SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6229719 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97815631 | CAGGGGCTGCTCAGT[G/T]ATAAGAGAAGCTCAG | 16796 |
rs6230292 | snp | C/T | 0.487535 | 0.077957 | synonymous-codon | Lasp1 | Mm_Celera | 11:97815746 | CGACACTCCGGAAAA[C/T]CTCCGCCTCAAGCAA | 16796 |
rs6230876 | snp | A/C | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97815818 | GGCTGGTGGAAGGGG[A/C]GNGGGGTTGTGTAAC | 16796 |
rs6230889 | snp | G/T | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97815820 | CTGGTGGAAGGGGNG[G/T]GGGGTTGTGTAACAG | 16796 |
rs6231943 | snp | A/G | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97809404 | GACAAGTGTGAGGGG[A/G]AGTCAGGGTCATGAA | 16796 |
rs6233529 | snp | A/T | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97809702 | TAGAGAAATATTTAT[A/T]CCCTGAGTTATTTGT | 16796 |
rs13468536 | snp | G/T | 0.465374 | 0.126941 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837638 | GGACAGTACTCACTC[G/T]GCTTCATTCATCTCT | 16796 |
rs13468537 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837394 | AGGCCCTCCCGCCTC[G/T]CTGGGGAGGTGGGAG | 16796 |
rs13468538 | snp | A/G | 0.465374 | 0.126941 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837467 | GAGGCTACAGAGCCC[A/G]GTACCAGAAGGGCCG | 16796 |
rs13468540 | snp | C/T | | | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97838250 | CCATAGTCTCTTCCT[C/T]TGTAAAGGTCTTTTC | 16796 |
rs27074205 | snp | A/C | 0.391111 | 0.206368 | upstream-variant-2KB, downstream-variant-500B | B230217C12Rik, Lasp1 | Mm_Celera | 11:97839223 | TACTGCCACGTTTGA[A/C]TTGTAAATTGATAGC | 16796 |
rs27074206 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB, downstream-variant-500B | B230217C12Rik, Lasp1 | Mm_Celera | 11:97839150 | CTTGGGAAGCAGGCT[A/G]CTCTGCAAGAGTTCA | 16796 |
rs27074207 | snp | C/T | 0.42 | 0.183303 | upstream-variant-2KB, downstream-variant-500B | B230217C12Rik, Lasp1 | Mm_Celera | 11:97839088 | TTCTAGCCACCAGTG[C/T]CCTCCTGGACAGTTG | 16796 |
rs27074208 | snp | A/G/T | 0.336735 | 0.234472 | utr-variant-3-prime | Lasp1 | GRCm38.p3 | 11:97838145 | GAAGAGGGGAGAGGA[A/G/T]CTACCTAAGGTGCTG | 16796 |
rs27074209 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97838079 | CCTCCCTTCCCAACG[A/T]CAAGTCAGCTGTTCT | 16796 |
rs27074210 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837772 | TTTGAACCTGAAGAC[C/T]TTGATCAGGCCAGCA | 16796 |
rs27074211 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837556 | GGAGAGTCCAGGGCT[C/T]CAAAGCTGGCGGCAC | 16796 |
rs27074212 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837445 | GTGCTTTTCTGTCGT[C/T]GTGTCTGAGGCTACA | 16796 |
rs27074213 | snp | A/G | 0.492188 | 0.0620098 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837311 | TGGCCTTCCTTCCCC[A/G]GAACAAGGCTGGACT | 16796 |
rs27074214 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837285 | GGGAAAAGGTCTCCG[A/C]GTCTCTCCTGTGGCC | 16796 |
rs27074215 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837284 | TGGGAAAAGGTCTCC[A/G]CGTCTCTCCTGTGGC | 16796 |
rs27074216 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97837000 | GTGCAGTCCTCCACA[G/T]AACAGAGTGTGCCCA | 16796 |
rs27074217 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97836967 | AGTTCCTGCTTCAGA[C/T]TGAATCCTTGCCCCT | 16796 |
rs27074218 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97836881 | GGGTCGGTATTAAGG[C/T]CTCGTGCTGACCTTT | 16796 |
