SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4226342 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Strap | Mm_Celera | 6:137750511 | TAGATTTTCTTCTTC[C/T]CTTTATTAAATTGAC | 20901 |
rs4226343 | snp | C/T | 0.453686 | 0.144955 | utr-variant-3-prime | Strap | Mm_Celera | 6:137750672 | AAGCAGAGACAAGCA[C/T]CCGCCTTCAGAGTTA | 20901 |
rs4226344 | snp | A/T | 0.46875 | 0.121031 | utr-variant-3-prime | Strap | Mm_Celera | 6:137750761 | CACGAACAGCTACTC[A/T]GTGTTGCCCGTGAGT | 20901 |
rs6411307 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Strap | Mm_Celera | 6:137733899 | GCCATTCACTGTTAG[A/G]TTCCAGGCTGATACA | 20901 |
rs13473516 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Strap | Mm_Celera | 6:137745588 | GGAGTTTCTTGTTGC[A/G]GGTGGAGAAGACTTT | 20901 |
rs13473517 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751230 | CTAAACATTTCCTAA[A/T]TTTGAAATTGAATTA | 20901 |
rs13473518 | snp | C/T | 0.473373 | 0.11227 | synonymous-codon | Strap | Mm_Celera | 6:137742042 | TCCTGAAGGAGAGAT[C/T]TTGGTTATTACTTAT | 20901 |
rs29828453 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Strap | Mm_Celera | 6:137750222 | AAGCAGTGTTTAATG[C/G]TTAAGGTTTTGAACT | 20901 |
rs29833847 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strap | Mm_Celera | 6:137739500 | ACACTGCTTGCATAG[C/T]ACAAAAAGCCTTGAA | 20901 |
rs29874497 | snp | C/T | 0.5 | 0 | intron-variant | Strap | Mm_Celera | 6:137749464 | CTTTTCTAAGAGCCC[C/T]GGGTATGTAAAAATT | 20901 |
rs29923519 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strap | Mm_Celera | 6:137749795 | ATGGGCAGGAGGGCT[C/T]AGCAGAAAGCAGAAG | 20901 |
rs29968840 | snp | C/T | 0.475309 | 0.108333 | downstream-variant-500B | Strap | Mm_Celera | 6:137751989 | TATTTTGTGCCATTG[C/T]TTTCCTATTGCTGCA | 20901 |
rs29973609 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Strap | Mm_Celera | 6:137733977 | CCAGGGTCAGACATA[G/T]CAAAGTCTGGAACCA | 20901 |
rs29975826 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Strap | Mm_Celera | 6:137750411 | GGAGTCCTGGGATAA[G/T]GCCATGTTTAGTAGC | 20901 |
rs29982283 | snp | A/C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Strap | GRCm38.p3 | 6:137751176 | TCTATATCATACACA[A/C/G]CCAGCCAGAGCAAAG | 20901 |
rs30064237 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Strap | Mm_Celera | 6:137752151 | CCCTCATGCTAGAAG[C/T]CTTTCCTCAGCTAAA | 20901 |
rs30115902 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Strap | Mm_Celera | 6:137734287 | ACCCCAACTTTCCTG[G/T]CTTCTTTATTTCTGA | 20901 |
rs30128112 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, downstream-variant-500B | Strap | Mm_Celera | 6:137748978 | GATTCTAACTGAGCA[A/G]TGTCCTTTATGTGAT | 20901 |
rs30169900 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strap | Mm_Celera | 6:137739584 | GGAGGAGGGGAATGG[C/T]AGACTGGCAAGGCAG | 20901 |
rs30217901 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Strap | Mm_Celera | 6:137750276 | ATTACTACAGGACCC[A/G]AAAAAGCGTGATTTA | 20901 |
rs30226613 | snp | A/G | 0.375 | 0.216506 | intron-variant | Strap | Mm_Celera | 6:137739442 | GGATTTCACACAGGT[A/G]TGAGAAAATGGAATT | 20901 |
rs30270583 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strap | Mm_Celera | 6:137750354 | GGGAGAGGGGTGGGG[C/T]TAAACAATTGGTGAA | 20901 |
rs30373335 | snp | A/G | 0.492188 | 0.0620098 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751913 | CCTAAATAAAATTGA[A/G]TGCATCTTTTGTAAT | 20901 |
rs30559308 | snp | C/T | 0.493827 | 0.0552116 | downstream-variant-500B | Strap | Mm_Celera | 6:137752310 | CTGTTAATCCTTCCT[C/T]GTGCTGCCCATGGTT | 20901 |
