SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs29970418 | snp | A/G | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121167880 | TCCTGATCCACCTCC[A/G]TCCTAAAGAGCTCAT | 66568 |
rs29972496 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, intron-variant | Rwdd3 | Mm_Celera | 3:121171349 | TGTCAGGGACGTGAT[A/G]CACAAATGCTTATGG | 66568 |
rs30149426 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121163699 | CTGTATCACATTTTC[G/T]TTTTGCTCTCTCCTT | 66568 |
rs30215359 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171820 | ATGGGCGTGTTTATG[C/G]GCGTGGCATGTGTCC | 66568 |
rs30255299 | snp | C/T | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121166973 | TTCTTCCTCCCCCTC[C/T]TCCTCTTCCTCCTCT | 66568 |
rs30308755 | snp | C/T | 0.5 | 0 | synonymous-codon, missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121156514 | CTGAAGAATCAGGTA[C/T]TCCTAAAGAATAATC | 66568 |
rs30355136 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121166838 | GTAACCCGGTACTCT[A/G]CTGCATAAAAAGCCA | 66568 |
rs30356906 | snp | A/G | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121167123 | GACCAGGCTGGCCTC[A/G]AACTCCTAGATCTAC | 66568 |
rs30367734 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167958 | GCTCCAAGACTAGGC[A/G]CTCTTACCTCTCCCA | 66568 |
rs30456541 | snp | C/T | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121167002 | CTTTTTCCTTTTCTC[C/T]TCCTCCCCCTTCTTC | 66568 |
rs30459980 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155550 | TTCCACCAAAAAAAA[A/T]AAAAAGGGTTCACTT | 66568 |
rs30557545 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155147 | AAGACATCCAACATT[A/G]ATTTTTGCCCTCTAC | 66568 |
rs30651293 | snp | C/T | 0.32 | 0.24 | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158890 | CATATTTAGTCCTCG[C/T]TCTCATGTGATCTAA | 66568 |
rs30654018 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121168108 | TTACTCTTTCTAGCC[C/T]GGGCACACACAGAGC | 66568 |
rs30749828 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121171232 | AAACAACAAAAAAAA[A/T]TAATAATAAAGTCAA | 66568 |
rs30754580 | snp | A/G | 0.396694 | 0.202437 | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155773 | CTTAAAACATAATAA[A/G]CAGAGTGGGGAGGAA | 66568 |
rs30770901 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121161915 | CCCTGTCTGAAGAAG[C/T]GGGTCTCTGTGGAGT | 66568 |
rs30795271 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rwdd3 | Mm_Celera | 3:121157441 | GGTTTCTTACTTTAT[C/T]CATACCAGAACCCAG | 66568 |
rs30796824 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167902 | AGAGCTCATGCCTGC[C/T]CTACCAAAGCAAAAC | 66568 |
rs30894166 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rwdd3 | Mm_Celera | 3:121157276 | GCTGATTAGACAATC[A/G]GGGCCTTAGGTAAAT | 66568 |
rs30909572 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155706 | TGTATTTAATCCAAC[A/G]ATTTATGCAACCGCA | 66568 |
rs30991235 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rwdd3 | Mm_Celera | 3:121164069 | AAGCACCATTCTCAA[A/G]CATGACCCACGACCT | 66568 |
rs31010859 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121161884 | TGGAAGGTTGTGGAA[C/T]TTTAGAAATATGGGG | 66568 |
rs31048919 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Rwdd3 | GRCm38.p3 | 3:121164228 | GATTTACACTTCACC[A/C/G]TGGTACTGCAGTGAA | 66568 |
rs31056684 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155823 | AACATAAACATGAGA[A/C]AGTAAACATGAAAAC | 66568 |
rs31056905 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121163768 | CAGCAAACCCTACCA[C/T]CCCTAGGTGGTTATT | 66568 |
rs31127742 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158945 | ATCGTCCCCCGTCGC[A/G]CTTTCTGGCAAAGTG | 66568 |
rs31141343 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121159328 | TAATCAGTTAAAAAA[A/T]TTTCCCTTTCAAACC | 66568 |
rs31193608 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121157479 | CTTGTTAAGCAAATG[C/T]CAATGAAGGCTGGGC | 66568 |
rs31233483 | snp | C/T | 0.345679 | 0.230967 | synonymous-codon, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121159092 | AAGTAACTTCTCCTT[C/T]GCGGTAACACACTGG | 66568 |
rs31238822 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167832 | TTTGCCTGGTCCCCC[A/G]CGCCAGGACAACTAT | 66568 |
rs31263694 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121171672 | TGCCGCACCTCCTCC[A/G]CCATATCCGTGCGAC | 66568 |
