SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs80385714 | snp | C/T | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927698 | TATAACGGTAGAAAC[C/T]GTTAACTTTACTTTT | 31037 |
rs202249117 | snp | A/C | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:926464 | AGCTGCCGGCCACCA[A/C]CGCCGAGTGGTGGTA | 31037 |
rs202265896 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:928143 | ACGTGGTCACACTGT[A/T]CATATAAAAAACGAC | 31037 |
rs202508315 | snp | C/T | | | upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927978 | CAAACACAATTATTA[C/T]GATTTTAACCAACCG | 31037 |
rs202701580 | snp | A/C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923080 | ATTTATATTCGAAGT[A/C/T]GAAAGAACTTCCGGC | 31037 |
rs202725241 | snp | A/T | | | intron-variant, missense | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925852 | AAGGCACATCCGAAT[A/T]CTGTTCAGGCTGGAT | 31037 |
rs202902188 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927520 | CGGTTTTCACAAATT[A/C]CAGATTTTATATGCA | 31037 |
rs202912056 | snp | C/T | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927796 | GAAATGGGTTCAATG[C/T]GGGGCAGGCGTGTCT | 31037 |
rs202953642 | snp | C/T | | | intron-variant, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923265 | ACCAATTAAAACGAG[C/T]AGATTTAGATCTATA | 31037 |
rs203076418 | snp | A/G | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:924793 | GCCCTGAAAGTAGGT[A/G]CAGCGCGATGACAAC | 31037 |
rs203160492 | snp | A/G | | | intron-variant, synonymous-codon, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927178 | GATCCCGGCAGGAGT[A/G]CTGCCACCGCTGATG | 31037 |
rs203177304 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B, missense | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:929140 | TCCCGAGGCATGACC[A/T]TGGTGACTCGGTGTG | 31037 |
rs203445493 | snp | C/T | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927821 | GTGTCTCTTTGCCCA[C/T]TCTTTTTAAATTTTT | 31037 |
rs203464872 | snp | A/T | | | upstream-variant-2KB, missense | CG43867, CG3711, CG3708 | Release_6_plus_ISO1_MT | X:929368 | TGAAAGATGACCATG[A/T]AGCTGTCCTGGTCGT | 31037 |
rs203541032 | snp | A/T | | | intron-variant | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925206 | CGATCCAAAGGCTAT[A/T]TCTGCTCTCACTTGC | 31037 |
rs203563663 | snp | G/T | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:926899 | TGGTCCGCTGCTGCA[G/T]CTGCTGCCCGGAGGA | 31037 |
rs203605015 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:928662 | TTCGCAGCTGTTCAG[A/G]AACACACAGAGCGAG | 31037 |
rs203714758 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923102 | ACTTCCGGCAAATCA[G/T]TAAAAACACAACGCT | 31037 |
rs203751384 | snp | A/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:922893 | ATGTGTATAATAATA[A/T]TGTTTATTCTGAATT | 31037 |
rs203753157 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925772 | TCTCACACTATTGTC[C/T]ACGGTTCCGCCAAAT | 31037 |
rs203804410 | snp | G/T | | | intron-variant, downstream-variant-500B | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:922826 | TTTAGCCACGTTTTT[G/T]TGGTAAGCCCACAAA | 31037 |
rs203819871 | snp | C/T | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927714 | GTTAACTTTACTTTT[C/T]CAATAAAGAACTTGG | 31037 |
rs203851530 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925592 | GTTCCTCAGATACTT[C/T]GAGCGCGCCGCCACA | 31037 |
rs204218530 | snp | A/G | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927633 | CACACTGTTCGCTAT[A/G]GTTCACACACATACA | 31037 |
rs204256580 | snp | A/G | | | intron-variant, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923850 | ACTGAGTGCATATAG[A/G]GGGTTTATATATATG | 31037 |
rs204301684 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:926102 | TATCTGCAAGCCACT[C/T]TGCCCCGAAAAGACG | 31037 |
rs204378699 | snp | A/T | | | intron-variant, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923412 | TATTATGAAATGTTT[A/T]GACATTCGGTTTTCG | 31037 |
rs204402107 | snp | A/G | | | intron-variant, synonymous-codon, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927163 | AGCGGGGCAATAAAG[A/G]ATCCCGGCAGGAGTG | 31037 |
rs204616092 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, missense | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:928954 | CTGTCCGGAGAGGCC[A/G]CGCTCAGGCTGTCAA | 31037 |
