SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3654432 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91782731 | TGCTCTTAGGTGGTG[C/T]GCCCCTCCGCATGTT | 16443 |
rs3654484 | snp | C/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91782757 | ATGTTGCTTGCATGG[C/G]CTTGATGGATCATGT | 16443 |
rs3654487 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91782761 | TGCTTGCATGGGCTT[A/G]ATGGATCATGTTGTG | 16443 |
rs3655085 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Itsn1 | Mm_Celera | 16:91782809 | TTTGAAGCACGCCAT[C/G]TTTGCTGTTTGAAAG | 16443 |
rs3671778 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91837009 | GCATCCTCGTGAACA[A/G]TTCAGTGTCCATCTG | 16443 |
rs3684385 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91833874 | GAAGTGATTTATCCC[A/T]CTTGGACATAGGGAA | 16443 |
rs3687287 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Itsn1 | Mm_Celera | 16:91837229 | CTGTGGCATTCATTC[G/T]CCCTGTTCTCAGACG | 16443 |
rs3692607 | snp | C/T | 0.385633 | 0.210009 | intron-variant | Itsn1 | Mm_Celera | 16:91774923 | CCAAAAATCAGTTGG[C/T]AAACAGGTATGGCTG | 16443 |
rs3693923 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902296 | TAATTGTTTTAACCT[C/T]CCTTCTAGCCCACCA | 16443 |
rs3695773 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902613 | TGATCAGGGAAGAAG[A/G]CAAGGAGAACCAATG | 16443 |
rs3712349 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897673 | TATTTGCTGTGTGGA[A/G]TTTTGCCTGCATGTG | 16443 |
rs3712364 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897679 | CTGTGTGGAATTTTG[C/T]CTGCATGTGTGTCTG | 16443 |
rs3713005 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91897777 | GAGCCCACATGTGAG[C/T]ACTGGGAACCCAGGG | 16443 |
rs3713023 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897779 | GCCCACATGTGAGTA[C/T]TGGGAACCCAGGGCT | 16443 |
rs3713211 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91782615 | TTTAGGTATAAATTA[C/T]AGCTATAAAATTTAC | 16443 |
rs3713261 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Itsn1 | Mm_Celera | 16:91782641 | TTTACCTTATGTCCA[C/T]GTAGGCTTTAGGCAA | 16443 |
rs3718712 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91786299 | CCCCAGGAAGGTAGG[A/G]CTTAGCATCAGAGAT | 16443 |
rs3719314 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Itsn1 | Mm_Celera | 16:91786374 | TGAGTGACCAACACA[C/T]GGACACCGGAAAGGC | 16443 |
rs4138168 | snp | A/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91786586 | TAACGTCCGAGTCCC[A/T]TGCTGGACTGGGCTG | 16443 |
rs4138387 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91897516 | ATACTCCAGAAGAGG[A/G]CATCAGATTTCGTTA | 16443 |
rs4219320 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727644 | CTGGATTCGGAGAGC[A/G]GCGAATAGCCACAGG | 16443 |
rs4219321 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728441 | CAGGGCATCTCTGAG[A/G]TCGGCGTGTGATGCG | 16443 |
rs4219322 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729341 | GAGGGAGATGAGGAG[A/T]TAGGCGGGAGTGAGG | 16443 |
rs4219323 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Itsn1, Cryzl1 | Mm_Celera | 16:91730288 | AGCAAGGAGGAGCTG[A/G]CTGGATCTCCCTTCA | 16443 |
rs4219324 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91731609 | CCACATCCATCCTTC[C/T]TTCCTTCCTTTTTTC | 16443 |
rs4219325 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91732585 | ATTTTATAAATGATG[A/G]TAATCCCAACATAAA | 16443 |
rs4219326 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91734444 | ACAGCTCTAGTTTCA[A/G]CAGTAGACTATCTCA | 16443 |
rs4219327 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91734513 | CTCAATGCCAGCCAC[A/G]TACACCCACTCGAGC | 16443 |
rs4219328 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91734766 | AGCTTTCACCGATGT[C/T]TTTCTTTGTTGGTGG | 16443 |
rs4219329 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91737296 | TCTCCATGTCCCAGA[C/T]AGTCCACCACACGGA | 16443 |
rs4219330 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91737512 | TTGAAGGAGAACAAG[A/G]GAAATACTGGATCAG | 16443 |
rs4219331 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91738711 | GCCTGGGAGACTGAA[C/G]ACCTGTTGTCTGTGG | 16443 |
rs4219332 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Itsn1 | GRCm38.p3 | 16:91743273 | ACAGAGCGTTGTTGA[C/G]AAACTCCCTCTCCTA | 16443 |
rs4219333 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746216 | GGAGTGTCAGTGTTC[C/G]ACAAAGCAAGCAGAA | 16443 |
rs4219334 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91750687 | TGGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT | 16443 |
rs4219335 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91751773 | CTTGAAAAAGTGGCC[A/G]GGCCATTCAAAGCCT | 16443 |
rs4219336 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Itsn1 | Mm_Celera | 16:91752703 | TGAGGTATGATGCTG[C/T]TTCTCTGTGCTTTTG | 16443 |
rs4219337 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91758563 | TTTATTTTATCTTTT[A/G]AGGCAAGGATTCAGT | 16443 |
rs4219338 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91758995 | AGATCAGGCTGGCCT[C/T]GAACTCAGAAATCCG | 16443 |
rs4219339 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91759036 | CCTCCCAAGTGCTGG[A/G]ATTACAGGCGTGTGC | 16443 |
rs4219340 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91760432 | CAAGGTATGTGTTCC[C/T]TTAAGCAGTAGGGTC | 16443 |
rs4219341 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91760468 | CTGTTAACTCTGATG[A/C]ACCGGAGAATTAGGT | 16443 |
rs4219342 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91760650 | TCAGTGTTGTAAGTC[C/T]TCCAGTGAGGCTGCG | 16443 |
rs4219343 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91760834 | CCACACTGGAACTGG[A/G]GCTTTTGTTTAGTCA | 16443 |
rs4219344 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | Mm_Celera | 16:91761081 | GTATTAAGCTCTATT[A/T]GAAGCCAAAATTGAG | 16443 |
rs4219345 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | Mm_Celera | 16:91761884 | TCAGGCGAGTGTGTC[A/T]CTGTATGTCCAGCCT | 16443 |
rs4219346 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91762695 | GTCTGATTCCATTTG[C/T]TTGTTGTCTGGCCAT | 16443 |
rs4219347 | snp | A/G | 0.287335 | 0.247197 | intron-variant | Itsn1 | Mm_Celera | 16:91763311 | GTAATCGAGACAGTT[A/G]CCCGTGGCTTCTAGA | 16443 |
rs4219348 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91763384 | AGGCATCCTTGACAG[A/G]CACCCTGTTTTTTCA | 16443 |
rs4219349 | snp | C/T | 0.287335 | 0.247197 | intron-variant | Itsn1 | Mm_Celera | 16:91763560 | TAGATCGAGAGGAAC[C/T]TTTCACCTTGTGACT | 16443 |
rs4219350 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Itsn1 | Mm_Celera | 16:91764052 | GCCACATGGCTCACT[C/T]AGGACTTTATTCAGC | 16443 |
rs4219351 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91764403 | GCTTTTTTTTCTTTT[C/T]CCATATATTTTTGCT | 16443 |
rs4219352 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91766737 | ACTTATGTTCTTTAT[G/T]CGAGGCGTGGGGCTG | 16443 |
rs4219353 | snp | A/G | 0.433884 | 0.169371 | intron-variant | Itsn1 | GRCm38.p3 | 16:91766792 | TTGACACTGATTGAA[A/G]TCCGGGCACACAGGG | 16443 |
rs4219354 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Itsn1 | Mm_Celera | 16:91766819 | AGGGCTAACAGTGTG[A/C]CCCACCTCGCTGCCC | 16443 |
rs4219355 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Itsn1 | Mm_Celera | 16:91766972 | CTCTTGGTTTATGTA[A/G]TGACATGGAAGCAGA | 16443 |
rs4219356 | snp | A/G | 0.30839 | 0.243086 | intron-variant | Itsn1 | GRCm38.p3 | 16:91767135 | GATTATGTGGCGGAC[A/G]TAACCTATTCTATGA | 16443 |
rs4219357 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91767412 | ACTCTGCCCCCCACA[C/T]ATGTGCTGAAGCCCG | 16443 |
rs4219358 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91767494 | GTAATGACACCATGG[C/T]GACTGTCAATTGACA | 16443 |
rs4219359 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91767779 | GATTCCTCAGTAAAG[C/T]TTCCCTCCCTCTGAC | 16443 |
rs4219360 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91770208 | CATGGTGTCTTCTGT[A/G]CTATACCTGAGCAGG | 16443 |
rs4219361 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91770211 | GGTGTCTTCTGTGCT[A/G]TACCTGAGCAGGGAC | 16443 |
rs4219362 | snp | C/T | 0.35124 | 0.228584 | intron-variant | Itsn1 | Mm_Celera | 16:91770482 | GAGACTGTCAAGATC[C/T]ACTTTCTCCTGAGCA | 16443 |
rs4219363 | snp | A/G | 0.42344 | 0.180051 | intron-variant | Itsn1 | GRCm38.p3 | 16:91770985 | GCCACGTGACTAGAC[A/G]GCATTGATCAGGATG | 16443 |
rs4219364 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91771174 | GTTTCTCACTTACTG[A/G]GCAGGGTACAGTCAC | 16443 |
rs4219365 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91771183 | TTACTGAGCAGGGTA[C/T]AGTCACCTCTGTTTC | 16443 |
rs4219366 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Itsn1 | GRCm38.p3 | 16:91771484 | GCCTCCCCATTCCAG[A/G]CTCTGTTGTTTGCCT | 16443 |
rs4219367 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Itsn1 | GRCm38.p3 | 16:91771530 | AGTAGTAGGGCCCTG[A/C]GTCCCTTGCCCTTCC | 16443 |
rs4219368 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91771886 | TGTGGGTGTAGATTT[C/T]GATGATGTTTGATAG | 16443 |
rs4219369 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91772042 | ATAGTCATGTTACCC[C/T]CTGGCACATCTGGCC | 16443 |
rs4219370 | snp | G/T | 0.471655 | 0.115624 | intron-variant | Itsn1 | GRCm38.p3 | 16:91772139 | CTGTTTGCCCTCAAT[G/T]TTTCATTAATGCAAA | 16443 |
rs4219371 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91772311 | GACCCATAACCTCAG[C/T]CTCTTATCATTTCTT | 16443 |
rs4219372 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91772509 | AATTGATTGCTTTTT[A/T]AAAAAAGATCCCCTA | 16443 |
rs4219373 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91772510 | ATTGATTGCTTTTTA[A/T]AAAAAGATCCCCTAA | 16443 |
rs4219374 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91772649 | AGCTCAGTGGATGAG[C/T]GCTTCGCTGGCTTGC | 16443 |
rs4219375 | snp | A/C | 0.42 | 0.183303 | intron-variant | Itsn1 | GRCm38.p3 | 16:91772751 | GGAGAGCGTGTGCTT[A/C]CTTGGTGTGAACCCG | 16443 |
rs4219376 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91772837 | GACGATAGTGGTGCC[A/G]AGCTTCCTTGTGCAT | 16443 |
rs4219377 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91772953 | GAAAGCTTAATATGT[A/G]TTCACAATCTACTTT | 16443 |
rs4219378 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91776583 | ATTTAATGATGTTGC[A/G]TCATATTTCTAGCTA | 16443 |
rs4219379 | snp | A/C | 0.413194 | 0.189387 | intron-variant | Itsn1 | Mm_Celera | 16:91776612 | TATGCTGCTGTGCAG[A/C]AATTTCCATTCTTTT | 16443 |
