SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4214184 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Ltn1 | GRCm38.p3 | 16:87377232 | CTACTGGGGCTTTGG[A/G]TCCAAAGTCAAGAAC | 78913 |
rs4214185 | snp | C/G | 0.46281 | 0.131194 | utr-variant-3-prime | Ltn1 | Mm_Celera | 16:87378844 | TACTGACAGATGGCA[C/G]TTTGTCATGCTCACT | 78913 |
rs4214186 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, downstream-variant-500B | Ltn1 | Mm_Celera | 16:87379599 | TCTTACTGGCCCGAC[A/G]CACAATCTTTCAAAT | 78913 |
rs4214187 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Ltn1 | GRCm38.p3 | 16:87381752 | TAGACTAGCTGATGC[A/G/T]CCTTAGAAAGCCACT | 78913 |
rs4214188 | snp | C/G/T | 0.408163 | 0.193609 | intron-variant | Ltn1 | GRCm38.p3 | 16:87383000 | AGAGAGAGACAGAGA[C/G/T]AGAGAGAGAGCTATA | 78913 |
rs4214189 | snp | C/T | 0.453686 | 0.144955 | intron-variant | Ltn1 | Mm_Celera | 16:87383109 | CTTCATTGTTAGAGA[C/T]ATAGTTCTAATATCT | 78913 |
rs4214190 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87383492 | GTAACACTCCTGTGT[G/T]GTAACGGCTTTGGTG | 78913 |
rs4214191 | snp | G/T | 0.5 | 0 | intron-variant | Ltn1 | Mm_Celera | 16:87384571 | CCACCTGTTACTCTA[G/T]CTCAAAGGATCTGAC | 78913 |
rs4214192 | snp | C/G | 0.5 | 0 | intron-variant | Ltn1 | Mm_Celera | 16:87384686 | TAAACACTTTTAAAA[C/G]ACTGGATCATGTCTC | 78913 |
rs4214193 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87385081 | TTCTAAAAGAGAGCA[A/G]GCTGAGCAAGCCAGG | 78913 |
rs4214194 | snp | G/T | 0.5 | 0 | intron-variant | Ltn1 | Mm_Celera | 16:87388081 | GTAGCAGTAGATCTG[G/T]ACAGTGTGCAGTTAC | 78913 |
rs4214195 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87388389 | TGCAGCTTGGTCTTC[A/G]TGTGGGTCCCACACA | 78913 |
rs4214196 | snp | A/G | 0.5 | 0 | intron-variant | Ltn1 | Mm_Celera | 16:87389090 | ATGCCCTTCTGGTGT[A/G]CCTGAAGAAAGCGAC | 78913 |
rs4214197 | snp | C/T | 0.5 | 0 | intron-variant | Ltn1 | Mm_Celera | 16:87389091 | TGCCCTTCTGGTGTA[C/T]CTGAAGAAAGCGACA | 78913 |
rs4214198 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87389141 | CCAAATAAATCTTTT[A/T]AAAAAAAAAGGAAAA | 78913 |
rs4214199 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87389733 | GGGAAAGCTAGTCTC[A/G]AAACAAAATAAAACA | 78913 |
rs4214200 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87389798 | GAGAAGGGGGAAACA[C/T]ACATAGGACTGTTCC | 78913 |
rs4214201 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87389799 | AGAAGGGGGAAACAC[A/G]CATAGGACTGTTCCC | 78913 |
rs4214202 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87390025 | CTGGGCACAGGTCTG[C/T]GCCAGTTGGGCTCTT | 78913 |
rs4214203 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87390068 | AGAAGTAGGCCCACA[C/T]ACCCATCCTAACCCA | 78913 |
rs4214204 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87390100 | AAGCTATCTCCAATC[A/G]AGAACCACTTGCAAA | 78913 |
rs4214205 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87390163 | TGGGGAAACAAACTA[C/T]ACTAAGGGGTAGGTC | 78913 |
rs4214206 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87390292 | GTCCTTTGTGTATAT[C/T]ATGGGTTCCAGTTTT | 78913 |
rs4214207 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87390501 | ATCACAGAGAAAGGA[A/G]CTTCAGTTGAGGAAA | 78913 |
rs4214208 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87393160 | ACGACTCTTAAAATA[A/C]ATCAGCAAATAATAG | 78913 |
