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 |
rs48330125 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169220 | TGCACCAGCCCCTTT[C/G]CTACAGAGGAGTGGG | 66568 |
rs48390444 | snp | A/G | 0.18 | 0.24 | synonymous-codon, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121159002 | CGGCTGGCTGAGGAC[A/G]AGTCTGAGATTCTGC | 66568 |
rs48392282 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161929 | GTGGGTCTCTGTGGA[A/G]TGGACCTTCAAGTTT | 66568 |
rs48402674 | snp | A/G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158381 | TTAAAAAAACAACTG[A/G/T]GGAAAGATGGTTGGG | 66568 |
rs48462862 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rwdd3 | Mm_Celera | 3:121156955 | AGCACACTGCTCAAT[A/G]GTAGCAACCGCTGCT | 66568 |
rs48500025 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Rwdd3 | Mm_Celera | 3:121157874 | CTCAGGCACTACAGG[G/T]ACAACACTGAAGTGT | 66568 |
rs48558430 | snp | A/G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121164958 | GGTTGTGAACCACCA[A/G/T]GTGATTGCTGGGAAA | 66568 |
rs48588215 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168055 | TTGGAACAATATTGA[C/T]GTTACAGCTACAACT | 66568 |
rs48628118 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163653 | CTTGCTGAAGCCAGA[A/G]AAGCTGCCCCTGACC | 66568 |
rs48670708 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163728 | TTCTCATTCTTCTCA[C/T]TGAGAAAGAAGTATC | 66568 |
rs48672535 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170662 | AAAGCCATTACAATC[A/G]TAGTTACATTGTAAC | 66568 |
rs48677148 | snp | G/T | 0.197531 | 0.244432 | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158988 | CTGCTGGCGGTCTCC[G/T]GCTGGCTGAGGACAA | 66568 |
rs48686007 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165499 | CCCATCCAAATTTAT[A/G]TGTCCGTTTGTTTAT | 66568 |
rs48808905 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164678 | TTGCAGCTCCTGTCA[C/T]TTTAAATTAACATAA | 66568 |
rs48906393 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rwdd3 | Mm_Celera | 3:121163632 | ACTTGGGGGTGCTGC[C/T]GCCTTCTTGCTGAAG | 66568 |
rs48960963 | snp | C/G | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171409 | TTCACGAGGAGGGCA[C/G]TGCGCACCGTCTAGT | 66568 |
rs49001272 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170167 | CACCACCATTTTTTT[A/T]AAATGTCATAGGACA | 66568 |
rs49067938 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160405 | TGTATATAGTATTTT[A/T]AAAAAAACTTCTCTA | 66568 |
rs49164038 | snp | A/G | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171368 | AAATGCTTATGGTGG[A/G]TGCCGACTATTTGGA | 66568 |
rs49165085 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173780 | CCCACCTCCCACAAA[C/T]ACGCACACCAGTGTG | 66568 |
rs49227621 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160960 | CACAGATCTGCCACC[A/G]TGGTTCAGTCCAGGG | 66568 |
rs49257408 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170716 | CCTCAAAATGTACAT[A/G]ACATATTTGACAGCT | 66568 |
rs49387306 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166290 | GACATGGGGAGAGTG[C/T]CTGGAATTACTAACA | 66568 |
rs49418530 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161771 | ACAATGTGTGTACAC[C/T]CACCAGCACACTACC | 66568 |
rs49422147 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169429 | CCCTGATTTGGCTAC[C/T]CCACTGCTTTCCCAA | 66568 |
rs49438270 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169652 | TGGGGTCAACCCAGG[C/T]CTTCCTGTCTTACAG | 66568 |
rs49468983 | snp | C/T | 0.297521 | 0.245442 | synonymous-codon, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158987 | GCTGCTGGCGGTCTC[C/T]GGCTGGCTGAGGACA | 66568 |
rs49474564 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121154991 | GAGGCACAAGCAGGT[A/G]GATCTATGAGTTCGA | 66568 |
rs49514250 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rwdd3 | Mm_Celera | 3:121156727 | TTAAATCTGGACTGG[A/G]CCACTGCTAGAGTGA | 66568 |
rs49573730 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171427 | CGCACCGTCTAGTTG[C/T]GGGAGAGCACGGGGT | 66568 |
rs49600057 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168296 | CCGGATTCCACTCTG[A/G]TCTGTTTTAAAGTTT | 66568 |
rs49628608 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165419 | AAGAAATAAAGACAG[C/T]GTGGTGTGGTGTGCT | 66568 |
rs49628874 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169472 | GTGTTTACATTATTT[C/T]CAGCCCTAAGAGACT | 66568 |
rs49632992 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121169154 | TATTGCCACTGTTTT[G/T]TTTTTTTTTTTTCTC | 66568 |
rs49803886 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163115 | CTCATTATTCCTCTT[A/C]TTTTCTCTCTGGCTC | 66568 |
rs49853781 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167875 | ACCATTCCTGATCCA[C/T]CTCCGTCCTAAAGAG | 66568 |
rs49989187 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165401 | TACAAAAAGGCCAGA[A/G]AAAAGAAATAAAGAC | 66568 |
rs50013682 | snp | G/T | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171365 | CACAAATGCTTATGG[G/T]GGATGCCGACTATTT | 66568 |
rs50056613 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164529 | CGCATGGGTTCCCCT[C/G]TACCTTCCTCTTGAC | 66568 |
rs50166036 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166425 | AATCTGATGATGGAG[A/G]AAGAGGAGTCTTAGT | 66568 |
rs50219945 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169786 | GAAACCCGAACTGCC[G/T]CTGGCAGCGAGGGTA | 66568 |
rs50383674 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168254 | CGGCAGACGACAGAA[A/G]TTCAAACAAAGAAAC | 66568 |
rs50403724 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170525 | ATGCAAGAAGGCATA[A/G]GAGAAAGGGGTCACT | 66568 |
rs50412439 | snp | C/G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170764 | ATTTGCATCAGCACA[C/G/T]TTTCCCAAAAGGGGG | 66568 |
rs50665732 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164951 | TACAGATGGTTGTGA[A/G]CCACCAGGTGATTGC | 66568 |
rs50746942 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161560 | CAGCAACTTTCATAA[A/G]ACTGAAAGGTCTATC | 66568 |
rs50748314 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168122 | CCGGGCACACACAGA[A/G]CTTAGGAAGCTGAGG | 66568 |
rs50794019 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167246 | CTAGTAATCACTTTA[G/T]AAAACTAGGGAAGGA | 66568 |
rs50797107 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161830 | CATACCACAAGCTCA[C/T]CTGTTTGCACACTTG | 66568 |
rs50822871 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160623 | GCAAGCACCTCCACA[A/C]ACGGAAACATCTCAC | 66568 |
rs50835072 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164455 | ACAGTCACACACTGC[C/T]GCTGCGATGATCTGC | 66568 |
rs50856718 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164988 | ATGAACTCAGGACCT[C/T]TGGAAGAGGAGTCAG | 66568 |
rs50891778 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158299 | ATAATCTTATGCTAA[C/T]CCTGAACCTTGCAAG | 66568 |
rs50991169 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156988 | CACCAAGCCGCCTGC[A/G]AAAGGGGCCTTCCGG | 66568 |
rs51023961 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156535 | AAGAATAATCGGTAC[A/G]TTAAGGGCAGAGCGA | 66568 |
rs51029622 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164962 | GTGAACCACCAGGTG[A/G]TTGCTGGGAAATGAA | 66568 |
rs51039390 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170547 | GGGGTCACTGACTTA[C/T]CTTATGGAAACCCAA | 66568 |
rs51051204 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165033 | GAGCCACCTCCCCAG[C/T]CCAGAAGAAAAGTTT | 66568 |
rs51054643 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160915 | GTCAACCCTGTGCAC[C/T]GTGCTGTTCAGAAAA | 66568 |
rs51204596 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167761 | TAAAGTTATTAACAG[C/G]TTAGCAAGAGAATGG | 66568 |
rs51286391 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165227 | CCAAGAAAAAGCATT[A/C]AGGGCCAAGGATGAA | 66568 |
rs51291357 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163103 | TACTTGAATTCTCTC[A/T]TTATTCCTCTTCTTT | 66568 |
rs51316852 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162943 | AAATGTATATGTGTG[A/G]CTGTCTATAGGTACA | 66568 |
rs51388379 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163750 | AGAAGTATCTTCCTC[C/T]TACAGCAAACCCTAC | 66568 |
rs51388992 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160622 | TGCAAGCACCTCCAC[A/C]AACGGAAACATCTCA | 66568 |
rs51460863 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170246 | AACTCGGAGACACGA[A/G]TGATCCCTTTAAATA | 66568 |
rs51474316 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170219 | ATATTGGCAAGTAAG[C/T]CACGATACAAGAACT | 66568 |
rs51475411 | snp | C/T | | | splice-acceptor-variant, intron-variant | Rwdd3 | Mm_Celera | 3:121171420 | GGCACTGCGCACCGT[C/T]TAGTTGCGGGAGAGC | 66568 |
rs51502009 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170937 | AGGTCTATACAGGCA[G/T]GCAAAACACTCATAC | 66568 |
rs51607473 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162507 | AGCACCGCTTTGAAC[A/G]TACTATCAGCGTCCT | 66568 |
rs51633354 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168810 | ATATGTCACTGTAAC[A/G]GTTTTGCAGGGGGAC | 66568 |
rs51695583 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Rwdd3 | Mm_Celera | 3:121161731 | CAGGGGACCTCATGG[C/T]GACGAAAACCCTTGG | 66568 |
rs51712348 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rwdd3 | Mm_Celera | 3:121159812 | GAACTGAAACTGGGC[A/G]GACATCCGTTCAGCC | 66568 |
rs51749268 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161799 | ACCTCATGCATTACA[A/G]TTTGGAGGTAAATAG | 66568 |
rs51825244 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166478 | AGAAAGGCAGGCAAA[C/G]GGACTGCCCAGAGCT | 66568 |
rs52003721 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170415 | AAAAATATACAAGAC[A/T]GGTCTAGGCACTTAA | 66568 |