rs27074219 | snp | A/G | 0.456747 | 0.140554 | utr-variant-3-prime | Lasp1 | Mm_Celera | 11:97836475 | TTGATTTTTCTCTCT[A/G]GATGGAACAGGCTGG | 16796 |
rs27074220 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lasp1 | Mm_Celera | 11:97834951 | GCCTTTGAGACTAGT[A/G]ATGTACACTCCACTC | 16796 |
rs27074221 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Lasp1 | Mm_Celera | 11:97834926 | GACTTGTGGGCCCAG[A/G]AGAAGGAAAGCCTTT | 16796 |
rs27074222 | snp | C/G | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97834594 | TGTGCCAGCCAGGCT[C/G]ATCTCCACGCTGGGA | 16796 |
rs27074223 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97833902 | CCCTGGCATGAAGTC[C/T]GAGACACTAATGAAT | 16796 |
rs27074224 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Lasp1 | Mm_Celera | 11:97833356 | GCTTGTCATGGTCAA[A/G]TCACTTAGACACACA | 16796 |
rs27074225 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Lasp1 | Mm_Celera | 11:97833240 | CTGTGCAATAGCACA[C/T]AGCATTAAGGAGGTG | 16796 |
rs27074226 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Lasp1 | Mm_Celera | 11:97833178 | ATATGGGGCTTTGTG[A/G]CCAACCAGTCCTCGC | 16796 |
rs27074227 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97833010 | TCGGGTAGCCAAGCC[A/G]TTTTGCACTTTCTGT | 16796 |
rs27074228 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lasp1 | Mm_Celera | 11:97832849 | GCAGCAGCCTAGGGC[C/T]GTAAGTAGGAGCGGC | 16796 |
rs27074229 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97832809 | TGGCACAGTCATTGT[A/G]TCATGTGCTGACCAT | 16796 |
rs27074230 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Lasp1 | Mm_Celera | 11:97832760 | TAAAGTCACCCAGGG[G/T]AGTATTTGGCCTGTC | 16796 |
rs27074231 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97832646 | CCTCATGTTTTGTCC[A/G]TCACTTAAGTGTGCA | 16796 |
rs27074232 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97832244 | ACTAGGACTCTTGGG[C/T]CTCCAGAGCTCTGGG | 16796 |
rs27074233 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97832028 | GCTCTCTGCTTCTAG[A/G]CAACACCCTTCCCAC | 16796 |
rs27074234 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97831828 | AGGTCCCCTGCGTCT[A/G]TGCGTACCTCACACC | 16796 |
rs27074235 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97831787 | CTTCCTATTGGCCAC[A/G]GAGCAGGGTCCCTAA | 16796 |
rs27074236 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97831414 | AACCTGGAAATACTC[C/G]TGTCCACATACCTGC | 16796 |
rs27074237 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97831160 | GGATTGTCTTCCACT[A/G]TTCAAGATGCCGGAG | 16796 |
rs27074238 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97831109 | TGGCGAGTACACTGA[C/T]GGTGGTGAGTGGCGT | 16796 |
rs27074239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97831060 | GCCTTGGTGTTAAGG[A/G]CTGCGCAGATGTTAA | 16796 |
rs27074240 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97830875 | TCACTTATTTAGTGC[G/T]TGTGTTATCGAGGTC | 16796 |
rs27074241 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97830593 | ACAGAGCCTCCTAAC[A/G]TTTCAGCCACTATAC | 16796 |
rs27074242 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Lasp1 | Mm_Celera | 11:97830470 | GGACCCTCGGGAGGG[C/T]AAAGAAACACCCTCC | 16796 |
rs27074243 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lasp1 | Mm_Celera | 11:97829828 | CTAAGGCTCTTAAGT[A/G]CTAACAGTAGATTCA | 16796 |
rs27074244 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97829576 | TGCTGCGGTTACATG[C/T]CCAGCCTATGTGTGT | 16796 |