rs4214209 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87393534 | AGTATCTGAGGACAG[C/T]TACAATGCATTTACA | 78913 |
rs4214210 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87393539 | CTGAGGACAGCTACA[A/G]TGCATTTACATATAA | 78913 |
rs4214211 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87393632 | GACATTCTCTGCTAA[A/G]TACTTCTGTATTGAT | 78913 |
rs4214212 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87393734 | CACTCGTGAGGCTGA[A/G]GCAGGGGGATGCATG | 78913 |
rs4214213 | snp | C/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87394037 | CTGAGCCGGTTCTTC[C/T]GACATGTGAAATAAC | 78913 |
rs4214214 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87394130 | AGGCTACCTGGCTGG[A/G]CTAGTGTCATGATCG | 78913 |
rs4214215 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87394144 | GACTAGTGTCATGAT[C/G]GGGGAAATACTGCTT | 78913 |
rs4214216 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87394200 | CTGTCTTCAGATCTC[G/T]GGTTTTCCGTGACAT | 78913 |
rs4214217 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87394214 | CTGGTTTTCCGTGAC[A/G]TAACAACTGCATCTG | 78913 |
rs4214218 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87394830 | TCCAAATACGGCTGT[A/G]GAAAACAGCAATCCC | 78913 |
rs4214219 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87395022 | AGATCACAGTTCATC[C/G]GAAGGTTAAACTCGT | 78913 |
rs4214220 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ltn1 | Mm_Celera | 16:87395256 | GTCTGACCTTCGCTA[C/T]TGTCTTACAAACATC | 78913 |
rs4214221 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87395306 | ACGGCCATCCAATAC[A/C]GTCATCTCACTTCTG | 78913 |
rs4214222 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87395690 | GGCTTTTATGTAAGT[A/C]CTGGGGATTCCAACC | 78913 |
rs4214223 | snp | C/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87395937 | CTGTGCAAAGTGCAA[C/T]AGGGGACAGAAATCC | 78913 |
rs4214224 | snp | A/C | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396319 | AGCATATTGAATATG[A/C]TTCAGGAGTGATTAA | 78913 |
rs4214225 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87396395 | CTGAAGCTCGATTCC[C/T]AGCGCCCACATGGCA | 78913 |
rs4214226 | snp | A/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396596 | TTTTCGAGACAGGGT[A/T]TCTCTGTATAGCCCT | 78913 |
rs4214227 | snp | A/G | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396696 | TAAGCAAATCATATA[A/G]GCATGCGCCACCACT | 78913 |
rs4214228 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ltn1 | Mm_Celera | 16:87396755 | TTTGGAACTTCCAAC[A/G]GGTATGAATGCAGAA | 78913 |
rs4214229 | snp | A/G | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396887 | CTGGGGTGCCTGAGT[A/G]TATAAGGTACCTTCT | 78913 |
rs4214230 | snp | G/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396938 | CTTGGATCCCCAGAG[G/T]GTAAAGCTGGATGTG | 78913 |
rs4214231 | snp | C/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87396977 | CCTCTGACCCCAGCC[C/T]CATAAAGCAAGAGGT | 78913 |
rs4214232 | snp | C/T | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87397111 | CCCAAGGTGGTCCTG[C/T]AACCTGCACTCACAC | 78913 |
rs4214233 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87397443 | TAGGATACGTATAAT[C/T]CAGTCTCCTTTCTCA | 78913 |
rs4214234 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87397574 | CCCAGCAACCACATG[C/G]TGGCTCACAGCCGTC | 78913 |
