SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3662278 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Strn | Mm_Celera | 17:78701102 | GAAAAAATATCCACA[A/G]GAGCCCTGAGCAGTG | 268980 |
rs3663966 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strn | GRCm38.p3 | 17:78701360 | ACTCAGCACAGAAGG[A/G]AGGAGGGCTTCATGC | 268980 |
rs4136942 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strn | GRCm38.p3 | 17:78701439 | CTGCCCTTCTTGGGG[C/T]GTGCAGAGGGCACTG | 268980 |
rs4231664 | snp | A/G | 0.15879 | 0.232768 | utr-variant-3-prime | Strn | Mm_Celera | 17:78650254 | GTGGTTCTTCCTAAA[A/G]CAGGCATTGGATCAT | 268980 |
rs4231665 | snp | A/C | 0.456104 | 0.141496 | utr-variant-3-prime | Strn | Mm_Celera | 17:78650295 | CGGGAATGGGGGACA[A/C]GCCTTAAGCGGAAAT | 268980 |
rs4231666 | snp | G/T | 0.21875 | 0.248039 | utr-variant-3-prime | Strn | Mm_Celera | 17:78650310 | CGCCTTAAGCGGAAA[G/T]AAAAATAGCGTGAAG | 268980 |
rs4231667 | snp | A/C | 0.21875 | 0.248039 | utr-variant-3-prime | Strn | Mm_Celera | 17:78650334 | CGTGAAGGGGGCTCT[A/C]TTTGTTTTCTCACAA | 268980 |
rs6156167 | snp | C/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78697562 | CCTTGCTCCTTGCTC[C/T]GAGCACAGCTCTCCT | 268980 |
rs6156231 | snp | A/C | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78697595 | CCCTCCTAAGCCACA[A/C]TGTTTTGTTCCTGCC | 268980 |
rs6169467 | snp | C/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78697733 | AGAAACCTGGGGCTT[C/T]TTCTTAACTCTGCTT | 268980 |
rs6169985 | snp | G/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78697794 | TTTTATACCTCCAAA[G/T]TTTAGAGTCTTTGTA | 268980 |
rs6170554 | snp | G/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78697883 | TCATTTATTATAATT[G/T]TCCTGCCCTGATAAG | 268980 |
rs6170599 | snp | C/G/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78697908 | GATAAGAAGGAAATA[C/G/T]CTCCTGTTCATGGAG | 268980 |
rs6276717 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Strn | GRCm38.p3 | 17:78676888 | CAAGCTGCACAACCC[A/G]CGACTGTGCTGTGTA | 268980 |
rs6301186 | snp | G/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78672464 | AGTGAGGAGGGAAGA[G/T]GTCAGGAGCAGAAAT | 268980 |
rs6302280 | snp | A/C | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78666087 | CGTAAGACCCGCAGC[A/C]AGGACTACACCCAGT | 268980 |
rs29498226 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78699262 | TTAAGAATGCTCGCT[A/G]CTCTTCCAGAGGCCA | 268980 |
rs29498688 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Strn | GRCm38.p3 | 17:78700718 | CTACAGCATGTCACC[C/T]GCCTTACTGCACTGC | 268980 |
rs29498781 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78734845 | GTATTCCTAAGTTTC[A/C]TCGGAGATAGACATA | 268980 |
rs29500580 | snp | C/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78729073 | ACCCCGGTAAGAATC[C/T]CCCAGGACCCCAAGG | 268980 |
rs29500910 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78671263 | GCCTTGTTTTAATGT[C/T]CCCTTTCTCGCTCTG | 268980 |
rs29501702 | snp | A/T | 0.46281 | 0.131194 | intron-variant, missense | Strn | GRCm38.p3 | 17:78670365 | CTTACCTGGGCTTTG[A/T]CTCTTCATTCTCCCA | 268980 |
rs29502068 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78729128 | AAGGGCCCGACACTG[A/G]AACGGGAACACCATT | 268980 |
rs29503040 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78692076 | ATGAAATGAGTTAAT[A/G]CTTTAAAAGATAAGT | 268980 |
rs29503494 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78699494 | GCCAGTAAGCAGAAT[C/T]CTTCCATGATCTCTG | 268980 |