rs27074245 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97828560 | TAATGACCCACAGGA[C/T]GGTAAAACCATAAAA | 16796 |
rs27074246 | snp | A/T | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97828442 | GTAGAGCCTTAGTTC[A/T]GGGACCCTCTTAGCC | 16796 |
rs27074247 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lasp1 | Mm_Celera | 11:97828158 | TTCCTTCCAGTATAC[A/G]TGTCTACACATGCAG | 16796 |
rs27074248 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97828089 | TGTTTGCTCCAGAGC[A/G]CTGAGGGCTTGAGTG | 16796 |
rs27074249 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97828065 | AGAGCCTTCCATTTG[A/C]AGTCTTTGTGTTTGC | 16796 |
rs27074250 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97827820 | CGTCCCACAGATGCT[A/G]GAATGCTCGGGAAGT | 16796 |
rs27074251 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Lasp1 | Mm_Celera | 11:97827787 | GTCTTGTTCCAGGCA[C/G]GCTGGGCTCCCACCT | 16796 |
rs27074252 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97827691 | CTAAGTGACTATTTT[C/T]CTGGAGTGGTCATCT | 16796 |
rs27074253 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lasp1 | Mm_Celera | 11:97827528 | TTCCAAAATAGCATC[C/T]TTGTTCGTGGCTCAT | 16796 |
rs27074254 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Lasp1 | Mm_Celera | 11:97827382 | CCCCTAAGTCCGAGG[A/C]CACTGGGCATGACTA | 16796 |
rs27074255 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97827352 | TTATCGCTTAAACTC[A/G]TACGGTCTTACCAAC | 16796 |
rs27074256 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97827265 | AGCATTCCAGATTGG[C/T]ACCCCTGGACCGGAG | 16796 |
rs27074257 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Lasp1 | Mm_Celera | 11:97827245 | AACTCAGGCCTCTGT[C/T]TCCCAGCATTCCAGA | 16796 |
rs27074258 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Lasp1 | GRCm38.p3 | 11:97827201 | CCATACACAAAGGAT[C/T]CCCTTCTGTCATCTG | 16796 |
rs27074259 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97827122 | GTCCCGCACAGTCAG[C/T]TGGGCTGCAGAGCTC | 16796 |
rs27074260 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Lasp1 | Mm_Celera | 11:97827084 | GTTTTAGGGAGTGTG[A/T]CCAGGGTCTGTCTCT | 16796 |
rs27074261 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Lasp1 | Mm_Celera | 11:97826934 | GCCTACAGTAGCCAC[C/G]GTATCTACACTACCG | 16796 |
rs27074262 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Lasp1 | Mm_Celera | 11:97826782 | TTTGGAAGAGAGAAG[C/T]AGCCCTAGCCATCTC | 16796 |
rs27074263 | snp | C/T | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97826589 | CCTTTCTGCCTCAGA[C/T]CACACAAAGGGTAAA | 16796 |
rs27074264 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97826454 | TGAACAGCCTGTTGA[A/C]TGACTTCTCCTGAGC | 16796 |
rs27074265 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Lasp1 | Mm_Celera | 11:97826204 | CATGCACACGAAACA[A/C]AGAAAACTTCTTAAA | 16796 |
rs27074266 | snp | C/G | 0.18 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97825989 | CCCGGCACAGAAGCA[C/G]CCTCTTGCAGGGTGG | 16796 |
rs27074267 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Lasp1 | Mm_Celera | 11:97825789 | GATACCCTCGTGTCT[A/G]TCACAGGAAAGGGTC | 16796 |
rs27089568 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Lasp1 | Mm_Celera | 11:97825744 | TTGGCAACAGACTCC[A/T]TATAAATGAAGGATG | 16796 |
rs27089569 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Lasp1 | Mm_Celera | 11:97825730 | AACATGCCCCGTCAT[C/T]GGCAACAGACTCCTT | 16796 |
rs27089570 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Lasp1 | Mm_Celera | 11:97825702 | GGGCACAAGCCTGAA[A/T]GCCGAGTTATAGAAC | 16796 |