rs204682914 | snp | A/T | | | intron-variant, synonymous-codon, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:926486 | GTGGTGGTATCGCGG[A/T]GCAGGCGGAGTTCCT | 31037 |
rs204701402 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:928397 | AGAAATACTCAAGCT[A/G]GCGCGCCGTGAGAGC | 31037 |
rs204710945 | snp | A/G | | | upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:928031 | TTGTGACGCTTTGCA[A/G]TTGGCGGGCGGCATG | 31037 |
rs204810699 | snp | C/T | | | intron-variant, synonymous-codon, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927226 | CCTGTCGCGATCCCG[C/T]TCAAATCCACCTCCG | 31037 |
rs205274382 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925019 | CAGCTTGCTGGGATA[C/T]AGGCGCTTGCGGATG | 31037 |
rs205284808 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:929340 | ATCGTGCAGGAAGCT[A/G]TTGGGCCGAAACTGA | 31037 |
rs205321816 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | CG43867, CG3711, CG3708 | Release_6_plus_ISO1_MT | X:929390 | CCTGGTCGTAAGCCA[A/G]GCGCACATCCATTAG | 31037 |
rs205326840 | snp | A/T | | | intron-variant, downstream-variant-500B | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:922859 | TTTGCCATTTAACAC[A/T]GATCAACAGTGCTAG | 31037 |
rs205327406 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923025 | CACAATGCAATCATA[A/G]ATAAACTGATTTATC | 31037 |
rs205391552 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925640 | TATGCGAATCTCCTC[C/T]GCTCCGACAATAAAC | 31037 |
rs205471961 | snp | A/G | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927717 | AACTTTACTTTTCCA[A/G]TAAAGAACTTGGAAT | 31037 |
rs205861727 | snp | C/T | | | intron-variant, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923503 | ACATATACAACTTTG[C/T]AAGGACCTAGAGTAG | 31037 |
rs205923501 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927956 | TCGAACGTAGGATAT[G/T]TAAGCACAAACACAA | 31037 |
rs205985300 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925814 | ATCGCAGATGACTGC[C/T]GAGGCATGGAACACT | 31037 |
rs206027035 | snp | C/T | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:926805 | AGCTACCCGGGGAAG[C/T]GGCCTTTCCGCTTCC | 31037 |
rs206036737 | snp | C/T | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:928599 | CGACCTAAAACAGTA[C/T]CTAATCCTCAACGAC | 31037 |
rs206229501 | snp | A/T | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:926440 | TGTAACCCCCAAAGA[A/T]GAACATAGAGCTGCC | 31037 |
rs206260766 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:923128 | ACGCTATAGTAAATT[C/G]AAACAATCGTAAACA | 31037 |
rs206262248 | snp | A/G | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925427 | CAATATGATTTCAAA[A/G]GCCTCGGGGGAGGCG | 31037 |
rs206405816 | snp | C/G | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927171 | AATAAAGGATCCCGG[C/G]AGGAGTGCTGCCACC | 31037 |
rs206432960 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:928992 | GCCCGTGTAAAAGAG[C/T]ACCGCCTTCGGGACG | 31037 |
rs206890359 | snp | A/T | | | intron-variant, missense | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:924384 | ACTCCTTAATATCAT[A/T]GATCTTTGTGATGTC | 31037 |
rs206898727 | snp | A/G | | | upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:928106 | CGTCGGTGAGTTAGG[A/G]CGGTATTTATGGTCG | 31037 |
rs206942334 | snp | A/G | | | intron-variant, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927699 | ATAACGGTAGAAACT[A/G]TTAACTTTACTTTTC | 31037 |
rs207356602 | snp | C/T | | | intron-variant, missense, upstream-variant-2KB | CG43867, CG3711, MED22 | Release_6_plus_ISO1_MT | X:927363 | CAGAGGCGCTTCCTC[C/T]TGCTCCACCTCCTCC | 31037 |
rs207419539 | snp | C/T | | | intron-variant, downstream-variant-500B | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:922871 | CACAGATCAACAGTG[C/T]TAGCGTATGTGTATA | 31037 |
rs207456095 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | CG43867, CG3711, MED22, CG3708 | Release_6_plus_ISO1_MT | X:929343 | GTGCAGGAAGCTATT[C/G]GGCCGAAACTGAAAG | 31037 |
rs207457567 | snp | C/T | | | intron-variant, synonymous-codon | CG43867, CG3711 | Release_6_plus_ISO1_MT | X:925688 | TTTGTCCTGGAAGAA[C/T]TTTCCGAAGTCATCG | 31037 |