rs29512284 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Strn | GRCm38.p3 | 17:78654535 | AGAAACAGCAAGGCT[C/T]ACTTGAACTAGTTAT | 268980 |
rs29514301 | snp | G/T | 0.444444 | 0.157135 | utr-variant-3-prime | Strn | GRCm38.p3 | 17:78655435 | CTGGTCTTCCGTATC[G/T]CTGTTGTGCAGTTGA | 268980 |
rs29514334 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78691896 | AGGTATCATGCATGC[A/G]CACACAATTCAAAAG | 268980 |
rs29515836 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Strn | GRCm38.p3 | 17:78700663 | ATGCCAGTCTAAATC[G/T]AGGAAGAAGCAGAGT | 268980 |
rs29517830 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Strn | GRCm38.p3 | 17:78655556 | CTTGGAAGGGTGGAA[C/T]GCTACATCGTGGATC | 268980 |
rs29518213 | snp | C/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78717895 | GAGTGAAATCTATGC[C/T]AGCTGGGGTCTGACA | 268980 |
rs29518487 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Strn | GRCm38.p3 | 17:78651144 | TCCTAAGTACTGTAA[C/T]ATAAACATGGTAGTA | 268980 |
rs29518498 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant | Strn | GRCm38.p3 | 17:78670544 | AAGCAATTTTAACTA[A/G/T]TACCTAGAAAAATTT | 268980 |
rs29518638 | snp | A/C | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78703089 | AGACTGACTAGTGCT[A/C]TATTAACTTTACAGT | 268980 |
rs29519843 | snp | A/G | 0.456747 | 0.140554 | intron-variant, utr-variant-3-prime | Strn | GRCm38.p3 | 17:78653815 | AGAGTAATCAGGGAC[A/G]TTCAACACGAATCTT | 268980 |
rs29522830 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Strn | Mm_Celera | 17:78672020 | TTTGGCTTCTATTTC[C/T]GATGTGGCATACATT | 268980 |
rs29524950 | snp | C/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78691932 | AAGTAAGAAAAAGAG[C/T]AAAATCTCAGAGAAG | 268980 |
rs29533919 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Strn | GRCm38.p3 | 17:78701977 | TACAGGCAGGAAGGA[G/T]CTCTATACAAGATGT | 268980 |
rs29534472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78725127 | TCTGCACTTGGGAGG[C/T]AGAGGCAGGTAGGTT | 268980 |
rs29540121 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Strn | GRCm38.p3 | 17:78702008 | GTCTAAGATAACCAC[C/T]GATTTACTATTTGCC | 268980 |
rs29540681 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Strn | GRCm38.p3 | 17:78701520 | ATGACTGGACTCTGT[C/T]GGGTGTTTTTTAAAA | 268980 |
rs29541353 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Strn | Mm_Celera | 17:78683686 | AAATTATGTATATGT[C/T]AATGATATGGGGTCT | 268980 |
rs33044504 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Strn | GRCm38.p3 | 17:78690450 | CTCCTGCTGCCTTCA[C/G]ATTAAGATGTAGAAC | 268980 |
rs33044932 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78715017 | AGAGAGGGAGTGGGG[C/T]GGGGGAGAGTGGGAG | 268980 |
rs33046396 | snp | G/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78691033 | CACTTAGAGTGAATG[G/T]GTAGAAAGAAGGTCT | 268980 |
rs33049796 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78717334 | GATGCTCTACAGTCA[C/T]CTGCAATATGGCAGT | 268980 |
rs33057373 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Strn | GRCm38.p3 | 17:78668016 | ACCGTATCAACAGGC[C/T]GTGGCTACTTCTGAT | 268980 |
rs33060527 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78714644 | AAAGTCAGTTAAGAA[A/G]AAAAGAGAGAGCTAG | 268980 |
rs33062099 | snp | C/G | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78717598 | GTCAACTGACATGCT[C/G]GCTCAACAAATCATG | 268980 |
rs33068639 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78671915 | GTGTTGATATGTAAG[A/G]ACTTGTATTTCCTTA | 268980 |
