SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3725732 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16322932 | tgtgtgtgtgtgtgt[A/G]ngacagagaacaact | 56459 |
rs3725733 | snp | G/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16322933 | gtgtgtgtgtgtgtn[G/T]gacagagaacaactt | 56459 |
rs3727037 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16323162 | AGAATATTCATTTGG[A/T]TAATTTATACCATGT | 56459 |
rs3727041 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16323165 | ATATTCATTTGGTTA[A/T]TTTATACCATGTGTT | 56459 |
rs4137465 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Sae1 | GRCm38.p3 | 7:16322746 | CTTGTGTACCATAGT[C/T]CAGACCTTGAGATCA | 56459 |
rs4137488 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Sae1 | Mm_Celera | 7:16322759 | GTTCAGACCTTGAGA[C/T]CATTTCTCACAAGAG | 56459 |
rs4137510 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16322765 | ACCTTGAGATCATTT[C/T]TCACAAGAGGTTATG | 56459 |
rs4138799 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16322910 | tgtgtgtgtgtgtgt[A/G]tgtgtgtgtgtgtgt | 56459 |
rs6184212 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Sae1 | Mm_Celera | 7:16364878 | CCAAGGCCCTCTCTC[C/T]CCAAATAGAGAAGTT | 56459 |
rs6215368 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16377882 | TTTTTAAATTTTTTT[A/T]AAAAATTACATACCT | 56459 |
rs6288477 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Sae1 | GRCm38.p3 | 7:16382173 | TTGTCAACCTCAGGG[G/T]CCCTTCCTACCATGC | 56459 |
rs6288945 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16382251 | TATTTAAAATCTCTA[A/T]NGGTCCTAAtggtgc | 56459 |
rs6288946 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Sae1 | Mm_Celera | 7:16382252 | ATTTAAAATCTCTAA[A/C]GGTCCTAATGGTGCA | 56459 |
rs6290044 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Sae1 | GRCm38.p3 | 7:16382448 | GGGCGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 56459 |
rs6297439 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16356081 | CAGGGGTGCAATCTA[C/T]AGGAAAGGGAACAAG | 56459 |
rs6407136 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Sae1 | Mm_Celera | 7:16328658 | ATGACCCATATCTAT[A/T]TCCTTCATGGCTCTG | 56459 |
rs6407540 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16328701 | GTCTGGTCTCCTGGG[C/T]TCCCTGGCTCCAGCC | 56459 |
rs6408652 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16328900 | GTGTTGGGATTCATG[C/T]GCCACCACTGCTGGG | 56459 |
rs13465098 | snp | A/T | | | intron-variant, utr-variant-3-prime | Sae1 | Mm_Celera | 7:16327461 | GAGACTGTCACCCAG[A/T]TGTCATGTCTTTTGG | 56459 |
rs31037464 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Sae1 | GRCm38.p3 | 7:16385450 | CTACTGAAGTCTGCT[A/G]GGCATAGGAGTTGTA | 56459 |
rs31043173 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16338162 | ACTGCCATGCTCCCA[C/T]CTTGATGATAATGGA | 56459 |
rs31050930 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Sae1 | GRCm38.p3 | 7:16360013 | GAAAATGCAATGGGG[C/T]GTACTGGATTTTTAT | 56459 |
rs31055163 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16361798 | CAAAAATCCTTAGAG[C/T]AACAACAGCATCTGC | 56459 |
rs31055238 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16381165 | ATGTATGCAAGAAAG[A/G]CAAGCCCCTGCGCTA | 56459 |
rs31055441 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16371340 | TTCTGGTAAGATGGA[A/G]TTGAAGAGTTGGCTG | 56459 |