rs4219380 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91776898 | CCAGAGTATGGAGCG[G/T]CTGGTCACTGGATGT | 16443 |
rs4219381 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91777228 | CTTAGTTCCCTGTGT[C/T]TAGTCGGGCTTTATT | 16443 |
rs4219382 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91778609 | CTGACTATAACTTAA[C/T]TGAGGGCACCTCAGT | 16443 |
rs4219383 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91778838 | CATGATACCTAGCTG[C/T]AGGGCTGGTGAGATG | 16443 |
rs4219384 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91778873 | AGCAGTTAGGAGTGC[C/T]GACTGCTTTTCCTAA | 16443 |
rs4219385 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91778881 | GGAGTGCCGACTGCT[C/T]TTCCTAAGGTCCTGA | 16443 |
rs4219386 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91779545 | GGTTAATAATTTGCC[C/T]TTGCTTTGCAGTAAA | 16443 |
rs4219387 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91779719 | GGGTGAGAGAACACA[G/T]GCTAAAAGCTGCTGG | 16443 |
rs4219388 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91779753 | AAGATGACACGTGCA[A/G]GTACGCCGGGAAGAG | 16443 |
rs4219389 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91779841 | TTTCTTGCCTTAATC[A/G]GAATCAGCGTGTCAC | 16443 |
rs4219390 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Itsn1 | Mm_Celera | 16:91780160 | ACGTTCTGTGTAGGG[C/T]CCTTACCACAGTCTA | 16443 |
rs4219391 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91780187 | TCTAAGGCAGCATGA[A/G]GGTGGATGGTGCCAC | 16443 |
rs4219392 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91780713 | TTCCTCTTTCTATGT[A/C]TGTGCTGGTCTTAGG | 16443 |
rs4219393 | snp | A/G | 0.4032 | 0.19756 | intron-variant | Itsn1 | Mm_Celera | 16:91783288 | CTTCACCTTTTCAGC[A/G]AGCGCTGCTGGTCTA | 16443 |
rs4219394 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91783458 | GTGAAACATGGCCAT[C/T]GGATGTTCCCACCTC | 16443 |
rs4219395 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91783507 | TCACAGAGTGTTTTG[G/T]CCATCACCTCGGATT | 16443 |
rs4219396 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91784192 | TACATTCCTACCGAG[C/T]GGCAGGAAATCCGTT | 16443 |
rs4219397 | snp | G/T | 0.30839 | 0.243086 | intron-variant | Itsn1 | GRCm38.p3 | 16:91785430 | AAGTTTGGTTTCTTC[G/T]GTAGAAAGAGAGCAT | 16443 |
rs4219398 | snp | A/G | 0.340265 | 0.233136 | intron-variant | Itsn1 | GRCm38.p3 | 16:91785473 | TAGGGCAAACATTAA[A/G]TGGCAGTGCAGAAGT | 16443 |
rs4219399 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91785481 | ACATTAAGTGGCAGT[A/G]CAGAAGTTAAATTGT | 16443 |
rs4219400 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91785579 | AATTTGAATGTCCCC[A/G]TTTCTTCTCTCTAAT | 16443 |
rs4219401 | snp | G/T | 0.42 | 0.183303 | intron-variant | Itsn1 | Mm_Celera | 16:91785694 | AGTTTGGCCACAATC[G/T]CGAGTAAAACAGGCT | 16443 |
rs4219402 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91785771 | GCTGAATTCTACTGA[C/T]CTGAAAGAAGTCACA | 16443 |
rs4219403 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91787768 | GGACTGTGAGACTGG[C/G]AAGCTGCCCTTCATT | 16443 |
rs4219404 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91788026 | CACCTCTGGCCTCCA[A/T]GGACACTGGTGTTTA | 16443 |
rs4219405 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91788060 | CCATGCTTAGATGCA[C/T]ACCCACAATTGAAAA | 16443 |
rs4219406 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91788185 | TCAAAAATGAACCCC[A/G]CCCCTCAGGAAACAA | 16443 |
rs4219407 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91788191 | ATGAACCCCGCCCCT[C/T]AGGAAACAAACATAC | 16443 |
rs4219408 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91788306 | CCCAGCACCAACATG[A/G]TGGCTCACAACTGTT | 16443 |
rs4219409 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91788596 | TGTTCCTCACCAGGG[C/T]AGGTCTCCCCTTGCC | 16443 |
rs4219410 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91788610 | GTAGGTCTCCCCTTG[C/T]CTCAGGACCACTGGA | 16443 |
rs4219411 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91788611 | TAGGTCTCCCCTTGC[C/T]TCAGGACCACTGGAT | 16443 |
rs4219412 | snp | G/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91788633 | CCACTGGATTGCTGT[G/T]TCTCCTTCCTGCAGT | 16443 |
rs4219413 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91792916 | TCTGCCTTTTGCCTC[A/C/T]TTTTCCACTGAAAAC | 16443 |
rs4219414 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91793468 | CCTGTAAAGATGCCG[G/T]TAAAGATGCTTCACT | 16443 |
rs4219415 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91793518 | GGGAAAGGAGCCAGC[A/C/G]ATTTGCTTAGTGCTG | 16443 |
rs4219416 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91794407 | TTGTTGTTGTCCTTG[C/T]TTGGCTCATGTTTAG | 16443 |
rs4219417 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91794931 | TGCCAGTTCCTGTCA[C/T]GGTTGTGGCTTGTGA | 16443 |
rs4219418 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91795423 | CTTTCTTTCTTTCTT[C/T]CTTTCTTCCTTCCTT | 16443 |
rs4219419 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91795427 | CTTTCTTTCTTTCTT[C/T]CTTCCTTCCTTCCTT | 16443 |
rs4219420 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91801342 | AGCAGATCCGAGTGT[A/G]TTAGCCAAGCAAGCA | 16443 |
rs4219421 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91801819 | CCAGCGTATGACATG[A/G]CGCGTGCTAAGACTG | 16443 |
rs4219422 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802276 | GCCTAACAAATCATA[A/C]CGAATATATAGAAGA | 16443 |
rs4219423 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802370 | GCTTTACCGTTAGAT[C/T]TGTGTCACTATTGCT | 16443 |
rs4219424 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802933 | TGCTAGGGGAAGGAG[A/G]GGCCACTGCTTCAGA | 16443 |
rs4219425 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802986 | TTTGAACTAAGGGAC[A/G]TTTCTTAATTTTATA | 16443 |
rs4219426 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91803252 | GATGGTTCTGAGCCA[C/G/T]CATGTGGTTGCTGGG | 16443 |
rs4219427 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803629 | CTAACGCACTGGACC[A/G]TCTGTCCAGCCCCAG | 16443 |
rs4219428 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803676 | GTTTAATTTTATAGA[A/G]TGCTAATAACACCTT | 16443 |
rs4219429 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91804094 | TCAGATGACTGTCCC[C/T]GGTCACATATGTGGC | 16443 |
rs4219430 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91804277 | AGTTTCATGTGTTTT[C/T]GACTTTTCTCACATG | 16443 |
rs4219431 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804424 | CTGTGAAGTTGTGAC[A/G]ATTTCATAATGGAGC | 16443 |
rs4219432 | snp | G/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804436 | GACGATTTCATAATG[G/T]AGCTCCCTAGCTTTC | 16443 |
rs4219433 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804464 | TTCAGGTAAGGTGCT[C/T]TTGAGTTTTCAGTCT | 16443 |
rs4219434 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91808177 | AAAAACTATAGCAAA[A/G]CATAAGATTTGAAGT | 16443 |
rs4219435 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91808256 | GCCAGATACTGGCAG[G/T]CATTGGTATGCTTGG | 16443 |
rs4219436 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91808350 | GTGGTCTTATGTCCT[A/G]AACAGCAGGCCAGTG | 16443 |
rs4219437 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91808483 | CATAGACATAGAAAA[A/G]GATTATTTGAACTGA | 16443 |
rs4219438 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91808765 | GCGGGCAGCAAATGC[A/C]CATGGCTGCTGCGTG | 16443 |
rs4219439 | snp | A/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91808786 | CTGCTGCGTGTGCCA[A/T]CATCTGTTCTGAATG | 16443 |
rs4219440 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91808927 | CTCTCTTCCTCTGAG[C/T]ATGTCCCGGTGACTT | 16443 |
rs4219441 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91809187 | ACTGAGCAGGTTATA[A/G]TTATTTAGGAATTTG | 16443 |
rs4219442 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91809378 | GAGAGCACGTGTGTG[C/T]GTGTGCTGCTACAGA | 16443 |
rs4219443 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91811533 | GGTATTTGTAGTGGT[A/G]CCGTTAGAGGACCTG | 16443 |
rs4219444 | snp | A/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91811608 | AAATCAGCTGGTGGT[A/T]TCTGAGGCAGAAGAT | 16443 |
rs4219445 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91811730 | CGCTCTAGTCTTTGG[G/T]TTTTTTTTTGAGACA | 16443 |
rs4219446 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91811828 | CCTGCCTTTGTGCCC[C/T]ACGTGCTGGGACTAA | 16443 |
rs4219447 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91811830 | TGCCTTTGTGCCCCA[C/T]GTGCTGGGACTAACA | 16443 |
rs4219448 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91811876 | CCAGCCTGAAGCTCA[C/T]GTCTTCAGTGTGCTT | 16443 |
rs4219449 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91812994 | ATTGGGGCTGGCTTA[C/T]AGGTTCAGAGGCTCA | 16443 |
rs4219450 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91813026 | TCCATTATTATCAAG[G/T]TGGGAGAATGGCAAT | 16443 |
rs4219451 | snp | G/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91813059 | CTAGGCAGGCATGGT[G/T]CAGGAAGAACTGAGA | 16443 |
rs4219452 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91813089 | AGTTCTACATCTTCA[C/T]CCAAAGTCTGCTGAA | 16443 |
rs4219453 | snp | A/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91813105 | CCAAAGTCTGCTGAA[A/T]GACTGGTTCTCAGGT | 16443 |
rs4219454 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91813257 | TTAATCCCAGGTGTG[A/G]GATATGGGGCTGCTT | 16443 |
rs4219455 | snp | A/G | 0.42 | 0.183303 | intron-variant | Itsn1 | Mm_Celera | 16:91813343 | TTTTGCCAGCTGCAC[A/G]TACTTTCTGCCCTTG | 16443 |
rs4219456 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91814120 | CAAAATTATTTTCTC[C/T]TCCCCCTCCCCCTTC | 16443 |
rs4219457 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91814441 | TCCAACCAGCACCCC[A/G]GGGCCCTCTGAGACA | 16443 |
rs4219458 | snp | C/T | 0.226843 | 0.248925 | intron-variant | Itsn1 | Mm_Celera | 16:91814809 | GTTCATCTTTAAGGC[C/T]GATGATCATTGGATT | 16443 |
rs4219459 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91815546 | TTCCTTCAGGTAAGT[A/G]ACGTTTTATTCTTGA | 16443 |
rs4219460 | snp | A/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91815569 | ATTCTTGAAAGAATT[A/T]TGCATGCATTCCAAA | 16443 |
rs4219461 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Itsn1 | Mm_Celera | 16:91815672 | AGCCTGGTCTCGCTC[C/T]GGTCTACTGTAATCC | 16443 |
rs4219462 | snp | A/C | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91815684 | CTCTGGTCTACTGTA[A/C]TCCCTACAGCAGGAG | 16443 |
