SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6201838 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907387 | CTCCCCCTCCCATCT[C/T]AGTTCTCCAAATCCG | 73998 |
rs6202344 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907481 | GGTACATTTCCAAGC[C/T]TGACTGCGTCTTAAA | 73998 |
rs6215207 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907569 | ACAGTGCGTGCCTGT[A/G]TCTGCGCAGACCATC | 73998 |
rs6215336 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907645 | CTCGTGGCAAATTGT[G/T]NCGGGAGGGACCTTG | 73998 |
rs6215337 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907646 | TCGTGGCAAATTGTN[A/C]CGGGAGGGACCTTGG | 73998 |
rs6215876 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907728 | AGTAGGTTTCACACA[A/G]TTGCCTCTGAAAAGA | 73998 |
rs6216349 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907770 | GGTGAACAGAAGAAA[A/T]GCAAAGCCCTAGAAG | 73998 |
rs6216389 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907788 | AAAGCCCTAGAAGTG[G/T]CCAACCGTGTGACAT | 73998 |
rs6216912 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nap1l5, Herc3 | Mm_Celera | 6:58907857 | AATTCAGTTTTTGGG[G/T]GGAGGCACACTGCTT | 73998 |
rs6238470 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Herc3 | Mm_Celera | 6:58909482 | taatttcagactata[C/T]tgaataaaaactggg | 73998 |
rs6238544 | snp | A/G | 0.5 | 0 | intron-variant | Herc3 | Mm_Celera | 6:58909524 | CCCTTTTCCATGCCC[A/G]ATTATTGGATAAATG | 73998 |
rs6252515 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Herc3 | Mm_Celera | 6:58849691 | AGGGATCCTTTACTG[A/G]CTCCATGTTATTGAA | 73998 |
rs6342324 | snp | A/G | 0.5 | 0 | intron-variant | Herc3 | Mm_Celera | 6:58849448 | CAATTCATACACTCT[A/G]NATTCCATTTAAGCA | 73998 |
rs6342336 | snp | A/T | 0.5 | 0 | intron-variant | Herc3 | Mm_Celera | 6:58849449 | AATTCATACACTCTN[A/T]ATTCCATTTAAGCAC | 73998 |
rs6355059 | snp | A/T | 0.5 | 0 | intron-variant | Herc3 | Mm_Celera | 6:58894740 | GGGGAGGGCAATAGA[A/T]CAAGAACTTGAAGAT | 73998 |
rs6356499 | snp | A/T | 0.5 | 0 | intron-variant | Herc3 | Mm_Celera | 6:58894989 | TATTTGAATTAAAAA[A/T]ATAAATGACCAGCAT | 73998 |
rs13469407 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Herc3 | Mm_Celera | 6:58919095 | TAGTGAATAGTCTTT[C/T]TGAAAAAATCAGTGG | 73998 |
rs13478779 | snp | C/T | 0.21875 | 0.248039 | synonymous-codon, nc-transcript-variant | Herc3 | Mm_Celera | 6:58843788 | GTTCCTGCTGGAGGA[C/T]GGGGAGGTTTACACG | 73998 |
rs30340074 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847180 | ACTTTGTGATAAGCC[A/G]GACTCCTAGGGAAAT | 73998 |
rs30340075 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58847191 | AGCCAGACTCCTAGG[A/G]AAATGAAGAGAGTCC | 73998 |
rs30340076 | snp | A/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58847246 | TAGTATGTTAATTAT[A/T]AACTTCACAGCAACT | 73998 |
rs30340078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847301 | AGATGTGTAGGTGGG[C/T]GCCTCCCTCTAATGC | 73998 |
rs30340080 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58847361 | GCTACCATTGGATTT[A/C]TTTTTAATGATTGGA | 73998 |
rs30340081 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58847384 | TGATTGGAAGAAAGA[A/G]ACTGAGCTTTCATGC | 73998 |
rs30340082 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58847412 | TGCTCCGTGTGCTTG[C/T]TGGGAATCCTTACCG | 73998 |
rs30340524 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58857344 | GGATCAATGGGCAGG[A/G]ATCTGTTGGAAGGTA | 73998 |
rs30340526 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Herc3 | Mm_Celera | 6:58857699 | ATTTATCTTAGACCG[A/G]GAGTCTCCATGCCAC | 73998 |
rs30340528 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Herc3 | Mm_Celera | 6:58857838 | GAGATGGGCAATTTC[A/C]TATGTCGCAGAGTAG | 73998 |
rs30340529 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Herc3 | Mm_Celera | 6:58857944 | TAGAGTGAAGACTGT[A/T]TTTTAAAAACATGTC | 73998 |
rs30340530 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58858709 | CTACATCACCTCGCT[G/T]TTACATACTCTTAAA | 73998 |
rs30340532 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58858745 | CAATGGCAACCACTC[A/C]TTTAAGCAGTGCGGA | 73998 |
rs30341054 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58847558 | GGCAGACGGGCTCTA[C/T]TGGAGAGACCTTGCT | 73998 |
rs30341056 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847675 | AGGTTGAGATCTCAG[C/T]TCATATCATACACAC | 73998 |
rs30341058 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847751 | TGATGTACCACAAGG[A/C]GTTGAGGTCATGAGG | 73998 |
