SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3660661 | snp | A/T | 0.5 | 0 | intron-variant | Cnot4 | GRCm38.p3 | 6:35054829 | agaaagagagaaaga[A/T]agaCTGATTGCATCT | 53621 |
rs3706355 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Cnot4 | GRCm38.p3 | 6:35109923 | CTAAATTTTAGTCTA[A/G]TTGGAAAGTTAATAT | 53621 |
rs4137979 | snp | A/G | 0.5 | 0 | intron-variant | Cnot4 | GRCm38.p3 | 6:35054821 | agaaagaaagaaaga[A/G]agaaagatagaCTGA | 53621 |
rs6175453 | snp | C/T | 0.5 | 0 | intron-variant | Cnot4 | Mm_Celera | 6:35122361 | ggctgcaaagatggt[C/T]aggtggctaagagga | 53621 |
rs6189994 | snp | C/T | 0.5 | 0 | intron-variant | Cnot4 | Mm_Celera | 6:35122787 | ccagcctggactata[C/T]agcaagaacctgtca | 53621 |
rs6263991 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Cnot4, Gm33046 | Mm_Celera | 6:35132615 | AGCAAAACATTCCTT[C/T]CCCGAGTAGCCCGAA | 53621 |
rs6264080 | snp | C/T | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Cnot4, Gm33046 | Mm_Celera | 6:35132673 | GTCTCCCACTCACTT[C/T]ATTCACTTCCTAACT | 53621 |
rs6301039 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Cnot4 | GRCm38.p3 | 6:35062681 | AAAACACTATCAATT[C/T]TTTGGAAGCTACAAC | 53621 |
rs6309274 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Cnot4 | Mm_Celera | 6:35115040 | TGTAGAGTCAGCCAA[A/G]TGGGAAGAATTATTC | 53621 |
rs6310900 | snp | A/G | 0.5 | 0 | intron-variant | Cnot4 | Mm_Celera | 6:35115351 | aggaagcaggaagaa[A/G]gacaagttcaaggcc | 53621 |
rs6324201 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cnot4 | Mm_Celera | 6:35115505 | CAGCAGTAGTAAAAG[C/T]TGCTTGGGGAGAAAG | 53621 |
rs6349082 | snp | A/G | 0.5 | 0 | intron-variant | Cnot4 | Mm_Celera | 6:35084445 | AACTAAAATTGTAgg[A/G]ctgaagagatggctc | 53621 |
rs30939734 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cnot4 | GRCm38.p3 | 6:35102102 | TGCTGTAAATGTACC[C/T]CTGGCCTCCATTTCA | 53621 |
rs36241052 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Cnot4 | Mm_Celera | 6:35022655 | TGCAATAGTGAAAAG[C/T]TGAATACAAGATGGA | 53621 |
rs36242251 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35050522 | TGTCTGTGACATATA[A/C]TAGGCTTATAAAACA | 53621 |
rs36245894 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35041395 | TTATGAAATCTAATG[C/T]CACTGACTGCCCTTC | 53621 |
rs36251781 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cnot4 | GRCm38.p3 | 6:35066525 | CTTAAGTATATCTTG[C/T]GGCAAAATAAAAATA | 53621 |
rs36254426 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35063437 | TTTCCTTATTAAGCA[C/T]CCCAGACACTGTAGG | 53621 |
rs36255367 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cnot4 | GRCm38.p3 | 6:35074296 | ACACACTCAAGTTTG[A/G]CTAAACAACTGATAA | 53621 |
rs36256237 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cnot4 | Mm_Celera | 6:35073643 | CACATTTGATACGTC[C/T]ATCTGATAGCCAAAA | 53621 |
rs36260555 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35113617 | CTAGCATATGTGATG[C/T]CCAGGTTTGGGGAAG | 53621 |
rs36264678 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35054297 | CAGCTTTGCTGAATC[C/T]TCCTGCCCCTAGCCT | 53621 |
rs36265005 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35040544 | AGATGAAGAGACACG[C/T]GCGTACACACACCTT | 53621 |
rs36268237 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35123104 | AAAGCTTTTGGTTTC[A/T]GTGTGTCTACCTGCC | 53621 |
rs36276969 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cnot4 | Mm_Celera | 6:35050796 | CCTTTTTTGTGTTTA[C/T]ATATGATCTGAATGT | 53621 |