rs52011685 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170314 | TGTGGAGACAGGAGA[C/T]GCTAACCGATCAGGA | 66568 |
rs52021212 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163687 | AAGTTGCAATTACTG[G/T]ATCACATTTTCGTTT | 66568 |
rs52070426 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164878 | ATTTATTTATTTTAT[C/G]TACATAAATACATTA | 66568 |
rs52177169 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rwdd3 | Mm_Celera | 3:121161439 | TCCCCATGGCCTGAG[G/T]TCCTCAGAGTCTGTG | 66568 |
rs52285712 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161378 | TGTGTGTGTGTGTCT[C/G]TGTGTGTGTGTGTGT | 66568 |
rs52286448 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164904 | CATTATTGCTGTCTT[A/C]AGACACACCAGAAGA | 66568 |
rs52294371 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157154 | TAGAGAATGTTATTT[A/T]AAAAATGCACTTCTC | 66568 |
rs52335044 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162533 | GTCCTTCTGTAACTC[C/T]CCTTTGTGCAACATT | 66568 |
rs52379227 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162660 | GTTTTTGTTTTTTGG[G/T]TTTTTTTTTTTTTTT | 66568 |
rs52385149 | snp | A/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161092 | GTGTGTGTGTGTGTA[A/T]GAGAGAGAGAGAGAG | 66568 |
rs52388356 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161075 | TGTTTGTGTTTGTGT[G/T]TGTGTGTGTGTGTGT | 66568 |
rs52399040 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161376 | TGTGTGTGTGTGTGT[C/G]TCTGTGTGTGTGTGT | 66568 |
rs52401731 | snp | A/G | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171150 | ATGCTGCGTCCAGCA[A/G]AAGTCTGGAATCGGC | 66568 |
rs52414528 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161054 | GGGTTTTTTAGGGGG[A/T]TTGTGTGTTTGTGTT | 66568 |
rs52505435 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162657 | TTGGTTTTTGTTTTT[G/T]GGTTTTTTTTTTTTT | 66568 |
rs52569251 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161091 | TGTGTGTGTGTGTGT[A/G]AGAGAGAGAGAGAGA | 66568 |
rs211805035 | in-del | -/AAAG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167676 | CAACAAAAAAAAAAA[-/AAAG]AAAGAAAGAAAAGAA | 66568 |
rs212176863 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158364 | AGATAGATATGTATA[-/T]TTTAAAAAAACAACT | 66568 |
rs212256420 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166895 | GAGCCGGAGAACACT[C/T]CAGGGAAAGCTGCAG | 66568 |
rs212275310 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167471 | GTGAGAGACCAAAAA[G/T]AAAAAAGAATAAAAT | 66568 |
rs212283813 | in-del | -/AC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160268 | CCTAGCACATCTGTT[-/AC]AGAGTTTTTCTTTAA | 66568 |
rs212499073 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165658 | CTTAATTCTTTTCCT[C/T]TCCTTCCTCTCTGGT | 66568 |
rs212575869 | in-del | -/CT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163901 | CAACAAGCTTCAGAC[-/CT]CTCTCTCTCTCTACT | 66568 |
rs212823882 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170992 | TGTGTGAGTGGAGCG[G/T]CTGGGTTCCTTAACG | 66568 |
rs212863632 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165230 | AGAAAAAGCATTAAG[C/G]GCCAAGGATGAAGCC | 66568 |
rs212877649 | in-del | -/TCA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168015 | ACCTCAGACCCACAT[-/TCA]TCACTATTTGCACGA | 66568 |
rs213067002 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163883 | AACCCAATGCTAATT[C/T]CTCAACAAGCTTCAG | 66568 |
rs213151445 | in-del | -/TACATACA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162955 | GTGACTGTCTATAGG[-/TACATACA]TACATACATACATAC | 66568 |
rs213206430 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156831 | GTACCTTAGTTAGCC[A/G]ACTCCGCACAACTAG | 66568 |
rs213677583 | in-del | -/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170161 | CAAACCACCACCATT[-/G]TTTTTAAAATGTCAT | 66568 |
rs213739118 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157344 | ATGTTACTCTAAAGG[A/G]TCAAGGGCTATAGTG | 66568 |
rs213781658 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167679 | CAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 66568 |
rs213838718 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155257 | TCAGATCACCCCAAC[A/G]CCAACTACACTGTTA | 66568 |
rs213958241 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165873 | ACTTGCAAAACCAAG[-/C]CCCCCCCCAACCTCC | 66568 |
rs213995748 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162517 | TGAACATACTATCAG[C/T]GTCCTTCTGTAACTC | 66568 |
rs214556372 | snp | C/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171864 | TGAGTTTTGGCCTCT[C/G]TGGTTTTCTGGATCA | 66568 |
rs214594679 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172664 | TAACATTCTGTGAGT[A/T]CATCAAAGAATTTAA | 66568 |
rs214661689 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167932 | CTCCCAAAAGACCCG[A/C]GTCTTATTTGGCTCC | 66568 |
rs214767234 | snp | C/G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161212 | CTGGGGCTTACTATA[C/G/T]AGACCAAGCTGCTTC | 66568 |
rs214937738 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166781 | TGTTTTAAGCCACCC[A/T]CACGTGAGGACCGGA | 66568 |
rs214964481 | in-del | -/ATAAATAA | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121157066 | CTAGTATACAATCTT[-/ATAAATAA]ATAAATAAATAAATA | 66568 |
rs214967129 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166094 | AACATGGTTTATAGC[A/G]ATACAGGCCTTGAGT | 66568 |
rs215000676 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158032 | AGTTTACCATTAATA[G/T]GAAACAAATACATGT | 66568 |
rs215100469 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160286 | AGTTTTTCTTTAATG[A/G]ATGTCAATACCAGCT | 66568 |
rs215232700 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156772 | TGTTGTTTAGACCAG[C/T]TATTTAAACCAGTTA | 66568 |
rs215242196 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164861 | GTTTTGTTTTGTTTC[A/C]GATTTATTTATTTTA | 66568 |
rs215399642 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162766 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 66568 |
rs215559006 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155997 | TCTTTTCTGGCAAAC[A/G]TTAGAATATATGGGA | 66568 |
rs215711472 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170888 | CCTAGCCCCTGAACG[C/T]CCTATTCAGGCCTCC | 66568 |
rs215882776 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165139 | TACTAGTAAGTAAAG[A/T]CTGCATCATCAGAAA | 66568 |
rs215948054 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167374 | GCACACCAGAGCTGC[-/A]AAACTAAGGCTGCAC | 66568 |
rs215996925 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168975 | TAAACTGCGACTCCA[C/T]TTATAACAGGCACTG | 66568 |
rs216355823 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160046 | ACACAGGGCTATGTG[A/G]CCAGTCTGCCTCTCT | 66568 |
rs216667332 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165779 | TTAGGCAAAAGGTGA[C/T]AATTCCTCTGGGGCT | 66568 |
rs216695819 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121159095 | TAACTTCTCCTTCGC[A/G]GTAACACACTGGGCC | 66568 |
rs216892753 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157407 | GGTTAGGCCCCACTG[C/T]AGGCTATAGATTAAA | 66568 |
rs216919595 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168508 | ACATATCCTCAAAAC[C/T]TTTGCACAGAAAAGC | 66568 |
rs217057979 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169809 | CGAGGGTAGAAGCCA[C/T]GAAGCCTGCTACACT | 66568 |
rs217163244 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164004 | CTGCTTAAACTGCAA[C/G]TTCTCCTCATAACTG | 66568 |
rs217214646 | snp | C/G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167571 | ATTTGCTCTCCCTTG[C/G/T]GGTACAGCAATAACT | 66568 |
rs217389630 | in-del | -/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171443 | GGAGAGCACGGGGTA[-/G]GGGGGGCGGAGAGGG | 66568 |
rs217652678 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167957 | GGCTCCAAGACTAGG[C/T]GCTCTTACCTCTCCC | 66568 |
rs217775824 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168338 | CATCCCTACAGCACA[C/T]GGTAGATACACACTC | 66568 |
rs217808976 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162604 | TTGTTGTTTTGGTTT[G/T]GGGGTTTTTGGAGGG | 66568 |
rs217901838 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169155 | ATTGCCACTGTTTTG[-/T]TTTTTTTTTTTCTCA | 66568 |
rs217908767 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121171696 | GTGCGACCAGAACCC[A/G]AAGCCACTTCCGCCG | 66568 |
rs217940764 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167360 | AGTGTGTTCCAAACC[A/G]CACACCAGAGCTGCA | 66568 |
rs217968316 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167706 | AGAAAGAAAAAGAAA[A/G]TTGTTCTGCTCGAAA | 66568 |
rs218309453 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171986 | GTAAAAAAAACCTAA[A/T]CAAACAAGAAAAGCC | 66568 |
rs218812642 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170321 | ACAGGAGATGCTAAC[A/C]GATCAGGATGCTACC | 66568 |
rs218850149 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168112 | TCTTTTTAGCCCGGG[C/G]ACACACAGAGCTTAG | 66568 |
rs218856146 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156855 | CAACTAGACTGCTAA[C/G]AGGATCCACCCCCTG | 66568 |
rs219039416 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169858 | CAGCTCCCGAGTGTG[C/T]CAATCATTCCTGCTT | 66568 |
rs219129578 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168555 | CACACACACACACAC[A/G]CTCTCCTCTCATACA | 66568 |
rs219145271 | snp | C/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155337 | CTTTCACATCCCAGC[C/T]TCCTATTTTAGATGC | 66568 |
rs219306811 | snp | C/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155723 | TTTATGCAACCGCAC[C/T]AAGAAATGAGTGTTA | 66568 |
rs219688497 | in-del | -/TATTTGTCA | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173173 | AAATATTAATTTGAT[-/TATTTGTCA]TATTTGTTAAATGGT | 66568 |
