SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657315 | snp | A/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702729 | AGTTTCTACTGTATT[A/T]GGTTTCCATATAACC | 17997 |
rs3657420 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702789 | TCTCCCCCCATCTTC[A/G]CTTCCTCATTCCCCT | 17997 |
rs3657964 | snp | A/C | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702847 | CTGTTCTAGTCCCTA[A/C]CCCACCCCTACCCAC | 17997 |
rs3657979 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702854 | AGTCCCTACCCCACC[C/T]CTACCCACCCATCTA | 17997 |
rs3658006 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702866 | ACCCCTACCCACCCA[C/T]CTATTCATAACTATC | 17997 |
rs3658067 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702902 | TATTACCTATTACAC[A/G]GTCCTAGAGAATGTA | 17997 |
rs3658530 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92702909 | TATTACACAGTCCTA[A/G]AGAATGTATTGTTTC | 17997 |
rs3659829 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92703150 | AGTCTGCTTACCTTT[A/G]ATTTAACAACTAACA | 17997 |
rs3659868 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92703170 | AACAACTAACATCCA[C/T]TCACAAGTGAATACA | 17997 |
rs3665100 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713486 | TTATATTAACTACTT[A/G]TAAGTGACAAACTTA | 17997 |
rs3665553 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nedd1 | Mm_Celera | 10:92713518 | AAATAACTTTGTAAT[A/G]CCTTCTAAATACTTA | 17997 |
rs3665589 | snp | G/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713543 | TACTTAAAAAAGCTG[G/T]ATGTCAAGCTACGGA | 17997 |
rs3665590 | snp | A/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713545 | CTTAAAAAAGCTGGA[A/T]GTCAAGCTACGGAAG | 17997 |
rs3666199 | snp | A/C | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713646 | TGATTTTAATTAGTA[A/C]ATTATTTTAAGAACT | 17997 |
rs3680895 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | GRCm38.p3 | 10:92713734 | AACCCACTGAAGAAC[C/T]AAGAAGCTGAACCAT | 17997 |
rs3680942 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nedd1 | Mm_Celera | 10:92713764 | TCAACTCTGGTTACT[A/G]AAGTCCAGAACCACA | 17997 |
rs3681008 | snp | A/C | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713805 | CAAAATCCTTAAAAA[A/C]AAGATCCCTGATGAC | 17997 |
rs3681012 | snp | A/C | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92713807 | AAATCCTTAAAAACA[A/C]GATCCCTGATGACAA | 17997 |
rs3682273 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd1 | GRCm38.p3 | 10:92704511 | TTATTAAGCAATTAT[C/T]TTGTTTAGCACTTTC | 17997 |
rs3697598 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Nedd1 | Mm_Celera | 10:92704709 | CTGAAGACATCACGT[A/C]AATGAATGACAATAA | 17997 |
rs3698237 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd1 | Mm_Celera | 10:92704827 | AAAAAAAATGAAGTA[A/G]CAAAGACAGTAAATT | 17997 |
rs3698280 | snp | C/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92704845 | AAGACAGTAAATTCA[C/G]CTGTCACCTCAGCAA | 17997 |
rs3698811 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92704916 | AGTACCTTTCTGTAC[A/G]TGCATCTGTGCTGAG | 17997 |
rs3698822 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92704921 | CTTTCTGTACGTGCA[C/T]CTGTGCTGAGTGTAA | 17997 |
rs4139750 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Nedd1 | Mm_Celera | 10:92704963 | CCTGGGATTACATTC[C/T]ACTGCGACACAGTCA | 17997 |
