SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs104937658 | snp | C/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66674191 | TTCCAGTCTACTTAA[C/G]AAAACCGGCTGTTTT | 171329 |
rs104959130 | snp | A/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66623481 | TTTTTTTTTTTTTTT[A/T]ACTATAAATTATATG | 171329 |
rs105187832 | snp | A/C | 0.486966 | 0.07967 | intron-variant | Usp15 | Rn_Celera | 7:66622059 | CGTTTATGAATAAAC[A/C]CCCAAGCGGTGAGCA | 171329 |
rs105387974 | snp | C/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66683027 | TTCAGTTCTTTGTAT[C/T]TCACGGCCTTCTCTC | 171329 |
rs105485398 | snp | G/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66658992 | AGAGATTTTAGACAC[G/T]TATTTTGTAAAATTT | 171329 |
rs105596732 | snp | C/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66639211 | AATCTACAAAATTTA[C/T]ATTTAGCCTTTATAG | 171329 |
rs105866962 | snp | A/T | 0 | 0 | intron-variant, downstream-variant-500B | Usp15, Mir3084d | Rn_Celera | 7:66663616 | TTCCCTTCTGAACAA[A/T]GGGCATACTCTCTGC | 171329 |
rs105873668 | snp | A/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66636914 | AAGGAGAAGGAGAAG[A/G]AGAAGAAGAAGAAGA | 171329 |
rs105978455 | snp | G/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66607181 | TTATCACAAGGCCAT[G/T]AGACAGTTAAGTGGG | 171329 |
rs106037795 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | Usp15 | Rn_Celera | 7:66686556 | TGTTCCCACAGTGAG[C/T]GAGATAAACGTAATG | 171329 |
rs106054321 | snp | A/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66674184 | CTACTTAACAAAACC[A/G]GCTGTTTTAACTCAA | 171329 |
rs106133850 | snp | A/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66682533 | GCCTTTCTTTGGCTC[A/G]ATGCCTTCCAGCCCC | 171329 |
rs106930300 | snp | A/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66636920 | AAGGAGAAGGAGAAG[A/G]AGAAGGAGAAGAAGA | 171329 |
rs107576476 | snp | C/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66674211 | AGCTTGTTATAAAAT[C/T]AACTTTCCAGTCTAC | 171329 |
rs197047402 | snp | A/C/G/T | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66677038 | AAACACTGTCAATCA[A/C/G/T]GAAACCTCTCCCTGT | 171329 |
rs198277638 | snp | C/G | 0 | 0 | intron-variant | Usp15 | Rn_Celera | 7:66676886 | AACACAGTGCTTATT[C/G]TACACTTTCTCAATT | 171329 |