SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023700 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Dcun1d1 | Mm_Celera | 3:35918963 | AGACGAGGTGCTCTC[C/G]GAGATGATGGAGCTT | 114893 |
rs3723789 | snp | A/C | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35899641 | GCTGTGCACAGACAC[A/C]ATGACCAAGGCAACT | 114893 |
rs3724421 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | Mm_Celera | 3:35899735 | AAGATGGGAACATGG[C/T]AGCATCCAGGTGCAG | 114893 |
rs3724504 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35899778 | GTAGGAGGTGAGAGT[C/T]CTACATCTTTCAGAT | 114893 |
rs6277424 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | Mm_Celera | 3:35899229 | ggtcttcctgtgtgc[C/T]ccccatgcttcccac | 114893 |
rs6313310 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | Mm_Celera | 3:35901295 | acaattaggttgatt[C/T]taattttttactaca | 114893 |
rs30003537 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35912553 | GAATTTAATGAAAAG[A/G]AAGGTACAACATACC | 114893 |
rs30018823 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35921286 | TTTTCCCACAAAACA[C/T]GGAAACATTTTTACT | 114893 |
rs30020214 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Dcun1d1 | Mm_Celera | 3:35897283 | TTTCTATCACGCGTT[C/T]GCACATACACATACA | 114893 |
rs30258165 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35915000 | AGTCAGAATGGCTAA[A/G]ATCAAAAACTCAGGT | 114893 |
rs30261986 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35921679 | CAACCTTTAGAAAGG[G/T]TCTTTTAATTATATA | 114893 |
rs30300623 | snp | C/T | 0.42 | 0.183303 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35898369 | CGCTCAATTTCTAAT[C/T]TTCAACTTCTTACAC | 114893 |
rs30305456 | snp | A/G | 0.290657 | 0.246672 | utr-variant-3-prime | Dcun1d1 | GRCm38.p3 | 3:35893153 | CAGTTTACTATTTAA[A/G]AAGCATTACATTTAA | 114893 |
rs30309722 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35939183 | ACACATGGGTGTGCA[C/T]GTGTATATGCCTGCC | 114893 |
rs30324835 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35907502 | AACAAAATCATTCAA[A/G]ACAAAAACAAAACAA | 114893 |
rs30355510 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35916709 | AATGCGCTCTGGCAC[A/G]CCTTCATTGCCAGCA | 114893 |
rs30359992 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dcun1d1 | Mm_Celera | 3:35919808 | AAATATACAATTCAA[C/T]CTTTAATCTCAACAG | 114893 |
rs30363024 | snp | G/T | 0.277778 | 0.248452 | intron-variant, utr-variant-3-prime | Dcun1d1 | GRCm38.p3 | 3:35909056 | TTCCCCTTTCTTTGC[G/T]GAATGCCAAAATCCT | 114893 |
rs30401826 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35918545 | CCTGAGAGTCAACTA[A/G]CAATTGTCAGCAAAC | 114893 |
rs30409140 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35917075 | ACAAAAAGATGACAA[A/T]GCCCACAGTGATGGA | 114893 |
rs30411796 | snp | A/G | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35920031 | GTAACCCCATGAAAA[A/G]ATGAGCAGTCTCAAC | 114893 |
rs30500895 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dcun1d1 | Mm_Celera | 3:35917348 | TTTTAATAAATACTA[A/G]CTAAGACCTGTAGTA | 114893 |
rs30504145 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Dcun1d1 | Mm_Celera | 3:35924598 | CCTAGACTGTGAACA[C/T]GTGCCACTCGGTGCT | 114893 |
rs30505673 | snp | C/T | 0.455 | 0.143091 | intron-variant | Dcun1d1 | Mm_Celera | 3:35898308 | ATTCTAGAGGACAAA[C/T]CTGCCCCAGTTAAGA | 114893 |
rs30523461 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | Mm_Celera | 3:35915120 | AGTTTGGTGGTTCCT[C/T]AGAAAATTATACATA | 114893 |