rs27089571 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lasp1 | Mm_Celera | 11:97825582 | ATCATCGCTCAGTTC[C/T]ACCCTTACATAGCCG | 16796 |
rs27089572 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Lasp1 | Mm_Celera | 11:97825573 | GGGTTAGGGATCATC[A/G]CTCAGTTCCACCCTT | 16796 |
rs27089573 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97825032 | AGCAAAGGCCCACGC[C/G/T]GCAGTGGTCAGATCA | 16796 |
rs27089574 | snp | A/G | 0.465374 | 0.126941 | synonymous-codon | Lasp1 | Mm_Celera | 11:97824859 | GCGCTACAAGGAGGA[A/G]TTTGAGAAGAATAAG | 16796 |
rs27089575 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lasp1 | Mm_Celera | 11:97824548 | TTCTTTTGTGTTCTA[C/T]GTAATTATTGCAGGT | 16796 |
rs27089576 | snp | A/C/G | 0.492188 | 0.0620098 | intron-variant | Lasp1 | GRCm38.p3 | 11:97824416 | CAGTTGGTGCACAGC[A/C/G]AGCCATCACGTCCAT | 16796 |
rs27089577 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Lasp1 | Mm_Celera | 11:97824405 | CTATGCAAACCCAGT[C/T]GGTGCACAGCAAGCC | 16796 |
rs27089578 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97824384 | GGCACGAGCAGATTG[C/T]AAGTCCTATGCAAAC | 16796 |
rs27089579 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Lasp1 | Mm_Celera | 11:97823341 | TTGCTGCAGAACTGC[C/T]TCTCAGAGGCCGGCT | 16796 |
rs27089580 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97823252 | AGTGTGTTTTTCATA[C/G]AGTTCTCAGGAGAGC | 16796 |
rs27089581 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lasp1 | Mm_Celera | 11:97823217 | CTGACTTCTGTTCGT[A/G]TTGGAGAAGCCCTTT | 16796 |
rs27089582 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97823176 | CCCAGAGTAGGATGA[A/G]CGATGAGCTGAGCCT | 16796 |
rs27089583 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Lasp1 | Mm_Celera | 11:97823135 | CTACAGCCAAGAAAC[C/G]GTTCCCAGCCTCGGC | 16796 |
rs27089584 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Lasp1 | Mm_Celera | 11:97823116 | GGTGGTGGACAGTGA[C/G]CTGCTACAGCCAAGA | 16796 |
rs27089585 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97822911 | GATGATCCTGACCCT[G/T]GAGGGCCTGACTGGA | 16796 |
rs27089586 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lasp1 | Mm_Celera | 11:97822826 | CTAATTTAGCAGCCC[A/G]TTGAATGCCGGATTA | 16796 |
rs27089587 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Lasp1 | Mm_Celera | 11:97822712 | CAAGGGAGGTGAAGC[A/C]TATGTCAGTCCGGGT | 16796 |
rs27089588 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Lasp1 | Mm_Celera | 11:97822592 | GGACCCTTCTGGATT[C/G]CTGCAGTCTCCATTC | 16796 |
rs27089589 | snp | A/G | 0.5 | 0 | intron-variant | Lasp1 | Mm_Celera | 11:97822030 | TGTGCTCACGTGTAC[A/G]CGCGCATATTTTGAA | 16796 |
rs27089590 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Lasp1 | Mm_Celera | 11:97821116 | TCCTGTCACAGCTGG[C/T]GAGCCATCCAAATGC | 16796 |
rs27089591 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Lasp1 | Mm_Celera | 11:97821076 | TTGTGGCCAAACTGA[C/T]AAGAGGCTTGAGTGA | 16796 |
rs27089592 | snp | A/G | 0.32 | 0.24 | intron-variant | Lasp1 | Mm_Celera | 11:97820819 | CACTGGTCATACTGT[A/G]TGCTGCCAAGCTACT | 16796 |
rs27089593 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Lasp1 | Mm_Celera | 11:97820078 | TGGCAGTGACCTCTC[C/G]GGTTTGCCTGTGGGA | 16796 |
rs27089594 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Lasp1 | Mm_Celera | 11:97819662 | CTAATAGTCTGAGCC[A/C]GGTTTGACAATGTGT | 16796 |