rs30341060 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847849 | CTGGCTGCAGGGAAT[G/T]TGAGACTGGACTGTT | 73998 |
rs30341061 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58847894 | TCATTACACTCATGT[C/T]GCCTACAGCACTGTG | 73998 |
rs30341063 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Herc3 | Mm_Celera | 6:58848078 | GCCTCCAGTCTGACT[A/C]GCTAGCTGTCAGGTT | 73998 |
rs30341564 | snp | A/T | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Herc3 | Mm_Celera | 6:58875302 | TTTTATCAGACTTTT[A/T]AATTTTTGGCATTTT | 73998 |
rs30341566 | snp | C/T | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Herc3 | Mm_Celera | 6:58875344 | ATTTCCTAGGCCAGA[C/T]AGCACAAAACAGAAC | 73998 |
rs30341568 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Herc3 | GRCm38.p3 | 6:58875354 | CCAGATAGCACAAAA[A/C/T]AGAACGGGATTATTC | 73998 |
rs30341570 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Herc3 | Mm_Celera | 6:58875800 | ATGAAGATACAGTGA[C/T]ATAATCCTGCTTGAA | 73998 |
rs30341572 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58875965 | TCAGTCTTGAAAGGT[C/T]GAGGGTACACAAATA | 73998 |
rs30341584 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58868785 | TGAGTTTGTCTGCCT[A/C]CATTTTTGCTTTTTC | 73998 |
rs30341586 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58868898 | ATTTACAGAATCATT[C/T]TTGTATATTTATTTG | 73998 |
rs30341588 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58868996 | CGGACGTATTATGGC[A/C]AGATCTGTGACACCC | 73998 |
rs30341590 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58869112 | TTCAAGGGATCTTGA[A/C]TATTAACAGCCTCTT | 73998 |
rs30341592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58869173 | AGGTTTGCCATTCAG[C/T]GTGATTAGTTGAAGT | 73998 |
rs30341614 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58858756 | ACTCATTTAAGCAGT[A/G]CGGACCCATTCCCTA | 73998 |
rs30341616 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58858879 | AGACCCGTGAGATGG[A/G]ATTTTATGAGTAAGT | 73998 |
rs30341618 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc3 | Mm_Celera | 6:58859358 | CTTTAGGAAGTCTCA[A/G]CTGCACGGTCACCTG | 73998 |
rs30341620 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc3 | Mm_Celera | 6:58859580 | TCACAGATTTTCACT[C/T]GATCTGTAGGCACAT | 73998 |
rs30341622 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58860223 | CATCGCCAGAAGGAA[A/T]TCTGCCAATGAGTTC | 73998 |
rs30341623 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc3 | Mm_Celera | 6:58861231 | CATCCTGAAATCATA[C/T]ATCCAGGGGTAGAAT | 73998 |
rs30341873 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58840376 | AACATTCAGCAGTTC[A/G]TTGTAGGTTCCTGGC | 73998 |
rs30341915 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58848215 | GGGGCTGCATGTTTT[A/C]CTCAGACTGCCATTT | 73998 |
rs30341917 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58848569 | TTCAAGCTGCAAGAC[A/G]GGTTTATTTCAAGAA | 73998 |
rs30341919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58848752 | GAAGCTTTTACCTAA[C/T]AACTTATTAAACCTC | 73998 |
rs30341920 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc3 | Mm_Celera | 6:58848818 | CTCTTCAGTATTCCG[C/T]CTTTTCTTTCCTTTC | 73998 |
rs30341922 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58848893 | TGGTAGTTCTGCTGA[G/T]TAGATGATGGTAGGA | 73998 |
rs30341923 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58849079 | CTGTTGCTTATATCC[C/T]GTTATCAGCATCTCA | 73998 |
rs30342074 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58888329 | AGCCATTCTGGACAA[C/T]GTGGATAGATTTTTG | 73998 |
rs30342076 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58888410 | ACACTCGCTTCTCCT[A/G]TGTGTGACTCCTGTT | 73998 |
rs30342078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58888523 | TTCTGAGTTTTATAA[C/T]ACACAGCCACTGTTT | 73998 |
rs30342080 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58888543 | AGCCACTGTTTTCAG[C/T]TACTCAGACAGGCCT | 73998 |
rs30342082 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Herc3 | GRCm38.p3 | 6:58888570 | GCCTCCTGCTTTGTC[A/G/T]CATAGTTGAGTCTTT | 73998 |
rs30342124 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Herc3 | Mm_Celera | 6:58883603 | AGAGTTCAAGAAGCC[A/G]GAGTTCAGAGGCCAT | 73998 |
rs30342126 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Herc3 | Mm_Celera | 6:58883643 | AGCTGCTCCCAGGGC[C/T]GCTGAGTCCAGAGGG | 73998 |