rs30572327 | snp | A/G | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35915122 | TTTGGTGGTTCCTTA[A/G]AAAATTATACATAGT | 114893 |
rs30600332 | snp | G/T | 0.5 | 0 | intron-variant | Dcun1d1 | Mm_Celera | 3:35922211 | CCACTGCACTCTTCC[G/T]CCTGTTAGGTCCCAA | 114893 |
rs30698665 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35928741 | ATCAACTGTCATGGC[C/T]GACACCACCGTGGCC | 114893 |
rs30751371 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35923877 | TTCCCAGCTCCTTCC[C/T]CAGGCCACACAGGTG | 114893 |
rs30759045 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35921274 | TTAGTAAGGGGTTTT[A/T]CCCACAAAACACGGA | 114893 |
rs30760810 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35931285 | AACTCCTAACAGTCT[C/T]ACCAAACCATTTTAT | 114893 |
rs30796668 | snp | C/T | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35919435 | AGGCTTGGTGCTACA[C/T]GCCTTTAGTCCCAGT | 114893 |
rs30841852 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35915551 | CCTCTTCTTTGGAAC[C/T]CTCTCTTTACTACTC | 114893 |
rs30845730 | snp | A/C | 0.32 | 0.24 | intron-variant | Dcun1d1 | Mm_Celera | 3:35920669 | TGCCACTGATCTCAG[A/C]TGTTCGGCTTTTTAA | 114893 |
rs30847748 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Dcun1d1, Gm35804 | Mm_Celera | 3:35896681 | GACAAGGTTAGGAGG[A/G]AAAAAAAAAAAAAAC | 114893 |
rs30855365 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Dcun1d1 | Mm_Celera | 3:35923951 | GAAAAGGGTTACTAG[A/T]TTAAACAGAATTCTT | 114893 |
rs30860236 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcun1d1 | Mm_Celera | 3:35915099 | GGTACAACCACTCTG[A/G]AAATCAGTTTGGTGG | 114893 |
rs30939166 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, downstream-variant-500B | Dcun1d1, Gm35804 | Mm_Celera | 3:35897129 | GTCCAGACACCACAA[A/G]TGTTCTGTACCTAAG | 114893 |
rs30953995 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcun1d1 | Mm_Celera | 3:35920675 | TGATCTCAGCTGTTC[A/G]GCTTTTTAAAAGAGC | 114893 |
rs30954910 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Dcun1d1, Gm35804 | GRCm38.p3 | 3:35895798 | CCTTTTTTTTTTATA[A/G]CTTTCTTGTAAGAAT | 114893 |
rs30988877 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35934418 | AACAGCCAACAGTGC[A/G]GCCTGGGATTGCAGG | 114893 |
rs30993110 | snp | A/G | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35910792 | CCAGGACCTAAAATT[A/G]GAAACAGAATCAATA | 114893 |
rs31006949 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35892736 | GATGGTTTCAGTGAG[C/T]GAATTTACCAACACT | 114893 |
rs31047927 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35939164 | TGTGTGTGTGTGTGC[A/G]TGCACACATGGGTGT | 114893 |
rs31058326 | snp | G/T | 0.415225 | 0.187619 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35893320 | TGTGTGAGTGAGTGT[G/T]CCCTTCCTCTGGAAG | 114893 |
rs31084550 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Dcun1d1 | Mm_Celera | 3:35922300 | AAACACATTAAAGAT[A/G]CAGTATTCTGCAGTT | 114893 |
rs31094704 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35906941 | TTACTGAACATGAGA[C/T]ATAACAGTAGTTATC | 114893 |
rs31200212 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | Mm_Celera | 3:35911574 | TTTTTTGGTTTTTTC[A/G]AGACAGGGTTTCTCT | 114893 |
rs31234759 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Dcun1d1 | Mm_Celera | 3:35927300 | GCACCAGGAATACTA[C/G]TTTAAGTCATCTAAG | 114893 |
rs31236193 | snp | G/T | 0.5 | 0 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35904418 | AGGAAAGAGATAGTT[G/T]TTTTGTTTGTTTGCT | 114893 |
rs31238746 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Dcun1d1 | GRCm38.p3 | 3:35893359 | ACGCCCCGCCCCCAA[C/T]AGGGTAAGCATTTGT | 114893 |
