SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3089611 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rnf130 | Mm_Celera | 11:50029601 | ATGCCACAGCTGGTA[A/G]ATTCTCCTGTCTTTG | 59044 |
rs3089612 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rnf130 | Mm_Celera | 11:50029713 | GTTAATTCTGATTAC[C/G]AGTTGTAAGAGACAG | 59044 |
rs6317370 | snp | C/G | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50079509 | ggcctgttgaccaga[C/G]ttcagtccttggaat | 59044 |
rs6317405 | snp | A/C | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50079538 | attgataaatatagg[A/C]gagaactgacttcac | 59044 |
rs6317805 | snp | C/G | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50079558 | actgacttcacagat[C/G]ngtcttctcgtttct | 59044 |
rs6317813 | snp | A/G | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50079559 | ctgacttcacagatn[A/G]gtcttctcgtttcta | 59044 |
rs6332784 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Rnf130 | Mm_Celera | 11:50079957 | GAGACAGGCACAAAT[A/G]TAAGCTGAGTGCTCC | 59044 |
rs6332908 | snp | G/T | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50080025 | AAATTTTGGGATTTT[G/T]AAATACTTNTTTAGA | 59044 |
rs6332921 | snp | A/G | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50080034 | GATTTTNAAATACTT[A/G]TTTAGACCTTACTTT | 59044 |
rs6370171 | snp | C/T | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50048920 | tttatttattattaa[C/T]attattttagttttc | 59044 |
rs6370662 | snp | A/G | 0.5 | 0 | intron-variant | Rnf130 | Mm_Celera | 11:50048998 | acatacatgccttgt[A/G]cacaagcattataga | 59044 |
rs6404429 | snp | A/G | 0.415225 | 0.187619 | utr-variant-3-prime | Rnf130 | Mm_Celera | 11:50122577 | AGAGTGCAGCCTACC[A/G]AGTCTGGGTAGAGAC | 59044 |
rs6404962 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Rnf130 | Mm_Celera | 11:50122663 | CCGCTTCTGGGCCCA[A/G]GGAAGCTCTAGGGTC | 59044 |
rs13469741 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf130 | Mm_Celera | 11:50052850 | CAGTGGATCGCCTTG[C/T]TACAAAGAGGAAATT | 59044 |
rs13469742 | snp | A/C | | | stop-gained | Rnf130 | Mm_Celera | 11:50095909 | AGCCACTGAGAACTT[A/C]GGGGATATCGCCTCT | 59044 |
rs16787283 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50024881 | GGGCAGTTCACTGAA[A/C]CCAGTGCCAGCAAGC | 59044 |
rs16787284 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf130 | Mm_Celera | 11:50052361 | TTACTTTGGCCTCTT[A/C]ACTTACTCCAAGCAA | 59044 |
rs16787285 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50052438 | AAGTTGGAAGTGCAG[A/G]TGAATAAACTAGAAG | 59044 |
rs16787286 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50052656 | GTGTTGCCCTTTGTG[A/G]NAATCCATACAGCCC | 59044 |
rs16787287 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf130 | Mm_Celera | 11:50052657 | TGTTGCCCTTTGTGN[A/C]AATCCATACAGCCCT | 59044 |
rs16787288 | snp | G/T | 0.393491 | 0.20472 | intron-variant | Rnf130 | Mm_Celera | 11:50052686 | CTGCTGCAGTGAGCT[G/T]CGGATGTGCGTAGTA | 59044 |
rs16787289 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50087646 | AAGAATTGTTTGTAT[A/G]AGAAAACATGACAAC | 59044 |
rs16787290 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50087665 | AAACATGACAACATT[C/G]AGGCATATTATAACC | 59044 |
rs16787291 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50087708 | TTCAGTAACCCTCCC[A/G]ggctaggctgtagcg | 59044 |