rs31103228 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16332030 | TTCCATAGTACTTTG[G/T]TTTTTTTTTGCCTCC | 56459 |
rs31106591 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16326414 | ACGTAGGTTAGGAGT[A/G]TCTGCTCCCCCTTGT | 56459 |
rs31108510 | snp | A/C | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16326843 | TGTTAGTACTGAGAC[A/C]CTCAGCACACAGGCA | 56459 |
rs31109363 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Sae1 | GRCm38.p3 | 7:16365786 | ATGAAACTTTAAATG[A/G]ATGTTCCAACCAACG | 56459 |
rs31127210 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Sae1 | GRCm38.p3 | 7:16338687 | GGTCTGGAAACAAAG[C/T]CTAAACTGTGGTAGA | 56459 |
rs31142151 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16380843 | CACAAACAAAAGCAT[C/T]GTCTATACTCTGAAG | 56459 |
rs31150028 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16337702 | TGTATGGAAAGCATT[A/T]AAAAAAAAAAAAAAA | 56459 |
rs31157085 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16340492 | TAGAAGACAATGAAG[A/T]GTCACAAATTAGCCC | 56459 |
rs31172842 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sae1 | Mm_Celera | 7:16361756 | AGTGAGACTGCTACA[C/T]GCTATTGGCCACGGA | 56459 |
rs31187194 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16338203 | GAACCTGTAAGCCAG[C/G]CCCAATTAAATGTTT | 56459 |
rs31189744 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Sae1 | GRCm38.p3 | 7:16325588 | AGGTTGACCTCAAAC[A/G/T]CAGACGTCCACCTGC | 56459 |
rs31193784 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Sae1 | GRCm38.p3 | 7:16331391 | GTCACCTATACACAT[A/G]ATAACATAAACCCAA | 56459 |
rs31199204 | snp | A/G | 0.375 | 0.216506 | intron-variant | Sae1 | Mm_Celera | 7:16325859 | TCAACTCAGAAATCT[A/G]TCTGCCTCTGCCTCC | 56459 |
rs31200474 | snp | A/G | 0.484429 | 0.0868505 | intron-variant, downstream-variant-500B | Sae1 | GRCm38.p3 | 7:16330344 | TGACACCACTCTGAC[A/G]GATGTCGGTTAGGGT | 56459 |
rs31249731 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16363023 | AAGAAGAGAAAGGAA[A/G]AGAAGGAAAGAATGG | 56459 |
rs31259494 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16354134 | CATTTTTTCAGGTGC[G/T]TCTCTGCCATTCGGT | 56459 |
rs31264257 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16333155 | GTGGTGCCATTTCTG[G/T]GCTGGTAGTCTTGGG | 56459 |
rs31278496 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16337352 | AGATTGACAAACAGC[C/T]TGGCAGATGAGCATC | 56459 |
rs31287179 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16375428 | TCATCTCCTATATCT[A/C]TTCTTGGCTTTGAGT | 56459 |
rs31304740 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Sae1 | Mm_Celera | 7:16361776 | TTGGCCACGGAATGG[A/G]TATTGGCAAAAATCC | 56459 |
rs31314794 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Sae1 | GRCm38.p3 | 7:16347299 | TAGAAAGGAAACACA[A/G]CTCTCCACTCCTGAG | 56459 |
rs31328724 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16346402 | GCTGGGATTAAAGGC[A/G]TGTGTCACCACTGCC | 56459 |
rs31330544 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Sae1 | Mm_Celera | 7:16320231 | GTGCCAAGTCTGGGG[C/T]GTGATGTGGTAGCAC | 56459 |
rs31345136 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Sae1 | Mm_Celera | 7:16376333 | AACAACTTTATACCT[C/T]CTCCTCCAACGGTGT | 56459 |
rs31348969 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Sae1 | GRCm38.p3 | 7:16341458 | CATCCCAAATTCTCA[C/T]ATTACAGGAATGTGT | 56459 |
