SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3710867 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Eml6 | GRCm38.p3 | 11:30010484 | TCTTTTCTATATGTC[A/G]AGAATGGCCCACCTT | 237711 |
rs3711503 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:30010584 | TAAAGGGAAGATCCT[C/T]TGAAACATAGTCTCA | 237711 |
rs3720479 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866027 | AATCTATAATGAAAA[A/G]GAGCAAGCTGAGCAA | 237711 |
rs3720970 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866057 | AGTAAAACATTTTTT[A/T]AAAAAAGTACAATTT | 237711 |
rs3722277 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866307 | ATTAGAGGCCAGCTT[A/G]GTCTACAGAGAAAGT | 237711 |
rs3722907 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866427 | CTCATCAAGTAGCAG[A/G]ATTTGGCAGCTTCAG | 237711 |
rs3723433 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770526 | GCAGTCTGTTTTAGG[C/T]TGCCATGACACTGTT | 237711 |
rs3724126 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770647 | AGAAACAATTCACAG[C/T]GTAAAATTTATTCCT | 237711 |
rs3724130 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770650 | AACAATTCACAGTGT[A/G]AAATTTATTCCTCAG | 237711 |
rs6162931 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882764 | CATTTTAAAGTATGT[A/G]CATATATTTTACAAA | 237711 |
rs6162996 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882804 | AGGCTGGTTGGTGGA[A/G]TTGGTTAGAGCATAG | 237711 |
rs6163412 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882846 | ATAATTCCTTTTTAA[C/T]CAAAATATTATAGTT | 237711 |
rs6165034 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29883184 | GGAGCACAGGTTCAG[A/T]CAGATTCTGCTACTC | 237711 |
rs6286383 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29862743 | TGCCACCCCCTTCTT[C/T]CCTTGATGGGCAGCT | 237711 |
rs6286818 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29862798 | TTTATTATCTTAATG[A/T]GCTAGCATTGTGAAC | 237711 |
rs6286875 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29862833 | AGAAAGCAGAGTGGT[A/G]GATTAGCACAGAAAA | 237711 |
rs6287858 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29862952 | CACATGGCAAAGAGC[A/G]CAGGGCACCCTTCCC | 237711 |
rs6288438 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29863078 | CATGGGCAGTGGTAG[A/G]TGGGTTGAACACTAA | 237711 |
rs6288475 | snp | A/G/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29863097 | GTTGAACACTAAGAC[A/G/T]GAAAAACATTGCCTC | 237711 |
rs6310062 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801709 | AAGATTCTGAACTTT[A/G]TACATGCATTATCAA | 237711 |
rs6310518 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801756 | AGACTGTAGACATTG[G/T]TTTTACACGTGGCTG | 237711 |
rs6310524 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801764 | GACATTGTTTTTACA[C/T]GTGGCTGGGATATTT | 237711 |
rs6311079 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801866 | CATAACCACCTCCTC[C/T]TGAGTGTGGCATGAC | 237711 |
rs6339303 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872102 | tggggaatcactgga[A/G]ggttttgaaaaaaga | 237711 |
rs6339752 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872154 | ACACAAAACAATTTT[G/T]AAAGCTGCTGGACAC | 237711 |
rs6339814 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872200 | TGTTGAAATCCATGT[A/G]CTCCATGATGCTCCA | 237711 |
rs6340315 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872249 | AAACCTTGTGTCCCG[C/T]AGAGCCCAGCCCCAG | 237711 |
rs6340901 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872402 | TCTAGTCCTTTGGCA[C/T]ACATCTCAACAGATG | 237711 |
rs6341293 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872447 | ATTGAATGGGAAAAT[A/G]ATAGATCTTGCATTG | 237711 |
rs6341435 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872535 | TTGGTTGACACTTTT[A/T]AAGAAATTNTTTTTA | 237711 |
rs6341800 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872544 | ACTTTTNAAGAAATT[A/G]TTTTTACCTTTTCTT | 237711 |
rs6341954 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872631 | CAATTTGCTTTAAAA[A/T]GTTGGANGCAACATA | 237711 |
rs6341967 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872638 | CTTTAAAANGTTGGA[C/T]GCAACATATGCTGTT | 237711 |
rs6352018 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29855853 | ATACCAGTCCAGGCT[A/G]CTATAACCAGCAAAA | 237711 |
