SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6290869 | snp | A/T | 0.5 | 0 | intron-variant | Hltf | Mm_Celera | 3:20092279 | ATACTATAGTTAAAA[A/T]TCTCAATNTTCTAGA | 20585 |
rs6290887 | snp | A/G | 0.5 | 0 | intron-variant | Hltf | Mm_Celera | 3:20092287 | GTTAAAANTCTCAAT[A/G]TTCTAGAAAGAATGT | 20585 |
rs30110097 | snp | C/T | 0.5 | 0 | intron-variant | Hltf | GRCm38.p3 | 3:20107636 | CCACAAGGTGGGAAC[C/T]GCTACACTAGGGACT | 20585 |
rs31316542 | snp | A/T | 0.5 | 0 | intron-variant | Hltf | Mm_Celera | 3:20093573 | GTGTGTGTGTGTGTG[A/T]GAAAGTGTACACATG | 20585 |
rs31670999 | snp | C/G | 0.5 | 0 | intron-variant | Hltf | Mm_Celera | 3:20093536 | CAATTCAGAAATTAC[C/G]TGTGTGTGTGTGTGT | 20585 |
rs33562195 | snp | C/T | 0.18 | 0.24 | missense, nc-transcript-variant | Hltf | Mm_Celera | 3:20082926 | GCAAGCTGAAAAATG[C/T]ACAGTTAAATACTAA | 20585 |
rs33562198 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20083325 | CACAGTAGTGAACAG[A/G]TTTGGAGTATCTTCT | 20585 |
rs33562201 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20083354 | CTTGGCAGCATTCAC[A/G]TTATGCACATATTAA | 20585 |
rs33563084 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20083407 | TTCATCTTTGAAACA[C/T]GCTTTATATCCCTGT | 20585 |
rs33563087 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Hltf | Mm_Celera | 3:20083518 | CAGCTTCACACTGGG[G/T]GAGACGCACTCCATC | 20585 |
rs33563090 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20084398 | TTGTTTTAGAAAGGG[C/T]CAAGGTGTAATGGGA | 20585 |
rs33563093 | snp | C/T | 0.18 | 0.24 | intron-variant | Hltf | Mm_Celera | 3:20084464 | TGTAAATCAACAAAG[C/T]CATTTATGATTGGTT | 20585 |
rs33563816 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Hltf | Mm_Celera | 3:20084537 | ACTGGGATTAAGATT[A/T]ACTTTTCTTAATGTC | 20585 |
rs33563818 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hltf | Mm_Celera | 3:20084638 | CTATGGTCTCCATTT[A/G]TAGCACAAGATCTTA | 20585 |
rs33563821 | snp | C/T | 0.260355 | 0.249785 | missense, nc-transcript-variant | Hltf | Mm_Celera | 3:20086099 | TTGTTCTTTTAGGCA[C/T]GTCTATGATGGAGTG | 20585 |
rs33563864 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20099492 | ATTGTGTATGGACTG[A/G]TAAGTTGATAAGAAG | 20585 |
rs33563867 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20099508 | TAAGTTGATAAGAAG[C/G]CATTTGAGAAAAAAG | 20585 |
rs33563870 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20099992 | TAACATTGTATGGCT[C/T]TGTCTACTTTAGCTG | 20585 |
rs33563873 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20100343 | AAGTAATTTCTTGGC[C/G]CTGCAAAAAATAAAA | 20585 |
rs33564496 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20100390 | GATTTCAGAGGTCAG[A/C]GGGCCTTGCTTGCTT | 20585 |
rs33564498 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hltf | Mm_Celera | 3:20100475 | TGGGCTTTTATATTC[A/G]TTTTCTCTTTTGACA | 20585 |
rs33564501 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103145 | TAGCCCACCTACACC[A/G]GAAAGCCTAGTGTTT | 20585 |
rs33564664 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hltf | Mm_Celera | 3:20086318 | TATTTGTTGAAGTAA[G/T]TACCTTTTTTTTGAA | 20585 |
rs33564667 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20086345 | TGAAGGCTTATTTGA[G/T]TAACTTAATTGCTGA | 20585 |
rs33564670 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20086497 | CTTCTATAACTGTTT[A/G]TAACATCACATGTGC | 20585 |