rs30567039 | snp | G/T | 0.426035 | 0.177515 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751184 | ATACACAGCCAGCCA[G/T]AGCAAAGACAGTTTG | 20901 |
rs30710356 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Strap | Mm_Celera | 6:137739580 | GAGGGGAGGAGGGGA[A/G]TGGCAGACTGGCAAG | 20901 |
rs30750698 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751240 | CCTAAATTTGAAATT[C/G]AATTATTTAAACTTG | 20901 |
rs30803966 | snp | A/G | 0.5 | 0 | intron-variant | Strap | Mm_Celera | 6:137749504 | AACGTTTTGGTCCAT[A/G]GCAAAAGAAATTTAA | 20901 |
rs30818338 | snp | C/G/T | 0.5 | 0 | intron-variant | Strap | GRCm38.p3 | 6:137749243 | AGAGTGGCTGTTGTA[C/G/T]TAAAGGTGACTTTGA | 20901 |
rs30852664 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Strap | Mm_Celera | 6:137749263 | GGTGACTTTGAGATG[C/T]CTTTTAGAATCACAG | 20901 |
rs30860024 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Strap | Mm_Celera | 6:137734307 | TTTATTTCTGATCCG[G/T]TCGGTCCCTCCTCTC | 20901 |
rs30932894 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Strap | Mm_Celera | 6:137733990 | TAGCAAAGTCTGGAA[C/T]CAGGCCCCCCAGAGT | 20901 |
rs30953943 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137749777 | GAGGATGCGCTGTGG[A/G]TGATGGGCAGGAGGG | 20901 |
rs31003394 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Strap | Mm_Celera | 6:137749639 | CCTCGCATACACTCA[A/G]GGACAGGGTCTAAAA | 20901 |
rs31972494 | snp | A/G | 0.345679 | 0.230967 | upstream-variant-2KB | Strap | Mm_Celera | 6:137735078 | TACCGCCTTCCCGCC[A/G]GTCGTCACTTCCGGC | 20901 |
rs31972496 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Strap | Mm_Celera | 6:137735676 | AGGATTTACGGGAAG[A/G]AGAAATTAGGCCAGG | 20901 |
rs31972498 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Strap | Mm_Celera | 6:137735694 | AAATTAGGCCAGGCC[A/G]AGAGGAGTGCCCTTT | 20901 |
rs31972500 | snp | A/G | 0.42 | 0.183303 | intron-variant | Strap | Mm_Celera | 6:137735809 | TGGTCCAAAGTAAAA[A/G]GCGGCTATCTAGATC | 20901 |
rs31972502 | snp | A/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137736507 | CATTCTGTTTGAATT[A/T]TGTGGTGACATGGCC | 20901 |
rs31972864 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Strap | Mm_Celera | 6:137744733 | CATGTTTGTAGAAAA[A/T]ATAGAGTGAAATTTT | 20901 |
rs31972866 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137744763 | TCAAAAGAAAAATAA[C/T]CTGGCATTGTCACTG | 20901 |
rs31972868 | snp | C/T | 0.18 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137744976 | CATAATAGCAACAAG[C/T]AGTAATGAATAATCT | 20901 |
rs31972870 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Strap | Mm_Celera | 6:137745000 | ATAATCTGAAGTAAA[A/G]ACATCGCTATCCACT | 20901 |
rs31972872 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137745156 | CCTGACCCCAGAGAG[C/T]GGCTAAGGCAAGGAG | 20901 |
rs31973234 | snp | C/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137736817 | CTGGCTCTAGATAAT[C/T]TAAAACCGGACCTCA | 20901 |
rs31973236 | snp | C/G | 0.18 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137737251 | ATCTCAGTTCACTTT[C/G]TCTTTTGATACAGTC | 20901 |
rs31973238 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Strap | Mm_Celera | 6:137737610 | AGTAGACCAGAGCCT[A/G]GAGAGTGAAAATGGC | 20901 |
rs31973240 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Strap | Mm_Celera | 6:137738212 | CTGAGGAATGGGTCA[C/T]GGTTAGAACCCTGGG | 20901 |