rs219741654 | in-del | -/AAAA | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155071 | GAAACCCTGTCTCAG[-/AAAA]AAAAAAAAAAAAAAA | 66568 |
rs219755782 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173538 | AAATCCCTCGAATAC[A/G]TTTCTTGCACTCTGA | 66568 |
rs220030591 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172217 | CAGGGCCTCTTTCCA[A/G]TCCAAGATGAAGAAG | 66568 |
rs220066563 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173387 | TATCATACTTAAAAT[A/T]TTCTGGTCAGTGGGT | 66568 |
rs220134940 | snp | A/C | | | missense, intron-variant | Rwdd3 | Mm_Celera | 3:121171361 | GATACACAAATGCTT[A/C]TGGTGGATGCCGACT | 66568 |
rs220314889 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159521 | AAATTATCAAAAAAA[A/G]GCAGTTTGATTTATA | 66568 |
rs220414069 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156979 | CGCTGCTATCACCAA[A/G]CCGCCTGCAAAAGGG | 66568 |
rs220425392 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157809 | CTGACAGTCCTGGCG[A/C]CCCTGCTTCCTCTGA | 66568 |
rs220456828 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158410 | GGTGCCTAGAGAGAT[A/G]GCTCAGTGGTTAGAA | 66568 |
rs220462029 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158307 | ATGCTAATCCTGAAC[C/G]TTGCAAGTTTATAGC | 66568 |
rs220743929 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156549 | CATTAAGGGCAGAGC[A/G]AATTCTAAAAGGCAC | 66568 |
rs221015165 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164880 | TTATTTATTTTATGT[A/T]CATAAATACATTATT | 66568 |
rs221068274 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157583 | AATCCTCTGTAACGG[G/T]GCATGACTCACTCTG | 66568 |
rs221354830 | snp | C/T | | | intron-variant, downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121156081 | AGAATGATTTTGCTT[C/T]AGAGAAATTTCAGAT | 66568 |
rs221381757 | snp | C/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155403 | ACACAAGAGTCCTTT[C/T]ACATTTCATCATAAA | 66568 |
rs221458683 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160520 | CATTATTATTGGTGT[A/G]TGTGGCCATGGGGAG | 66568 |
rs221473501 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156998 | CCTGCAAAAGGGGCC[A/T]TCCGGCACACCACCT | 66568 |
rs221627920 | in-del | -/TT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170159 | TGCAAACCACCACCA[-/TT]TTTTTTTAAAATGTC | 66568 |
rs221701829 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159666 | TTGTGGTGAGTCACA[C/T]GGAACCTGGGTGGTG | 66568 |
rs221941706 | in-del | -/CTCTGC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160071 | CTCTCTGCCTTCTTT[-/CTCTGC]CCCTGTTCTATTTCT | 66568 |
rs222323218 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162828 | GGCATGCACCACCAC[A/G]CCTGGCGGGGTAATT | 66568 |
rs222363091 | snp | A/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155519 | GAAAATTGTAGAGCT[A/T]CAGTTTGGTTTGTTT | 66568 |
rs222555729 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167234 | CCCAGTTAGTACCTA[A/G]TAATCACTTTAGAAA | 66568 |
rs222602111 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160648 | TCTCACTAGCTGCAC[A/G]TCTCTCCTTTCTTTC | 66568 |
rs222645031 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158289 | TTTTTACATTATAAT[C/T]TTATGCTAATCCTGA | 66568 |
rs222647926 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168630 | CCTAAGAGATTGTTA[C/T]ACACGGTGTCTCTGG | 66568 |
rs222686912 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162871 | TTTGTCTAAGAAGGT[A/T]TAAATTGCCAAAGAG | 66568 |
rs222690291 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169204 | CTGTAAGAACGTTTC[C/T]TGCACCAGCCCCTTT | 66568 |
rs222841714 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164388 | AAGCTAATTCCCTCC[C/T]AACTGCTACAGTGTG | 66568 |
rs222909136 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167608 | CTTTGCTCCAGAATC[C/T]TTGTGGGCCTCGATC | 66568 |
rs222945104 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161590 | CTTTTTATTAAATAT[A/G]TTTACGAGATACACA | 66568 |
rs223189326 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159398 | TGAAGAGACACACAA[A/G]GCAAAAAAGCCATGA | 66568 |
rs223321747 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165453 | ATGTGATGTGGTGTG[A/G]TGGCTTGGAGAGCTC | 66568 |
rs223676544 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161660 | TGATATTTTGATCCC[C/T]GTAAAGTTTAAATCA | 66568 |
rs223776849 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164594 | GCAATTATGAGTTTA[A/G]CAGATTCTCTGAGTC | 66568 |
rs223786891 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170750 | CGAGGGTGAGAATAA[G/T]TTGCATCAGCACATT | 66568 |
rs223791675 | in-del | -/TT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160414 | TATTTTTAAAAAAAC[-/TT]CTCTAAATATTACAG | 66568 |
rs223828927 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164981 | CTGGGAAATGAACTC[A/G]GGACCTTTGGAAGAG | 66568 |
rs223964543 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166558 | CTGTTGCTGTCTTCA[A/G]CCGCACCAGAAGAGG | 66568 |
rs224135003 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169317 | TCAATGCAAACTAAG[C/T]TAAGCAAGCCTCTCC | 66568 |
rs224153960 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121171681 | TCCTCCACCATATCC[C/G]TGCGACCAGAACCCA | 66568 |
rs224194952 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172367 | ATGCATATAACATAA[A/T]GTGTCTATTACCTCT | 66568 |
rs224200792 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165689 | TTACCAAGAGTTAAC[C/T]AGCAAGGCAAGTGAA | 66568 |
rs224229106 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165267 | GTGCACTACGATAGG[A/C]CATGGGAAACTGCTG | 66568 |
rs224416338 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168677 | ATCGTTCTTAGAGAA[A/G]GAAACAAAACAACTA | 66568 |
rs224678546 | in-del | -/CACTACCT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161780 | GTACACTCACCAGCA[-/CACTACCT]CATGCATTACAGTTT | 66568 |
rs224736354 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167997 | GGGTTTGTCTTCTAG[C/T]CCAACCTCAGACCCA | 66568 |
rs225088713 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168809 | AATATGTCACTGTAA[C/T]AGTTTTGCAGGGGGA | 66568 |
rs225249464 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167823 | ATGTTACTTTTTGCC[C/T]GGTCCCCCGCGCCAG | 66568 |
rs225459174 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172900 | AGGCAATTAGGAACC[A/G]TGCTGTGCAAATAAT | 66568 |
rs225542753 | in-del | -/CTGGCTGTAAAGGACAAGCCTT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157834 | CTCTGAGGCTGGCTC[-/CTGGCTGTAAAGGACAAGCCTT]CCTCTCAGGCACTAC | 66568 |
rs225590335 | snp | G/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172177 | TTGGTCACTAGCCTC[G/T]GGATTACACACAAGG | 66568 |
rs225835120 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168537 | GCACTCAGAAGCCCC[-/A]CACACACACACACAC | 66568 |
rs225880463 | snp | A/C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170055 | AGAGCCGCAGTGTTC[A/C/G]GAGTATTAAGACAAC | 66568 |
rs226238188 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170892 | GCCCCTGAACGTCCT[A/C]TTCAGGCCTCCCAGG | 66568 |
rs226282890 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171481 | AGGGGAGGGCACTGC[A/G]AGCGCAGGCCAACCC | 66568 |
rs226371219 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173284 | ACGAACAGCGTGATT[C/T]CATTGTCAGCAGGAT | 66568 |
rs226435420 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156529 | CTCCTAAAGAATAAT[C/T]GGTACATTAAGGGCA | 66568 |
rs226672319 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157219 | CATGTTAGTAACTCA[G/T]GAGTCTGTCGGCAAT | 66568 |
rs226723021 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155558 | AAAAAAATAAAAAGG[A/G]TTCACTTTGTTGGAC | 66568 |
rs226768083 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155231 | CTCAGGCATGCATGG[A/G]CTTGTCATGCTCAGA | 66568 |
rs226802510 | snp | A/C | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155647 | CACTGTGTATTCTTC[A/C]AGCTCTCCAGAAAGC | 66568 |
rs226826704 | in-del | -/AAATAAATAAATAAATAAATAAATAAATAAATAAA | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121157099 | AATAAATAAATAAAT[lengthTooLong]AAGATAAAATAACAG | 66568 |
rs226951334 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156811 | GTTGGCTCCTCAAAC[A/T]CTCGGTACCTTAGTT | 66568 |
rs227841997 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159843 | TCCACTGACTCCACA[A/G]GGGGCAGAGCACGCC | 66568 |
rs227852513 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157907 | GGATGCGCTTCTAAG[C/T]GCCTGCATGTTAGGA | 66568 |
rs227882256 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158534 | CAGAGGCTTTTCTAA[A/G]CGTTTACACGAGGTG | 66568 |
rs227978304 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166676 | TTAACCACTGAGCCA[C/T]CTCTCCAGCCCCCAA | 66568 |
rs227995972 | in-del | -/GAGGA | | | frameshift-variant, intron-variant | Rwdd3 | GRCm38.p3 | 3:121171399 | GGAGCTGGGTTTCAC[-/GAGGA]GGGCACTGCGCACCG | 66568 |
rs228081858 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160103 | TTCTCAGCACAGAAG[C/T]AGCCAGATCCTACAC | 66568 |
rs228088021 | in-del | -/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155146 | AAGACATCCAACATT[-/G]AATTTTTGCCCTCTA | 66568 |
rs228113653 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165005 | GGAAGAGGAGTCAGT[A/G]TTCTTAACCTCTGAG | 66568 |
rs228245260 | in-del | -/AA | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158613 | TAAAGAATAGAGGAG[-/AA]AAAAAAAAAAAAACA | 66568 |
rs228561508 | in-del | -/AGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158336 | CTGTTGTTAGGGACA[lengthTooLong]AGATAGATAGATAGA | 66568 |
rs228590924 | in-del | -/AAAGA | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172979 | AATTTGTATTAGAAG[-/AAAGA]AAAAAAAAATAGTTC | 66568 |