rs16787292 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50087800 | caagaaaGACGCAAA[A/C]CAAACCAAACACCAT | 59044 |
rs16787293 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50087876 | TTCATGAGTTATCCT[C/T]CACTTNCTCTGGGTT | 59044 |
rs16787294 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50087882 | AGTTATCCTNCACTT[G/T]CTCTGGGTTCCACAG | 59044 |
rs16787295 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Rnf130 | Mm_Celera | 11:50087930 | ATGCAGAATGGAAGA[C/G]NAGCCATTTGTCTTG | 59044 |
rs16787296 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Rnf130 | Mm_Celera | 11:50087931 | TGCAGAATGGAAGAN[A/C]AGCCATTTGTCTTGT | 59044 |
rs16787297 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf130 | Mm_Celera | 11:50087169 | ATGGAAAAATTAGAG[C/T]TNCGGCTTANTGTAA | 59044 |
rs16787298 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf130 | Mm_Celera | 11:50087171 | GGAAAAATTAGAGNT[C/T]CGGCTTANTGTAANA | 59044 |
rs16787299 | snp | A/T | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50087179 | TAGAGNTNCGGCTTA[A/T]TGTAANACACATCAT | 59044 |
rs16787300 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50087185 | TNCGGCTTANTGTAA[A/G]ACACATCATAAANNG | 59044 |
rs16787301 | in-del | -/A/T | 0.162571 | 0.245019 | intron-variant | Rnf130 | GRCm38.p3 | 11:50087195 | AANACACATCATAAA[-/A/T]NGAGTCAGTATGAAT | 59044 |
rs16787303 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50087285 | TTTAGTTCCTTTCCC[C/T]TTATAGCCACCTGCT | 59044 |
rs16787304 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf130 | Mm_Celera | 11:50087308 | CACCTGCTCATGGTA[A/G]AGTGTTCTTAGCTGG | 59044 |
rs16787305 | snp | A/G | 0.277778 | 0.248452 | missense | Rnf130 | Mm_Celera | 11:50087391 | CAGGAAACAGACCCA[A/G]ACTTCGATCACTGTG | 59044 |
rs16787306 | snp | A/G | 0.277778 | 0.248452 | missense | Rnf130 | Mm_Celera | 11:50087418 | TGTGCAGTCTGCATA[A/G]AAAGCTATAAGCANA | 59044 |
rs16787307 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon | Rnf130 | Mm_Celera | 11:50087432 | ANAAAGCTATAAGCA[A/G]AATGATGTTGTTCGG | 59044 |
rs16787308 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf130 | Mm_Celera | 11:50095658 | CGATTGTTTGAGGGA[A/C]GTTTCTTAGGNGACA | 59044 |
rs16787309 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50095669 | GGGANGTTTCTTAGG[G/T]GACAGTAGGGAAGGA | 59044 |
rs16787310 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf130 | Mm_Celera | 11:50095737 | CTCCGCAGAGGGTGA[A/C]CATGNTCTTATGAAC | 59044 |
rs16787311 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50095742 | CAGAGGGTGANCATG[C/T]TCTTATGAACTTGTT | 59044 |
rs16787312 | snp | A/G | 0.165289 | 0.235211 | missense | Rnf130 | Mm_Celera | 11:50095956 | CTCACTCCTCGCACG[A/G]GTGAAATCAACATTG | 59044 |
rs16787313 | in-del | -/T | 0.197531 | 0.244432 | intron-variant | Rnf130 | Mm_Celera | 11:50096046 | AGTACCTGATGACTG[-/T]CAAGAAGAAAGTTGC | 59044 |
rs16787314 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50096098 | TGTAAAGGATAATGT[A/G]TACATTTAAACATGT | 59044 |
rs16787315 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50095185 | TACTGTCTACTGCAG[A/G]CAGGANCAGCCTCTT | 59044 |
rs16787316 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50095191 | CTACTGCAGNCAGGA[A/G]CAGCCTCTTCCTCTT | 59044 |
rs16787317 | snp | A/G | 0.3648 | 0.222083 | intron-variant | Rnf130 | Mm_Celera | 11:50095245 | CACAGGTAGACGGCC[A/G]GCTGGAGCTGGGTAC | 59044 |