rs36285448 | snp | A/G | 0.5 | 0 | intron-variant | Cnot4 | GRCm38.p3 | 6:35069657 | AGCTCATTAAAAGCT[A/G]TAAGTGGATTATAAC | 53621 |
rs36292424 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cnot4 | Mm_Celera | 6:35034208 | TATAAATTAACAACA[A/G]TCTCAAATGAAACAA | 53621 |
rs36294210 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Cnot4 | GRCm38.p3 | 6:35038326 | AAGCATTAATCTCAA[A/G]TATATGAATGAAGTG | 53621 |
rs36305089 | snp | C/G | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35102585 | ACATGTAAACACACT[C/G]GAGAACTCATCTCTG | 53621 |
rs36319179 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cnot4 | Mm_Celera | 6:35081236 | GGTTACACTGAAGAG[C/T]ACTTGAGAATAACTG | 53621 |
rs36321572 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cnot4 | Mm_Celera | 6:35052050 | AATGCTCTGCTTGGC[C/T]ATTCACTCAACACCA | 53621 |
rs36324236 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Cnot4 | GRCm38.p3 | 6:35086119 | AAACAAATAGAAAAA[C/T]CAGGGCTACTTATAC | 53621 |
rs36329938 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35041410 | TCACTGACTGCCCTT[C/T]CACATCACTCACATC | 53621 |
rs36331407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35032346 | ACAAATCACGTCAAA[A/G]TAATCTGTTTGGATA | 53621 |
rs36336245 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Cnot4 | GRCm38.p3 | 6:35021863 | TAGCCACTGGGAGAG[A/G]AGTGTTGAGAGCAAG | 53621 |
rs36348914 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35028366 | ACCAGAGAGCCTATG[A/T]CAAGTTAAATTACTT | 53621 |
rs36351071 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35053774 | CCTCCTCTATCCGGG[C/G]ACTATTTATACAAAC | 53621 |
rs36351974 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, nc-transcript-variant | Cnot4, Gm33046 | Mm_Celera | 6:35134386 | CATGTGGACTTACCT[A/G]CAAACTGTTGCTGGC | 53621 |
rs36354426 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cnot4 | GRCm38.p3 | 6:35076983 | AAAGCCTACAAGAAA[A/G]CATGAGCTCAGAGTA | 53621 |
rs36357146 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35031960 | ACAAGAGCAAGAGGC[A/C]GACTGCAGCAATGGC | 53621 |
rs36361756 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | GRCm38.p3 | 6:35035593 | TTCAGATATTCTGGA[A/C/T]CTTCAAGTTGAATTA | 53621 |
rs36363885 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35038557 | CAAGACAGTAGGACT[A/C]TGACTGCCATTTCAA | 53621 |
rs36364720 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Cnot4 | Mm_Celera | 6:35078821 | ACATCTTCAGCCCAT[A/C]TCCTTTTTGGCCCTG | 53621 |
rs36371960 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Cnot4 | GRCm38.p3 | 6:35030925 | GTAAGGAGGAAGGAA[A/G]TCGAACTCTGCCCAA | 53621 |
rs36377704 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35063971 | TATGCCAAAGTATAG[A/T]TTAAGAAAGGAAGAT | 53621 |
rs36380601 | snp | C/T | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35079826 | CATCTGGCCTTGGCT[C/T]TCAATCCACTGCTCT | 53621 |
rs36381585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35115300 | ACATTTAAACCTAAA[A/G]TATGGTGGTGAGGCA | 53621 |
rs36393609 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Cnot4 | Mm_Celera | 6:35035777 | AAAACTGAGTATCAA[A/G]ACTTTCCAATGTAAA | 53621 |
rs36395683 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35027940 | CCTGGGTAGACAGAA[C/T]GAAAGAAGGAAACAT | 53621 |
rs36396723 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Cnot4 | Mm_Celera | 6:35089204 | ATCCTAATAAAGAAA[A/G]TTAGCAGATTTAAAC | 53621 |