rs33564672 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20086542 | CTTCATTTCTTCTCA[C/T]AGATTTTTCTCACTT | 20585 |
rs33564875 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20113830 | TCTGGACTTACACTT[C/T]ATTCTCCTTTGTACT | 20585 |
rs33564878 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20114000 | GTACATCTTTGTGCA[C/T]GTATTCCAGTAATTC | 20585 |
rs33564881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20114293 | TCTGCTGCTCATGGT[C/T]GTATTTCCTGCTGTG | 20585 |
rs33565055 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20108198 | AAAATAGTAATTCCA[A/T]TTCTGCTTTTAGTCT | 20585 |
rs33565058 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20108354 | TAAATTATATGAAAA[C/T]CTTCTCAATAAAAAA | 20585 |
rs33565061 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20108599 | AGAAAGGATAGATTG[A/G]TTGTTGGAGATTTGT | 20585 |
rs33565364 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103263 | TCAAAAGCTCTGCAT[C/T]AGACCTGTCATGTGA | 20585 |
rs33565367 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103318 | TGGAGAGGCAGGTAT[A/G]GAGTTCAGTGCTCCC | 20585 |
rs33565370 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103344 | CTCCCAGTTTGACTC[G/T]TAAGTTTCTGTTATT | 20585 |
rs33565372 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103435 | TCCGAAAAGGTACTA[A/G]CGTGGCTGGTAAAAC | 20585 |
rs33565694 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20114322 | TGACCTGCTTGTTCA[C/T]TTCTTCTTTGCTTTT | 20585 |
rs33565697 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20114654 | AGGGGCAGTCTGTAT[A/G]ATTCTTCTGGAAGAT | 20585 |
rs33565700 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20114718 | CTTTTCCAAATGAAG[A/C]GGTTATTGTTCTGTC | 20585 |
rs33565703 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20115182 | ACACACACACACAAA[C/T]AAAAGTAACTTCAGT | 20585 |
rs33565725 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20087223 | CCCGAATTGGCTTCT[C/G]TTTTCAGCTGTCAGA | 20585 |
rs33565728 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20087613 | CAAATAAAATTATGC[A/G]AAACTGTAAAGGCAT | 20585 |
rs33565731 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20088519 | TCTCCTTAACTGGAT[C/T]TCTTCTCTACCAGAC | 20585 |
rs33565733 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20088797 | TTCTACTCCTTGTCT[C/T]CTGTGGGTGTTCATG | 20585 |
rs33565954 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hltf | Mm_Celera | 3:20108984 | GTTTAGTCATTTCAT[C/T]TATTTAAAATGATAT | 20585 |
rs33565957 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20109087 | GTACCTGGCAGATGG[C/T]CAGATGCTCAGTAGG | 20585 |
rs33565959 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20109158 | CATTCACTTGGAAGC[C/T]GTTTACTTAGCTTGT | 20585 |
rs33565962 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20109242 | AATTTGGTTTAACGA[A/C]TATTTGTTAACCTTT | 20585 |
rs33566265 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103573 | GAGTGCTGAGGAAGC[G/T]GTCTGTTTGAATTGT | 20585 |
rs33566268 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20103604 | GTTCTCAGGGATGTT[A/G]TTGTTAAAGTAACCT | 20585 |
rs33566271 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20104204 | TTTGAAAAAAAAATA[A/T]TAGTCAGTTTTGCCT | 20585 |