rs31973242 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Strap | Mm_Celera | 6:137738462 | GCCCTTGGCGTTCCT[A/G]TCTCTGATTGCTCCT | 20901 |
rs31973774 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Strap | Mm_Celera | 6:137745290 | CGTGTCTCCCTGAGA[C/T]GACATCCACTTGGGT | 20901 |
rs31973776 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Strap | Mm_Celera | 6:137745378 | GAAATCCATTTATAC[G/T]TAGCTGAATCTATGT | 20901 |
rs31973779 | snp | C/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137745654 | GTTAGGTGAGCCTCG[C/T]TCTCTCTCTCTTTAA | 20901 |
rs31973781 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137746031 | AGAATTATAGACCCT[C/T]AGACAAAATATACTG | 20901 |
rs31973783 | snp | C/G | 0.5 | 0 | intron-variant | Strap | Mm_Celera | 6:137746059 | CTGAGCTCATTTCCT[C/G]TTAATTGAGTCTTAT | 20901 |
rs31974044 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Strap | Mm_Celera | 6:137738463 | CCCTTGGCGTTCCTA[C/T]CTCTGATTGCTCCTG | 20901 |
rs31974046 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Strap | Mm_Celera | 6:137738624 | TTTGAGAAAAGTTTG[A/G]CTGAGTACTTAAGGC | 20901 |
rs31974048 | snp | C/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137739061 | GAATTGGTTAAGATA[C/T]TTTGCAGATATGGTA | 20901 |
rs31974050 | snp | C/T | 0.489796 | 0.070696 | synonymous-codon | Strap | Mm_Celera | 6:137739809 | CTGCGCATATATGAC[C/T]TGAACAAACCTGAAG | 20901 |
rs31974052 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Strap | Mm_Celera | 6:137739869 | TGCTTTTCCTTTTCC[A/G]TTAGGTAGCGACTAA | 20901 |
rs31974695 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137746120 | TTTGGATGCTTTATT[G/T]GGATGGATTATTTAT | 20901 |
rs31974697 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Strap | Mm_Celera | 6:137746163 | ATACAAAACATATAC[A/G]AGGATATTTTGTTCT | 20901 |
rs31974699 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137746195 | CCTAAGGAGAGAACA[A/G]ATAACAAAATCCTGC | 20901 |
rs31974701 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Strap | Mm_Celera | 6:137746272 | GAGAATGGTGGGGTC[C/T]CACTGGTTTATCAAG | 20901 |
rs31974703 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Strap | Mm_Celera | 6:137746310 | TAGAAAGAGTAATGT[A/G]TATAGGATTAGAATA | 20901 |
rs31974984 | snp | G/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137739890 | TAGCGACTAAAGAAC[G/T]CTAAACCATTATCTA | 20901 |
rs31974986 | snp | C/T | 0.18 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137739908 | AAACCATTATCTATT[C/T]TCCTTCATTGTTAAT | 20901 |
rs31974988 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137740023 | GCTCATAGCCTTCTG[A/G]CACTGTAAACATCAC | 20901 |
rs31974990 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137740084 | AGGTTTTGTAAAGGT[A/T]CTAGAGCAATGCTGC | 20901 |
rs31974992 | snp | C/G | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137740190 | GATTTAGCTGTATTG[C/G]TTGTTCAAAAGAAAC | 20901 |
rs31975455 | snp | C/T | 0.375 | 0.216506 | intron-variant | Strap | Mm_Celera | 6:137746511 | GAGTCTTGCTATTTC[C/T]CTAAGTTTCATAGTT | 20901 |
rs31975457 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137746551 | TAGAATGGCTGATGT[A/G]TGATTAATTTGAAGC | 20901 |
rs31975459 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747063 | TTACTTACCAAGTCC[A/C]ACTATGTTTTGCTTT | 20901 |
rs31975461 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747246 | AACAGGTGGACTGGG[A/G]CTGCTTAAGTCAGTT | 20901 |
rs31975463 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Strap | GRCm38.p3 | 6:137747290 | GTCACACATTCCGTT[A/C]TTCTCAGCTTGAGAG | 20901 |