rs36397102 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35033772 | CTCTTGCAATAGCCA[A/C]GCTGTTCTGCTTGCT | 53621 |
rs36404597 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, intron-variant | Cnot4 | GRCm38.p3 | 6:35045979 | TAATCTCCTCTGGGA[C/T]CTTAATTAGTACTCT | 53621 |
rs36408273 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35030962 | AACAGTTACCTACTG[C/T]AAAAATTCAGGTTTT | 53621 |
rs36425873 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35039047 | AGTACTAAAAAGAAT[C/T]CTTTGTGGCAGCACC | 53621 |
rs36426114 | snp | A/G | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35130862 | TTAAATGTTACAAAT[A/G]AAGACTACACAAAAA | 53621 |
rs36437379 | snp | A/C | 0.142012 | 0.225474 | upstream-variant-2KB, nc-transcript-variant | Cnot4, Gm33046 | Mm_Celera | 6:35134416 | CTGCACAGAACTCTT[A/C]CAGCCTGCACAGAAG | 53621 |
rs36437591 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35122076 | ATAATAAAAAGCAGC[A/G]TCTAGGACTAGGGAT | 53621 |
rs36438728 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Cnot4 | GRCm38.p3 | 6:35032178 | AGGAAATAGCTTTTT[C/T]CTGTATCTTGTGACT | 53621 |
rs36438732 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant | Cnot4 | GRCm38.p3 | 6:35044376 | GAAGGAAAGCAGCTT[C/T]GCTCAGTAGCTCCCT | 53621 |
rs36454473 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35047718 | CATCAGTGTAGCAAG[A/G]CAAAAACCACTTCCA | 53621 |
rs36460690 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Cnot4 | GRCm38.p3 | 6:35066204 | TAGTGGAAGACAGTG[A/G]CAGAGACTACAACTG | 53621 |
rs36469202 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Cnot4 | GRCm38.p3 | 6:35042490 | ttattattattatta[A/T]ACAAGCTCTTTTTCT | 53621 |
rs36472356 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Cnot4, Gm33046 | Mm_Celera | 6:35135361 | GAGACAGTTCAGTGG[C/T]GAGAGTACAATTCCC | 53621 |
rs36473910 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cnot4 | Mm_Celera | 6:35124796 | AGCCTCCAATATTAC[G/T]TCGGTAAAATGAAGC | 53621 |
rs36484793 | snp | C/G | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Cnot4 | GRCm38.p3 | 6:35086062 | TTTACTCCAGCATAA[C/G]CCAGCAAATTAAAGC | 53621 |
rs36498600 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35123008 | GACAGGTCAAAAATC[A/G]AGACTAGTGCAGCTA | 53621 |
rs36502043 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35036909 | TGCAACCCAGCACTC[A/C]GTTTAAGGTGATGCA | 53621 |
rs36502117 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Cnot4 | GRCm38.p3 | 6:35030843 | AACCATGTTAGCACC[C/T]CGAGGTCTACATCTG | 53621 |
rs36503158 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Cnot4 | Mm_Celera | 6:35045231 | GTTTTGCATTATCAA[A/C]GCATCACTTTACATT | 53621 |
rs36509497 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cnot4 | Mm_Celera | 6:35116100 | GAAGCAAGACCTGCT[C/G]TGTGAATAACACTAA | 53621 |
rs36520071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35063281 | TACACATTACAGCTG[C/T]GTGGCTTCCTTGTTT | 53621 |
rs36520840 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Cnot4 | Mm_Celera | 6:35021722 | ATGCTACTGGGCTGC[C/T]GCTGCCGCTGCCACC | 53621 |
rs36522688 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35037127 | CAGTGAAGTTCCAGA[C/G]CACTCTGTTCTGTTC | 53621 |
rs36541803 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cnot4 | Mm_Celera | 6:35028690 | TGTGACTCTAATATA[A/C]AGGAATATGCCAAAC | 53621 |
rs36544351 | snp | A/G | 0.497778 | 0.0332592 | utr-variant-3-prime, intron-variant | Cnot4 | GRCm38.p3 | 6:35044338 | TTCTGTACAAATTAG[A/G]AATGAAAAGGAGCAG | 53621 |