rs4214235 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87397587 | TGCTGGCTCACAGCC[A/G]TCTGTAATGGGATCT | 78913 |
rs4214237 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87398059 | ACACACACACACAAC[C/T]CATAAGAACACACAT | 78913 |
rs4214238 | snp | A/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Ltn1 | Mm_Celera | 16:87400305 | TGGGCCCACATTTTA[A/T]TGTGGGAATAAAGTA | 78913 |
rs4214239 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | Ltn1 | Mm_Celera | 16:87400337 | TACCTACCAGCTAAA[A/G]AGAAAAATATCTTCA | 78913 |
rs4214240 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87400473 | AAGGCTCCTAAAGGA[A/G]AATCAGAGCGAAAAG | 78913 |
rs4214241 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87400522 | CCGTCTAAGACCAAC[A/G]GCAGTCTGCGCTGGA | 78913 |
rs4214242 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87400601 | AGCCTGGTGTGGTGC[C/G]TGCTCCTGCAATCCC | 78913 |
rs4214243 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87400637 | TTCAGAGGTGGAGGC[A/G]GGAGGATGCTGGTAT | 78913 |
rs4214244 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87400764 | GATGAGCGCCTCAGC[A/G]CTCTGGGCAGAGCTG | 78913 |
rs4214245 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87401076 | ATTCTACCATAAAAA[C/T]ACAAAGTCTACTTTG | 78913 |
rs4214246 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Ltn1 | Mm_Celera | 16:87402528 | AAAACTAAACAAGTA[A/C]GAACCCAAAATGTAC | 78913 |
rs4214247 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ltn1 | Mm_Celera | 16:87402580 | GTAAAACAGGCCATA[C/T]AGAGCAGTAAGGTTT | 78913 |
rs4214248 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87402942 | AGTTTCCAGCACCCA[C/T]ATGGCTGTTACAATC | 78913 |
rs4214249 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403006 | CTTTTCTGGACTCCA[C/T]GGGCACCAGACACCC | 78913 |
rs4214250 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403066 | ACACATGAAAGAGTT[A/C]AATGAGTCTGGGGGG | 78913 |
rs4214251 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403081 | CAATGAGTCTGGGGG[A/G]AAAAGTGGAGGTTGT | 78913 |
rs4214252 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403435 | AATTAGGCTTATAAA[A/T]TTTTTTTCTGAAATA | 78913 |
rs4214253 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403530 | AACAACAAAAAACCC[A/G]TTAGTTCCAGCACTC | 78913 |
rs4214254 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87403941 | ACTGTTCACTAACCA[C/T]AGACGGCCAAAGTAA | 78913 |
rs4214255 | snp | C/T | 0.433884 | 0.169371 | intron-variant | Ltn1 | Mm_Celera | 16:87403945 | TTCACTAACCATAGA[C/T]GGCCAAAGTAACCCA | 78913 |
rs4214256 | snp | C/T | 0.487535 | 0.077957 | synonymous-codon, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87404026 | TTTTCTTTTATAGTA[C/T]GGTTTCACTTCATCA | 78913 |
rs4214257 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ltn1 | Mm_Celera | 16:87404168 | AGATAGAGATTGGAT[C/T]AATCATTCTGAAAAT | 78913 |
rs4214258 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ltn1 | Mm_Celera | 16:87404238 | TAAAATTAAATAAAT[C/T]TGGATCACTAAGTCA | 78913 |
rs4214259 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87404508 | AGCTGTGAGTATCTG[A/G]GGTTGGCTTTTCTCT | 78913 |
rs4214260 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87404522 | GGGGTTGGCTTTTCT[C/T]TTCTTCTGTTTTCTT | 78913 |
rs4214261 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87404817 | AGGCAGAGGCAGGCG[A/G]ATTTCTGAGTTCGAG | 78913 |
