Usp46 | GRCm38.p3 | 5:74003057 | GTGTGCAGAGGCCCA[A/G]TGGGGAAAACAAATT | 69727 |
rs33353281 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74054255 | GTGAATCTAAAATTT[A/T]AAAAAAAATTAATAA | 69727 |
rs33374251 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74039652 | ACTGGGAGCCAGTCC[A/G]AGTGGTCACTTGCCA | 69727 |
rs33394471 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74062466 | TACCTTTCTGGATGT[C/T]TAAAGTTCACCTCCA | 69727 |
rs33403297 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Usp46 | GRCm38.p3 | 5:74036391 | CTCTTGGTTCTTGAT[C/T]GGCAGCCCTCCTCTA | 69727 |
rs33424624 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | Mm_Celera | 5:74025273 | ACATACACACACACA[C/T]ATCATATACATATAA | 69727 |
rs33430930 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74018469 | CTGGTGATTGTGGGG[C/T]ACTGGTGGTGGTGAT | 69727 |
rs33438054 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Usp46 | GRCm38.p3 | 5:74000324 | GCAAGGTCCATTTTT[A/G]TCACTTGCATAAGAG | 69727 |
rs33448398 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Usp46 | GRCm38.p3 | 5:74052437 | GTGGCACAGAGTCGC[C/T]CTACTCGGTGAAGGA | 69727 |
rs33460798 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp46 | GRCm38.p3 | 5:74018471 | GGTGATTGTGGGGTA[C/G]TGGTGGTGGTGATGG | 69727 |
rs33481753 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp46 | GRCm38.p3 | 5:74002977 | AGAACCGTGGACTAG[C/T]TTTTGTCTAAGTCCA | 69727 |
rs33486859 | snp | C/T | 0.5 | 0 | intron-variant | Usp46 | GRCm38.p3 | 5:74027332 | TTACAGTTACTGACT[C/T]GAGCTTCTTTTAAAT | 69727 |
rs33500127 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Usp46 | Mm_Celera | 5:74068461 | GCGGCGCGGGGCGGG[A/G]AGTGGCGGAGCGACG | 69727 |
rs33507771 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Usp46 | GRCm38.p3 | 5:74062321 | AAAAGTACGAAACAC[A/G]CGATAAATGCCAAAT | 69727 |
rs33509384 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Usp46 | Mm_Celera | 5:74036585 | AGCAAAGTGGGTTTG[A/G]CCACACACTAATGAC | 69727 |
rs33517546 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp46 | Mm_Celera | 5:74032957 | CAGGACCCACAGGAT[A/G]TTCAGAGGGGTCGCA | 69727 |
rs33523112 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp46 | GRCm38.p3 | 5:74032560 | AATCATCGCCCGGGC[A/G]TAAGCCACTGCCGGA | 69727 |
rs33528312 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp46 | GRCm38.p3 | 5:74052903 | GAGTATTAGCTGCCC[A/G]GTCACCTCTAGGAAT | 69727 |