rs31975774 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Strap | Mm_Celera | 6:137740332 | GCGTTTGTAATGTAG[C/T]AGACTGTACTGAACA | 20901 |
rs31975776 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137740395 | TTTCCCTCTGCTTAC[A/T]TTTTGGTGGACTTCT | 20901 |
rs31975778 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137740434 | ATCAAAGTGATGTTG[A/G]GCTTGTGTGACACAG | 20901 |
rs31975780 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137740477 | TCAGGGTTGGATGGA[C/T]GCTTTTCTTCATCCT | 20901 |
rs31975782 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137740792 | AGTAGTTACTACCAA[C/T]AGTGACTTTGACAAA | 20901 |
rs31976255 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137747346 | AGCCTTAGCATTGCT[C/G]ACCCAGACTGTGAAG | 20901 |
rs31976257 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Strap | Mm_Celera | 6:137747411 | CAGCTGTTCTCATCT[C/T]GGTCTCTGTTCATGG | 20901 |
rs31976259 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747645 | ATTAAAATGTAAGGT[C/T]AGTAAGGTCCCTATT | 20901 |
rs31976261 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747689 | AGCATTGTGGTGGAA[C/T]TAGGAAGCCTAGATA | 20901 |
rs31976263 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Strap | Mm_Celera | 6:137747837 | ATGGAGTTCACAGAC[G/T]TGAGCTCTAGTCTGT | 20901 |
rs31976614 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Strap | Mm_Celera | 6:137740849 | GATTAGCTTAATACA[C/G]TGTTGTTCCTGGGCC | 20901 |
rs31976616 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Strap | Mm_Celera | 6:137741460 | ACCTTGTGGTTTATA[A/G]ATACTTTTAATAATC | 20901 |
rs31976618 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Strap | Mm_Celera | 6:137741481 | TTTAATAATCATGTA[C/G]GAAAATGTGTGTAAC | 20901 |
rs31976620 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Strap | Mm_Celera | 6:137741545 | TGGACTTACTCTTAT[C/T]GTCACCTGGAGTAGA | 20901 |
rs31976622 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137741693 | AAAAGATGCATAGCT[G/T]CGAGATAGACCCAAG | 20901 |
rs31976870 | snp | C/T | 0.486111 | 0.0821678 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751297 | TCATTTATTTCCTTC[C/T]GGATGGATACAATTG | 20901 |
rs31976872 | snp | C/T | 0.42 | 0.183303 | utr-variant-3-prime | Strap | Mm_Celera | 6:137751316 | TGGATACAATTGCTT[C/T]TCTTGTCTCTTTAAA | 20901 |
rs31977045 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747863 | TCTGTAGAATTAAGT[C/T]TTTATTGACAGCCTC | 20901 |
rs31977047 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Strap | Mm_Celera | 6:137747959 | TCAAAAGAGTGATGT[A/G]CAGTGAATAACACCT | 20901 |
rs31977049 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137747960 | CAAAAGAGTGATGTA[C/T]AGTGAATAACACCTT | 20901 |
rs31977051 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Strap | Mm_Celera | 6:137748006 | GCTGCAGGAAAGATG[A/G]CAGACGGCCGTTTCC | 20901 |
rs31977053 | snp | C/T | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137748107 | CATGTTTCTTCTTGT[C/T]GGCTGTCAGAGCGCA | 20901 |
rs31977384 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Strap | Mm_Celera | 6:137741849 | AATGAAAATTGCTTC[A/G]TTACAATTGTGATTG | 20901 |
rs31977386 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Strap | Mm_Celera | 6:137741927 | ATTTACTTATGTGCT[C/T]ATTCATTTGCTTATT | 20901 |
rs31977388 | snp | A/G | 0.32 | 0.24 | intron-variant | Strap | Mm_Celera | 6:137741940 | CTCATTCATTTGCTT[A/G]TTCATTTGCAGGCTC | 20901 |
rs31977392 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Strap | Mm_Celera | 6:137742471 | TTTCGTGATTCTTTT[A/G]AAGGCAGATTCTTAC | 20901 |