rs228685763 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157142 | AAAATGACATTTTAG[A/G]GAATGTTATTTTAAA | 66568 |
rs228759177 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157882 | CTACAGGTACAACAC[G/T]GAAGTGTCAGGATGC | 66568 |
rs228854468 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163244 | TTAATCACCAGAAGG[C/T]AGGGGCTGTTGGCCT | 66568 |
rs229008000 | in-del | -/CCCCCT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170070 | AGAGTATTAAGACAA[-/CCCCCT]CCCCCTCTCTCTCAG | 66568 |
rs229031859 | snp | A/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121156641 | GAGTTACACAGTGCC[A/T]TTACATAGGTGGCAG | 66568 |
rs229037131 | snp | C/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155701 | GGTTTTGTATTTAAT[C/T]CAACGATTTATGCAA | 66568 |
rs229160137 | in-del | -/TC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168639 | TTGTTACACACGGTG[-/TC]TCTGGATTTTCACAT | 66568 |
rs229166030 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168130 | ACACAGAGCTTAGGA[A/G]GCTGAGGCAGGAGGA | 66568 |
rs229406637 | in-del | -/GAAAG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167675 | CAACAAAAAAAAAAA[-/GAAAG]AAAGAAAGAAAGAAA | 66568 |
rs229745503 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161368 | TGTCTCTGTGTGTGT[C/G]TGTGTGTCTCTGTGT | 66568 |
rs229804665 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170526 | TGCAAGAAGGCATAG[A/G]AGAAAGGGGTCACTG | 66568 |
rs229827780 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171034 | AAGAATGAAATTTTA[G/T]CTTTTTAAAACAATT | 66568 |
rs229828160 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164882 | ATTTATTTTATGTAC[A/G]TAAATACATTATTGC | 66568 |
rs229854844 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165296 | TGCTTTGAACTTATA[A/T]TGAGCTTTGGACTTA | 66568 |
rs229870442 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171230 | AAAACAACAAAAAAA[-/T]ATTAATAATAAAGTC | 66568 |
rs229912960 | snp | A/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121154904 | AATAAATAAACCTTT[A/T]AAAAAAAATAAAAAG | 66568 |
rs230113065 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167456 | GTGATGTCAAATGTG[C/G]TGAGAGACCAAAAAG | 66568 |
rs230160709 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161224 | ATACAGACCAAGCTG[C/T]TTCCCAAATGCTGAA | 66568 |
rs230394405 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165882 | ACCAAGCCCCCCCCC[-/A]ACCTCCATAACACCC | 66568 |
rs230399319 | in-del | -/TG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161379 | GTGTGTGTGTGTCTC[-/TG]TGTGTGTGTGTGTGT | 66568 |
rs230408081 | in-del | -/CACCATC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166307 | TGGAATTACTAACAA[-/CACCATC]CTCAGTGTCCCGATG | 66568 |
rs230421960 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168571 | CTCTCCTCTCATACA[C/T]ACTTGCTTTATGCAA | 66568 |
rs230455594 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169171 | TTTTTTTTTTTCTCA[A/G]CATCATGGATTGTCT | 66568 |
rs230490280 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169774 | GAGTGACACCCTGAA[A/G]CCCGAACTGCCGCTG | 66568 |
rs230523425 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163975 | CATTTTCCCATTAAC[C/T]GGCCTCCCCATAACT | 66568 |
rs230836745 | snp | A/C | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173307 | AGCAGGATTAGGAGG[A/C]GATCACCGGAGCCTA | 66568 |
rs230908687 | snp | C/T | | | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158935 | TCCACGGTCCATCGT[C/T]CCCCGTCGCACTTTC | 66568 |
rs230995267 | in-del | -/CT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161433 | GGAGTTCCCCATGGC[-/CT]CTGAGTTCCTCAGAG | 66568 |
rs231040397 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167623 | TTTGTGGGCCTCGAT[C/T]ACTCAAAGTCTGTTT | 66568 |
rs231089560 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167933 | TCCCAAAAGACCCGA[C/G]TCTTATTTGGCTCCA | 66568 |
rs231231051 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163834 | TCCCTGCCTTCTCTT[A/G]TTTAGAAAATGTTTG | 66568 |
rs231516686 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171865 | GAGTTTTGGCCTCTG[A/T]GGTTTTCTGGATCAG | 66568 |
rs231575891 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170177 | TTTTTAAAATGTCAT[A/G]GGACATCACAGGTTC | 66568 |
rs231882856 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157499 | GAAGGCTGGGCTTGG[A/G]GAAACTCTAGGCTGC | 66568 |
rs231994150 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163243 | GTTAATCACCAGAAG[C/G]CAGGGGCTGTTGGCC | 66568 |
rs232051724 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161905 | AAATATGGGGCCCTG[C/T]CTGAAGAAGTGGGTC | 66568 |
rs232347736 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167413 | GCTATCTGCACAAGA[A/C]AACAAGAAGACCTGA | 66568 |
rs232845471 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170332 | TAACCGATCAGGATG[C/G]TACCCAATCACAAGA | 66568 |
rs232949216 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161536 | AAGATCAAAAGCTGA[A/G]AAAATTTTCAGCAAC | 66568 |
rs232970912 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172596 | ATTCTGCAGCTCCCA[A/G]GAGTCCTTTGGCTCA | 66568 |
rs233064291 | in-del | -/ACATACATACATACAT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162954 | GTGACTGTCTATAGG[-/ACATACATACATACAT]TACATACATACATAC | 66568 |
rs233240562 | snp | A/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155406 | CAAGAGTCCTTTTAC[A/T]TTTCATCATAAATTT | 66568 |
rs233290426 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121156008 | AAACGTTAGAATATA[C/T]GGGATCTTTTCATGT | 66568 |
rs233433511 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168893 | TATCGCCAGCCTATT[A/G]TGTGATGCAGTTAAG | 66568 |
rs233726911 | in-del | -/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162736 | GGCCCTGGCTGTTCT[-/G]GAACTCACTATGTAG | 66568 |
rs233756948 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170861 | GGCAAGGCTCTCAAA[C/T]CCTCGGTAACTCCTA | 66568 |
rs233866882 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121154967 | CACACATTTAATCTC[A/G]GCACTTGGGAGGCAC | 66568 |
rs234015944 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164006 | GCTTAAACTGCAACT[C/T]CTCCTCATAACTGCT | 66568 |
rs234051822 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164710 | AAACCCTGGGCATTA[C/G]TGTACTGAGCAGATT | 66568 |
rs234053753 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156930 | CTAGAGTGACTGCCT[A/T]CCAGAGGACAGCACA | 66568 |
rs234246552 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161247 | ATGCTGAAATTAATG[A/G]CATGCACCTACCACA | 66568 |
rs234289074 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162174 | CAAACTTCCTGCAGA[G/T]CAACATGAAGATGTA | 66568 |
rs234369695 | snp | C/G | | | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121159014 | GACAAGTCTGAGATT[C/G]TGCTGGATCCAAAGA | 66568 |
rs234489799 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169344 | CTCCTTAAAACCCAC[A/G]TGAAGATCAAGGTGA | 66568 |
rs234682492 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158295 | CATTATAATCTTATG[C/T]TAATCCTGAACCTTG | 66568 |
rs234717002 | snp | A/G | | | missense, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121159180 | ACTGGTAAATGGAAC[A/G]CCAACTCTAAGGGCA | 66568 |
rs235239001 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163596 | ACGCTGGGTGTGCAG[G/T]GAGCAGTACTGCCCA | 66568 |
rs235278865 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121156170 | AGGCTGTTTTACCAA[C/G]GGATCCTGTCATTCA | 66568 |
rs235289465 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166904 | AACACTCCAGGGAAA[A/G]CTGCAGGAAGCCAGG | 66568 |
rs235327872 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167536 | GGAACCCTTCAGATG[C/T]GTCTATCTCACCCTT | 66568 |
rs235703092 | in-del | -/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169751 | CAGGGAAGAAATGAT[-/G]GGGTACAGAGTGACA | 66568 |
rs235853183 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168405 | TGAGAAAGAGGTCGT[C/T]AGGATTTGTTGAGTG | 66568 |
rs235907924 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162702 | TTTTTTTGGTTTTTC[A/G]AGACAGGGTTCCTCT | 66568 |
rs236206370 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158220 | AAAACACGCATACAC[A/G]TTTTTAAGAAAATAA | 66568 |
rs236314175 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121171684 | TCCACCATATCCGTG[C/G]GACCAGAACCCAAAG | 66568 |
rs236378897 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166795 | CACACGTGAGGACCG[A/G]ATGCAGTAGCCACAG | 66568 |
rs236591956 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167824 | TGTTACTTTTTGCCT[C/G]GTCCCCCGCGCCAGG | 66568 |
rs236629232 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168123 | CGGGCACACACAGAG[C/T]TTAGGAAGCTGAGGC | 66568 |
rs236650368 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156837 | TAGTTAGCCGACTCC[A/G]CACAACTAGACTGCT | 66568 |
rs236732321 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158080 | ACTGGGGCTGGTGCT[A/G]GAGAGATAACTCGGC | 66568 |
rs236866854 | in-del | -/CACACACACA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168535 | AGCACTCAGAAGCCC[-/CACACACACA]CACACACACACACAC | 66568 |
rs236907414 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169850 | CTCACTCACAGCTCC[C/T]GAGTGTGTCAATCAT | 66568 |
rs236943736 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164120 | ATGGGGAGAACTTAA[A/C]AGGCCTGGGTTGCGT | 66568 |
rs237066850 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164274 | GTTGACGTCAGCCAT[A/G]CAGGGGTGTATTCCT | 66568 |
rs237222570 | in-del | -/A | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155797 | GAGGAAGGCACGATT[-/A]AAAGGCAAAAAACAT | 66568 |
rs237270092 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162818 | TGGGACTAAAGGCAT[A/G]CACCACCACACCTGG | 66568 |