rs31281057 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167833 | TTGCCTGGTCCCCCG[C/T]GCCAGGACAACTATT | 66568 |
rs31383646 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167561 | ACCCTTTCAGATTTG[A/C]TCTCCCTTGCGTCTA | 66568 |
rs31430844 | snp | A/G | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121156614 | AAGAGCATTCTCAGA[A/G]TGTAGCAGGGGGAGT | 66568 |
rs31473253 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155700 | TGGTTTTGTATTTAA[C/T]CCAACGATTTATGCA | 66568 |
rs31545322 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121167441 | TGAACAGACCCTGTT[C/G]TGATGTCAAATGTGG | 66568 |
rs31594530 | snp | A/G | 0.5 | 0 | intron-variant | Rwdd3 | Mm_Celera | 3:121167319 | ACACTGGAGAGTCAC[A/G]GTCTTCCTAGTTGAT | 66568 |
rs31639509 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121168539 | ACTCAGAAGCCCCAC[A/C]CACACACACACACAC | 66568 |
rs31682782 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121167573 | TGATCTCCCTTGCGT[C/G]TACAGCAATAACTGG | 66568 |
rs33861476 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rwdd3 | Mm_Celera | 3:121168102 | CAAACCTTACTCTTT[C/T]TAGCCCGGGCACACA | 66568 |
rs45682246 | snp | C/T | 0.32 | 0.24 | intron-variant | Rwdd3 | Mm_Celera | 3:121157368 | TATAGTGCACACAGA[C/T]TGCCTCAAAATCTGC | 66568 |
rs45726812 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170049 | AGATAAAGAGCCGCA[A/G]TGTTCAGAGTATTAA | 66568 |
rs45809185 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121163530 | TCCCTCCCGTTTTCT[C/T]GTGCGGTCTTTGCTC | 66568 |
rs45831604 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169390 | CACCTGGACTGACTC[A/G]TGGGATGGAGAAGAA | 66568 |
rs45881852 | snp | C/G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161783 | CACTCACCAGCACAC[C/G/T]ACCTCATGCATTACA | 66568 |
rs45951352 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165532 | AGGTACATGTGTATG[A/T]ATGCAAGCATGCATG | 66568 |
rs46040816 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168142 | GGAAGCTGAGGCAGG[A/G]GGATCTAGTGTTCCT | 66568 |
rs46092942 | snp | A/G | 0.32 | 0.24 | intron-variant | Rwdd3 | Mm_Celera | 3:121159621 | CAGCAGCATGTATAG[A/G]GAAGGTGTAAGGAGT | 66568 |
rs46291360 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168240 | ACCATATTCCAACAC[A/G]GCAGACGACAGAAAT | 66568 |
rs46352667 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164328 | CATTTTAAATTGTCC[C/T]GAAACACCTAATATC | 66568 |
rs46378299 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rwdd3 | Mm_Celera | 3:121157752 | GAAGGCAGCTGCTGG[A/G]ACAAGTCAGGTGGAA | 66568 |
rs46475104 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162039 | GATTTCTGGAGATGG[C/G]TGAGCTCTGAGATGC | 66568 |
rs46508344 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173480 | GCTTAAATAAAAAGT[C/T]CATGTGAATTGTCTT | 66568 |
rs46514682 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162486 | TATAATGAGTTTATC[A/G]AAGGAAGCACCGCTT | 66568 |
rs46544200 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165617 | GAACATATATGTGTC[A/G]GTGCAAACTTGCCTG | 66568 |
rs46567968 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170481 | TGGCCTGAAACGTCA[A/G]ATCACCACAAAGATC | 66568 |
rs46577169 | snp | A/G | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171402 | GCTGGGTTTCACGAG[A/G]AGGGCACTGCGCACC | 66568 |
rs46579532 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163168 | GCAAGGGGCCAAAGA[A/G]AAAGTAAGTTTTTTG | 66568 |
rs46678279 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158212 | ATGCAAGCAAAACAC[C/G]CATACACATTTTTAA | 66568 |
rs46720213 | snp | A/G | 0.32 | 0.24 | intron-variant | Rwdd3 | Mm_Celera | 3:121159802 | GCAGCAGGATGAACT[A/G]AAACTGGGCGGACAT | 66568 |
rs46749553 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162441 | GACATATGATAACAA[C/T]GTGCCCATGTGAAAC | 66568 |
rs46761035 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170582 | CTCCTAATCATAGAT[A/G]TAGCTTCCTTAGGTC | 66568 |
rs46762744 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160987 | AGGGTGGACACAGAG[C/T]TTCCTGAGTCTACGC | 66568 |
rs46810947 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167808 | TTAAATGTACCTATG[A/C]TGTTACTTTTTGCCT | 66568 |
rs46815512 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173712 | TACTGAAATTCTAGA[A/T]ATTTAAATGTGAAGT | 66568 |