rs31238817 | snp | A/C | 0.46875 | 0.121031 | utr-variant-3-prime | Dcun1d1 | GRCm38.p3 | 3:35892409 | TAAACGCTCACTGAA[A/C]GGTCATTCATGTTAC | 114893 |
rs31272463 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35913978 | GAAATTAGGGAAACA[A/G]CACCCTTCCCAGTAG | 114893 |
rs31289426 | snp | C/G | 0.5 | 0 | intron-variant | Dcun1d1 | Mm_Celera | 3:35922241 | ATTCTGTCTTCTCAG[C/G]AAAATACTTGGGCTC | 114893 |
rs31292549 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35912718 | ATATACCCAAGAGGA[G/T]TAGATGGCATGAAAT | 114893 |
rs31310668 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35919706 | ATATTTTATTAAGTA[C/T]TCAAAATTAACCAAT | 114893 |
rs31332322 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Dcun1d1, Gm35804 | GRCm38.p3 | 3:35895790 | TGATAGAATCCTTTT[A/T]TTTTTATAGCTTTCT | 114893 |
rs31362969 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35923818 | ACAGGCTGCCTGCTC[A/G]CCCAGCTAAATGACA | 114893 |
rs31378870 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35923089 | AAATTTTCTGAAGCA[C/T]AGCCTATTTTCTGCT | 114893 |
rs31387174 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35923596 | AAAAAGGAGCTACTC[A/G]TATGAAACCTCCTAA | 114893 |
rs31390311 | snp | C/T | 0.432133 | 0.171253 | intron-variant, nc-transcript-variant | Dcun1d1, Gm35804 | GRCm38.p3 | 3:35896246 | GGAAGGATTAGCTGA[C/T]ATGCTACTGAATGAG | 114893 |
rs31396551 | snp | A/C | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35935013 | GACCAGATCATATCC[A/C]TCTTTGAGATAATTT | 114893 |
rs31473091 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dcun1d1 | Mm_Celera | 3:35912604 | AAAGCAGGCTAAGAG[A/G]AAAACTCATAGCTCT | 114893 |
rs31480696 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Dcun1d1, Gm15952 | GRCm38.p3 | 3:35936236 | CTAACATGTAAGTGG[C/G]TGCTGGCGTCTGAAC | 114893 |
rs31489643 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Dcun1d1 | Mm_Celera | 3:35926931 | GGAACTTACGGCATC[A/T]ATTTAGGACTCTGCT | 114893 |
rs31559621 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcun1d1 | Mm_Celera | 3:35915108 | ACTCTGAAAATCAGT[C/T]TGGTGGTTCCTTAGA | 114893 |
rs31572940 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35898461 | TTTGTTTGTTTAAGC[G/T]TATAAGTCTGTTGCT | 114893 |
rs31575742 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Dcun1d1, Gm35804 | GRCm38.p3 | 3:35896044 | AGCTGTCTAGTCCCT[C/T]CCTCATGAGCACCTC | 114893 |
rs31581847 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35918474 | CTGACCCTCGTGCAT[C/G]TGCCTTCCAAGGGCT | 114893 |
rs31645791 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35912160 | ACTCAAAGCACACAT[C/T]GGACCTCAGACAATA | 114893 |
rs31670555 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | Mm_Celera | 3:35913844 | ATGTTAGTAAGCGAC[C/T]ACAAAAATTCCACCA | 114893 |
rs31741083 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35928415 | AATGCAGCAACCTAA[A/C]AAGGAGGTAAGTAGT | 114893 |
rs31742234 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcun1d1 | Mm_Celera | 3:35921742 | CTCTCCCCTCTCTCC[A/G]TTTCTGTCTGTCTGT | 114893 |
rs33861108 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcun1d1 | GRCm38.p3 | 3:35912199 | AGATTTTAACACCCC[A/T]CTCTCATCAATGGAC | 114893 |
rs36240343 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35892550 | GGTTTCCAAACAGTC[C/T]TTAACAGCAACACAC | 114893 |
rs36249305 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcun1d1 | Mm_Celera | 3:35915756 | AATGTTCACTGCTTT[C/T]CCAGTAAGATTATTA | 114893 |