rs16787318 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50095384 | CTTAACTAGGTACCA[A/C]GTAAATGGAGCNTTT | 59044 |
rs16787319 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50095396 | CCANGTAAATGGAGC[A/G]TTTTAGAGAAGTTAC | 59044 |
rs16787320 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50095523 | TAGCTTTGTACATGA[C/T]ATCAGCCTCCCTCTG | 59044 |
rs16787321 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf130 | Mm_Celera | 11:50096156 | GGGAATGTGTATGCT[A/G]GTGATGATGTGTTAG | 59044 |
rs16787322 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50096221 | TTTTGAGATCGTTGC[A/G]TTGCATATAGTCATG | 59044 |
rs16787323 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50096276 | GGCTGGCAGGCAGCA[A/G]TGTTGGTGTGCTACA | 59044 |
rs16787324 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50096380 | AAAAAGCATTCTGAG[A/C]TAGTTATGAATGTTT | 59044 |
rs16787325 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50096424 | GTTAATAAGCAAAAA[C/T]CTATCGAGGGCAGTG | 59044 |
rs16787326 | snp | A/C/G | 0.260631 | 0.270007 | intron-variant | Rnf130 | GRCm38.p3 | 11:50096430 | AAGCAAAAACCTATC[A/C/G]AGGGCAGTGCCTGAC | 59044 |
rs16787327 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50096442 | ATCGAGGGCAGTGCC[C/T]GACTGTGTACAGTGT | 59044 |
rs16787328 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50096443 | TCGAGGGCAGTGCCT[A/G]ACTGTGTACAGTGTG | 59044 |
rs16796618 | snp | A/T | 0.21875 | 0.248039 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023401 | TATGTGGGGGCAGAA[A/T]ATCAGACTAGGAATT | 59044 |
rs16796619 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023456 | TGATAAAATGAGAGC[A/G]GGGCTTTGTATGACC | 59044 |
rs16796620 | snp | A/T | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023491 | GGGGTCATTTAGAAA[A/T]TTTAAGAACACAAAC | 59044 |
rs16796621 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023660 | GCCCATGGGGCCATG[C/T]TTAGGCTTTGACCCC | 59044 |
rs16796622 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023783 | TCTTAATAGAATCTG[A/G]GACCTGCAAAGGTGG | 59044 |
rs16796623 | snp | A/G | 0.165289 | 0.235211 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023815 | AGCTGAGATCTTAGT[A/G]GAGCTTGGCAAGAAG | 59044 |
rs16796624 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023969 | AGGTGGGCATGAGGG[C/T]AGCTCACTGACAGGC | 59044 |
rs16796625 | snp | A/T | 0.165289 | 0.235211 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50023986 | GCTCACTGACAGGCA[A/T]CTGAGGGCTCTATTC | 59044 |
rs16796626 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50024088 | TATACTGTTACACca[A/G]tngttctcaaccttc | 59044 |
rs16796627 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50024090 | TACTGTTACACcant[A/G]gttctcaaccttcct | 59044 |
rs16796628 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50024188 | tttactccTTCCTCT[A/G]CCCTGGTTTTGTATC | 59044 |
rs16796629 | snp | A/C/G | 0.535503 | 0.0872656 | upstream-variant-2KB | Rnf130 | GRCm38.p3 | 11:50024319 | TAGACCAACAAATGG[A/C/G]NNGGGNAAAGGAGAT | 59044 |
rs16796632 | in-del | -/G | 0.375 | 0.216506 | upstream-variant-2KB | Rnf130 | Mm_Celera | 11:50024324 | AACAAATGGNNNGGG[-/G]AAAGGAGATTCATAT | 59044 |
rs16796633 | in-del | -/T | 0.46281 | 0.131194 | intron-variant | Rnf130 | Mm_Celera | 11:50070758 | CTTAGAGCAGTCCTT[-/T]GCTCAGCAGTGCGTG | 59044 |
