SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8145852 | snp | G/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cuedc2, Fbxl15 | Rn_Celera | 1:266078023 | AGCTTTTTACCCCTT[G/T]TTGCATGGTGCATAG | 294009 |
rs8146932 | snp | A/G | | | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Cuedc2, Fbxl15 | Rn_Celera | 1:266078390 | GTTGTCAATGTATCG[A/G]ATCAGCTTCTTGGGG | 294009 |
rs8159365 | snp | C/G | 0.333644 | 0.235592 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cuedc2, Fbxl15 | Rn_Celera | 1:266077881 | TGTGCTCCCACCCAA[C/G]GAAAGTCAGTCAGAC | 294009 |
rs8167477 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Cuedc2, Fbxl15 | Rn_Celera | 1:266078160 | GAAGCTCCAAGAATA[A/G]ATTAACACTAGAGCA | 294009 |
rs105215751 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266081910 | TTCTAAGATCACAGC[C/T]TCTGGTGGCCTCCCC | 294009 |
rs105243676 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266081837 | CCCCAATTTTGTTTC[A/G]AACACTTTATATATA | 294009 |
rs105306905 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266082922 | GGTTTTTTTGTTTTG[C/T]TTTTGTTTGTTTGAG | 294009 |
rs105373072 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266083877 | CCAGCTCCGAAAAAA[A/G]GAAAAAAAAAAAAAT | 294009 |
rs105447676 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mir146b | Rn_Celera | 1:266089069 | CAAATTTTGGCTTTT[C/T]CCCCAGTCCCTCAGC | 294009 |
rs105551654 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266081684 | GGATCAAACCAAGTC[C/T]TACCGACTACACCCT | 294009 |
rs105726763 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266081962 | GCCTCCTGCTTCTGA[C/T]CCCTTCTCTGCTGCC | 294009 |
rs105878703 | snp | G/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266082594 | AAAGGCATGAGCCTT[G/T]GGGGTTTTTTTGATA | 294009 |
rs106087818 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266079369 | ATACCCCTGAAAGGG[C/T]AGAGAGGTAGTGGGA | 294009 |
rs106423247 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266082719 | CTGTCTCTGCCTCCC[A/G]AGAGCTGGGATTAAA | 294009 |
rs106434076 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266084358 | TGTTGACAGTGGCCT[A/G]GAAACCTCTGCAGGG | 294009 |
rs106531584 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | Cuedc2, Fbxl15 | Rn_Celera | 1:266077636 | GCCCTACAGACAGAC[C/T]GCGAGAGGGCCTTCA | 294009 |
rs106744233 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266085294 | GCCTGTTACCTGAAC[A/G]GAAATGAAGGCACTG | 294009 |
rs106774474 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266082097 | CCCCTGGTTCAGCCT[A/G]TGAGCTGTTCTCTCT | 294009 |
rs106915065 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266083400 | ATCCACACCAGGAGG[C/T]TCCCGATAGGGCCTG | 294009 |
rs107051836 | snp | A/G | 0 | 0 | upstream-variant-2KB | Cuedc2, Mir146b | Rn_Celera | 1:266087875 | ACCCCCGACCATAAA[A/G]TTATTTTTACTACTA | 294009 |
rs107055621 | snp | C/T | 0 | 0 | upstream-variant-2KB | Mir146b, Cuedc2 | Rn_Celera | 1:266089054 | ATATGTCATCAGGTG[C/T]AAATTTTGGCTTTTT | 294009 |
rs107435339 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266084034 | GCATGTGCGATGCCC[A/G]AGGCTGGACTCCCCA | 294009 |
rs197331612 | snp | C/G | 0 | 0 | upstream-variant-2KB | Mir146b, Cuedc2 | Rn_Celera | 1:266088503 | CACTCATCAGGCACT[C/G]AAATAAGGAAGGAGA | 294009 |
rs197429530 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | Cuedc2 | Rn_Celera | 1:266078654 | ACTTCAACTCCTCCT[C/T]CCGGGGGCCTCTGAG | 294009 |
rs198674966 | snp | G/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266080836 | AGAGTTCCACAGTCT[G/T]GTCCTTGCCCACTCT | 294009 |
rs198750723 | snp | A/G | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266078759 | GAGGGTAGGCAGGGC[A/G]TGTGCCTCACAAGAA | 294009 |
rs199036722 | snp | C/T | 0 | 0 | intron-variant | Cuedc2 | Rn_Celera | 1:266080594 | GCCCCCAACTCCAAT[C/T]ACAAGGGGCCCCATT | 294009 |