rs33072397 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78668825 | CCTCAGCTACTACCC[A/G]GGACTAAGGAAGCTC | 268980 |
rs33075668 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78728918 | GATCTGTGTGTCATC[A/C]CCAGCAGTTTGTAAA | 268980 |
rs33078940 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Strn | GRCm38.p3 | 17:78685060 | GATATGGAACTTTCT[A/C]TTAAACTTTTTATTC | 268980 |
rs33084414 | snp | A/G | 0.455 | 0.143091 | intron-variant | Strn | GRCm38.p3 | 17:78701681 | TCTAAATTTTACAAG[A/G]GAGTCCTTAACTTAA | 268980 |
rs33087661 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78669151 | GTATAATATGTAGCA[C/T]TAAGGCTGAACTTGA | 268980 |
rs33089953 | snp | G/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78683985 | CAGGGTTTCAAGATA[G/T]TAAGATCTATGTTAA | 268980 |
rs33091711 | snp | A/G | 0.375 | 0.216506 | intron-variant | Strn | Mm_Celera | 17:78675221 | TTGAGAGATAAGCTC[A/G]GTCAGAAAAAGACAG | 268980 |
rs33094662 | snp | C/G | 0.375 | 0.216506 | intron-variant | Strn | Mm_Celera | 17:78675241 | GAAAAAGACAGAAGA[C/G]AGACCTATAAAACCA | 268980 |
rs33095308 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Strn | GRCm38.p3 | 17:78667251 | AGGGGGGAATGTCAG[C/T]GCTTCCACTGAGGAG | 268980 |
rs33098135 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78667669 | CTAGTGAGTCTAAAA[C/G]TAAGGTTTTTCTCTA | 268980 |
rs33098138 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78708720 | GCCATAGAATGGACT[A/G]TGTTTTTATTAATAC | 268980 |
rs33110827 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strn | Mm_Celera | 17:78667941 | GGCCACAGAGGACGC[C/T]ACATTAGTAATATCG | 268980 |
rs33118202 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Strn | Mm_Celera | 17:78715303 | CTGGCATGGGCGGGC[C/T]CCTGCCCCCACATGC | 268980 |
rs33121306 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Strn | Mm_Celera | 17:78683614 | GATTTATGACAATTT[A/T]AAAATAAAGAATAAT | 268980 |
rs33122101 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Strn | GRCm38.p3 | 17:78651155 | GTAACATAAACATGG[C/T]AGTAACATACTTATA | 268980 |
rs33123704 | snp | A/G | 0.475309 | 0.108333 | synonymous-codon | Strn | GRCm38.p3 | 17:78700945 | CCCCTGAAGGAAAGC[A/G]ATCTGAGCCTGAAAA | 268980 |
rs33123837 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78732565 | GTGCCACCAGACACA[A/G]CCAAAATTCAAAGTC | 268980 |
rs33127974 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Strn | Mm_Celera | 17:78725876 | GAGATGGGTAGGAGG[A/T]TTCTGGGAAGGCAGG | 268980 |
rs33131131 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78687059 | AAAAACCAAAAAAAA[A/G]AAAGAAAAAAAGAAA | 268980 |
rs33133853 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Strn | Mm_Celera | 17:78655173 | ATGCCCTGTTTACTT[A/G]AAAGGGAGAAGAAGC | 268980 |
rs33136370 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime | Strn | GRCm38.p3 | 17:78653862 | TTGCCTGCACTGGAG[A/G]ATTCTAAAGATAGAT | 268980 |
rs33140324 | snp | A/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78735498 | TTTATCTGGCAGGTT[A/G]TGCAAGGGGGCAACG | 268980 |
rs33141122 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78691423 | ATGGAGTTTGGTGCC[A/G]GCAGAGGCCTTGAGT | 268980 |
rs33148073 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78733553 | AGATTTTTTTTTAAA[C/T]GCTTTTATATGCTGT | 268980 |
rs33148203 | snp | C/T | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78675342 | CTGTTGTGTTTCTTA[C/T]TGTAGTTGCCTGAAC | 268980 |