rs4219463 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Itsn1 | Mm_Celera | 16:91815753 | CTCCTGTTGCCAAAG[C/T]TCACCAGAAATTGTA | 16443 |
rs4219464 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91816040 | GTTCCGTTTCCCTGG[G/T]GAGAGACAACTTAAG | 16443 |
rs4219465 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Itsn1 | Mm_Celera | 16:91817221 | TTCTTGGTAGCACCA[A/G]TGCAGCAGTGAAAAC | 16443 |
rs4219466 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Itsn1 | GRCm38.p3 | 16:91817275 | TTGCTAACCTAAGGA[A/G]CATACAGTGGTTTTA | 16443 |
rs4219467 | snp | G/T | 0.255 | 0.24995 | intron-variant | Itsn1 | Mm_Celera | 16:91817998 | TCACTCCGGAGACCC[G/T]TGTGTGCATGCTAAG | 16443 |
rs4219468 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91818299 | TTCTGCAGTAGTCAC[A/G]GACATCCTAGGAACC | 16443 |
rs4219469 | snp | C/G | 0.5 | 0 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91818472 | GCTGGAGAAGCGCCG[C/G]CAAGCGCTCTTGGAG | 16443 |
rs4219470 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91818708 | CGCCCGCGGCAGGGC[C/T]GAGATTCAGGCGCCG | 16443 |
rs4219471 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91819413 | TAGTCCCTGAAGATA[A/C]AGAGATGGCCCAAGG | 16443 |
rs4219472 | snp | C/T | 0.329861 | 0.236901 | intron-variant | Itsn1 | Mm_Celera | 16:91819469 | AGTATATCTGAAAGC[C/T]TGCTTCGTGAGAGGT | 16443 |
rs4219473 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91819644 | AGGGTTTTTATCACT[A/G]CAACAGAACAGCGTG | 16443 |
rs4219474 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91819944 | ACACAAAACTAGCCA[A/G]TACAGATATGTTTGG | 16443 |
rs4219475 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91820065 | ATGCAGGCACCTAGG[A/G]ATGGTCTCCGTCATC | 16443 |
rs4219476 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91820187 | TGATTTTATTAGATA[C/T]AAAAATTCCCTTCTT | 16443 |
rs4219477 | snp | A/G | 0.453686 | 0.144955 | intron-variant | Itsn1 | GRCm38.p3 | 16:91820348 | TGAGCCCTGCAATGG[A/G]AGATGTTTCACCTTT | 16443 |
rs4219478 | snp | A/C | 0.340265 | 0.233136 | synonymous-codon | Itsn1 | Mm_Celera | 16:91820502 | GAATGGGAACGGAAC[A/C]GGAGACAGGAACTCC | 16443 |
rs4219479 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91821211 | GAAATTATGTCTTAC[A/G]TGAATGGCCTGAAAA | 16443 |
rs4219480 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91821518 | TCAGGCAGCTAGGAG[A/G]AGGGTCTCCAAGCCC | 16443 |
rs4219481 | snp | A/G | 0.385633 | 0.210009 | intron-variant | Itsn1 | GRCm38.p3 | 16:91822090 | TGGGTACAGGGGAGC[A/G]CTGGAGCATCTCTGC | 16443 |
rs4219482 | snp | C/T | 0.255 | 0.24995 | intron-variant | Itsn1 | Mm_Celera | 16:91822511 | AAGTTTGGTGAGCAA[C/T]CTTCGGTGGTGTTTG | 16443 |
rs4219483 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91822749 | TTCACTGATGTATGG[C/T]ATTTTCAGCCCCAGA | 16443 |
rs4219484 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | Mm_Celera | 16:91824383 | GCTACCATTGCCTCG[C/T]ACTCTCTTCCACTGG | 16443 |
rs4219486 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828653 | GTGATCGTCTGGAGT[A/G]TGACCTGTCTTATCT | 16443 |
rs4219487 | snp | C/T | 0.304688 | 0.243945 | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829666 | GCTAGGGAAAGATGC[C/T]CAGGCAAAGGCTTGT | 16443 |
rs4219488 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830305 | GCGTTTCTGCAGCAG[A/G]CAGCAGTGCTTCCGG | 16443 |
rs4219489 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830644 | TCACCGCACTACACA[C/T]GGCTTCCTTTTGTAG | 16443 |
rs4219490 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832304 | TATGGGTGTTTTCTA[C/T]GTAAGGTTGGAAAAA | 16443 |
rs4219491 | snp | G/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91832492 | AGTCGGCATGCTGTA[G/T]TAGGTGGCATGCTCC | 16443 |
rs4219492 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Itsn1 | Mm_Celera | 16:91833328 | AAGTTCAGGAAATTA[C/T]AGTCAGTGGTCTGAG | 16443 |
rs4219493 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91836069 | CTCCCTCCAGCTCTC[C/T]ACCACCCAATTTCCA | 16443 |
rs4219494 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91836357 | GATCGCTAGGAAGAG[C/T]TGGCAGCTTCATAAA | 16443 |
rs4219495 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Itsn1 | GRCm38.p3 | 16:91837505 | GAAAGCAAAGCCCCC[A/G]GTCTACTGCCACAAG | 16443 |
rs4219496 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91837612 | GGTGGAGATCGCCGC[C/T]ACTGCCTGGAAGACA | 16443 |
rs4219497 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91837684 | TACCTTTTCCATGTA[A/G]TGTTCTGTGGTCACT | 16443 |
rs4219498 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91837728 | TGCGACCTTGTACTT[C/T]GTGGCTTTGTGCTAT | 16443 |
rs4219499 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91840973 | TCTTCAATTTTTTTT[A/C]ATTTGATTTAAATTC | 16443 |
rs4219500 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91841134 | CTTCCTCTTTCCCTG[A/C]AAGAGTGCTTTCTGG | 16443 |
rs4219501 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91843108 | GGAACGGTGGAGCTC[A/G]ACAGGCTGACTGTGG | 16443 |
rs4219502 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91843945 | AGCTTCCACACGCTC[C/T]CTGCCACCCCCACCA | 16443 |
rs4219503 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91844033 | TCTGTCTGTCTGCTC[C/T]TTCTTTCATCTATGC | 16443 |
rs4219504 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91844125 | GTAGGCCTTCCATTA[A/G]GGAATGTAGCCCCGC | 16443 |
rs4219505 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91844139 | AAGGAATGTAGCCCC[A/G]CCCCTCTGTCCTGCC | 16443 |
rs4219506 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91844957 | GCAGGCAAAATGTCC[A/C]TGTACAAACGTGAAA | 16443 |
rs4219507 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91845204 | AGGGTTGTCAGGGAT[C/T]GGGGCGTAGGGTGGG | 16443 |
rs4219508 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91845695 | AATGTACCCCAGGGT[A/G]GGAGAGGGTGAAGAA | 16443 |
rs4219509 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91845712 | GAGAGGGTGAAGAAT[A/G]GACCCAGAGTCCCAT | 16443 |
rs4219510 | snp | A/G | 0.226843 | 0.248925 | intron-variant | Itsn1 | Mm_Celera | 16:91846891 | TGAATGTTCCAGAAA[A/G]GCAGTAATCAGATAC | 16443 |
rs4219511 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91847020 | AAATGAGGTACCAGA[A/G]CCAATGTCTAGATGT | 16443 |
rs4219512 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91847024 | GAGGTACCAGAACCA[A/G]TGTCTAGATGTGAGA | 16443 |
rs4219513 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91847031 | CAGAACCAATGTCTA[C/G]ATGTGAGAACACCGT | 16443 |
rs4219514 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91847087 | AATTGTGGTTTTAAA[C/G]TTTTATTTGTGCCCG | 16443 |
rs4219515 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Itsn1 | GRCm38.p3 | 16:91847971 | GACTCACTGGACTCT[A/G]GTATTGGAGCCAGCT | 16443 |
rs4219516 | snp | A/G | 0.35124 | 0.228584 | intron-variant | Itsn1 | GRCm38.p3 | 16:91848112 | GGCAGAACTAAGGAC[A/G]GACACAAGCACTGGC | 16443 |
rs4219517 | snp | A/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91848139 | TGGCTGCACTCGGCA[A/T]AGCAGATGGCCCCTT | 16443 |
rs4219518 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91848243 | AATTAAAGTAGTGAT[A/C]GCTCTGAATATGCTG | 16443 |
rs4219519 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91848558 | AAAGTCAGTAGGAAC[G/T]CGCGTGCTTACGGAG | 16443 |
rs4219520 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91848568 | GGAACGCGCGTGCTT[A/G]CGGAGCTTGCCACTT | 16443 |
rs4219521 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91850854 | GGACAACTGGGATAC[A/G]TGGGCGGCTCAGCCT | 16443 |
rs4219522 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Itsn1 | GRCm38.p3 | 16:91851416 | TCCTTTAATTAATGT[A/G]ATGATAATAAAGGAA | 16443 |
rs4219523 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91855030 | TCCAAGATATTACTC[A/G]CCAGGCTATGAAGAA | 16443 |
rs4219524 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91869315 | CCCTGCCTGTGTGCT[A/G]TGCTGTGGGAACTGA | 16443 |
rs4219525 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91869325 | GTGCTATGCTGTGGG[A/G]ACTGAGTGGTACAGC | 16443 |
rs4219526 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91880681 | CTGCAGGATAGTATG[A/C/T]GAACATTGAGGAACA | 16443 |
rs4219527 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Itsn1 | GRCm38.p3 | 16:91881669 | TGAACAGCATCGTCC[A/G]CTTTTCTTACAGAAC | 16443 |
rs4219528 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91883466 | GAAAGAAAGAAAGAA[A/T]GAATGAATGAATCTA | 16443 |
rs4219529 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91885200 | ATATGCCTTCCACAG[C/T]TCAAGCGTTTCCTAG | 16443 |
rs4219530 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91885223 | TTTCCTAGGTGACTT[C/T]CTCAAAAAGAAAGGT | 16443 |
rs4219531 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91885469 | TTTGAGGTCAGGCTC[A/C]GTGGTGGATGGGAAG | 16443 |
rs4219532 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91885483 | CAGTGGTGGATGGGA[A/G]GGCGTGGAGAGCGTT | 16443 |
rs4219533 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91885664 | CCAGTTCACCAAGAT[C/G]TGATACCACGATTCC | 16443 |
rs4219534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91886662 | CGAGTACCCCACAGC[A/G]TCCTCGCCTGAAGAG | 16443 |
rs4219535 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91886801 | AAAGAAGCCTGCTGT[A/G]GACATAGGGTCTAGA | 16443 |
rs4219536 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91886967 | AACCACTCAAGGCAG[C/G]GGTCAGCTCCCGAAA | 16443 |
rs4219537 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91887691 | GTTTTTTTCCCACAC[A/G]GCCACCATGTGAGAC | 16443 |
rs4219538 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91888068 | TGTCTGAAAGGATGA[A/T]ACGGAGTTTGTGATC | 16443 |
rs4219539 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91888275 | GAGGGAGAGTGATTG[C/G]CTCTTTGGTGTTATG | 16443 |
rs4219540 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91888330 | TCCACAAGGGTTTCC[C/T]CAATTATGTTGTCTC | 16443 |
rs4219541 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91888501 | CCACAAACAGGCCAC[A/G]TTCCTGTGCCCAAAG | 16443 |
rs4219542 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91888618 | TCAGCTTTGAGCTAT[A/C]TGCTCACCCACCCAG | 16443 |
rs4219543 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91890149 | AGGAAGCAGTAGGCA[C/T]GGGCTCTCCTCCCTC | 16443 |
rs4219544 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91891523 | CTTTGTTATAGAACC[C/T]AGGACCACCAGCCCA | 16443 |