rs237279932 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169342 | CTCTCCTTAAAACCC[A/G]CGTGAAGATCAAGGT | 66568 |
rs237335120 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170041 | TTAAGAGCAGATAAA[A/G]AGCCGCAGTGTTCAG | 66568 |
rs237395564 | snp | C/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155265 | CCCCAACACCAACTA[C/T]ACTGTTAGGGTGTGC | 66568 |
rs237606897 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168515 | CTCAAAACCTTTGCA[C/T]AGAAAAGCACTCAGA | 66568 |
rs237913935 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170735 | TATTTGACAGCTCAG[C/G]GAGGGTGAGAATAAT | 66568 |
rs237950295 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167573 | TTGCTCTCCCTTGCG[C/G]TACAGCAATAACTGG | 66568 |
rs238041521 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159429 | TTACAGGTTAATCCC[-/T]CCCTGCCATAAACAC | 66568 |
rs238256953 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166198 | AACAGACCTATGAAT[A/G]TATGCACCCTGTTTC | 66568 |
rs238306466 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159477 | CAAATGTACTTGCAA[C/T]TCACTCTCTTTATCA | 66568 |
rs238320462 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156593 | AGGGACCCAGCCAGC[A/G]TTTTCAAGAGCATTC | 66568 |
rs238343868 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167314 | TCCTAACACTGGAGA[C/G]TCACGGTCTTCCTAG | 66568 |
rs238545483 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171814 | GGGGAGATGGGCGTG[C/T]TTATGGGCGTGGCAT | 66568 |
rs238546798 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172266 | ACTCCTTAGAGATGG[A/G]GTCCAAAGCCAAAAA | 66568 |
rs238582983 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165780 | TAGGCAAAAGGTGAC[A/G]ATTCCTCTGGGGCTT | 66568 |
rs238584823 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173466 | ACTTCATTTAGCATG[C/T]TTAAATAAAAAGTTC | 66568 |
rs238983673 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164862 | TTTTGTTTTGTTTCC[A/G]ATTTATTTATTTTAT | 66568 |
rs239184433 | in-del | -/TTTG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162575 | TAATTTTATTTGTTT[-/TTTG]TTTGTTTGTTTGTTT | 66568 |
rs239299278 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168999 | GGCACTGGGCACAGC[A/C]ATATACTCTCCGTGT | 66568 |
rs239345085 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163455 | GAGAGCCACTCTCAG[A/G]GCCACTCTGCCCCAC | 66568 |
rs239480180 | in-del | -/AA | | | upstream-variant-2KB | Rwdd3 | GRCm38.p3 | 3:121172983 | TGTATTAGAAGAAAG[-/AA]AAAAAAAATAGTTCC | 66568 |
rs239552371 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159758 | CTACTCTTCTGATTC[C/T]GATCCACTCACGTCA | 66568 |
rs239875931 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155357 | ATTTTAGATGCCCAG[A/G]GAGCTTTATGGACAT | 66568 |
rs240381698 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173130 | AATTTTCAGTTTAAA[A/G]TCCAATGTTACTGCT | 66568 |
rs240383312 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167070 | CCCAAGACATGGTTT[C/T]TCTGTGTAGCTCTAG | 66568 |
rs240488949 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161908 | TATGGGGCCCTGTCT[G/T]AAGAAGTGGGTCTCT | 66568 |
rs240500780 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163655 | TGCTGAAGCCAGAAA[A/G]GCTGCCCCTGACCCG | 66568 |
rs240504718 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155613 | TTATTTTTTTCACAT[A/G]TGAATTTCGATTTGA | 66568 |
rs240540121 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156534 | AAAGAATAATCGGTA[C/T]ATTAAGGGCAGAGCG | 66568 |
rs240769139 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162882 | AGGTATAAATTGCCA[A/G]AGAGAAGAAATAAAA | 66568 |
rs240854822 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165420 | AGAAATAAAGACAGC[A/G]TGGTGTGGTGTGCTG | 66568 |
rs240878458 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168112 | CTTTTTAGCCCGGGC[-/C]CACACAGAGCTTAGG | 66568 |
rs241001279 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156697 | TACAGAGCAACAAAA[A/T]CAAATCGTTCACCTT | 66568 |
rs241014130 | in-del | -/TAAAAA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171193 | GCAGCCTGGAAAACG[-/TAAAAA]TAAAAATATTTTTAA | 66568 |
rs241114041 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157610 | TCTGACACTGCAAAA[C/T]GTATGAAGTGATCTG | 66568 |
rs241148978 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157801 | GTGACAAGCTGACAG[C/T]CCTGGCGACCCTGCT | 66568 |
rs241331915 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167516 | AAGAACTCCTTTTCT[-/C]CCCAGGAACCCTTCA | 66568 |
rs241350843 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164411 | ACAGTGTGTGAAAAT[A/G]TGCACTTTCCTGGCT | 66568 |
rs241386735 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164907 | TATTGCTGTCTTAAG[A/G]CACACCAGAAGAGGG | 66568 |
rs241613104 | in-del | -/AA | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155097 | AAAAAAAAAAAAAGG[-/AA]AAAAAAAAAGAGTAA | 66568 |
rs241621621 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166292 | CATGGGGAGAGTGTC[C/T]GGAATTACTAACAAC | 66568 |
rs241659104 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159545 | ATTTATACAATTTCC[A/G]TCCATAATTTACTGG | 66568 |
rs241684503 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169810 | GAGGGTAGAAGCCAC[A/G]AAGCCTGCTACACTT | 66568 |
rs241800182 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170759 | GAATAATTTGCATCA[A/G]CACATTTTCCCAAAA | 66568 |
rs241852409 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121154939 | AAATAGCAGCCAGGT[A/G]GGGGTGGTGACACAC | 66568 |
rs241862234 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165504 | CCAAATTTATGTGTC[C/T]GTTTGTTTATATAGG | 66568 |
rs242140595 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164001 | TAACTGCTTAAACTG[C/T]AACTTCTCCTCATAA | 66568 |
rs242228799 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161407 | GTGTGTGGCAGGGGG[G/T]AGAGGGTGGAAGGAG | 66568 |
rs242473670 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167408 | ATGGTGCTATCTGCA[C/T]AAGACAACAAGAAGA | 66568 |
rs242509018 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167708 | AAAGAAAAAGAAAAT[C/T]GTTCTGCTCGAAAGT | 66568 |
rs242715103 | in-del | -/AACT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165993 | ATTATATTTAACCCA[-/AACT]AACTTTTTCTCTACC | 66568 |
rs242937558 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167458 | GATGTCAAATGTGGT[A/G]AGAGACCAAAAAGAA | 66568 |
rs242963837 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163200 | TTTTTTTTTTTTTTT[-/C]CTTAATCCCTTCCTG | 66568 |
rs243063383 | in-del | -/AA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159322 | GAATACTAATCAGTT[-/AA]AAAAATTTCCCTTTC | 66568 |
rs243152507 | snp | G/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173018 | GAGTTATTTCCAAAA[G/T]AGCAGTTCAAGCAAG | 66568 |
rs243267781 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165460 | GTGGTGTGGTGGCTT[A/G]GAGAGCTCTGCCCCA | 66568 |
rs243450076 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172135 | TCAGAAAAGAGAACG[A/G]TAATGACCTCCAGGA | 66568 |
rs243610295 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163236 | AGCAGAAGTTAATCA[C/T]CAGAAGGCAGGGGCT | 66568 |
rs243690309 | in-del | -/AAC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158620 | AGAGGAGAAAAAAAA[-/AAC]AAAAAAACAAAGTAC | 66568 |
rs243899315 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157033 | CCCACCTGTAAATGT[A/T]CCTGCACGGTCCTGA | 66568 |
rs244072092 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169564 | CCTCAAAACTCTTAA[A/C]AGAAATTACTCCCCA | 66568 |
rs244280387 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168705 | CTAGAAAGACTGGAA[A/G]GTAAAGGTGGCACTC | 66568 |
rs244347605 | in-del | -/AA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167669 | TTCCTAACAACAAAA[-/AA]AAAAAAAAGAAAGAA | 66568 |
rs244395643 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158245 | AAATAAGAAATAAAA[A/C]AAAACTGTCATTTCA | 66568 |
rs244452343 | snp | A/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155249 | TGTCATGCTCAGATC[A/T]CCCCAACACCAACTA | 66568 |
rs244485988 | snp | C/G | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155650 | TGTGTATTCTTCCAG[C/G]TCTCCAGAAAGCAAC | 66568 |
rs244682688 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162836 | CCACCACACCTGGCG[A/G]GGTAATTTTATAAAG | 66568 |
rs244687508 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171500 | GCAGGCCAACCCCAC[C/T]CCCCAGTCCCCTCCT | 66568 |
rs244830352 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161753 | AACCCTTGGTGTACA[A/G]TGACAATGTGTGTAC | 66568 |
rs245069808 | in-del | -/AGGACA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165263 | GGTGTGCACTACGAT[-/AGGACA]AGGCCATGGGAAACT | 66568 |
rs245287283 | in-del | -/AAAA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167553 | CTATCTCACCCTTTC[-/AAAA]AGATTTGCTCTCCCT | 66568 |
rs245357160 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160401 | GTAATGTATATAGTA[-/T]TTTTAAAAAAACTTC | 66568 |
rs245514583 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157991 | ATTAATATGGACAAG[C/T]TTTTTGTTCTTGTTT | 66568 |
rs245548918 | snp | C/T | | | intron-variant, nc-transcript-variant | Rwdd3 | Mm_Celera | 3:121158712 | ACACACTTAAAAATG[C/T]ACCATATTTAAGAGA | 66568 |
rs245608791 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172180 | GTCACTAGCCTCGGG[A/G]TTACACACAAGGTCT | 66568 |
rs245656925 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166490 | AAACGGACTGCCCAG[A/G]GCTTGGAGGGAGCAA | 66568 |
rs246081302 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157870 | TCCTCTCAGGCACTA[C/T]AGGTACAACACTGAA | 66568 |
rs246330474 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160266 | GGACCTAGCACATCT[C/G]TTAGAGTTTTTCTTT | 66568 |