rs36269650 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Dcun1d1 | Mm_Celera | 3:35926089 | TAAGGTGAGAGTAAA[C/G]TGTCCCGGAAGAGGT | 114893 |
rs36277326 | snp | C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35892731 | CTCCCGATGGTTTCA[C/G]TGAGCGAATTTACCA | 114893 |
rs36311650 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, upstream-variant-2KB | Dcun1d1, Gm35804 | Mm_Celera | 3:35894844 | ATGTGGTGTGTGATG[A/C]ACGAGTGTGGAGTCT | 114893 |
rs36312954 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dcun1d1 | Mm_Celera | 3:35898623 | CCATGACAACATAAA[A/G]GGCTTTTTAGTGGGA | 114893 |
rs36313811 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35893134 | GGGTACTTCTCATTT[C/T]ATACAGTTTACTATT | 114893 |
rs36334445 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Dcun1d1 | Mm_Celera | 3:35925463 | GCAATTCTAGTTGTT[C/G]TCTAGTTTACAAGAG | 114893 |
rs36335333 | snp | C/G | 0.18 | 0.24 | intron-variant | Dcun1d1 | Mm_Celera | 3:35924599 | CTAGACTGTGAACAC[C/G]TGCCACTCGGTGCTT | 114893 |
rs36340283 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Dcun1d1 | Mm_Celera | 3:35891939 | TGCCCAGAGGAGACC[A/G]TGGGTGACAGTTCCA | 114893 |
rs36343051 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Dcun1d1 | Mm_Celera | 3:35923412 | CTAACAGAAAGCTAG[G/T]TATTAGAAAATGGTG | 114893 |
rs36376576 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Dcun1d1 | Mm_Celera | 3:35930113 | ACAAAAGCTCTTTCC[A/G]TCTTCTTCGACTCCC | 114893 |
rs36378292 | snp | C/G | 0.142012 | 0.225474 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35893039 | ATATGACAGGGATTG[C/G]AAACGACACACTTGA | 114893 |
rs36402466 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcun1d1 | Mm_Celera | 3:35902273 | AAACTCTGTAACCTA[C/T]TACGACTGGTTGCTG | 114893 |
rs36423880 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dcun1d1 | Mm_Celera | 3:35922640 | TCTCACAACATAAAA[C/T]ACGTTTATGCCCTTG | 114893 |
rs36435224 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Dcun1d1 | Mm_Celera | 3:35926221 | TTCAGTAAACCAAGT[A/G]CTACAGTTCTAGGCA | 114893 |
rs36436255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcun1d1 | Mm_Celera | 3:35915860 | TTGTGCCCTATATCT[A/G]TGACACAGTGACCTT | 114893 |
rs36438715 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Dcun1d1 | Mm_Celera | 3:35891920 | ACAGAAAAGAAGCCA[A/G]GAGTGCCCAGAGGAG | 114893 |
rs36467526 | snp | C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Dcun1d1 | Mm_Celera | 3:35892566 | TTAACAGCAACACAC[C/G]TAAACACACAAGCAG | 114893 |
rs36514007 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Dcun1d1 | Mm_Celera | 3:35924906 | TAGTAAGAGTTAAGT[A/C]GAGAAAGTACCCCTA | 114893 |
rs36563014 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dcun1d1 | Mm_Celera | 3:35919670 | TATACAGGGACAAGA[A/G]ACTTTTAAGTCAAGG | 114893 |
rs36571824 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcun1d1 | Mm_Celera | 3:35917133 | ATTGGCTATGCTTTT[A/T]AAATATATTAATTCA | 114893 |
rs36576017 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dcun1d1 | Mm_Celera | 3:35926443 | CTTTATGCTAGCCAC[A/G]TACTCTACTCTTCTC | 114893 |
rs36584657 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Dcun1d1 | Mm_Celera | 3:35925876 | AGCATGTGCTTAACA[A/T]TCCTATGAGATTTTT | 114893 |
rs36608327 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcun1d1 | Mm_Celera | 3:35902246 | GAAGGTCTGTGTCCA[C/T]GCAGAACACATAAAC | 114893 |
rs36608757 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcun1d1 | Mm_Celera | 3:35905005 | CACCAGCCTCTTTAC[C/T]GCCTCGTGTCCCATG | 114893 |