rs4219545 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91891919 | CCTGTGAGCTACAAT[A/T]ACGGCTGGCCTGAGA | 16443 |
rs4219546 | snp | A/C | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91891992 | ACTCTATGACTGTCG[A/C]TGTCTGCTCAGCCCG | 16443 |
rs4219547 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91891997 | ATGACTGTCGCTGTC[C/T]GCTCAGCCCGAGGAC | 16443 |
rs4219548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892083 | TTAGCTGGTTCCTCC[C/T]CATGTTGATCATGGC | 16443 |
rs4219549 | snp | C/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91892258 | CAATTGAACCTAGCA[C/G]GTGGTAAGTCAGGCC | 16443 |
rs4219550 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91892261 | TTGAACCTAGCACGT[A/G]GTAAGTCAGGCCATG | 16443 |
rs4219551 | snp | A/G | 0.499055 | 0.0217186 | intron-variant | Itsn1 | Mm_Celera | 16:91892309 | CTGGTTAGACAACTT[A/G]ATTCTAGCATGGTGA | 16443 |
rs4219552 | snp | A/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91892318 | CAACTTAATTCTAGC[A/T]TGGTGATAGAATAGA | 16443 |
rs4219553 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91892385 | ATAATGAGCTTTGTG[C/T]CCCAGACCCACCTTC | 16443 |
rs4219554 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Itsn1 | Mm_Celera | 16:91892719 | TGTCCCCCAGGTTAC[C/T]TTCCTTGGCTTTCCC | 16443 |
rs4219555 | snp | A/G | 0.59375 | 0.121031 | intron-variant | Itsn1 | Mm_Celera | 16:91892760 | ACCCTTCTTTAGCAG[A/G]AAAAAAAAAATGTGG | 16443 |
rs4219556 | snp | C/T | 0.476371 | 0.106096 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893094 | AGCTGAACACTTGGT[C/T]TTGCTCTCCTTGCCA | 16443 |
rs4219557 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Itsn1 | Mm_Celera | 16:91893759 | CACCAGGGCAGTGAC[A/G]GCGGGCGACTCACCT | 16443 |
rs4219558 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Itsn1 | Mm_Celera | 16:91894517 | GGAGTCCACCTCTTC[A/G]TGTAGCATCAACGTT | 16443 |
rs4219559 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91894641 | GACCAAAGGCAGCTT[A/G]GGGAAGTGGAGTTTA | 16443 |
rs4219560 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91894650 | CAGCTTGGGGAAGTG[A/G]AGTTTATCTGGCTTA | 16443 |
rs4219561 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91894683 | GGTTAGAGTCTATCG[C/T]AGAGGGGAATGGGGC | 16443 |
rs4219562 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91894807 | GCCACCTTTCTTAGT[C/T]CCCACCTACCTGCTA | 16443 |
rs4219563 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91894846 | TGCTGCCCAGAGGGC[A/G]CCCAGCCTTCTACAT | 16443 |
rs4219564 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Itsn1 | Mm_Celera | 16:91901123 | ACCTCCACTCTCTTC[C/T]TTTCTGCCTGTTTTC | 16443 |
rs4219565 | snp | G/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91901626 | CAGCTGAGAGCACTG[G/T]TTGCTCTTATAGAGG | 16443 |
rs4219566 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Itsn1 | Mm_Celera | 16:91902031 | ATAGGGTAGAGGGCG[A/G]CCACGCTGGATGAGG | 16443 |
rs4219567 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902745 | CTTTGTAAACATCAC[A/G]TGGGGTCTGCTCTAG | 16443 |
rs4219568 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902960 | CCAGGCGGTGGTGGC[G/T]CATGCCTTTAATCCC | 16443 |
rs4219569 | snp | A/C | 0.498866 | 0.0237825 | intron-variant | Itsn1 | Mm_Celera | 16:91903616 | ATAAACGACTCAATA[A/C]CCCAGTCTCTGGTCC | 16443 |
rs4219570 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Itsn1 | GRCm38.p3 | 16:91904125 | GAGTTCCATGGCCTC[C/T]TTCCAATGCTTTCCT | 16443 |
rs4219571 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | Mm_Celera | 16:91904338 | TGTCAAAAGTGGGGC[A/G]TTTGCCAAGTCTGTT | 16443 |
rs4219572 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91904370 | GCCTCGGATGAGCTG[A/G]CTTGACATGACAACC | 16443 |
rs4219573 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Itsn1 | GRCm38.p3 | 16:91904383 | TGGCTTGACATGACA[A/G]CCCCCGGGTAGATGT | 16443 |
rs4219574 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91906669 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 16443 |
rs4219575 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91921016 | TTTTTTGACCCTGGC[A/G]TTCCCCTGTACTGGG | 16443 |
rs6164774 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Itsn1 | GRCm38.p3 | 16:91770394 | GACTTTACTTGCTTA[C/G]AAAATGGTTTTTCAC | 16443 |
rs6214493 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91845215 | GGATNGGGGCGTAGG[A/G]TGGGAAAGGTGAGGG | 16443 |
rs6216160 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91845528 | ccaggcagtggtggc[A/G]cangcctttaatccc | 16443 |
rs6216161 | snp | C/G/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91845531 | ggcagtggtggcnca[C/G/T]gcctttaatcccagc | 16443 |
rs6216593 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91845553 | aatcccagcagttgg[A/G]aggcagaggcagacg | 16443 |
rs6235450 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91813209 | tgccactccttggcc[C/T]aagcatattcaaacc | 16443 |
rs6236619 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91813432 | aggggtgatgggtta[C/T]tgtttgcaatttgtt | 16443 |
rs6237125 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91813499 | gaaattcgatatcct[A/G]atggcaaagatcaaa | 16443 |
rs6238833 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91813869 | TTAATTGATATATTT[C/T]AAAAATCCGCTTTAA | 16443 |
rs6282917 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91900425 | CTTGTATGAGAGCCA[C/T]CTGGCGGTCACGGGG | 16443 |
rs6283438 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Itsn1 | Mm_Celera | 16:91900494 | CCTTGCTTTTCTTTG[C/T]GGAGAGTCACCCTGC | 16443 |
rs6283967 | snp | A/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91900567 | GCCACACAGTGGGGC[A/T]CAGTGTCACCAGGTC | 16443 |
rs6284114 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Itsn1 | Mm_Celera | 16:91900651 | ATAACTTCATTTTCA[C/T]TCTGGTTTAAGGATC | 16443 |
rs6298438 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91900897 | atacataagtacact[A/G]tagctgtctccggat | 16443 |
rs6298479 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91900928 | gcaccagaagagggc[A/G]tcagatccctttaca | 16443 |
rs6298511 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91900945 | cagatccctttacag[A/G]nggttgtgagccacc | 16443 |
rs6298512 | snp | G/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91900946 | agatccctttacagn[G/T]ggttgtgagccacca | 16443 |
rs6298950 | snp | C/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91900969 | agccaccatgtggtt[C/G]ctgggatttgaactc | 16443 |
rs6393468 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91755842 | gcaagacacaggttt[A/G]tgacccggatcttga | 16443 |
rs6394101 | snp | A/C | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91755993 | aggacaaagcaaatc[A/C]cagatctaggtatgg | 16443 |
rs6394578 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91756061 | gaggcctgcgtaagg[A/G]ctttggaagaagaaa | 16443 |
rs6407297 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | GRCm38.p3 | 16:91841762 | GTGTTTCTATTGCTC[C/T]GTAGCCTGCTTTTAA | 16443 |
rs31417221 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899253 | TTATACAGAGTTTGT[G/T]CTGGGACATTCAAGG | 16443 |
rs31417223 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899281 | AGGGTTTGGGAGTGG[A/G]CTGAAGGCCCAAGGG | 16443 |
rs31418054 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899282 | GGGTTTGGGAGTGGG[C/T]TGAAGGCCCAAGGGC | 16443 |
rs31418055 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91899299 | GAAGGCCCAAGGGCA[A/G]GGCCACTCACTGCCT | 16443 |
rs31418056 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Itsn1 | GRCm38.p3 | 16:91899444 | TGGTTTCCATGACAA[C/T]GGGCCCAGGACCATC | 16443 |
rs31418057 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91899460 | GGGCCCAGGACCATC[C/T]ACACTGAGGGAAGTG | 16443 |
rs31418058 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91899579 | AAAGGCGGAGGAGCT[A/G]TGCTCCCAGGTGAAC | 16443 |
rs32626074 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91824484 | TCCTCCTGCCTCCCT[G/T]CTCTCCCTCCTCCTG | 16443 |
rs33595904 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914238 | CAGATCTGGATTGGT[G/T]TCATTTGTTGTGATT | 16443 |
rs33595905 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913996 | GTGCAAATGGCCAGT[A/G]TAGGGTCACCATTAC | 16443 |
rs33595906 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913958 | AGGACATGCTCCCAT[A/G]CTGTGAAACACAGAC | 16443 |
rs33595907 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913782 | TAACTTCGAGCATGC[A/G]TTGGCTTACCACTTT | 16443 |
rs33595908 | snp | A/C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913673 | TTGAAGATAGTGTTG[A/C/T]CTTTTGTATCAAGAA | 16443 |
rs33595909 | snp | A/C | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913648 | CCAAGAAGCACTTAG[A/C]GTTTATTTATTGAAG | 16443 |
rs33595910 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913521 | AAATCTGAATGCTCC[A/G]TGTGACCCCAGAAGG | 16443 |
rs33595911 | snp | G/T | 0.391111 | 0.206368 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913441 | TAGGTTCTCAGATTT[G/T]AACTAGGTTTCTAGA | 16443 |
rs33595912 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913278 | GTTTTGGTCCCTCGT[G/T]TGCATCTCCAGTCTG | 16443 |
rs33595913 | snp | C/G | 0.132653 | 0.220748 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913148 | GCGAGAATCAGGAGT[C/G]TATGACCATAGGCCA | 16443 |
rs33596704 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913110 | ACAACAACCTCTTAG[A/T]CATAGGAACACACGC | 16443 |
rs33596705 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912840 | CTGGAGACCAGTCCT[A/G]TCTGAGCCCATTCTG | 16443 |
rs33596706 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912803 | GCTTGGAGACCCTGG[A/G]ATGTTTCATGAGAAG | 16443 |
rs33596707 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912727 | AGTTAGGTCCTGCCG[C/T]GGGTCACTGCGGGTC | 16443 |
rs33596708 | snp | G/T | 0.396694 | 0.202437 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912514 | GGAGCAGACACCAAC[G/T]TACTTAACCCTCTGG | 16443 |
rs33596709 | snp | C/G | 0.35503 | 0.226867 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912415 | TTGGCCTATAATATC[C/G]TGTGTGTGTGTCCAA | 16443 |
rs33596710 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912241 | AGAGTCTCTGAAATC[C/T]GTGACCTTTAACTAG | 16443 |
rs33596711 | snp | A/G | 0.165289 | 0.235211 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912139 | CTAGGAGTCGTTCTC[A/G]ACAATCCTGCCCTTC | 16443 |
rs33596712 | snp | C/T | 0.297521 | 0.245442 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912095 | TCAGAGCAACGGGGA[C/T]GAAGCAAAGACGAAG | 16443 |