rs6363833 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29765278 | CTTAGTTTAGAGTGT[A/G]CTGGGGAGGGACTCA | 237711 |
rs6366634 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805253 | GAAAGGAACAAGGGG[A/G]TTGATTTATTACCCT | 237711 |
rs6366665 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29805272 | ATTTATTACCCTAGA[A/G]AGCTGAAGCTTCCCA | 237711 |
rs6367196 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805354 | GTCAAAGTAACAAAA[A/C]CAGCAAGGGCATCAT | 237711 |
rs6367302 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805408 | GTATCTATGACATTC[C/G]TACTTGCTGTCAAAT | 237711 |
rs6380698 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805558 | TCCTCACTCTTGGCA[A/T]CATAGAGTCTAACAG | 237711 |
rs6380736 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29805580 | GTCTAACAGAGACTT[A/T]TCCATTAAATAGTCC | 237711 |
rs13480936 | snp | C/T | 0.497041 | 0.0383476 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29749331 | TTTGCAGTAGCCGAT[C/T]CGGTTCAGACTTGTG | 237711 |
rs26821535 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30027006 | GACACTACTAAACAT[C/T]AAAACATGGCTTAGA | 237711 |
rs26821536 | snp | A/T | 0.18 | 0.24 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026496 | TCCCCTATTATTCCA[A/T]AGGATTCTGATTTAT | 237711 |
rs26821537 | snp | A/C | 0.48 | 0.0979796 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026459 | TTGCAGCACTTGACT[A/C]ACGCTGTTTCCTACT | 237711 |
rs26821538 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026397 | TTTCCTCAGGACTTT[C/T]ACTTGCGCCAGTCCC | 237711 |
rs26821539 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026322 | CATGGTGACCCAGGC[C/T]AGCGGCATGCGCGTC | 237711 |
rs26821540 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026191 | TGAGGCGAGCGCCTC[G/T]AGTGTACTACAAGTC | 237711 |
rs26821541 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026090 | GTTCGGAAACGCAGA[C/T]GCCTCCTAGGGCCGA | 237711 |
rs26821542 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026072 | CGCGGCGAAATTGCG[C/G]CGGTTCGGAAACGCA | 237711 |
rs26821543 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:30025519 | TCATAATTTTTTTTT[C/T]TCTGAATCGGAGGAA | 237711 |
rs26821544 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:30025422 | TCCAAACCCTCTATG[A/C]GCCTTCTCTTCACAG | 237711 |
rs26821545 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:30025265 | CCACCTTAATTATAG[A/G]AAATACTCCCTAAAC | 237711 |
rs26821546 | snp | A/G | 0.408163 | 0.193609 | utr-variant-5-prime | Eml6 | GRCm38.p3 | 11:30024999 | GCTTCGCAGCAGGCG[A/G]TGGGATTTATTCTGT | 237711 |
rs26821547 | snp | A/G | 0.459184 | 0.136902 | utr-variant-5-prime | Eml6 | Mm_Celera | 11:30024851 | GGTACCAGTACCCGC[A/G]CACACGCCTCACTGC | 237711 |
rs26821548 | snp | A/G | 0.408163 | 0.193609 | utr-variant-5-prime | Eml6 | Mm_Celera | 11:30024593 | ATAAGCCGACACCGC[A/G]CGACCCCCGGGTGCC | 237711 |
rs26821549 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:30023894 | TGCCTTAGGTCCAAC[A/G]CATATGGGATGAAGA | 237711 |
rs26821550 | snp | G/T | 0.375 | 0.216506 | intron-variant | Eml6 | GRCm38.p3 | 11:30013270 | TCTTCTGACGTCTCT[G/T]TAACTTGTTTTAATC | 237711 |
rs26821551 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011986 | CAGTTTCTCCAAATG[C/T]AAATGGCTCCTTTCT | 237711 |
rs26821552 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30011952 | AAATCTATTGTCTTG[A/G]CTGCAGCTTGCTCTA | 237711 |
rs26821553 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011875 | GACTCAATAGACTCA[C/T]CTCCAGCAACAGAGC | 237711 |
rs26821554 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30011785 | ACAACAAAACAACCA[A/G]TGGGGAATAGGAAGA | 237711 |
rs26821555 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011219 | CCAAGCTACAAACAA[A/G]ATGACTCAACCCTCA | 237711 |
rs26821556 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30010386 | CCATAACATACCACT[C/T]GTCTTTTGAATTTAA | 237711 |
rs26821557 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30010363 | TCCTCTTCTGGGGAC[A/T]GAAAACTCCATAACA | 237711 |
rs26821558 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Eml6 | Mm_Celera | 11:30010282 | CATCGGCAGAGTACA[A/C]AGAGGCATGTCAAGC | 237711 |
rs26821559 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30010170 | TGCACTGTGGTCTCA[C/T]GCCTGGAGAAAGGAA | 237711 |