rs33566273 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hltf | Mm_Celera | 3:20104292 | GCTCCAGAGGTGTCA[A/G]CCCATGGTAGTGGAA | 20585 |
rs33566486 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20115745 | TAATGTTCTGTAATA[C/G]AGCTCTTGTTGTTAT | 20585 |
rs33566489 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20116070 | ATATAATTTGTGTTT[A/G]TGATGTTCTCATGTG | 20585 |
rs33566492 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20116362 | GAAATACAAGTTCTT[A/G]TAAAGGTATGTATAT | 20585 |
rs33566654 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Hltf | Mm_Celera | 3:20056968 | ATTACCTTTACCTTG[C/G]CTGATACTGTTGCAT | 20585 |
rs33566656 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Hltf | Mm_Celera | 3:20057641 | CTCGATGTTTTACCG[C/T]GCAAGGCGTCTCGGA | 20585 |
rs33566659 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Hltf | Mm_Celera | 3:20057687 | GTAGAACCCGGACGC[A/G]CCGCACTGCCTTTGA | 20585 |
rs33566662 | snp | A/T | 0.5 | 0 | intron-variant | Hltf | Mm_Celera | 3:20060779 | TGTTTAGTAGTTGTA[A/T]GAGAGGTAGTATATA | 20585 |
rs33566686 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Hltf | Mm_Celera | 3:20088834 | TTCATCTTCTCTCTG[C/T]GTCTTGGGACTCTGG | 20585 |
rs33566688 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20088913 | CTCAGGAGCTTGAGA[A/G]TTTTGAGGCCATCTT | 20585 |
rs33566690 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hltf | Mm_Celera | 3:20089064 | TAATTGCATAGAGTG[A/G]TTCAGTGTTGGCAGG | 20585 |
rs33566693 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20090889 | CAGCCATCTGAAATA[A/T]AAGGACATCACTGTC | 20585 |
rs33566935 | snp | C/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Hltf | Mm_Celera | 3:20109485 | GTTCTTAATGGATCC[C/G]GTAAGTACTTATATA | 20585 |
rs33566937 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20109693 | TGTGTAAAACTAGTC[A/C]GCTTCTGTGTTTTTA | 20585 |
rs33566939 | snp | C/T | 0.32 | 0.24 | intron-variant | Hltf | Mm_Celera | 3:20109705 | GTCAGCTTCTGTGTT[C/T]TTAAGTACGGTTCTG | 20585 |
rs33566942 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20109780 | TTTAAGATTCAGTAA[A/G]CAGCAAATCAATGAG | 20585 |
rs33567245 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20104373 | GAGCACCGGAAACAA[A/G]TGCTCAAGTCAGGGC | 20585 |
rs33567248 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20104450 | CGTCAGTCAGTGCTG[C/T]AGCTGGAGACCTGGA | 20585 |
rs33567251 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20104500 | GGAGAGTGTTTCATA[A/C]GTAAAAAATAGCAAG | 20585 |
rs33567275 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Hltf | Mm_Celera | 3:20116418 | TTCATTCTGACTTTA[A/G/T]TGTGCAGTATTGTTA | 20585 |
rs33567278 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hltf | Mm_Celera | 3:20116489 | AGTAAAGGTTTCTTA[A/G]GAGCATTAAAAAACT | 20585 |
rs33567281 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Hltf | Mm_Celera | 3:20116583 | GCAGTTCATTGTGAA[A/G]GACTCTGTGGAAGAA | 20585 |
rs33567465 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20091021 | TTCTGCTCGTCTGGT[C/T]GTACAGTTGCAGTTC | 20585 |
rs33567467 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20091047 | AGTTCTCACCTAAGA[A/G]TCTACCAGCTTTTCT | 20585 |
rs33567469 | snp | A/G | 0.32 | 0.24 | intron-variant | Hltf | Mm_Celera | 3:20095852 | CATGAGTCTTTAATT[A/G]TATCTATTTCTTTAA | 20585 |