rs33596713 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912082 | CTGGTGGTCAGCCTC[A/G]GAGCAACGGGGATGA | 16443 |
rs33597374 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912018 | GCCGTAGCAGCCCTG[C/T]GATGATCGTAGATGA | 16443 |
rs33597375 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91911807 | CAGTGTCACGAGTGC[A/G]TGTCCTGGAGACAGA | 16443 |
rs33597376 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | Mm_Celera | 16:91911708 | ATTGACAACTCCATG[A/G]GGCAGTAAAATGGAA | 16443 |
rs33597377 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91910625 | AACTGGTCCCACTTG[C/T]TGCCCATTCTGTCAT | 16443 |
rs33597378 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91910231 | CTGCTCTCTCTTCTG[C/T]AGTGATTTTTGGCCA | 16443 |
rs33597379 | snp | C/T | 0.18 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91909630 | CCTGAGAGGTTGGCA[C/T]GGTGCAAGGAGCTGC | 16443 |
rs33597380 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon | Itsn1 | Mm_Celera | 16:91909278 | AATCCAGGACACGCT[A/G]AACCCCAAGTGGAAT | 16443 |
rs33597381 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91908998 | AGCACTTGTCAAAGA[G/T]ATGCACACATGTAGG | 16443 |
rs33597382 | snp | G/T | 0.35503 | 0.226867 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91908812 | GTTGATGGTGAACGT[G/T]GTAGAAGGCATTGAG | 16443 |
rs33597383 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91908716 | GAAGGGCATCAAGGC[A/G]AATGTGATGTGATAG | 16443 |
rs33597764 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896104 | AGGTATGCAGGCAGG[C/G]TGCGGGTAGGTCCTA | 16443 |
rs33597765 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896046 | TCATGAAGGTTTTCA[A/G]ACATCTGGAAGAAAT | 16443 |
rs33597766 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91895928 | TGTGCAGGCTACACC[C/T]TGAATGAGAGAATTA | 16443 |
rs33597767 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91895882 | CGGGTCTCTGCTCCA[C/T]GATGCAGCCCTGTCT | 16443 |
rs33597768 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | Mm_Celera | 16:91895857 | TGGCAGAGACTGGAG[C/T]TTTAGCCCTCGGGTC | 16443 |
rs33597769 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Itsn1 | Mm_Celera | 16:91895612 | CTAGAGGCATTAATA[C/G]AGTTGGTAAAAGTGG | 16443 |
rs33597770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91895503 | TCCAGATACCTGTGC[C/T]TAAACCGGCTTTAAA | 16443 |
rs33597771 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91895434 | GTGTTTCCAAGATGG[A/C]GGCATCCAAAAATTG | 16443 |
rs33597772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91895134 | GTGAGGTATCTCTGC[A/G]GCATCTTCTTGGTCA | 16443 |
rs33597773 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Itsn1 | Mm_Celera | 16:91895033 | TATGAGATGCCACAG[C/T]GGGTTAAGCATCTTT | 16443 |
rs33597794 | snp | A/T | 0.32 | 0.24 | intron-variant, stop-gained | Itsn1 | GRCm38.p3 | 16:91853196 | CTGTTCCTTGCACAC[A/T]AAGTTCCTCACTAGA | 16443 |
rs33597795 | snp | C/T | 0.32 | 0.24 | intron-variant, synonymous-codon | Itsn1 | GRCm38.p3 | 16:91853168 | ACCCAATGATACACG[C/T]GGCTGTTTCTATCTG | 16443 |
rs33597796 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91852820 | TCTTTAAGTCATTGT[A/C]ATGATCTGAAGCAGA | 16443 |
rs33597797 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91852737 | GCTACAGACCAGTTG[A/T]CCTTGGGCATTAACT | 16443 |
rs33597798 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91852519 | AATTAGTTGAAAAGG[C/T]TAGACAAGGCATAAT | 16443 |
rs33597799 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91852211 | TGGGACTGTAGCCTC[C/T]GAACTGTTAGTGCAG | 16443 |
rs33597800 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91852098 | TCGCGACCTTGTTGG[A/T]AGATAGGCTTAGGAA | 16443 |
rs33597801 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91848278 | TTCATCTCCTCATCT[C/T]GTATCTGTGGAGCTC | 16443 |
rs33597802 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91847908 | CCTGTGGTTGTTTGA[A/G]AAGTCAGTGGCCTCA | 16443 |
rs33597803 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91847565 | GTGCCCAGCAGTTGC[A/C/G]TGTGGTATGACGCCA | 16443 |
rs33598064 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91908676 | GGACAGATGCCTCGC[A/G]TAGATTGTGAGCGTG | 16443 |
rs33598065 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91908353 | TTGAGCAGACCCGAA[A/G]CCTGCTCTGTGCGTT | 16443 |
rs33598066 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91907645 | ATGGACGCAGGGAAC[A/G]TGAAGGAGATCTTCA | 16443 |
rs33598067 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91907304 | CTGTTCTGGAGCCAA[A/G]TGAAACAGATCGCTT | 16443 |
rs33598068 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91906089 | GCCACGCCATGTGAG[A/G]TTTTATTTTCTAATT | 16443 |
rs33598069 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Itsn1 | GRCm38.p3 | 16:91905891 | GTGAGCCGACATCAT[A/G]GCCAGTCCAAGCACC | 16443 |
rs33598070 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Itsn1 | GRCm38.p3 | 16:91905842 | AATCCTATAGGGGAC[C/T]TCACATGACAAAAAC | 16443 |
rs33598071 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91905121 | TTTGGGTACCTGGAA[C/T]CCTAGAACCTTTCTT | 16443 |
rs33598072 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91904759 | TCCTTAATTCCTAAC[A/T]CCTCACTTCTCACTC | 16443 |
rs33598073 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91904431 | ATTCACAGATGCCCT[C/T]GCTGTTGGTGAGTGG | 16443 |
rs33598364 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91779127 | TGGTGTTGGAGAAGG[C/T]GGAGTAGGATACTAA | 16443 |
rs33598365 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91778020 | GAGAAAGCCTTATAT[C/T]GCAGATGTTGGATGC | 16443 |
rs33598366 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91777967 | GCTATGATCAATGAC[C/T]GTCAGAGCCCCAAGC | 16443 |
rs33598367 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91777856 | GGAGGCTTCCAGCCC[G/T]GTTCTTAGTCCAGCT | 16443 |
rs33598368 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91777598 | CTGGGCTTGATGAGG[A/G]CCTGAGGGTCTGCAG | 16443 |
rs33598369 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91777179 | GTAGAGTGCTGACTG[C/T]GGGTTTCTCCTCCTG | 16443 |
rs33598370 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91776609 | AGCTATGCTGCTGTG[C/T]AGAAATTTCCATTCT | 16443 |
rs33598371 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91775563 | CCAATATGAAATAAT[C/T]CTGCTAATTTTTATT | 16443 |
rs33598372 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91775482 | TGTGTTTAAGTATTT[A/G]CCTGCTGATCCATCT | 16443 |
rs33598373 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91775036 | ACTCTTTAAACTCTC[A/G]GTGATCCTTCTGTTT | 16443 |
rs33598524 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91814208 | GCCTCTTTTAGTTGT[A/G]TGTTGCTGGCAGCCT | 16443 |
rs33598525 | snp | C/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91813995 | CTAGTGGTATAGAGC[C/G]TGTACGTCCTTTGAA | 16443 |
rs33598526 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91812546 | CTCCCAAAGACTTCA[A/G]ACCAAACCTCTATAT | 16443 |
rs33598527 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91812057 | GGGAATGTCTGATGA[C/T]TCACCTCGTGTCCTT | 16443 |
rs33598528 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91811262 | CTTAACAACAGAAAA[C/T]TCATTTTGAAAGGAA | 16443 |
rs33598529 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | GRCm38.p3 | 16:91811139 | GACCGTGCTACACTG[C/T]GACTGTTTGCGCTTC | 16443 |
rs33598530 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91811096 | CCTGTTCCTTGGTTC[A/G]TGAGTGTTCCTGGCA | 16443 |
rs33598531 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Itsn1 | Mm_Celera | 16:91810823 | ATGGGTGTCCAGCTC[A/G]GTGTTATGGTTCCTC | 16443 |
rs33598532 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Itsn1 | GRCm38.p3 | 16:91810443 | GAAGCCGCCTGAATG[C/T]CACTGAAGTCTAGTG | 16443 |
rs33598533 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91810408 | AGCAGACTGCTTACC[A/G]TTCATAAGAACCCTG | 16443 |
rs33598554 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91895020 | CCATTGGATTCGGTA[C/T]GAGATGCCACAGTGG | 16443 |
rs33598555 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | Mm_Celera | 16:91895004 | GTGAACTCTGGCCTT[C/T]CCATTGGATTCGGTA | 16443 |
rs33598556 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91894963 | CTTAGACATCATAAC[A/G]CCTTTCCCAACGGAA | 16443 |
rs33598557 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91894530 | TCATGTAGCATCAAC[A/G]TTGCCCCAGCCTCTG | 16443 |
rs33598558 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Itsn1 | GRCm38.p3 | 16:91894436 | GCCACCTCACCAGCC[C/T]TGTTTGTGGTATTTC | 16443 |
rs33598559 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91894205 | TTGTCCATGTATTTG[C/T]GGtctttctttcttt | 16443 |
rs33598560 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Itsn1 | Mm_Celera | 16:91894103 | TCAGTGGTACTGAAC[C/T]GGCAGGTGTGGGTCT | 16443 |
rs33598561 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893785 | CACCTCCCATGTTTC[C/T]GTGCAGAGCGCTGAG | 16443 |
rs33598562 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893745 | AAAGTGTGAGGTATC[A/G]CCAGGGCAGTGACAG | 16443 |
rs33598563 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893524 | ACCATAGGTAATGCA[A/G]TGGGACAGCCACACA | 16443 |
rs33598684 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91847539 | TAGGAGGATAGCAGC[A/C]GCCATTTCCAGTGCC | 16443 |
rs33598685 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91846862 | CAATACCAAGCAGTT[A/G]TCATTTGAGGCAGTG | 16443 |
rs33598686 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91846846 | AGATCCTAGGTCGTG[A/G]CAATACCAAGCAGTT | 16443 |
rs33598687 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91846294 | CTTGCCGTGTTACAG[A/G]GTGTATGTGCTTAAC | 16443 |
rs33598688 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91845829 | CCCTGATGAAGAAGA[C/T]GGTAGTGCATGGGAA | 16443 |
rs33598689 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91845056 | GACCTTCAGCCCTGC[C/T]TGTTCCTCCTGTGCT | 16443 |
rs33598690 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91844877 | CACACTACCTCTGCA[C/G]GCTTGCTTAGTTACA | 16443 |
rs33598691 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91843842 | CGGCTTAGGGAAGGA[G/T]CGTGCCATGCAAGCC | 16443 |
rs33598692 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91843744 | TTTACGTGAGGACCA[C/T]ACAGCAGCTGGCCAT | 16443 |
rs33598693 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Itsn1 | GRCm38.p3 | 16:91843706 | AATGAGAGAGACTTC[A/C]CTCATGGCCATTTTT | 16443 |