rs26821560 | snp | A/G/T | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30010120 | AAGAAGTCAATGAAC[A/G/T]CAATATAATACAATG | 237711 |
rs26821561 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30010017 | AGAGGAAGAAATCAA[A/G]GGGCAAATAAAAATA | 237711 |
rs26821562 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008630 | TCCCTGCCTGTCAAA[C/T]AGTCCTTCATCCTTC | 237711 |
rs26821563 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:30008492 | ATCCCCAACCCCACT[C/T]TCTTTCAGCTTCATG | 237711 |
rs26821564 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:30008339 | TTTAATATCAGAGGA[A/G]TAAGTAAATTAGAGG | 237711 |
rs26821565 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008229 | ATCCCCATGGACAAT[A/G]CTATTCTCTCTCTTT | 237711 |
rs26821566 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008166 | TTTAACTGAGGCCCA[A/G]AACAGTCACAGGCTT | 237711 |
rs26821567 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:30008115 | CCAAAAACCTCAGTA[A/G]GAACTTTAGAAAGTC | 237711 |
rs26821568 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008020 | ACTGGAGCAATTTCA[C/T]AGGAATCCCTGTGGC | 237711 |
rs26821569 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007411 | ATGCCCCTGATTTAT[A/G]TCCTACCATCGTGAA | 237711 |
rs26821570 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:30007322 | GCTGGTTTTCCAGGC[G/T]TTCTTTATCCTCCTC | 237711 |
rs26821571 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007221 | AACCTTTAAAAGCCA[G/T]ATGCAAGTACAAGCC | 237711 |
rs26821572 | snp | A/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:30007213 | TATAATGGAACCTTT[A/T]AAAGCCATATGCAAG | 237711 |
rs26821573 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | GRCm38.p3 | 11:30007135 | AGCATGCAACCCACC[A/G]GAGCATAAGCAGCAT | 237711 |
rs26821574 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007087 | GGCTGTGGATGGAAG[C/T]CATTAAGCCTAGATC | 237711 |
rs26821575 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007056 | CTTCTCTTATTTTCC[A/G]GGAGAGGAACAAGTT | 237711 |
rs26821576 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:30007030 | TCACAGAGAAGCAAT[A/G]TCTGTCACAGCTTCT | 237711 |
rs26821577 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:30006988 | GACTGTATTCTATCA[C/T]GCAGCACAGCAGACC | 237711 |
rs26821578 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006930 | TGACTTAGGAAATCA[C/T]TGTGAGCAGGCCAAG | 237711 |
rs26821579 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:30006601 | TTTTCTCCTATAGAT[G/T]ACACAGTTTGTACAA | 237711 |
rs26821580 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006458 | AAGCTGTAGGTCAGG[A/G]CAAGATGGTCTATAC | 237711 |
rs26821581 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006352 | TAGGTTTTAAGCAGG[A/G]ACTAAGACTGAAACG | 237711 |
rs26821582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:30003622 | GAACTTGCAGCTTGT[C/T]AGTTTTGAGTCTAAG | 237711 |
rs26821583 | snp | A/C | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:30003502 | GGTTTTTCTTTGAGC[A/C]TGTCCTAAGCACTGA | 237711 |
rs26821584 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:30003374 | TTGCACATGTCCAGT[G/T]CTTGTGACTGGCATG | 237711 |
rs26821585 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29996500 | GTATTCATTCCCACA[C/T]TATCAAATTGAGCTG | 237711 |
rs26821586 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29996468 | TCATACCCGGAGCCA[A/G]CCAGGATTGCTGATT | 237711 |
rs26821587 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:29996224 | CCTTATCTTGAGTGG[C/T]TCAGTGAAAGTGGCA | 237711 |
rs26821588 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml6 | Mm_Celera | 11:29996175 | CCAGGAACTAAAACA[A/G]TCAAAATCATCAAGT | 237711 |
rs26821589 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29996026 | AGATGGTCCCATGAT[A/G]ACAACAGGAGCCAGA | 237711 |
rs26821590 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29995491 | TGCGCACAGCACTCT[A/C]CAGAAAGATCGGAAC | 237711 |
rs26821591 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29995458 | TCTGCTATGGGCATC[C/T]AGGCTGTCCTCTCCA | 237711 |
rs26821592 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29995268 | TCCTGGTTTCATCTG[C/T]TAACTGAGCTCCTTT | 237711 |