rs4139767 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92704968 | GATTACATTCCACTG[C/T]GACACAGTCACCTCA | 17997 |
rs6340975 | snp | A/C | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92696586 | gatctctgtggcttg[A/C]tagccagctagcttg | 17997 |
rs6341381 | snp | A/G | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92696647 | tccaaaaataaggca[A/G]acagtccgcaaggaa | 17997 |
rs6354374 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | GRCm38.p3 | 10:92696714 | ctgcacacacacaca[C/T]acacacacacacaca | 17997 |
rs6411022 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd1 | Mm_Celera | 10:92700282 | CCCTTCCCCACTTCA[C/T]TCATGGTCTAAAAGT | 17997 |
rs6412118 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Nedd1 | Mm_Celera | 10:92700467 | TAAGTCACAAACGTC[A/T]GTTAATGAGCTATCT | 17997 |
rs6412133 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nedd1 | Mm_Celera | 10:92700478 | CGTCTGTTAATGAGC[C/T]ATCTGTCACTAAATT | 17997 |
rs13465010 | snp | C/T | | | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685931 | AAAACATAAACCTAT[C/T]CTTATGAACATTTTC | 17997 |
rs13465011 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Nedd1 | GRCm38.p3 | 10:92698897 | AGTGGCCGACACCCC[C/T]CTGACTGCAGTAGAT | 17997 |
rs13465013 | snp | A/C/T | | | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92684914 | ACGTTAAAATGCAGA[A/C/T]GTCTTTTGTCTATAT | 17997 |
rs13465014 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92685154 | GATGTTTACTAAAAT[A/G]TAGCTTAGATTGATA | 17997 |
rs13465015 | snp | A/G | | | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685055 | TATCTCCAAAAGTGG[A/G]ACAGGAGTAAGACTT | 17997 |
rs13465016 | snp | C/G | 0.260355 | 0.249785 | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685036 | GGAGTAAGACTTTTC[C/G]AAGTGACTCAGAAAG | 17997 |
rs29312542 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92714372 | TGTCACAGGTATAAT[C/T]ATTGTTAAGGGTTCA | 17997 |
rs29314466 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd1 | Mm_Celera | 10:92699068 | AAGCAGTTTGGATAC[A/G]TCTCACAGACACATC | 17997 |
rs29314535 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Nedd1 | Mm_Celera | 10:92690526 | ATGCATTCCTTTACC[A/G]TTATCTGGTCTATGG | 17997 |
rs29315062 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92718678 | CTAGAGAACTAAGAG[A/C]GCTACATCTGCCACT | 17997 |
rs29315190 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd1 | Mm_Celera | 10:92692320 | AGCCTGGGCTACATG[A/G]CAAGGATGTCTTAAA | 17997 |
rs29315587 | snp | C/G | 0.255 | 0.24995 | intron-variant | Nedd1 | Mm_Celera | 10:92695418 | ATCCACAAGGCATAC[C/G]CATGATGTCTAACAT | 17997 |
rs29316232 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92695762 | ATGCTGCTGTACATT[A/T]TAAAAGGAGTTTGAC | 17997 |
rs29316569 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Nedd1 | GRCm38.p3 | 10:92701777 | AGAACCCCACAAAAA[A/C]ACTGTAACTCATAAT | 17997 |
rs29316829 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd1 | Mm_Celera | 10:92701593 | CTTGATTAAAATTGA[C/T]TGAATTATACCTACC | 17997 |
rs29317520 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92714709 | AAAATAAGTAGGATG[A/G]GAATTTCTTTCCCCA | 17997 |
rs29318667 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nedd1 | Mm_Celera | 10:92699141 | TGCTCACATCACACC[A/G]GTGCAGCCCACATTT | 17997 |
rs29319154 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Nedd1 | Mm_Celera | 10:92713069 | TTTGCAGTCACTGAA[A/C]TAAACAGTAAGCACT | 17997 |