rs33157423 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78709520 | CAAATATGATAGAGG[A/G]ACTAGAAGAACTAGA | 268980 |
rs33162585 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime | Strn | GRCm38.p3 | 17:78653695 | GTGAGCTTTCCTTGG[C/T]AGTTATGTGTAACTC | 268980 |
rs33173670 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78700401 | CATGACCCTGGGTTC[A/C]ATCTTTAAAACCATG | 268980 |
rs33179662 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Strn | Mm_Celera | 17:78702395 | AAATCAAATTTGCCA[A/G]TATTCTCATAACCTC | 268980 |
rs33203455 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Strn | Mm_Celera | 17:78684806 | GAGAATGCTTCTTGT[A/G]TAAATGGTTTCTTTC | 268980 |
rs33203457 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Strn | GRCm38.p3 | 17:78669034 | CAATTGACAAACATT[C/T]CCAATCCTAAACTTT | 268980 |
rs33207690 | snp | C/G | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78714742 | GCCCAGCTGGCTGAC[C/G]CAACGGTACAAGGTC | 268980 |
rs33211756 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78656090 | TTTCATGTTCACTAA[C/T]TATGAGTTAGACATT | 268980 |
rs33213051 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Strn | GRCm38.p3 | 17:78723500 | AGCAAAGCTAGAGCT[A/G]CCATGGTGTAGAGAT | 268980 |
rs33213455 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Strn | GRCm38.p3 | 17:78701480 | TGGGCTTCAGTGGAT[A/G]AGCACACATGGGCTT | 268980 |
rs33218809 | snp | C/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78683943 | TAATTTCAATAACAT[C/G]TTTTATGAGATTCTA | 268980 |
rs33219665 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Strn | Mm_Celera | 17:78667847 | GAAAACTCTACAATG[A/T]GCCTATCTAAGAAAA | 268980 |
rs33221059 | snp | A/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78703799 | TAGTAGACATCTTTA[A/T]GGTAAAATTAGTTTT | 268980 |
rs33230039 | snp | A/T | 0.456747 | 0.140554 | intron-variant, utr-variant-3-prime | Strn | Mm_Celera | 17:78653944 | TACTTCAAAGAACAG[A/T]TCACCAGAAAAGCCA | 268980 |
rs33236194 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Strn | GRCm38.p3 | 17:78654517 | GACCGTGAAAGGCAG[A/G]GAAGAAACAGCAAGG | 268980 |
rs33237791 | snp | A/G | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78703449 | GTCATTCATCAGACT[A/G]GCAGACTGAAAACCT | 268980 |
rs33268219 | snp | C/T | 0.5 | 0 | intron-variant | Strn | GRCm38.p3 | 17:78703733 | GATCTGGCTGGAATG[C/T]AGACGCACCACACAC | 268980 |
rs33268998 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78675504 | GAAAAAATCTAATAA[A/G]TTATTACTACATTAG | 268980 |
rs33273112 | snp | A/T | 0.375 | 0.216506 | intron-variant | Strn | GRCm38.p3 | 17:78730371 | ATACATTAGCCAGAA[A/T]AAATCGGGGGAAATA | 268980 |
rs33274066 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Strn | Mm_Celera | 17:78684410 | TACCTGCACAAAACG[A/G]ATCCTTATAGTTCAG | 268980 |
rs33287792 | snp | A/G | 0.375 | 0.216506 | intron-variant | Strn | Mm_Celera | 17:78675233 | CTCGGTCAGAAAAAG[A/G]CAGAAGACAGACCTA | 268980 |
rs33292962 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78714372 | ATTCTCCATCAGGCC[A/G]GGCGTGGTGGTGCAT | 268980 |
rs33294432 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Strn | GRCm38.p3 | 17:78717368 | CAAGCTGAGTCTTTC[A/C]ATTAAAATATACATA | 268980 |
rs33315242 | snp | A/G | 0.5 | 0 | intron-variant | Strn | Mm_Celera | 17:78717863 | GGAATTAAAAAGCCA[A/G]GAAACAGAGGACACC | 268980 |
rs33323174 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Strn | Mm_Celera | 17:78725336 | CTCTGCCAGACCTTC[A/C]AAAATAAAAACCTCT | 268980 |