rs36549651 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35026770 | ACTATGAAGTAGCAT[C/T]ATAACACAACCAGAG | 53621 |
rs36550043 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35033642 | AGTTTATTCTCACTA[A/G]ATGATACCAAAGCTG | 53621 |
rs36552155 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cnot4 | GRCm38.p3 | 6:35031414 | GATTCAGGTTCTTTC[C/T]GACTCCTTCTGTGAT | 53621 |
rs36556653 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Cnot4 | Mm_Celera | 6:35083596 | ATCAGTAACTCTAGC[A/C]TGAACCTCCAAAGCA | 53621 |
rs36563884 | snp | A/T | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35024731 | CATCCTGTGAAGTTC[A/T]ATCTAGAAGCTCATT | 53621 |
rs36569033 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35027466 | TGTTTTTGTAGTAAG[C/T]GGTGGTGTTAGACAA | 53621 |
rs36572573 | snp | A/C | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35109564 | TCACTTTCACTAACC[A/C]TGGAAAACCAATTCA | 53621 |
rs36586645 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35048124 | GATAGGTCTCACATT[A/C]TGTCAGTGCTTTTAT | 53621 |
rs36592223 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35039211 | AGGTATCTGAAGAAT[A/G]TCACTTTAAAGAAGC | 53621 |
rs36593618 | snp | A/G | 0.345679 | 0.230967 | upstream-variant-2KB, intron-variant | Cnot4, Gm33046 | Mm_Celera | 6:35134811 | GGGACTGTGGATGTC[A/G]CACAGTGGTAGGGCG | 53621 |
rs36622675 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Cnot4 | GRCm38.p3 | 6:35051978 | CATCTTTCAGACTAA[A/T]AAGAAAATGTAAGTG | 53621 |
rs36623255 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cnot4 | GRCm38.p3 | 6:35039184 | AAGGGTATGCATATC[C/T]GCAAAGCCACCAGGT | 53621 |
rs36638248 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35037268 | TTCCCCCTTTGGAGA[C/T]GCTGATGGTACTATT | 53621 |
rs36643984 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35056393 | TGAGATACTATAATG[C/T]AAGATCTTATGTAAG | 53621 |
rs36644458 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Cnot4 | GRCm38.p3 | 6:35041033 | CAGCTCCTTTGCACA[C/T]TGAGCTTTCTCAAGC | 53621 |
rs36645604 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Cnot4 | GRCm38.p3 | 6:35086880 | CTCACATAAACAAAA[A/T]ATCTTCACAAACTTG | 53621 |
rs36646560 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35049795 | AAAGGAAAAAGCAGG[A/G]AGAAAAGGAAACCTT | 53621 |
rs36646863 | snp | C/T | 0.32 | 0.24 | intron-variant | Cnot4 | Mm_Celera | 6:35026374 | GAGAGTCTCTCCCTC[C/T]AGCTCCACCACTTTA | 53621 |
rs36658110 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35063045 | ATCTTCCCTTTGTTT[C/T]AGTCTTAACTTCACA | 53621 |
rs36659989 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cnot4 | GRCm38.p3 | 6:35029468 | AAAAGCTTCCCTCAA[C/T]GTAAACAAGAAAGAA | 53621 |
rs36661946 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Cnot4 | GRCm38.p3 | 6:35068546 | AATTTTAACTTGAAA[C/T]GTTGTTTTGTACTAA | 53621 |
rs36665963 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cnot4 | Mm_Celera | 6:35063014 | GATAAAAGAAGCACA[A/T]TAAAAGTTTATTTAC | 53621 |
rs36669050 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cnot4 | Mm_Celera | 6:35076863 | GACCTCAAATTCAGC[A/G]CTCTCCTACTGAAGC | 53621 |
rs36678617 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Cnot4 | Mm_Celera | 6:35081819 | AATAAAATAAAGTAA[A/T]ACTCAAAGCTGACTG | 53621 |
rs36684104 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Cnot4 | GRCm38.p3 | 6:35081007 | ACAGAGAACAAATGG[A/G]TCTTTCTTATTCAAA | 53621 |