rs246399805 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160184 | GAGCCTAACAGAACA[C/T]TGAAATCACTTCTTA | 66568 |
rs246534954 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170661 | AAAAGCCATTACAAT[C/T]GTAGTTACATTGTAA | 66568 |
rs246635837 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165270 | CACTACGATAGGCCA[A/T]GGGAAACTGCTGCTT | 66568 |
rs246725015 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169318 | CAATGCAAACTAAGC[G/T]AAGCAAGCCTCTCCT | 66568 |
rs246771204 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167555 | TATCTCACCCTTTCA[G/T]ATTTGCTCTCCCTTG | 66568 |
rs246773733 | in-del | -/TGATT | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172294 | AAACTAGCTTTACAG[-/TGATT]TGATTTGAGTTGATT | 66568 |
rs247291962 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163788 | AGGTGGTTATTCTAA[C/T]CATTATAACTTCCTG | 66568 |
rs247323191 | in-del | -/AAG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170802 | GGGCACTCAGTGGTT[-/AAG]AGCACTGACTATTCC | 66568 |
rs247326250 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156749 | CTAGAGTGAGTTATT[A/T]AACCCTCTGTTGTTT | 66568 |
rs247650136 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163286 | AGAGTTAAAGGAAGA[A/G]AAACTTTATACATAG | 66568 |
rs247687469 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164598 | TTATGAGTTTAACAG[A/T]TTCTCTGAGTCTTAT | 66568 |
rs247845362 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169178 | TTTTCTCAGCATCAT[G/T]GATTGTCTTACTGTA | 66568 |
rs247845464 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162839 | CCACACCTGGCGGGG[A/T]AATTTTATAAAGAAC | 66568 |
rs247923222 | in-del | -/TG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168076 | AGCTACAACTCAAAC[-/TG]AGAGAGACTCAAACC | 66568 |
rs248031758 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173562 | ACTCTGACATTTAGA[A/G]GTAATCATCACAGAG | 66568 |
rs248172316 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168610 | GTGTTTACATTGTCT[A/G]TAACCCTAAGAGATT | 66568 |
rs248209695 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157308 | GAACAAGGAACTGTT[-/C]CTCCACTTTCGTCGG | 66568 |
rs248453271 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166603 | TACAGATGGTTGTGA[A/G]CCACCATGTGGCTGC | 66568 |
rs248491685 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159844 | CCACTGACTCCACAA[C/G]GGGCAGAGCACGCCT | 66568 |
rs248588468 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168526 | TGCACAGAAAAGCAC[A/T]CAGAAGCCCCACACA | 66568 |
rs248625417 | in-del | -/ATGTGAAACTCTA | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163560 | ACAGTGCACCCTGAG[-/ATGTGAAACTCTA]ATATATGCAACACAC | 66568 |
rs248826731 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165695 | AGAGTTAACTAGCAA[A/G]GCAAGTGAAGGGCTT | 66568 |
rs248959961 | snp | C/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171867 | GTTTTGGCCTCTGTG[C/G]TTTTCTGGATCAGAG | 66568 |
rs248987581 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166285 | ATGCTGACATGGGGA[A/G]AGTGTCTGGAATTAC | 66568 |
rs249042851 | in-del | -/CA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170807 | CTCAGTGGTTAAGAG[-/CA]CTGACTATTCCCTGG | 66568 |
rs249166643 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162603 | TTTGTTGTTTTGGTT[G/T]TGGGGTTTTTGGAGG | 66568 |
rs249167427 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170107 | ACTTCTTTTTGGGGG[G/T]TTTCTCTGACCTATC | 66568 |
rs249189215 | snp | C/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155331 | GCCTTTCTTTCACAT[C/T]CCAGCTTCCTATTTT | 66568 |
rs249779571 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161240 | TTCCCAAATGCTGAA[A/G]TTAATGGCATGCACC | 66568 |
rs249895463 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167947 | AGTCTTATTTGGCTC[C/T]AAGACTAGGCGCTCT | 66568 |
rs250006943 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168635 | GAGATTGTTACACAC[A/G]GTGTCTCTGGATTTT | 66568 |
rs250396133 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165633 | GTGCAAACTTGCCTG[G/T]GTAAAGGGTCTTAAT | 66568 |
rs250529827 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168129 | CACACAGAGCTTAGG[A/G]AGCTGAGGCAGGAGG | 66568 |
rs250873032 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158366 | TAGATATGTATATTT[-/A]TAAAAAAACAACTGG | 66568 |
rs250991364 | in-del | -/A | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155541 | GTTTGTTTTTCCACC[-/A]AAAAAAAATAAAAAG | 66568 |
rs251075446 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169851 | TCACTCACAGCTCCC[A/G]AGTGTGTCAATCATT | 66568 |
rs251112363 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170508 | GATCTGTAGATGTGT[A/G]CATGCAAGAAGGCAT | 66568 |
rs251162405 | in-del | -/GACT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168696 | CAAAACAACTAGAAA[-/GACT]GACTGGAAGGTAAAG | 66568 |
rs251338125 | snp | A/C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169144 | CCACCCACACTATTG[A/C/T]CACTGTTTTGTTTTT | 66568 |
rs251401063 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169427 | TCCCTGATTTGGCTA[-/C]CTCCACTGCTTTCCC | 66568 |
rs251402443 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158469 | GATACCCAGCTCATA[C/G]CTCGAAGCTCCCAGG | 66568 |
rs251457986 | snp | C/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155427 | TCATAAATTTTAATA[C/T]AAATAATTATGCTGC | 66568 |
rs251490033 | snp | C/T | | | intron-variant, downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121156070 | TTCCTGAAATGAGAA[C/T]GATTTTGCTTCAGAG | 66568 |
rs251574994 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167931 | ACTCCCAAAAGACCC[A/G]AGTCTTATTTGGCTC | 66568 |
rs251609926 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161861 | GTCTCCAGTGGGTGG[C/T]GCTGTTTTGGAAGGT | 66568 |
rs251637718 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164057 | CATTTCTCCCTGAAG[C/T]ACCATTCTCAAGCAT | 66568 |
rs251713463 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157442 | GTTTCTTACTTTATC[C/T]ATACCAGAACCCAGC | 66568 |
rs251770665 | in-del | -/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121167572 | TTGCTCTCCCTTGCG[-/T]GTACAGCAATAACTG | 66568 |
rs251978656 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161738 | CCTCATGGTGACGAA[A/G]ACCCTTGGTGTACAG | 66568 |
rs252127551 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167707 | GAAAGAAAAAGAAAA[C/T]TGTTCTGCTCGAAAG | 66568 |
rs252135368 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172600 | TGCAGCTCCCAAGAG[C/T]CCTTTGGCTCACTCG | 66568 |
rs252168920 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166764 | GTACATTGGAGATGT[A/G]CTGTTTTAAGCCACC | 66568 |
rs252288935 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173330 | GGAGCCTACTGTCAG[C/T]AAGGGGTCCATGGGA | 66568 |
rs252684044 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160465 | TATCACATGCTTCAA[A/G]TGTCTTTGTTCCTCC | 66568 |
rs252795516 | in-del | -/CC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165872 | ACTTGCAAAACCAAG[-/CC]CCCCCCCCCAACCTC | 66568 |
rs252805946 | snp | A/G | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155071 | AGAAACCCTGTCTCA[A/G]AAAAAAAAAAAAAAA | 66568 |
rs252830449 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170878 | CTCGGTAACTCCTAG[A/C]CCCTGAACGTCCTAT | 66568 |
rs252867822 | in-del | -/TTTT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163177 | CAAAGAGAAAGTAAG[-/TTTT]TTGGTTTTTTTTTTT | 66568 |
rs252914255 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166351 | CGGGGAACAGGTGGA[A/G]ATGTGGATTTTATCA | 66568 |
rs253619573 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173261 | ATGTGTGATATGAAC[A/G]AAATAACACGAACAG | 66568 |
rs253847068 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161938 | TGTGGAGTGGACCTT[C/T]AAGTTTATTGTCTGG | 66568 |
rs253879530 | snp | A/C | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162730 | TCTGTGTGGCCCTGG[A/C]TGTTCTGAACTCACT | 66568 |
rs253901874 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162429 | AAAGCACAGGTGGAC[A/G]TATGATAACAATGTG | 66568 |
rs253909743 | snp | A/T | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155388 | AAATATCCTTCTCAG[A/T]CACAAGAGTCCTTTT | 66568 |
rs254184898 | in-del | -/TTTTGTTTTG | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121164837 | AATAAGAAAAGGGGT[-/TTTTGTTTTG]TTTTGTTTTGTTTCC | 66568 |
rs254354729 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162156 | TCAGCCCACCCTATC[A/G]TGCAAACTTCCTGCA | 66568 |
rs254818891 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170222 | TTGGCAAGTAAGTCA[C/T]GATACAAGAACTCGG | 66568 |
rs254822244 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165229 | AAGAAAAAGCATTAA[A/G]GGCCAAGGATGAAGC | 66568 |
rs254867990 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158096 | GAGAGATAACTCGGC[A/G]GTTAAGAGCACTTCT | 66568 |
rs254961881 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170744 | GCTCAGCGAGGGTGA[A/G]AATAATTTGCATCAG | 66568 |
rs255024425 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157891 | CAACACTGAAGTGTC[A/G]GGATGCGCTTCTAAG | 66568 |
rs255062719 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159427 | GATTTACAGGTTAAT[-/C]CCCCCTGCCATAAAC | 66568 |
rs255105610 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164884 | TTATTTTATGTACAT[A/G]AATACATTATTGCTG | 66568 |
rs255290492 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158263 | AACTGTCATTTCATT[A/G]AGTGGCATAATTTTT | 66568 |
rs255301458 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165904 | ATAACACCCACACCC[A/T]CACCCTCACCCATAC | 66568 |
rs255385932 | in-del | -/TTT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161041 | TGTGAACATAAAGGG[-/TTT]TTTTTTAGGGGGTTT | 66568 |
rs255512391 | in-del | -/TG | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158447 | TGCTCTTCCGGAGGC[-/TG]TGTTTGATACCCAGC | 66568 |
