SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs585274728 | snp | G/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11752705 | GCCTTGCTCAATCCC[G/T]AATAACACAAAAAGA | 50755 |
rs585340069 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11765978 | ACTCTGTGTAACCCA[A/G]CCCCTCCCTATCCCC | 50755 |
rs585383130 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11743508 | CCATAGAAAACTCTT[A/G]GGGAAGGAAGCATTA | 50755 |
rs585446867 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744669 | TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC | 50755 |
rs585474428 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744916 | TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC | 50755 |
rs585531167 | snp | A/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11751216 | AGAAGAAGAAGAAGA[A/T]AAAGAGGAGGAGGAG | 50755 |
rs585696399 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11751241 | GAGGAGGAGGAGGAA[A/G]AAGAAGAAGATGAGA | 50755 |
rs585757672 | snp | C/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11754695 | ACATCCCTCCATGGC[C/T]TCTGCATCAGCTCCT | 50755 |
rs585791806 | snp | C/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11750823 | ACAGTCAACACACAG[C/T]CAGGAGACCCTGGGG | 50755 |
rs585997475 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744935 | TCCTGTGTCCACTGC[A/G]TATTCCTGTCTCCAC | 50755 |
rs586126227 | snp | G/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11754662 | TTGAGCAAGCCAGGG[G/T]AAGCAAGCCAGTAAA | 50755 |
rs586132323 | snp | A/T | | | intron-variant, downstream-variant-500B | Fbxo18 | GRCm38.p3 | 2:11744628 | TATTCCTGTGTCCAC[A/T]GCGTATTCCTGTCTC | 50755 |
rs586235970 | snp | A/C | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11753748 | GTGATTAAGAAGAGA[A/C]CAGCATCATTGAGGT | 50755 |
rs586245668 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11753981 | GCCTCAGTTGCAATC[A/G]ACGGCCCAGGACTGA | 50755 |
rs586246747 | snp | A/G | | | intron-variant, downstream-variant-500B | Fbxo18 | GRCm38.p3 | 2:11744348 | CTGTCTCCACTGCGT[A/G]TTCCTGTCTCCACTG | 50755 |
rs586361833 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11753407 | TGACAACCTGACCAT[A/G]TTTTGGGGAGGACTG | 50755 |
rs586412262 | snp | A/C | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11771286 | ACACACACACACACA[A/C]ACACACACACACACA | 50755 |
rs586615489 | snp | C/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11774982 | ATTTTTCTCCATTTC[C/T]CAGATTTACTATGAA | 50755 |
rs586616266 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744751 | GTCCACTGCGTATTC[C/T]TGTCTCTACTGCGTA | 50755 |
rs586617694 | snp | A/G | | | intron-variant, utr-variant-3-prime | Fbxo18 | GRCm38.p3 | 2:11745000 | CCACTGCGTATTCCT[A/G]TCTCCACTGCGTATT | 50755 |
rs586631394 | snp | A/T | | | intron-variant, downstream-variant-500B | Fbxo18 | GRCm38.p3 | 2:11744400 | TATTCCTGTGTCCAC[A/T]GCGTATTCCTGTCTC | 50755 |
rs586719569 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11758484 | GACTGTGACCCTCTG[A/G]TTAGGTAATTGTGCA | 50755 |
rs586725546 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744688 | TCCTGTGTCCACTGC[A/G]TATTCCTGTCTCCAC | 50755 |
rs586739503 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11752650 | CATGAGGATTTTTAG[A/G]CTGGGGATCCAGAGC | 50755 |
rs586918999 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11772740 | CATTCTATGTTTGGA[A/G]CTATTGGTTATTGCA | 50755 |
rs587007411 | snp | A/C | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11765140 | ACAACACAACTTAAC[A/C]GACACCGTGGAAACA | 50755 |
rs587110849 | snp | C/T | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11751324 | ACTCCACAGGACTGT[C/T]TCACTAGCACAGAGT | 50755 |
rs587199008 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | Fbxo18 | GRCm38.p3 | 2:11744717 | ACTGCGTATTCCTGT[C/G]TCCACTGCGTATTCC | 50755 |
rs587291663 | snp | A/G | | | intron-variant, downstream-variant-500B | Fbxo18 | GRCm38.p3 | 2:11744517 | TCCTGTGTCCACTGC[A/G]TATTCCTGTGTCCAC | 50755 |
rs587307726 | snp | A/G | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11754373 | ATGTAAAGACTGTGG[A/G]ACGCTTAAAGTTATT | 50755 |
rs587324770 | snp | A/T | | | intron-variant, utr-variant-3-prime | Fbxo18 | GRCm38.p3 | 2:11744970 | TATTCCTGTGTCCAC[A/T]GCGTATTCTTGTCTC | 50755 |
rs587457890 | snp | A/C | | | intron-variant | Fbxo18 | GRCm38.p3 | 2:11754130 | GGGCATGGCTGGAGA[A/C]GTGACCCAAGCCCTT | 50755 |
rs587460932 | snp | A/G | | | intron-variant, downstream-variant-500B | Fbxo18 | GRCm38.p3 | 2:11744441 | TCCTGTCTCCACTGC[A/G]TATTCCTGTCTCCAC | 50755 |