rs30342128 | snp | G/T | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | Herc3 | Mm_Celera | 6:58883726 | GCATCGAGTTTATCT[G/T]CAGGGCTATAGATTC | 73998 |
rs30342130 | snp | A/C | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Herc3 | Mm_Celera | 6:58883882 | CCTGGTGTCTGCTGC[A/C]TGTCAGTCAGTCCCT | 73998 |
rs30342132 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Herc3 | Mm_Celera | 6:58884043 | CTACATATGGGTTTA[A/G]TTCCACCATGTGCTT | 73998 |
rs30342314 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58869381 | AACAAATGCACAGTG[A/G]GCCTTGCTTTATGAT | 73998 |
rs30342316 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58869423 | TAGAGCAAATGCCCA[G/T]GTCTTACCCTGAAGC | 73998 |
rs30342318 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58869540 | CAGCGGGTGACCTAG[A/C]TGCATGGGCTTTACC | 73998 |
rs30342320 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Herc3 | Mm_Celera | 6:58869582 | TTTTTTATTAACAGC[A/G]GAAGCTCGAGGAATC | 73998 |
rs30342321 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58869902 | TGGTGGTGAGAGAGT[A/G]CCCAAGCTTTTTATG | 73998 |
rs30342323 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58870059 | TGCACTGATGACCCA[A/G]TAGAGTCTGGCTAGG | 73998 |
rs30342364 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58898430 | GTTCACTTTGCATGG[C/T]ATCCTATAACACACA | 73998 |
rs30342366 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58899213 | TAATTTTGGTCACTG[A/C]GTTATAACAGATGGA | 73998 |
rs30342367 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58899873 | AGGTCACAGAGTGAT[A/G]AGACGACTTATGAGT | 73998 |
rs30342369 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58900149 | AACCCAGGTCAGGAC[A/G]GGCAGTTTGCAGTGT | 73998 |
rs30342371 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58900234 | AAATTATTTCCCTCA[C/G]GCTTTCCTTATTTAG | 73998 |
rs30342373 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Herc3 | Mm_Celera | 6:58900847 | CTTGCCAGCAATTCT[A/C]GCCCTTGGGAGCAAA | 73998 |
rs30342474 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58876011 | CATTCTGCATCCCGC[C/T]GGAGGATGTGTCTGG | 73998 |
rs30342476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58876435 | GAAGACAACCTAAGA[A/G]CACTTGTCCAGGGTT | 73998 |
rs30342478 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Herc3 | Mm_Celera | 6:58876529 | CAAATATTTCATGAA[A/G]CTGGTAACCCTGTAT | 73998 |
rs30342480 | snp | G/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | Herc3 | Mm_Celera | 6:58876824 | TATCCCTGAGATTTC[G/T]AGTCTTGTGGACATT | 73998 |
rs30342481 | snp | A/G | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Herc3 | Mm_Celera | 6:58876983 | TACACCTTGCCTTTG[A/G]CTTGAATGCTGCTAA | 73998 |
rs30342482 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Herc3 | Mm_Celera | 6:58877003 | AATGCTGCTAACACA[C/T]CTATCTATTTCACTC | 73998 |
rs30342774 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc3 | Mm_Celera | 6:58861667 | CCAAAGCAAAGAATA[A/G]CTTGGCGTCTTCTTT | 73998 |
rs30342775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58861975 | ATGTTTGACAAAATA[C/T]GGTGCAAATAGGAAA | 73998 |
rs30342776 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58862260 | AGGGGTATTGGAAGA[A/G]GTAATCATTCATATG | 73998 |
rs30342777 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc3 | Mm_Celera | 6:58862588 | CAACGCCGTACTGGG[A/G]AAAGAGGTCCTCATA | 73998 |
rs30342779 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58862866 | GGGCCTCTTTTCTGC[A/G]CACAATTAAAACAGA | 73998 |
rs30342781 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc3 | Mm_Celera | 6:58863102 | GACAATCATTGTTTT[G/T]TTTTTTTAATACCTA | 73998 |
rs30342782 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc3 | Mm_Celera | 6:58863187 | AATCAAACTAAACAA[C/T]GTTATCTCCGTTGAA | 73998 |
rs30342894 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58840390 | CGTTGTAGGTTCCTG[A/G]CTGGAGAGTTCAAGT | 73998 |
rs30342895 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc3 | Mm_Celera | 6:58840451 | CCAGCCACAGTGTGA[A/G]TCTGGTCCTGTGATT | 73998 |
rs30342896 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc3 | Mm_Celera | 6:58840588 | AAATCTTACAGAAGA[C/T]TAAACAGACCAATAC | 73998 |
rs30342898 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58840681 | AATTATTAATATTAT[C/T]AGTCAGGAGTTTATT | 73998 |
rs30342900 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc3 | Mm_Celera | 6:58840853 | AATACCACATTTGTG[A/C]CCCATGGAAAACTTA | 73998 |