rs255589844 | in-del | -/CT | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172092 | CATGTCCTCATGAGG[-/CT]GTCAGTGACCCTCGT | 66568 |
rs255642990 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163867 | TATAAACCACCACAA[A/G]AACCCAATGCTAATT | 66568 |
rs255682523 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156823 | AACACTCGGTACCTT[A/T]GTTAGCCGACTCCGC | 66568 |
rs255760962 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161604 | TATTTACGAGATACA[C/T]AGAAACATTACATTT | 66568 |
rs256326410 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171223 | TTTAAGTAAAACAAC[-/A]AAAAAAAATTAATAA | 66568 |
rs256349370 | in-del | -/AA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167665 | TTTTTTCCTAACAAC[-/AA]AAAAAAAAAAAAGAA | 66568 |
rs256393255 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168235 | AAGAAACCATATTCC[A/G]ACACGGCAGACGACA | 66568 |
rs256423978 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172334 | TGGTTCGGTTTGGTT[C/T]GGTTCAGGTGATATT | 66568 |
rs256452764 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158129 | TTCCCAATACCCAAA[-/T]GGCAGCTATCCAGTT | 66568 |
rs256496032 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159479 | AATGTACTTGCAATT[C/T]ACTCTCTTTATCACC | 66568 |
rs256554518 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166553 | GCACACTGTTGCTGT[C/T]TTCAGCCGCACCAGA | 66568 |
rs256638461 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159770 | TTCCGATCCACTCAC[A/G]TCAGTGTAACATGAA | 66568 |
rs256743222 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157526 | CTGCTGTCCTTCGAC[A/G]CTAAGATTACAGGTT | 66568 |
rs257173771 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167438 | ACCTGAACAGACCCT[A/G]TTGTGATGTCAAATG | 66568 |
rs257332554 | in-del | -/AAA | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121171972 | GGAAATGGAGAGAGT[-/AAA]AAAAAAAACCTAAAC | 66568 |
rs257335985 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163523 | CCCTTGTTCCCTCCC[A/G]TTTTCTCGTGCGGTC | 66568 |
rs257704151 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168760 | GTGGACTTTAGAGAG[A/G]TGAGTTCAGCCAAGA | 66568 |
rs257738725 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169336 | GCAAGCCTCTCCTTA[A/G]AACCCACGTGAAGAT | 66568 |
rs257881706 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164785 | TTTAGATGAATTAAT[A/G]ATTTCATAGAATTCC | 66568 |
rs257887659 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170380 | AATAAATCCTTTCAT[-/A]GGGGTCTTAAGGAAG | 66568 |
rs258121198 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155622 | TCACATATGAATTTC[A/G]ATTTGAACTCACTGT | 66568 |
rs258586794 | in-del | -/GACC | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163665 | AGAAAAGCTGCCCCT[-/GACC]CGGAAGTTGCAATTA | 66568 |
rs258610032 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168968 | TAGCTTCTAAACTGC[A/G]ACTCCATTTATAACA | 66568 |
rs258864013 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165444 | TGTGCTGTAATGTGA[C/T]GTGGTGTGGTGGCTT | 66568 |
rs259175801 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157155 | AGAGAATGTTATTTT[A/T]AAAATGCACTTCTCT | 66568 |
rs259184064 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164011 | AACTGCAACTTCTCC[C/T]CATAACTGCTTAAAC | 66568 |
rs259302921 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164994 | TCAGGACCTTTGGAA[A/G]AGGAGTCAGTGTTCT | 66568 |
rs259338345 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165505 | CAAATTTATGTGTCC[A/G]TTTGTTTATATAGGT | 66568 |
rs259339236 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157898 | GAAGTGTCAGGATGC[A/G]CTTCTAAGCGCCTGC | 66568 |
rs259370261 | in-del | -/CT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167143 | CCTAGATCTACCTGC[-/CT]CTGAGTCCCAAATGC | 66568 |
rs259479454 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158506 | AACCCCCTCCTCCAG[A/G]CTCTGTGAGCATCAG | 66568 |
rs259489045 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169812 | GGGTAGAAGCCACGA[A/G]GCCTGCTACACTTGG | 66568 |
rs259602716 | in-del | -/AACTTCT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160993 | ACACAGAGCTTCCTG[-/AACTTCT]AGTCTACGCCTGCAA | 66568 |
rs259722332 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168416 | TCGTTAGGATTTGTT[G/T]AGTGTGCACCAAGAA | 66568 |
rs259743237 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164556 | TGACTGACTTGCTCT[-/C]CCCTGCTAATATATA | 66568 |
rs259948395 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167727 | CTGCTCGAAAGTTAT[C/T]ATCTGCTTTGAGCTT | 66568 |
rs260010324 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121170888 | CTAGCCCCTGAACGT[-/T]CTATTCAGGCCTCCC | 66568 |
rs260211411 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172378 | ATAATGTGTCTATTA[C/T]CTCTCTGATCCCTGA | 66568 |
rs260346456 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167412 | TGCTATCTGCACAAG[A/G]CAACAAGAAGACCTG | 66568 |
rs260376417 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160932 | TGCTGTTCAGAAAAA[G/T]GAATAAGTAAGACAC | 66568 |
rs260431581 | in-del | -/CGCAGGCACACATGCACACA | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121155186 | GCAACTGTGCACGCT[-/CGCAGGCACACATGCACACA]CGCACGCACACTCAG | 66568 |
rs260479366 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157384 | TGCCTCAAAATCTGC[C/G]GTCCCTTGGTTAGGC | 66568 |
rs260480471 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161734 | GGGACCTCATGGTGA[C/T]GAAAACCCTTGGTGT | 66568 |
rs260490825 | snp | A/G | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172172 | CCTGGTTGGTCACTA[A/G]CCTCGGGATTACACA | 66568 |
rs260641801 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166638 | AACTGAACTCAGGAC[C/T]TTCAGAAGAGCAGTC | 66568 |
rs260857870 | in-del | -/TGC | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161233 | AAGCTGCTTCCCAAA[-/TGC]TGAAATTAATGGCAT | 66568 |
rs260895360 | in-del | -/GAGA | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161159 | AGGGGAGAGAGGGGG[-/GAGA]GAGAGAGAAAGAGAG | 66568 |
rs261082776 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156839 | GTTAGCCGACTCCGC[A/G]CAACTAGACTGCTAA | 66568 |
rs261103409 | in-del | -/G | | | upstream-variant-2KB | Rwdd3 | GRCm38.p3 | 3:121173286 | AACAGCGTGATTTCA[-/G]TTGTCAGCAGGATTA | 66568 |
rs261156768 | in-del | -/TC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169526 | GAACTTACTCTAACA[-/TC]TGAGTGGCCAGGATG | 66568 |
rs261252949 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155556 | CAAAAAAAATAAAAA[A/G]GGTTCACTTTGTTGG | 66568 |
rs261333871 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163760 | TCCTCCTACAGCAAA[C/T]CCTACCACCCCTAGG | 66568 |
rs261347303 | in-del | -/A | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121154904 | ATAAATAAACCTTTT[-/A]AAAAAAAATAAAAAG | 66568 |
rs261391433 | in-del | -/TTTT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162587 | TTTTTTGTTTGTTTG[-/TTTT]TTTGTTGTTTTGGTT | 66568 |
rs261431290 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160332 | TTTCAGACCCCATCC[A/G]GAATCAGAGGCAGTA | 66568 |
rs261583815 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165497 | CACCCATCCAAATTT[A/C]TGTGTCCGTTTGTTT | 66568 |
rs261586330 | snp | A/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168852 | TGAACAACAGTGTTA[A/T]TAAAACACAAAACCC | 66568 |
rs261845205 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121159840 | GCCTCCACTGACTCC[A/G]CAAGGGGCAGAGCAC | 66568 |
rs261944832 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164150 | TAGATGAGCCTGAGT[C/T]CTGATAGAAGTGTGT | 66568 |
rs262024822 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156996 | CGCCTGCAAAAGGGG[C/T]CTTCCGGCACACCAC | 66568 |
rs262272005 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121161596 | ATTAAATATATTTAC[G/T]AGATACACAGAAACA | 66568 |
rs262273541 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168551 | CACACACACACACAC[A/C]CACACTCTCCTCTCA | 66568 |
rs262354628 | in-del | -/TACACAGTGCCTTTACA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121156630 | TGTAGCAGGGGGAGT[-/TACACAGTGCCTTTACA]TAGGTGGCAGAACCC | 66568 |
rs262354909 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162827 | AGGCATGCACCACCA[C/T]ACCTGGCGGGGTAAT | 66568 |
rs262445543 | snp | A/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121157099 | AAATAAATAAATAAA[A/T]AAGATAAAATAACAG | 66568 |
rs262518559 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165562 | GAATACTTGTGGAGT[C/T]AATGGAGACAGACTC | 66568 |
rs262620079 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162158 | AGCCCACCCTATCAT[A/G]CAAACTTCCTGCAGA | 66568 |
rs262688230 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167588 | GTACAGCAATAACTG[A/G]CTCCCTTTGCTCCAG | 66568 |
rs262819999 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165862 | GCAACCTTTACACTT[A/G]CAAAACCAAGCCCCC | 66568 |
rs262920628 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158245 | AATAAGAAATAAAAA[-/C]AAAACTGTCATTTCA | 66568 |
rs262925949 | in-del | -/TC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166530 | CCCATCAAGCTAATG[-/TC]TATGTAAGCACACTG | 66568 |
rs263064121 | snp | G/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171470 | AGGGCGAGCTCAGGG[G/T]AGGGCACTGCAAGCG | 66568 |
rs263083016 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165581 | GGAGACAGACTCGGC[A/C]CAGCCCAAGTGTGGA | 66568 |
rs263278617 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169276 | GAGCTTGGTGGTGAT[A/G]TAATCTATGTGACCA | 66568 |
rs263491112 | snp | A/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168661 | ATTTTCACATGCTTT[A/C]ATCGTTCTTAGAGAA | 66568 |