rs31376831 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Sae1 | GRCm38.p3 | 7:16348554 | AGAGGAGGAAGTGTA[A/G]ATATCTACTGAGTCA | 56459 |
rs31385978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sae1 | GRCm38.p3 | 7:16325552 | AGCCCTGGCCGTCCC[C/T]GAACTCTCACAATGT | 56459 |
rs31389969 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16350073 | TCCATGTTAGTCTCC[A/G]TTTCCATGTGACCGA | 56459 |
rs31407310 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16378251 | AAGACTATATATTCA[C/T]GTAAACCTCCTCCCA | 56459 |
rs31409849 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16333145 | CCCATTGTGGGTGGT[A/G]CCATTTCTGTGCTGG | 56459 |
rs31428310 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16338518 | AGATGAGGCACAGTG[A/G]CTCATGACAGCAAGA | 56459 |
rs31429418 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Sae1 | GRCm38.p3 | 7:16384939 | GTGGCATCCGGAAGA[C/T]GAGGCACAGGTCAAA | 56459 |
rs31432775 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16364263 | GTACATGGAGTTGTA[C/G]CTCAGTGGTAAAAGA | 56459 |
rs31446994 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Sae1 | GRCm38.p3 | 7:16329574 | TTTCTCCAGCCCTTG[A/C]TGTCTAGAGTGTAGA | 56459 |
rs31454845 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16331260 | ATGATCCTCTCACAC[A/G]GGCACATATGCCTTT | 56459 |
rs31467869 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Sae1 | Mm_Celera | 7:16330156 | CAAATATTCTAGAAG[A/G]GCTACATAGTTCCTA | 56459 |
rs31470814 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Sae1 | GRCm38.p3 | 7:16338734 | GAGCCATGCTGAACA[C/T]GCTTCGTGTATGAGT | 56459 |
rs31473949 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16367451 | AAAGGTTGTCGTCGT[C/T]GTCCCCCTCCCCCAC | 56459 |
rs31475708 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16338105 | AGCCTTTGGGTGAAG[A/C]CATAGAACTCTCAGC | 56459 |
rs31495717 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16339757 | GCACTGAGAAAGCAG[C/T]GGCAGGTCAATAACT | 56459 |
rs31517238 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Sae1 | GRCm38.p3 | 7:16331236 | AGCAAAGTGGGACAT[C/T]AGGCCGCCATGATCC | 56459 |
rs31524536 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16332300 | AGACACACAGTCAGT[C/T]AGAGACGCTGTTTTA | 56459 |
rs31540221 | snp | A/G/T | 0.495 | 0.0497494 | intron-variant | Sae1 | GRCm38.p3 | 7:16349650 | CGTGTGCTGCTCCTC[A/G/T]ACTTGCAACACTATC | 56459 |
rs31549247 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sae1 | Mm_Celera | 7:16325860 | CAACTCAGAAATCTG[C/T]CTGCCTCTGCCTCCT | 56459 |
rs31555799 | snp | A/C/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16386181 | TTCAGAAGAGCAGTC[A/C/G]GGTGCTCTTACTCAC | 56459 |
rs31561117 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16378252 | AGACTATATATTCAC[A/G]TAAACCTCCTCCCAG | 56459 |
rs31569518 | snp | G/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16340190 | TGGTGGTGGCAGCAT[G/T]TCTTTAATCCCAGCA | 56459 |
rs31570975 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16382082 | CCAGAGGAAACTGGA[A/G]TCCATTCTGTTCTTC | 56459 |
rs31581236 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Sae1 | Mm_Celera | 7:16320292 | AGGCAGGCAGATCTC[C/T]GAGTATGGCTACAGA | 56459 |
rs31587710 | snp | A/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16369806 | CTTGATACTTCTATC[A/T]AATAAGTGCAGCTGG | 56459 |