rs33598934 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91904197 | CCTGGAGGCAGCTGG[C/T]TATCGTATCACACAA | 16443 |
rs33598935 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91904099 | TATTCAAACCACCAC[A/G]GACATGAGTTGAGTT | 16443 |
rs33598936 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902233 | GTGTGATAGCTCATA[A/C]CTGTCTGTGGGCATC | 16443 |
rs33598937 | snp | A/G/T | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91902111 | CAACAAAGCAGAAAT[A/G/T]CTGGGTGACAGTACC | 16443 |
rs33598938 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91901922 | AAGAATCATGAGGTG[C/T]GTCCAGAACAGAATC | 16443 |
rs33598939 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91901036 | TTTACTCTTTTGAAC[A/G]TTGCGTTGGTGAGTC | 16443 |
rs33598940 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91900520 | CCTGCTGAGTCCAGC[A/G]TCTCAGCCTGGGATT | 16443 |
rs33598941 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Itsn1 | GRCm38.p3 | 16:91900415 | CAGCGGTGGTCTTGT[A/G]TGAGAGCCACCTGGC | 16443 |
rs33598942 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Itsn1 | Mm_Celera | 16:91900353 | CCCGGGCCACTCCAA[A/G]TTAATATTTAGAGAG | 16443 |
rs33598943 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Itsn1 | Mm_Celera | 16:91900235 | ACTCTCAGCTCCTGC[A/C]TTAGGATTTTATTTA | 16443 |
rs33599274 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Itsn1 | GRCm38.p3 | 16:91810036 | GCAGTCCTGTGTGCC[A/G]TCATCTGCCAGCCGG | 16443 |
rs33599275 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91809357 | AAGAGCGGCACACAA[G/T]CGACAGAGAGCACGT | 16443 |
rs33599276 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91808379 | TGACTTAGAGGAGTA[A/G]CCAGGCTGTGCTTGT | 16443 |
rs33599277 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91807477 | GAAGTAGCAGTGCTT[C/T]GTGATTTTAGGCATA | 16443 |
rs33599278 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91807423 | AGATGCACACGTTCA[C/T]CTAACACTAATCAGC | 16443 |
rs33599279 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91807267 | AATTGTGGTTCTTTA[A/T]ACATTGCTTTGTATT | 16443 |
rs33599280 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91806977 | TGTCTGGACCAGCCA[A/G]TATGCAGAGAACATG | 16443 |
rs33599281 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91806570 | CGGGTGTGGAAGGAG[C/T]GACTCTGCTGTCCTC | 16443 |
rs33599282 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91805149 | CCAGCAGGAAATATC[C/T]GACTTTATTAAGAAG | 16443 |
rs33599283 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91804929 | GCCACTTTCCTGTCT[C/T]CGTTGTGTTGATGGA | 16443 |
rs33599394 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91843567 | CTGAGGCTGCCTAGC[C/T]GATCATCTCCATGTC | 16443 |
rs33599395 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91843129 | CTGACTGTGGCTCTC[G/T]TGTCATTGCAAAACC | 16443 |
rs33599396 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91841832 | ACATACTATGAAGGG[C/T]CTTTAAGAAATAGTT | 16443 |
rs33599397 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91841633 | AGTGTATGTCAGAGA[C/T]GGTCCTCTGTCCTCA | 16443 |
rs33599398 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91841618 | TAGTCATGGTAAGAA[A/G]GTGTATGTCAGAGAC | 16443 |
rs33599399 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91841448 | GCCTTGGCATTGTCC[A/G]TCAGTGCTTCCTGTA | 16443 |
rs33599400 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91841325 | ATCTGCTGATGAACT[C/G]CACGTGGTCTGAGTC | 16443 |
rs33599401 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91841139 | TCTTTCCCTGCAAGA[A/C/G]TGCTTTCTGGCTGAG | 16443 |
rs33599402 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91840883 | CAAGTTACATGCAGC[G/T]CAAGTGTAGAACAAT | 16443 |
rs33599403 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91840523 | TTGACACCATCTCAT[A/G]AACCATTTGTTTCCT | 16443 |
rs33599494 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893341 | TGCCGTGAGCAGAAG[A/G]GATACTTCACATGAT | 16443 |
rs33599495 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893312 | AGTCAGCTTTAAGTT[A/G]GACACACCAATGATG | 16443 |
rs33599496 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893207 | GCACACAGCAGGTAG[A/G]CCCAGGATCAGACAC | 16443 |
rs33599497 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893162 | TTACAAGGATGGCCA[C/G]TCCACCCTGGCCGTG | 16443 |
rs33599498 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91893160 | ACTTACAAGGATGGC[C/T]AGTCCACCCTGGCCG | 16443 |
rs33599499 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91893133 | CTGAGCTATATGCTG[G/T]TAAGACTACACACTT | 16443 |
rs33599500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91893110 | TTGCTCTCCTTGCCA[C/T]GGGGAAACTGAGCTA | 16443 |
rs33599501 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892482 | GAGCTGCTTTTGGGC[A/C/T]AACAATGAACTGAGG | 16443 |
rs33599502 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892437 | AAAGAGGAGGAAGCC[A/G]GTAATAGACCTTGTA | 16443 |
rs33599503 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892348 | ATTATCAGAACTCAG[G/T]GACTGACTGAACACC | 16443 |
rs33599564 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91774340 | TAGGCCTCTGGGGGT[C/T]TTTTTTCCCCCTCCA | 16443 |
rs33599565 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91774153 | CACCTGGACAGTAGA[A/C]TTACTGTTTTTGAAC | 16443 |
rs33599566 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91773676 | TTACGTAGATATAGG[C/T]GTGTTTGCCTCGCTC | 16443 |
rs33599567 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91773392 | ATCAAGTGACAAATT[G/T]TATTTCAATATGTTT | 16443 |
rs33599568 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | Mm_Celera | 16:91772173 | TATATTGATTTCAGT[A/G]TTCTATTTTGTAGGT | 16443 |
rs33599569 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91770974 | CACATGTAGGAGCCA[C/T]GTGACTAGACAGCAT | 16443 |
rs33599570 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91770745 | GGGCCTGACAGTGAT[A/G]CTGGACAGCGGACCT | 16443 |
rs33599571 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91770134 | TGCTGTATGAAATAA[C/G]CCAAAGAGTCTGCTA | 16443 |
rs33599572 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91768962 | TTTCTTAAAGAAGAG[A/C]GTGCGGCCCCTGCTG | 16443 |
rs33599573 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91767953 | TTTTCAAAATCTGTT[C/T]AGTCTTGGAACCTTG | 16443 |
rs33600004 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91900189 | CACCGAACCTCCTGC[A/C]TGCTGGTTAAGTACT | 16443 |
rs33600005 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Itsn1 | Mm_Celera | 16:91900156 | TGTATGAGCAGTGAT[C/T]TCTGTTTCTAGATTA | 16443 |
rs33600006 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Itsn1 | Mm_Celera | 16:91900102 | GTCATAGTCATCTGT[C/G]TGTTGTTTGTTAGCT | 16443 |
rs33600007 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91900061 | TGTATTTTAACATCT[A/G]ACAGTCCCAGTACCT | 16443 |
rs33600008 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91899522 | CCTGGAAAACACTCC[C/T]GAGAACCATCCAGAC | 16443 |
rs33600009 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Itsn1 | Mm_Celera | 16:91899445 | GGTTTCCATGACAAC[A/G]GGCCCAGGACCATCC | 16443 |
rs33600010 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91899374 | TGCTGCCAACAAGCC[A/G]TGGCCATGACACCCT | 16443 |
rs33600011 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91899355 | TGAGCCTGAGGCTGC[C/T]CACTGCTGCCAACAA | 16443 |
rs33600012 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91899208 | TGTGGTTTAGTGGCC[A/C]TGCTAGAAGCCACCA | 16443 |
rs33600013 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91899168 | GTTGTTCTGCATGCT[A/G]CCTAAGATCTGGGAT | 16443 |
rs33600034 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91804816 | CAGCGAAAACTTCAT[C/T]CTGTGCCTAAATCTT | 16443 |
rs33600035 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803144 | CAGGTAAGACTGCTT[G/T]GTTTTTATTTTTAAA | 16443 |
rs33600036 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802858 | TTAGCAGAGCAAATA[A/C]ATCTAGGAGTGTTTT | 16443 |
rs33600037 | snp | C/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802516 | AGCCAACATCGTTCA[C/T]GTAACTGTCCCAGTG | 16443 |
rs33600038 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802405 | CTGAGCAGCCTGCAC[C/T]TAGCATGCGTGTGTG | 16443 |
rs33600039 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802361 | GCAGCATAGGCTTTA[C/G]CGTTAGATCTGTGTC | 16443 |
rs33600040 | snp | C/G | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802240 | TAATTAAAGCATCAA[C/G]TATAACTATAGATAG | 16443 |
rs33600041 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91801347 | ATCCGAGTGTATTAG[A/C]CAAGCAAGCATGTAC | 16443 |
rs33600042 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91799142 | TGAAGTAAATGGGAG[C/G]CGAGACAGAGGTGAG | 16443 |
rs33600043 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91795823 | GGTGACTTTCAGTTT[C/T]GTCAACATTGCTGTT | 16443 |
rs33600124 | snp | A/C | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747603 | AATGGCAGAACAGGT[A/C]CTGTCACTTTCATTT | 16443 |
rs33600125 | snp | A/G | 0.152778 | 0.230321 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747562 | TAGGCAGTATTCTAG[A/G]TAATTCTGCGGGTAG | 16443 |
rs33600126 | snp | A/G | 0.391111 | 0.206368 | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747423 | TTTCAGGACATCATC[A/G]TTTCTTGTTTAGGCA | 16443 |
rs33600127 | snp | G/T | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747365 | CAGAGCCAGATGACT[G/T]TGTTACTGCTCAGGA | 16443 |
rs33600128 | snp | C/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746822 | AAGTAACAACTCCGT[C/G]CCTTTGTGGCCAGTG | 16443 |
rs33600129 | snp | C/G/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746734 | CGGAAGCAGCCTGCG[C/G/T]GCTCGCCTTGCTCTA | 16443 |
rs33600130 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745937 | TTCAAGCGGTCCACT[A/G]ACTCAGAAAATACTG | 16443 |
rs33600131 | snp | A/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745886 | TTTCCTTTAAGCTTG[A/G]AAGAAAGAAGAGGGC | 16443 |
rs33600132 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745666 | CAACAGGACTGATGG[C/T]GTTCTGGTCATGCTG | 16443 |
rs33600133 | snp | G/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745616 | AGCTTCTTTGCAGCC[G/T]TGGCATGTTTAACTG | 16443 |
rs33600294 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91840438 | CTGTCCCTTAGATAA[C/G]CTCAGCTGCACACTA | 16443 |
rs33600295 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91839715 | CAGACTGAAGAGGGA[A/G]GACAGTGTCAGGAAG | 16443 |