rs263671773 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167978 | TACCTCTCCCAGAGA[C/T]GCAGGGTTTGTCTTC | 66568 |
rs263994089 | snp | G/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173178 | TTAATTTGATTATTT[G/T]TCATATTTGTTAAAT | 66568 |
rs264007664 | snp | G/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172576 | CCCCAAAATAAAAAT[G/T]TTTAATTCTGCAGCT | 66568 |
rs264148771 | snp | C/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157719 | ATGAGAGCTCGGGAA[C/G]CTGAAGATGAGGGCT | 66568 |
rs264347937 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157057 | GTCCTGATCCTAGTA[C/T]ACAATCTTATAAATA | 66568 |
rs264469645 | snp | A/G | | | downstream-variant-500B | Rwdd3 | Mm_Celera | 3:121154941 | ATAGCAGCCAGGTGG[A/G]GGTGGTGACACACAC | 66568 |
rs264586052 | in-del | -/T | | | utr-variant-3-prime | Rwdd3 | Mm_Celera | 3:121155539 | TGGTTTGTTTTTCCA[-/T]CCAAAAAAAATAAAA | 66568 |
rs264676087 | in-del | -/CACACACA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168536 | GCACTCAGAAGCCCC[-/CACACACA]ACACACACACACTCT | 66568 |
rs264715572 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121160830 | AGCAAGCCTGCATTC[C/T]CTCTCATTGAGGGGG | 66568 |
rs265125050 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163200 | TTTTTTTTTTTTTTT[C/T]CTTAATCCCTTCCTG | 66568 |
rs265286821 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121167822 | GATGTTACTTTTTGC[C/T]TGGTCCCCCGCGCCA | 66568 |
rs265354691 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121166430 | GATGATGGAGAAAGA[A/G]GAGTCTTAGTGATGG | 66568 |
rs265452622 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172186 | AGCCTCGGGATTACA[C/T]ACAAGGTCTAGATTC | 66568 |
rs265526545 | snp | A/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121164941 | CAGATTCCATTACAG[A/G]TGGTTGTGAACCACC | 66568 |
rs265612158 | snp | C/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163789 | GGTGGTTATTCTAAC[C/T]ATTATAACTTCCTGT | 66568 |
rs265760606 | snp | C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161302 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTCTCTGT | 66568 |
rs265895046 | in-del | -/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157310 | ACAAGGAACTGTTCT[-/G]CCACTTTCGTCGGCT | 66568 |
rs265927727 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173647 | CAGATCTCTGAAGCT[A/T]CGGCACCATAATCAT | 66568 |
rs386853017 | in-del | -/G | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162737 | GCCCTGGCTGTTCTG[-/G]AACTCACTATGTAGA | 66568 |
rs386922861 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121158627 | GAAAAAAAAAAAAAA[-/A]CAAAGTACCATTTAA | 66568 |
rs386998684 | in-del | -/C | | | intron-variant | Rwdd3 | Mm_Celera | 3:121165881 | ACCAAGCCCCCCCCC[-/C]AACCTCCATAACACC | 66568 |
rs387102284 | in-del | -/A | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121172992 | AGAAAGAAAAAAAAA[-/A]TAGTTCCTTTGAGTT | 66568 |
rs387123506 | in-del | -/CT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168642 | TACACACGGTGTCTC[-/CT]GATTTTCACATGCTT | 66568 |
rs387179837 | in-del | -/A | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158613 | TAAAGAATAGAGGAG[-/A]AAAAAAAAAAAAAAC | 66568 |
rs387206233 | in-del | -/ACATACAT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121162972 | CATACATACATACAT[-/ACATACAT]GTGTAGGTATACGTG | 66568 |
rs387291890 | in-del | -/CTG | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161235 | GCTGCTTCCCAAATG[-/CTG]AAATTAATGGCATGC | 66568 |
rs387420542 | in-del | -/T | | | intron-variant | Rwdd3 | Mm_Celera | 3:121169166 | TTTGTTTTTTTTTTT[-/T]CTCAGCATCATGGAT | 66568 |
rs387495256 | in-del | -/ACACACAC | | | intron-variant | Rwdd3 | Mm_Celera | 3:121168549 | CCACACACACACACA[-/ACACACAC]CTCCTCTCATACACA | 66568 |
rs387546037 | in-del | -/ATAAATAA | | | intron-variant | Rwdd3 | Mm_Celera | 3:121157094 | TAAATAAATAAATAA[-/ATAAATAA]GATAAAATAACAGGC | 66568 |
rs387567770 | in-del | -/CATATTTGT | | | upstream-variant-2KB | Rwdd3 | Mm_Celera | 3:121173180 | AATTTGATTATTTGT[-/CATATTTGT]TAAATGGTCCACACA | 66568 |
rs387576016 | in-del | -/GTGAAACTCTAAT | | | intron-variant | Rwdd3 | Mm_Celera | 3:121163562 | AGTGCACCCTGAGAT[-/GTGAAACTCTAAT]ATATGCAACACACAC | 66568 |
rs387724985 | in-del | -/TTTTG | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121164837 | AATAAGAAAAGGGGT[-/TTTTG]TTTTGTTTTGTTTTG | 66568 |
rs387768779 | in-del | -/CATAACTGCTTAAACTGCAACTTCTCCT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121163984 | ATTAACCGGCCTCCC[-/CATAACTGCTTAAACTGCAACTTCTCCT]CATAACTGCTTAAAC | 66568 |
rs387806380 | in-del | -/A | | | intron-variant | Rwdd3 | Mm_Celera | 3:121171231 | AAACAACAAAAAAAA[-/A]TTAATAATAAAGTCA | 66568 |
rs387821662 | in-del | -/TGTT | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162593 | GTTTGTTTGTTTGTT[-/TGTT]GTTTTGGTTTTGGGG | 66568 |
rs578547317 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158140 | CCAAAGGCAGCTATC[C/T]AGTTCCTAGGGAGCC | 66568 |
rs579157193 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121167576 | CTCTCCCTTGCGGTA[C/T]AGCAATAACTGGCTC | 66568 |
rs579344938 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | GRCm38.p3 | 3:121155811 | TTAAAGGCAAAAAAC[A/G]TAAACATGAGAAAGT | 66568 |
rs579518914 | snp | A/G | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121154984 | CACTTGGGAGGCACA[A/G]GCAGGTAGATCTATG | 66568 |
rs579590192 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161053 | AGGGTTTTTTAGGGG[G/T]TTTGTGTGTTTGTGT | 66568 |
rs580221806 | snp | C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170980 | AAAATTTAAAAGTGT[C/G]TGAGTGGAGCGTCTG | 66568 |
rs580430811 | snp | A/C | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121160982 | AGTCCAGGGTGGACA[A/C]AGAGCTTCCTGAGTC | 66568 |
rs580574896 | snp | C/G | | | upstream-variant-2KB | Rwdd3 | GRCm38.p3 | 3:121172282 | GTCCAAAGCCAAAAA[C/G]TAGCTTTACAGTGAT | 66568 |
rs580742283 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121162740 | CCTGGCTGTTCTGAA[C/T]TCACTATGTAGACCA | 66568 |
rs580927823 | snp | C/G | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155014 | GAGTTCGAGGCCAGG[C/G]TGGTCTACAGAGTGA | 66568 |
rs581144255 | snp | C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161223 | TATACAGACCAAGCT[C/G]CTTCCCAAATGCTGA | 66568 |
rs581337737 | snp | A/G | | | utr-variant-3-prime | Rwdd3 | GRCm38.p3 | 3:121155794 | TGGGGAGGAAGGCAC[A/G]ATTAAAGGCAAAAAA | 66568 |
rs581678193 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161403 | GTGTGTGTGTGGCAG[A/G]GGGGAGAGGGTGGAA | 66568 |
rs581962100 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170162 | CAAACCACCACCATT[G/T]TTTTAAAATGTCATA | 66568 |
rs582053012 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158141 | CAAAGGCAGCTATCC[A/G]GTTCCTAGGGAGCCA | 66568 |
rs582368038 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121166516 | AGCAAAAGCATCAAT[C/T]CCATCAAGCTAATGT | 66568 |
rs582532916 | snp | A/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121160406 | GTATATAGTATTTTT[A/T]AAAAAACTTCTCTAA | 66568 |
rs583086556 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161067 | GGTTTGTGTGTTTGT[A/G]TTTGTGTGTGTGTGT | 66568 |
rs583095576 | snp | C/T | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121154995 | CACAAGCAGGTAGAT[C/T]TATGAGTTCGAGGCC | 66568 |
rs583519534 | snp | A/G | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155041 | GTGAGTTCCAGGACA[A/G]CCAGAGCTACACAGA | 66568 |
rs583665136 | snp | C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161324 | TGTCTCTGTGTGTCT[C/G]TGTGTGTCTCTGTGT | 66568 |
rs583903864 | snp | A/C | | | synonymous-codon, intron-variant | Rwdd3 | GRCm38.p3 | 3:121171412 | ACGAGGAGGGCACTG[A/C]GCACCGTCTAGTTGC | 66568 |
rs584183599 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161001 | GCTTCCTGAGTCTAC[A/G]CCTGCAAAGTCTTCT | 66568 |
rs584204680 | snp | C/T | | | upstream-variant-2KB | Rwdd3 | GRCm38.p3 | 3:121172329 | TGATTTGGTTCGGTT[C/T]GGTTCGGTTCAGGTG | 66568 |
rs584291814 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121157318 | ACTGTTCTCCACTTT[C/T]GTCGGCTAGCATGTT | 66568 |
rs584930122 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121167567 | TCAGATTTGCTCTCC[C/T]TTGCGGTACAGCAAT | 66568 |
rs585111917 | snp | C/T | | | utr-variant-3-prime | Rwdd3 | GRCm38.p3 | 3:121155810 | ATTAAAGGCAAAAAA[C/T]ATAAACATGAGAAAG | 66568 |
rs585224462 | snp | A/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170367 | GGCAAATCCCTACAA[A/T]AAATCCTTTCATAGG | 66568 |
rs585560766 | snp | G/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161051 | AAAGGGTTTTTTAGG[G/T]GGTTTGTGTGTTTGT | 66568 |
rs585738950 | snp | A/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121158238 | TTTAAGAAAATAAGA[A/G]ATAAAAAAAAACTGT | 66568 |
rs586247088 | snp | A/C | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121160411 | TAGTATTTTTAAAAA[A/C]ACTTCTCTAAATATT | 66568 |
rs586473530 | snp | C/G | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121154982 | AGCACTTGGGAGGCA[C/G]AAGCAGGTAGATCTA | 66568 |
rs586695054 | snp | G/T | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121155183 | GGGGCAACTGTGCAC[G/T]CTCGCAGGCACACAT | 66568 |
rs586870518 | snp | A/C | | | downstream-variant-500B | Rwdd3 | GRCm38.p3 | 3:121154997 | CAAGCAGGTAGATCT[A/C]TGAGTTCGAGGCCAG | 66568 |
rs587205536 | snp | C/T | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121170977 | AAAAAAATTTAAAAG[C/T]GTGTGAGTGGAGCGT | 66568 |
rs587291993 | snp | C/G | | | intron-variant | Rwdd3 | GRCm38.p3 | 3:121161366 | TGTGTCTCTGTGTGT[C/G]TGTGTGTGTCTCTGT | 66568 |
rs587495579 | snp | A/T | | | upstream-variant-2KB | Rwdd3 | GRCm38.p3 | 3:121172090 | TTCCATGTCCTCATG[A/T]GGGTCAGTGACCCTC | 66568 |