rs31590818 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16331682 | TGCAGTTCAAGCTGG[C/T]GCTGTCCTGAGTCCT | 56459 |
rs31612334 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Sae1 | GRCm38.p3 | 7:16333701 | TGTGGCATATTTAAA[A/G]AAAGATTCAAAGCAC | 56459 |
rs31655064 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16380726 | GAGAAACCCTGTTTC[A/G]AAAAACCAAAAACCA | 56459 |
rs31658722 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16360333 | GTTAAGAGCACATAC[C/T]GTCCTCGCAGAGGAC | 56459 |
rs31683947 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16375427 | ATCATCTCCTATATC[A/T]CTTCTTGGCTTTGAG | 56459 |
rs31698525 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16340327 | AATAAAGTACTACTA[C/T]AGCAGGGACTAGGGA | 56459 |
rs31699077 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Sae1 | GRCm38.p3 | 7:16374859 | TAGAAACAGTATAGA[C/T]ACTCATCATTCCACA | 56459 |
rs31703444 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Sae1 | GRCm38.p3 | 7:16359874 | CTCCTGTAGCAGGAC[C/T]GTGCTCTCATGACAC | 56459 |
rs31710585 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Sae1 | GRCm38.p3 | 7:16352031 | AGCTGAGATATGAAA[C/T]CCTGAGCTCCCAGCC | 56459 |
rs31714712 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Sae1 | GRCm38.p3 | 7:16338437 | GACTCTTGAGAAGAC[A/G]AGCACTAACGCCCAG | 56459 |
rs31738518 | snp | A/G | 0.32 | 0.24 | intron-variant | Sae1 | Mm_Celera | 7:16361760 | AGACTGCTACATGCT[A/G]TTGGCCACGGAATGG | 56459 |
rs31742784 | snp | C/T | 0.5 | 0 | intron-variant | Sae1 | Mm_Celera | 7:16348522 | GGATTTGAACTCCGG[C/T]CTTCATAATTAATTG | 56459 |
rs31742787 | snp | A/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16367833 | ATCTTTCTCTTGAAA[A/G]CGGTAGTAAGTAAAA | 56459 |
rs31758506 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16355774 | ACACACACACACACA[A/C]AAAAAAAAACCAAAC | 56459 |
rs31769888 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sae1 | Mm_Celera | 7:16326463 | CAACCAGAAAGGTGA[C/T]TTCTTTGGCCTTTCA | 56459 |
rs31777556 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16376813 | TTCTTTCTTTTTTAA[A/G]TGTTTGATGTATGAG | 56459 |
rs31777926 | snp | A/G | 0.42 | 0.183303 | intron-variant | Sae1 | Mm_Celera | 7:16387157 | AACAAACAACCCAAC[A/G]TCTGTAGCTGTGTGC | 56459 |
rs31805528 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | GRCm38.p3 | 7:16340808 | GTAGGACACAGCTGG[C/T]GGGGAAGATAGGGAT | 56459 |
rs31811205 | snp | C/G | 0.5 | 0 | intron-variant | Sae1 | GRCm38.p3 | 7:16377205 | GCACCGGAGGCAGAA[C/G]ACAGGCTGATCTCTG | 56459 |
rs31815282 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16357422 | TTGCCATTCTCAGAC[A/G]TGACATCCAGTTTTC | 56459 |
rs31834085 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Sae1 | GRCm38.p3 | 7:16370590 | ATCCCTACAGAATTC[A/G]GCCTGGCTACACTTC | 56459 |
rs31844044 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Sae1 | GRCm38.p3 | 7:16361407 | TGAACATTCTGTAGA[C/T]CAGGTCGGCCTCAAA | 56459 |
rs31844047 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Sae1 | GRCm38.p3 | 7:16363854 | CAAGTAACTGATCTA[C/T]GAAAACTAATGTGCT | 56459 |
rs31853972 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Sae1 | GRCm38.p3 | 7:16345940 | AATCTATGTAATACA[A/G]CAGAACCATTGGTGA | 56459 |
rs31858942 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Sae1 | Mm_Celera | 7:16326228 | GTCCCCACAGAGCTG[C/T]ATACCTTGCAGAGGT | 56459 |