rs33600296 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91839593 | GAGTTGCTTCCTCGG[A/C]AATCAAGCATCTTTG | 16443 |
rs33600297 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91839199 | GCATCTGTGCTCTGC[A/G]GCTTACACTCAGCTC | 16443 |
rs33600298 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91839158 | TCTCACAAAAGCAGC[A/G]TCAGGCACTTTCATA | 16443 |
rs33600299 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91839046 | AGCCCCAGATGTCTG[C/T]CTCGCCTTCAGGTTT | 16443 |
rs33600300 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91839002 | ATGTCAGTGCAGGGA[A/G]CCAAGAGTACTGGCT | 16443 |
rs33600301 | snp | A/G | 0.18 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91827660 | ACCTGCAGCCAGCTT[A/G]TGGCCTTTGTGCTGC | 16443 |
rs33600302 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91826128 | TCATGGCCAGAAGTC[A/G]TTTTCAAGTGTTAAA | 16443 |
rs33600303 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91826090 | TGAGGCTGTGATCAC[A/G]GAAAGTAACCAGGAT | 16443 |
rs33600444 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892228 | GGGCAGTAGAACATT[C/T]TAGAAAGAGATTCTC | 16443 |
rs33600445 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892167 | CTCATGGCTGTGGCT[A/G]CGACAGCCGACTCAC | 16443 |
rs33600446 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91892042 | CTGTGAGCTTAGTGA[A/G]CTTAGTGAGCGATCT | 16443 |
rs33600447 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91892013 | GCTCAGCCCGAGGAC[A/G]TCCGGTGGAGCCACT | 16443 |
rs33600448 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Itsn1 | GRCm38.p3 | 16:91883994 | ATTACTCCTGGGCCA[A/G]CCTGACAATTCCAGC | 16443 |
rs33600449 | snp | A/G | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91883761 | AGCTGGCCCTGAGCC[A/G]TGTTCCTGCACCTCC | 16443 |
rs33600450 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91882682 | TTATTTATTTCCCTC[A/G]GTGTTTAGCGGCTGT | 16443 |
rs33600451 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91880860 | GAAGGATTTACTTAC[A/C]GCCATTGCTAAGAAA | 16443 |
rs33600452 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91880801 | TCCCCATAGGAATAC[A/G]TCAACCCGTGCTGCT | 16443 |
rs33600453 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91880343 | AAAGCACCTAAGTCT[C/G]ATTCGCCCATGCTCC | 16443 |
rs33600964 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91767902 | ATAGGAATGATGTTT[A/T]GTGAGCCTTTCTACC | 16443 |
rs33600965 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91767872 | CGAAGGGTTAGTTTT[A/C]TAATGTCCATATTTA | 16443 |
rs33600966 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91767829 | TTTAACTCTCAGCCA[C/G/T]GTAAGAAAAGCTTGG | 16443 |
rs33600967 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91767784 | CTCAGTAAAGCTTCC[C/T]TCCCTCTGACAAAAG | 16443 |
rs33600968 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91767269 | AAGTGCTGAGTTACT[G/T]GTGTGTGCCTCTGTG | 16443 |
rs33600969 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91767147 | GACGTAACCTATTCT[A/G]TGATGTTGAACGTAT | 16443 |
rs33600970 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91766670 | CTCACCTTTAATCTC[C/T]GAAAACCAAAATAAA | 16443 |
rs33600971 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91766608 | AGGACTTCCCTAGGA[C/T]GCCTTCTTTGACTGA | 16443 |
rs33600972 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91766068 | ATTGCAAAGGTGCGC[C/T]TTCCCCTGCGGCATG | 16443 |
rs33600973 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91765956 | TGTTAAGCTGCTGCC[A/G]CTGTCACCTGCCCTT | 16443 |
rs33601044 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Itsn1 | Mm_Celera | 16:91899094 | TCTCTGGCTGAGTTG[C/G]TTGTTCTGTGAAATA | 16443 |
rs33601045 | snp | A/C/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | GRCm38.p3 | 16:91899014 | CATCCTTGGCTCCCT[A/C/T]GGGTAAGTGAGCCGG | 16443 |
rs33601046 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Itsn1 | Mm_Celera | 16:91898967 | TCACTCCTGAGTTAA[C/T]GGAGTACTGTTCAGT | 16443 |
rs33601047 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91898931 | TGCTCACCCAAAGGT[A/G]CCCTGCCTTCTCCTA | 16443 |
rs33601048 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | Mm_Celera | 16:91898908 | CACGTGGCGTAGGGC[A/G]CCTGTCCTGCTCACC | 16443 |
rs33601049 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Itsn1 | GRCm38.p3 | 16:91898867 | CACAGGCATCAGTGG[C/T]TCTGCGTGCTCTCAG | 16443 |
rs33601050 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91898849 | TAATTGATTTCCAGG[A/G]TGCACAGGCATCAGT | 16443 |
rs33601051 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Itsn1 | GRCm38.p3 | 16:91898827 | TATGTGAGCAGGGGA[A/G]CCATCCTAATTGATT | 16443 |
rs33601052 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Itsn1 | Mm_Celera | 16:91898120 | ACAGCCTGATAAGGG[A/C]TATGCTGTGGCATTT | 16443 |
rs33601053 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91898096 | CTGGATGGATACCCA[A/G]CCCTGCAAACAGCCT | 16443 |
rs33601054 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91743945 | CTTTACATCCTCACA[C/T]TTGTAGATAAGAAAC | 16443 |
rs33601055 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91743829 | CCCAGCTTAAACTAC[G/T]TATTCTTGTACAACT | 16443 |
rs33601056 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91743341 | TGAGGTTTCTTGGTC[A/G]TCTCTGCTTATATTT | 16443 |
rs33601057 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91743041 | ATATCTGCACTTAAA[A/G]AAATGCCCTTTTGTC | 16443 |
rs33601058 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91743003 | CTACTAACCATCTAT[A/G]ACTCAGAATTCAACT | 16443 |
rs33601059 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91741395 | TCCAGCATCTCAGAG[A/G]AGAAACCTTGGAAGT | 16443 |
rs33601060 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91741221 | TCCAGTCTTGTGCGC[C/T]GTCCTTGTCCTTGGC | 16443 |
rs33601061 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Itsn1 | GRCm38.p3 | 16:91736437 | GGATGTGGCTGGATT[G/T]TAGATTCAACAGAAC | 16443 |
rs33601062 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91735521 | CTTCGTAAACTCTAT[A/G]AGTATGCTTTGGAAA | 16443 |
rs33601063 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Itsn1 | GRCm38.p3 | 16:91735495 | CATTTCTGTGTGTTA[A/C]CTTACTCAGCCTTCG | 16443 |
rs33601084 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91795239 | TAGGAGGAGCACAAG[C/T]AAACAGTGTAGCAAT | 16443 |
rs33601085 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91793952 | CATTCCATCCGTGTT[C/T]AAGGACACGCTCGCA | 16443 |
rs33601086 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91793513 | ACAGCGGGAAAGGAG[C/T]CAGCGATTTGCTTAG | 16443 |
rs33601087 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91793080 | ATAGTAGTGTCCCAG[A/T]ATAGGATAGCATCCT | 16443 |
rs33601088 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91792967 | CCATGGATGCTTGAG[A/G]GTCATTTTGAAACAG | 16443 |
rs33601089 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91792776 | CTTTTAGAGAGCTTT[A/C]ATTTTTATTGCTATG | 16443 |
rs33601090 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91792339 | GTGCATAGCAACATG[G/T]AGAAAATGAGATAGT | 16443 |
rs33601091 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91791418 | ATTCTAAGCAGTGAA[A/G]CACTCGGTCCCTTCT | 16443 |
rs33601092 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91791201 | CATTAACAATGCTAA[C/T]ACCTAGTCAGCGAAC | 16443 |
rs33601093 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Itsn1 | Mm_Celera | 16:91791163 | GAGCTCAGCACCAGA[A/G]CTCTCGCACAACATA | 16443 |
rs33601137 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920862 | CTTCAGCCTCTCACC[A/G]TTTGGAAGCACACAG | 16443 |
rs33601138 | snp | A/G | 0.152778 | 0.230321 | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920799 | GCTCTAGTCAGGAAC[A/G]TGGCATGGTCAGAGA | 16443 |
rs33601139 | snp | A/G | 0.152778 | 0.230321 | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920695 | GTAGCCATGACCCGG[A/G]GTGAGACCATGTTAA | 16443 |
rs33601140 | snp | C/T | 0.260355 | 0.249785 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91920520 | CCAGGAGTAGAAATG[C/T]GTGATCAGGTCACTT | 16443 |
rs33601141 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91920498 | AGAAGAAACTTAAAA[C/T]CATATCCCAGGAGTA | 16443 |
rs33601142 | snp | A/C | 0.336735 | 0.234472 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91920331 | GTGTATACAGTATGT[A/C]AGAGGCTATGCTGTT | 16443 |
rs33601143 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920016 | GCCCCTCCGTCTGCC[A/G]CGGTGCACACAGGGG | 16443 |
rs33601494 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91825925 | AGGCCTTCCTTCTGC[C/T]TGCACTCTAGGCAAA | 16443 |
rs33601495 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91825847 | AAGCTGATTCATGGT[A/G]GAGTTCCAGCTTCCT | 16443 |
rs33601496 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91823430 | CAGCAGGGCCTTTGA[A/G]TACCCATGTAATCTT | 16443 |
rs33601497 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91823385 | AACACTATCAGATTA[C/T]ATGACCTCGTCTTGG | 16443 |
rs33601498 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Itsn1 | GRCm38.p3 | 16:91823246 | TACGCAATCCTTTAC[A/G]TTTCCAAATGTAGGA | 16443 |
rs33601499 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91823173 | CGCTTGGCACCATTG[C/T]CTGAAAACTCCCCTT | 16443 |
rs33601500 | snp | A/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91823111 | TCGAGTTGACAGTCC[A/T]TGCAGGTGAAGATGA | 16443 |
rs33601501 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91823059 | GTATCCTCTGTGCTG[C/T]CTTTGAGCTGTCATT | 16443 |
rs33601502 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91823012 | TCCAGTCTGCTAATT[G/T]TCCTTTGGTTCTAAG | 16443 |
rs33601503 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91822737 | CAGATGACTTGTTTC[A/G]CTGATGTATGGCATT | 16443 |
rs33601504 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91878726 | GTGTATTTGGTATTT[A/C]GTCTCCTCCGCAAGT | 16443 |
rs33601505 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91877323 | GGACATGTGGCAGGG[A/C]AGGCTCGGTTACCTC | 16443 |
rs33601506 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91876701 | GACTCCTCCAACCTG[C/G]AACAGCCAAGAGTCA | 16443 |
rs33601507 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91876649 | CCATGGTGCCAAATA[C/T]GGGAACACTACTCTG | 16443 |
rs33601508 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91876498 | TAGGAATGGGAAGAG[A/G]CACCAGTGAAGTCCA | 16443 |