rs33567472 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hltf | Mm_Celera | 3:20098237 | AAGTTTATGAGGTGA[C/T]CCATTAGTGACGATT | 20585 |
rs33567684 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20077798 | ATATAGCACTATTAG[A/G]TAGAATAGATCAGAT | 20585 |
rs33567686 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20078506 | TCCTGTTCGTCCCTC[A/G]GTCTTCTGGTGTAGT | 20585 |
rs33567689 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20078560 | TGGCCTAATCTTTTG[C/T]GTGTGTACAGGCCTT | 20585 |
rs33567692 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20078589 | TTTCACATTATCTTC[A/G]GTAGGTTGGCTTAGT | 20585 |
rs33567784 | snp | A/G | 0.142012 | 0.225474 | missense, nc-transcript-variant | Hltf | Mm_Celera | 3:20116698 | CAAGCTAAAATCAAC[A/G]AAATCAGAACTTTAA | 20585 |
rs33567786 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Hltf | Mm_Celera | 3:20116721 | AACTTTAATTGACTT[A/G]TAACTTGTGGGGTGT | 20585 |
rs33567788 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Hltf | Mm_Celera | 3:20116867 | ACTGACACATCTTCT[A/G]TACCTGAATCTCTTT | 20585 |
rs33567790 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Hltf | Mm_Celera | 3:20116986 | TCCCTTGCTGAGGGT[A/G]TTTTCCTACATTTCC | 20585 |
rs33567793 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Hltf | Mm_Celera | 3:20117044 | TGGTTGAAGCTTCTA[A/C]TTGTAACCACTTACT | 20585 |
rs33567924 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20109941 | AGACATAGAAGTTCC[C/T]GAGGAGACCTAAAGA | 20585 |
rs33567927 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hltf | Mm_Celera | 3:20109981 | AGACATGCATCCGCC[C/T]TGATTCAGGTTCAGA | 20585 |
rs33567930 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hltf | Mm_Celera | 3:20110033 | TAAGTTTCCCTGGCT[G/T]ACAACATGCACTTAA | 20585 |
rs33567933 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20110246 | AAAAAACTGTCAGCT[A/G]ATACAGCCTAAAGTC | 20585 |
rs33568084 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hltf | Mm_Celera | 3:20104801 | CATCCTTTATAACTA[A/T]TTTTTGTTTTCTTAG | 20585 |
rs33568087 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20105498 | TATGTACCACTTACT[C/T]TGAAGGGCCAGCTGA | 20585 |
rs33568090 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hltf | Mm_Celera | 3:20105880 | ACCTTTGCTGTAAGA[G/T]TTTTTTAAAATTATA | 20585 |
rs33568093 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20106236 | ATGATTTCTGCAAAT[A/G]CCAGAATAAAGATGA | 20585 |
rs33568545 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hltf | Mm_Celera | 3:20098313 | GTCTCCAAAGCATAA[A/G]CTTCCGTGTCACTGA | 20585 |
rs33568548 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hltf | Mm_Celera | 3:20098607 | TTAATGAACATTTCA[C/T]GTGGTTGATTTTGGT | 20585 |
rs33568550 | snp | C/T | 0.32 | 0.24 | intron-variant | Hltf | Mm_Celera | 3:20098684 | CACACACTTGGGTGC[C/T]GTAGTTTTAGAGCAG | 20585 |
rs33568552 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hltf | Mm_Celera | 3:20098732 | TTGGGACCCTAAGTG[A/G]GCCATACGGTCATTA | 20585 |
rs33568585 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hltf | Mm_Celera | 3:20080329 | CTCCAGCATTACTCT[C/T]AGGCTAGAATATGAA | 20585 |
rs33568588 | snp | G/T | 0.18 | 0.24 | intron-variant | Hltf | Mm_Celera | 3:20080399 | AAAAATACAGTAATA[G/T]CAATAAAAAATAACC | 20585 |