rs46911638 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164460 | CACACACTGCCGCTG[C/T]GATGATCTGCCATGC | 66568 |
rs46913989 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173071 | GTTAGAGAGATTTGG[A/G]GAAAAGATTACACTT | 66568 |
rs46962785 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169337 | CAAGCCTCTCCTTAA[A/G]ACCCACGTGAAGATC | 66568 |
rs47107329 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161763 | GTACAGTGACAATGT[A/G]TGTACACTCACCAGC | 66568 |
rs47138198 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rwdd3 | Mm_Celera | 3:121158367 | TAGATATGTATATTT[A/T]AAAAAAACAACTGGG | 66568 |
rs47150542 | snp | G/T | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171348 | TTGTCAGGGACGTGA[G/T]ACACAAATGCTTATG | 66568 |
rs47165900 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163683 | CCGGAAGTTGCAATT[A/G]CTGGATCACATTTTC | 66568 |
rs47270419 | snp | G/T | 0.42 | 0.183303 | intron-variant | Rwdd3 | Mm_Celera | 3:121163404 | AATCCACTCAGATAT[G/T]AGAAAAAGCAGCCTC | 66568 |
rs47337947 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164515 | TGTCCGGTAGCTTGC[A/G]CATGGGTTCCCCTCT | 66568 |
rs47349040 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160818 | CGGCAGTCATGCAGC[A/G]AGCCTGCATTCCCTC | 66568 |
rs47361435 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161814 | GTTTGGAGGTAAATA[A/G]CATACCACAAGCTCA | 66568 |
rs47370304 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168189 | ATGGGTAGGTTCTGT[A/C]TTAAAACAATCAAAC | 66568 |
rs47373787 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169829 | CCTGCTACACTTGGT[C/G]TTTGCCTCACTCACA | 66568 |
rs47387503 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161782 | ACACTCACCAGCACA[C/T]TACCTCATGCATTAC | 66568 |
rs47398296 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rwdd3 | Mm_Celera | 3:121157804 | ACAAGCTGACAGTCC[C/T]GGCGACCCTGCTTCC | 66568 |
rs47464615 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162250 | TTTCTGATAATGATT[C/T]TATAGAACTCTTAAA | 66568 |
rs47465492 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163089 | TGTGTCTATGTGTAT[A/G]CTTGAATTCTCTCAT | 66568 |
rs47572997 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160837 | CTGCATTCCCTCTCA[A/T]TGAGGGGGTAGAATC | 66568 |
rs47641793 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167656 | TTTCTTTTATTTTTT[C/T]CTAACAACAAAAAAA | 66568 |
rs47671664 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rwdd3 | Mm_Celera | 3:121161483 | GGTCAGAAAGCAGAT[A/G]TTTCCTGACCAGCAC | 66568 |
rs47812070 | snp | C/G | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171375 | TATGGTGGATGCCGA[C/G]TATTTGGAGGAGCTG | 66568 |
rs47854401 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162480 | TGAGCTTATAATGAG[C/T]TTATCAAAGGAAGCA | 66568 |
rs47870449 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163666 | GAAAAGCTGCCCCTG[A/G]CCCGGAAGTTGCAAT | 66568 |
rs47938691 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160331 | TTTTCAGACCCCATC[C/T]GGAATCAGAGGCAGT | 66568 |
rs47942825 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161776 | GTGTGTACACTCACC[A/T]GCACACTACCTCATG | 66568 |
rs48019405 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170477 | CACATGGCCTGAAAC[A/G]TCAAATCACCACAAA | 66568 |
rs48129597 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163208 | TTTTTTTCCTTAATC[C/T]CTTCCTGCTTACAGC | 66568 |
rs48150319 | snp | A/G | | | synonymous-codon, intron-variant | Rwdd3 | Mm_Celera | 3:121171339 | AGCGTCCTGTTGTCA[A/G]GGACGTGATACACAA | 66568 |
rs48151679 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166386 | AGAAGAAAACGTCCA[A/C]TGCCTGGTGAAGCTC | 66568 |
rs48234121 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160404 | ATGTATATAGTATTT[A/T]TAAAAAAACTTCTCT | 66568 |
rs48251211 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168199 | TCTGTCTTAAAACAA[C/T]CAAACCTTAACCTTT | 66568 |
rs48277031 | snp | G/T | 0.18 | 0.24 | intron-variant | Rwdd3 | Mm_Celera | 3:121156741 | GGCCACTGCTAGAGT[G/T]AGTTATTTAACCCTC | 66568 |
rs48289277 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169343 | TCTCCTTAAAACCCA[A/C]GTGAAGATCAAGGTG | 66568 |
rs48289958 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162505 | GAAGCACCGCTTTGA[A/T]CATACTATCAGCGTC | 66568 |