rs16796634 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf130 | Mm_Celera | 11:50070809 | ACCACCTGTTCAGAC[C/T]NTAAATGACAGTGCT | 59044 |
rs16796635 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50070810 | CCACCTGTTCAGACN[A/G]TAAATGACAGTGCTT | 59044 |
rs16796636 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50070826 | TAAATGACAGTGCTT[C/T]TCTGTCAGAACTTTC | 59044 |
rs16796637 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50070874 | AAAGGTTTTCTACTG[A/T]AGACTTAACCTGATT | 59044 |
rs16796638 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50070989 | GTTACCTGTTTGGAG[C/T]ACTGTACATGTTCTC | 59044 |
rs16796639 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50071019 | CATGCCTGTCAGTTT[A/G]CACAGCTGCAGCCTC | 59044 |
rs16796640 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50071035 | CACAGCTGCAGCCTC[A/G]TGTCAGTTNAACTGG | 59044 |
rs16796641 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50071044 | AGCCTCNTGTCAGTT[A/G]AACTGGAATCTATAA | 59044 |
rs16796642 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50071067 | ATCTATAAACCTTAG[C/T]GAAAATTATGGNNAN | 59044 |
rs16796643 | snp | A/C/T | 0.5862 | 0.228188 | intron-variant | Rnf130 | Mm_Celera | 11:50071079 | TAGNGAAAATTATGG[A/C/T]NANNNNTNTTNTCTA | 59044 |
rs16796651 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon | Rnf130 | Mm_Celera | 11:50071412 | CACAAATGCTCGGGA[C/T]AGGAACCAGGTGAGC | 59044 |
rs16796652 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50071442 | CTAACCAGTACTCTA[C/G]CCAGCCGTAATCCAT | 59044 |
rs16796653 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50071567 | gtaatacctgcactc[A/G]gggttttgaggccag | 59044 |
rs16796654 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50071701 | tcagtaaatgaatgt[C/T]ctttcagtacatttc | 59044 |
rs16796655 | in-del | -/C | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50071784 | ggcaacaaaaacccc[-/C]agattagttaggcca | 59044 |
rs16796656 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50085341 | TGATGCCGTGTCTGT[C/T]TCCAGTGCAGTAGTG | 59044 |
rs16796657 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50085359 | CAGTGCAGTAGTGAT[A/G]ACTTAGTGGGGATTT | 59044 |
rs16796658 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50085384 | GGATTTGGAGGTTTC[G/T]TTTGCTGTTCNAGTA | 59044 |
rs16796659 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Rnf130 | Mm_Celera | 11:50085395 | TTTCNTTTGCTGTTC[G/T]AGTACTCTGGGAAAG | 59044 |
rs16796660 | in-del | -/A | 0.46281 | 0.131194 | intron-variant | Rnf130 | Mm_Celera | 11:50085532 | ATTCAACTAGAATGC[-/A]AAANTCGATGGTATA | 59044 |
rs16796661 | in-del | -/A | 0.396694 | 0.202437 | intron-variant | Rnf130 | Mm_Celera | 11:50085535 | AACTAGAATGCNAAA[-/A]TCGATGGTATAGCTG | 59044 |
rs16796662 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50085591 | TTTCAGAAGGCACTT[A/G]CATAACATGGCAGAA | 59044 |
rs16796663 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50085627 | CTAGAATAATAGATG[C/T]CATACCTTTAATTAT | 59044 |
rs16796664 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf130 | Mm_Celera | 11:50085648 | CTTTAATTATTTAAA[A/T]TAAAGATCNTGTACT | 59044 |
rs16796665 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf130 | Mm_Celera | 11:50085657 | TTTAAANTAAAGATC[A/G]TGTACTACTTCAGCA | 59044 |
rs16796666 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf130 | Mm_Celera | 11:50085823 | ATAAGGTACAGTAAT[A/G]AAATTACTTTCCTCT | 59044 |