rs29319352 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92700277 | CTGCCCCCTTCCCCA[A/C]TTCATTCATGGTCTA | 17997 |
rs29319410 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92719713 | CCCTGATCTAAGGCA[A/G]GGATGTTACTTGTCC | 17997 |
rs29320344 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92701798 | AACTCATAATATACA[C/T]ATGCAAAATCTGTAG | 17997 |
rs29323092 | snp | C/G | 0.32 | 0.24 | intron-variant | Nedd1 | Mm_Celera | 10:92702253 | TCTCTGAGCCCAGAG[C/G]GGGAGGGATTTGATG | 17997 |
rs29323864 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92687796 | TCCCACCCTGCAGGT[A/G]TATTTATTTCAGTAT | 17997 |
rs29324087 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Nedd1 | Mm_Celera | 10:92698660 | TTTAGTTGACAAGAG[A/G]TAATTTTCATTTTCT | 17997 |
rs29325889 | snp | A/C | 0.18 | 0.24 | upstream-variant-2KB | Nedd1 | Mm_Celera | 10:92723902 | AAGCAGAAAACACAA[A/C]TCTCTAACACTGAAA | 17997 |
rs29326423 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92691780 | AGACACATATTCCAG[C/T]GGTCACCCCTTGACT | 17997 |
rs29326644 | snp | C/T | 0.5 | 0 | intron-variant | Nedd1 | Mm_Celera | 10:92714374 | TCACAGGTATAATTA[C/T]TGTTAAGGGTTCAGA | 17997 |
rs29327001 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92720312 | TGCTATAATCTAGCC[A/G]TCCTGGAAGTCTGAA | 17997 |
rs29327177 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Nedd1 | Mm_Celera | 10:92694892 | GCAAATACAGGAAAG[A/T]TCCAGTTCAGGAACT | 17997 |
rs29327585 | snp | A/G | 0.255 | 0.24995 | intron-variant | Nedd1 | Mm_Celera | 10:92692370 | AATACTTTGAAAACT[A/G]CAAACCACAATCAAT | 17997 |
rs29327777 | snp | A/G | 0.18 | 0.24 | intron-variant | Nedd1 | Mm_Celera | 10:92692200 | TGTGGACTTGAGGGG[A/G]TACATCCTTTCAATG | 17997 |
rs29328997 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92719059 | TCCACCCCGCTTATA[C/T]CCCCAAGCTCACGGA | 17997 |
rs29332300 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd1 | Mm_Celera | 10:92692852 | CAGCAGCAGCTCTAC[A/G]GTTTGTCTTCATGAA | 17997 |
rs29333120 | snp | A/C/G | 0.197531 | 0.244432 | intron-variant | Nedd1 | GRCm38.p3 | 10:92699202 | GTGCTCTCTGGCAGC[A/C/G]TGTGTGACAACAGGC | 17997 |
rs29333512 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nedd1 | Mm_Celera | 10:92707660 | CTCCGCAGGGATAGT[A/G]CAGTTCCTTTTCTTT | 17997 |
rs29333532 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92713157 | ACTCTTCAGTTTCCT[A/G]TTTTATTCTAAACAG | 17997 |
rs29334167 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92689831 | ATAATTAACTTGGAC[G/T]AAACAACATCAAGCA | 17997 |
rs29335765 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92700147 | CCTCCCAAGTGCTGG[A/G]ATTAAAGGCATGCAC | 17997 |
rs29337127 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nedd1 | Mm_Celera | 10:92699009 | TCTACTTATCAAGAA[C/T]ACTTAGAACTGGGCA | 17997 |
rs29337882 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92701550 | AGTTTATTTTCTGGA[C/T]CAGAAAATTCAGGCT | 17997 |
rs29338349 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Nedd1 | Mm_Celera | 10:92724895 | TGGCCCAGACTTAGG[A/G]TGTGTCCTCTGAGAT | 17997 |
rs29340815 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nedd1 | Mm_Celera | 10:92707609 | TGCTGGACTTGCCCA[A/G]TGCTGACACGAGGTT | 17997 |
rs29341476 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92707085 | ATGTTAAAGAAATAC[C/T]ACTACGATTATTAAG | 17997 |