rs4214262 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ltn1 | Mm_Celera | 16:87404819 | GCAGAGGCAGGCGGA[C/T]TTCTGAGTTCGAGGC | 78913 |
rs4214263 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87405199 | AGGTCTCATGCTCAA[G/T]CTATGCCCAGTATGG | 78913 |
rs4214264 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87405279 | CTTCTCAGCTCCTTG[C/T]CTGCCTGTATGTTGT | 78913 |
rs4214265 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87405340 | ACTGTAAGCCAGCCC[C/G]GATTAAATGTTTTCC | 78913 |
rs4214266 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ltn1 | Mm_Celera | 16:87405383 | ATCTTAGTCACAGTG[C/T]CTTTTCACAGCAATA | 78913 |
rs4214267 | snp | C/T | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87405636 | ACTTAGGAAAGATGG[C/T]GCATTGTCGAGTTCT | 78913 |
rs4214268 | snp | C/G | 0.499055 | 0.0217186 | missense, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87405638 | TTAGGAAAGATGGCG[C/G]ATTGTCGAGTTCTTC | 78913 |
rs4214269 | snp | A/G | 0.499055 | 0.0217186 | intron-variant | Ltn1 | Mm_Celera | 16:87406049 | TCTTGAGTTGATGGT[A/G]GCTGGACGGATAGAT | 78913 |
rs4214270 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Ltn1 | Mm_Celera | 16:87406312 | TCTGCTACTTCCATC[A/G]GGTACTTGTTGTAGA | 78913 |
rs4214271 | snp | C/T | 0.483471 | 0.0893938 | intron-variant | Ltn1 | Mm_Celera | 16:87406354 | CTAGCCCTTAGAGCA[C/T]TTTCACCTGTCTACC | 78913 |
rs4214272 | snp | A/G | 0.32 | 0.24 | intron-variant | Ltn1 | Mm_Celera | 16:87406363 | AGAGCATTTTCACCT[A/G]TCTACCCAATTCTAA | 78913 |
rs4214273 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Ltn1 | Mm_Celera | 16:87406490 | CTGGGGTGTGGTGTC[A/T]TGTACCTACAGTCCC | 78913 |
rs4214274 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ltn1 | Mm_Celera | 16:87408401 | ACTACTGTGTACAGG[A/G]CACACCTACAATACT | 78913 |
rs4214275 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Ltn1 | Mm_Celera | 16:87408404 | ACTGTGTACAGGGCA[C/T]ACCTACAATACTATG | 78913 |
rs4214276 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ltn1 | Mm_Celera | 16:87408431 | TATGAATGGAGAAAC[A/T]TGCTGAGGTTCGAAA | 78913 |
rs4214277 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ltn1 | Mm_Celera | 16:87408523 | AACACACAAAAGAAA[G/T]TTCAGAATCCTGACA | 78913 |
rs4214278 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ltn1 | Mm_Celera | 16:87408585 | AGGATCTCCTTACAT[C/T]CAGGATGTTATGCCA | 78913 |
rs4214279 | snp | G/T | 0.375 | 0.216506 | missense, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87408744 | ACTAATTTCTTTTTT[G/T]GGGCAACTAAGATCA | 78913 |
rs4214280 | snp | C/T | 0.375 | 0.216506 | missense, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87408751 | TCTTTTTTTGGGCAA[C/T]TAAGATCATTTTGCT | 78913 |
rs4214281 | snp | A/G | 0.42344 | 0.180051 | synonymous-codon, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87408833 | CTTAAAATCTGTCTT[A/G]AAGCATTCATAATTT | 78913 |
rs4214282 | snp | A/T | 0.471655 | 0.115624 | intron-variant | Ltn1 | Mm_Celera | 16:87409130 | CTTCCACTTTACATG[A/T]GGCTGACAACACCAG | 78913 |
rs4214283 | snp | A/G | 0.491493 | 0.0646602 | synonymous-codon, nc-transcript-variant | Ltn1 | Mm_Celera | 16:87409362 | GGGCATTACACTTCC[A/G]ATATAAACTCCAAGA | 78913 |
rs4214284 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Ltn1 | GRCm38.p3 | 16:87409656 | ACGGGGACCTGGGTG[A/G]TGCTTCTATCCCAGG | 78913 |