rs29343614 | snp | A/T | 0.255 | 0.24995 | intron-variant | Nedd1 | Mm_Celera | 10:92702320 | TCACTCTTGCTGTGT[A/T]TCGTCTGGCCGTGGG | 17997 |
rs29343967 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92691208 | GTAACCTCCCTTAAC[C/T]TGAGACCCCCAGGCG | 17997 |
rs29344646 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd1 | Mm_Celera | 10:92695510 | TGAAGTCTTCTTCTG[C/T]TAATAGTGGGAGCTT | 17997 |
rs29345305 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92685813 | TTACAATTATTTCTT[C/T]ATAAAATAGAAGGTA | 17997 |
rs29345822 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd1 | Mm_Celera | 10:92702295 | TTAGGGTGGAGAGTT[C/T]CAAGGTCTCTCACTC | 17997 |
rs29346030 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Nedd1 | Mm_Celera | 10:92691108 | AAACTAAGACATTTT[C/T]GTACGTCTCACTTGA | 17997 |
rs29346759 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Nedd1 | Mm_Celera | 10:92724853 | AACAACAAGCTTGTT[C/T]CTTTCCTGGGCTTCC | 17997 |
rs29347842 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Nedd1 | GRCm38.p3 | 10:92707047 | TGAGAACATAATACA[C/G]GGGCTAGGCAAGAAC | 17997 |
rs29347950 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92693052 | AACTTGGGCTTGCTG[C/T]TCCCTCTCCCAAGAG | 17997 |
rs29349141 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Nedd1 | Mm_Celera | 10:92690443 | CAAATGATCAAATCA[G/T]GGTTGATGGATTTAA | 17997 |
rs29349261 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92707090 | AAAGAAATACTACTA[A/C]GATTATTAAGGAAAT | 17997 |
rs29350077 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92719827 | TCCTTCCAAGAATCC[C/T]CTCTGCGACTACGAG | 17997 |
rs29350201 | snp | A/T | 0.255 | 0.24995 | intron-variant | Nedd1 | Mm_Celera | 10:92692410 | AGCACTAGTTCTTGA[A/T]AACTGAGAGCTGTAA | 17997 |
rs29350332 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723591 | GTCCCAGGTGCACAC[C/G]GGATGTGTTTCTCAA | 17997 |
rs29350422 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92719960 | TGAATCAAGCCAAGC[A/C]CATCCTCCACTTAGT | 17997 |
rs29352021 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92707271 | GAAATAGAACCCAGG[A/C]CTTCTTATCAAGTTT | 17997 |
rs29352222 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92700275 | GCCTGCCCCCTTCCC[C/T]ACTTCATTCATGGTC | 17997 |
rs29354351 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nedd1 | Mm_Celera | 10:92691237 | CGCTAATCCTTTACT[C/T]GTTCTTAGCAACCTC | 17997 |
rs29355388 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd1 | Mm_Celera | 10:92687878 | TGGTAGGGGATTGCT[A/G]AGAGCACGTGACTAC | 17997 |
rs29355395 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92720267 | TCCGCAGGGAAATAA[A/G]CTAAGTAATGTTCTC | 17997 |
rs29355464 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd1 | Mm_Celera | 10:92692839 | TACTACAGAGCAGCA[A/G]CAGCAGCTCTACAGT | 17997 |
rs29355517 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd1 | Mm_Celera | 10:92707277 | GAACCCAGGCCTTCT[C/T]ATCAAGTTTCTACAG | 17997 |
rs29359095 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Nedd1 | Mm_Celera | 10:92689879 | GTAAAGAAAGACTTC[A/G]GAAACTGCAAAAGAA | 17997 |
rs29360196 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685293 | GCCCTATCAAAGTGT[A/G]GGTTCCAGCAGGCAG | 17997 |
rs29362378 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd1 | Mm_Celera | 10:92694843 | ACCATGTACAGTGAC[C/T]AGCATTTGCTTGAAC | 17997 |