rs33601509 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91875911 | CTTGCTAGGCATGCC[A/G]ACTTGACCAGAGACC | 16443 |
rs33601510 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91874211 | GTTCTATTCATATAG[A/C]AAGCTACCAGGCATT | 16443 |
rs33601511 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91874081 | TAAATTCCAAGGTTC[G/T]GATACAACTATGTGA | 16443 |
rs33601512 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91873406 | ACAGATCAAACAACT[A/G]TAGAATACACCTGAT | 16443 |
rs33601513 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91873067 | GTGGTGCAGAGTCTC[C/T]CACAACTGCTCGTTT | 16443 |
rs33601834 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Itsn1 | GRCm38.p3 | 16:91898052 | TATGAAAACTATTTT[A/G]AACTATTTAATTCAT | 16443 |
rs33601835 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897960 | AGACCTAGAGTTATA[A/G]CAATATAAAAGAAAA | 16443 |
rs33601836 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91897419 | GCAACTGAACACAGA[C/T]TGGGGAAAGTATGAT | 16443 |
rs33601837 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91897240 | TTCTATGTTTAATTA[A/T]GTGCCGACTCTGGAA | 16443 |
rs33601838 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897137 | TCTCCCTTCCACATA[A/C]GCCTCAGCCCGACCC | 16443 |
rs33601839 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91897118 | GCTCCTCATGTGTAA[C/T]CAATCTCCCTTCCAC | 16443 |
rs33601840 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91897114 | TCAGGCTCCTCATGT[A/G]TAACCAATCTCCCTT | 16443 |
rs33601841 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Itsn1 | Mm_Celera | 16:91896926 | AGCCTTAGAACAAAA[A/G]ACAAAAGTGTGCTGG | 16443 |
rs33601842 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896884 | GAACGAGTGTTTCCA[C/T]ATCCACGCCGGCTCA | 16443 |
rs33601843 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896858 | CAAGAAAGCTAGTTC[C/T]AGAGAAAATAGAACG | 16443 |
rs33601894 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91790840 | TCACCACCTCACTTA[C/T]GTCTTTAATCTGAAA | 16443 |
rs33601895 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91790752 | CGTGTTATTGGTACC[A/G]GGAACCTTTCTCTCC | 16443 |
rs33601896 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | Mm_Celera | 16:91790728 | CTGTTTAACCATAGA[A/T]AGCGCATGCGTGTTA | 16443 |
rs33601897 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91790120 | TACCCTGTGTCTGAC[A/G]CCTGCCCCGCTAACC | 16443 |
rs33601898 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91789534 | TGTGATTTTTGATGA[C/T]ATGGTGGTTATAGAA | 16443 |
rs33601899 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91789347 | TGTAGTTTATTTCTT[C/T]TTTACATTAACAGTA | 16443 |
rs33601900 | snp | A/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91789291 | TTGTTTATTCTTGTG[A/T]TTAAATGCAGGCATA | 16443 |
rs33601901 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91789253 | GTTCTCACTTAGACC[A/G]CCGTTTCTTGTTATT | 16443 |
rs33601902 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91789102 | CTTGGACTTGCTTTT[A/G]TATTAGTGGGCACCA | 16443 |
rs33601903 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91788471 | ACAAAATCCAAAGCT[A/G]TCACCAAATGTCCAA | 16443 |
rs33602014 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | GRCm38.p3 | 16:91735437 | GAAAAGTCAGAGTAT[C/T]GTGCACCCGTAACAG | 16443 |
rs33602015 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91735316 | GCAACTTACACTCAT[C/T]GAGGCGTGGCAGTTC | 16443 |
rs33602016 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91733342 | CATTTTTGTGTGTGC[G/T]TATGGCTCTTCATGT | 16443 |
rs33602017 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91732300 | TTTCAGAAGAGCAGA[A/G]TTGGTGTGGCCTGCC | 16443 |
rs33602018 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91731998 | TATGTCAGACTTCTC[C/T]TTTTAGTGACTCCCT | 16443 |
rs33602044 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91765570 | TGGACACCTTAAGCA[A/G]CAGAGGGCGGTAGGC | 16443 |
rs33602045 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91764677 | GCTTACTTAGTGGAC[C/T]GCAGACATCTTGTCA | 16443 |
rs33602046 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Itsn1 | Mm_Celera | 16:91764641 | GTGAGTTTCTTAGTC[A/G]CTCTCTTTGGTGTGG | 16443 |
rs33602047 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91764270 | TCTCAAGGGGAAACG[C/T]TCTCTCTGAGGCTAC | 16443 |
rs33602048 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91763871 | GTACATTGTAAAATC[A/G]TTTCTTTTTGCTTTA | 16443 |
rs33602049 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91763091 | CAGCTTCATTGAGCG[C/T]ATCACAATCTCTAAC | 16443 |
rs33602050 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91763014 | CATGCTTCATGTGGG[C/T]TTTACAGATGTTTAG | 16443 |
rs33602051 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91762970 | CTTGCTGTTGGCTAA[C/G]CAGGTTGAGTATTTG | 16443 |
rs33602052 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91762827 | AGTCAGAACTGGATT[G/T]TTCATGCCCCGGGGC | 16443 |
rs33602053 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | Mm_Celera | 16:91762717 | TCTGGCCATCTTGTG[C/T]CCAGTATTTGTCTAG | 16443 |
rs33602054 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919692 | TTCAAAACTAGAAAC[A/G]CAGAAACTGAGAAGG | 16443 |
rs33602055 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919003 | GTTGATGGTTTCTCA[A/G]GTCTCCGTCCAGGGT | 16443 |
rs33602056 | snp | G/T | 0.391111 | 0.206368 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91918864 | ATTCTTAGAAAGTGA[G/T]GTGCTTTTCAAAACT | 16443 |
rs33602057 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918742 | CCTGGCAGGCTGCGC[A/G]GAGCTGAGATGGAAA | 16443 |
rs33602058 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91918359 | ACTTCGACTTTGGAC[A/G]TTTTAAGTGGCAAAT | 16443 |
rs33602059 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917964 | CTCTTCCTACCTAGA[C/T]GGTTCTATTGGCAGG | 16443 |
rs33602060 | snp | C/G | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917106 | AGCCAACTTGTAGAT[C/G]TAATTTTAAGTCACT | 16443 |
rs33602061 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916931 | CTCTAAGTTGAGAGC[A/G]TTGAAACTCCTATGT | 16443 |
rs33602062 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916888 | AGGAAAATACAACCC[A/G]TGAGAAAGATGGCCA | 16443 |
rs33602063 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916831 | GTGTATAATGACTTC[A/G]TGTCTGTAAGCGCCA | 16443 |
rs33602244 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91872868 | TCACACAACACTGTG[A/G]TCCATTCCCGTGTAG | 16443 |
rs33602245 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91869907 | GGTTTGCAGAACTGA[A/C]CGCAGACCACTGCTG | 16443 |
rs33602246 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91869160 | GAGAAGATCAGGTGA[C/G]AGCTGCACACCATCT | 16443 |
rs33602247 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91868233 | TAGCACTTCTACTTG[C/T]TGTCTGTGGCCTCTC | 16443 |
rs33602248 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91868182 | CTCGCTCGGGTCTCT[C/T]ATCTAAAGTCTTGTA | 16443 |
rs33602249 | snp | C/T | 0.277778 | 0.248452 | synonymous-codon | Itsn1 | Mm_Celera | 16:91868052 | CCAGATAGGGTGGTT[C/T]CCAGCAAATTATGTC | 16443 |
rs33602250 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91867203 | AGGGCAGTAGAAAGT[A/G]TAGCCAGTGCTCTGA | 16443 |
rs33602251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91866148 | TGAGCTGCTTCCTAG[C/T]CAGTGCTGATGGTGT | 16443 |
rs33602252 | snp | C/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91866098 | GTAGCTCTGCACTTT[C/G]CTCTGAACTCAGGGT | 16443 |
rs33602253 | snp | G/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91865389 | GAGAGCCCGTCCAGA[G/T]GTGCTGGCCAGGAGC | 16443 |
rs33602304 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91822708 | GTTCCTTACAGGTTT[C/T]CCTATCAGCAAGCCA | 16443 |
rs33602305 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91822513 | GTTTGGTGAGCAACC[G/T]TCGGTGGTGTTTGCA | 16443 |
rs33602306 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91822495 | GTGAATTGCTACTCC[C/T]AAGTTTGGTGAGCAA | 16443 |
rs33602307 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91821626 | CCATCACAGTGATTA[G/T]CTGGTCAGGTGCTGA | 16443 |
rs33602308 | snp | A/G | 0.124444 | 0.216185 | missense | Itsn1 | GRCm38.p3 | 16:91820743 | GACTGGCAACCCAGA[A/G]GCAAGAAATTGAGAG | 16443 |
rs33602309 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91820422 | ACGGTGTCAGAATTA[A/G]GGAATTAATAAGCTG | 16443 |
rs33602310 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91820258 | GTGATTTCTGGGAGG[C/T]GTGAGGAATGGGCTG | 16443 |
rs33602311 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91820105 | AGGAACCTTCAACTT[A/T]CAGATAGCAACTTCT | 16443 |
rs33602312 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91820075 | CTAGGAATGGTCTCC[A/G]TCATCATCGTGACAA | 16443 |
rs33602313 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91819968 | TGTTTGGAGTGTGCC[C/T]GGTGTGTAAATCTGA | 16443 |
rs33602614 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896825 | CTGTACCAGATGCCT[G/T]TTTTTCTCCTGTCCT | 16443 |
rs33602615 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91896693 | GGCATGGTGCCTGTG[A/C]GCAGAATTTGGAGCA | 16443 |
rs33602616 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896676 | GATGCTTTCCCAGAG[C/T]TGGCATGGTGCCTGT | 16443 |
rs33602617 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896299 | TTCTGAACCACATTT[A/T]AAAAAAAAATACCAT | 16443 |
rs33602618 | snp | A/G | 0.42 | 0.183303 | intron-variant | Itsn1 | Mm_Celera | 16:91896280 | GGCTTTGCATTTTGC[A/G]GATTTCTGAACCACA | 16443 |
rs33602619 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91896262 | AAAAAATGTAATGTT[A/T]CTGGCTTTGCATTTT | 16443 |
rs33602620 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896252 | GTCCTAAATGAAAAA[A/C]TGTAATGTTACTGGC | 16443 |
rs33602621 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | GRCm38.p3 | 16:91896217 | AGCCACTCTCCAGGT[A/G]GATGGGTAATAGGCA | 16443 |
rs33602622 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91896165 | CCTCAGCCTGGATTA[C/T]GACAGCTGGACAAGG | 16443 |
rs33602623 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91896149 | CTCCCTCTACATACC[A/G]CCTCAGCCTGGATTA | 16443 |
rs33602704 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91787532 | ATAGATCAAGAGTCC[A/T]GAAGCCAGTTACCTG | 16443 |
rs33602705 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91787097 | CAAAATACCAGAAAA[C/T]GTTGTTGCTGGGGAT | 16443 |
rs33602706 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | GRCm38.p3 | 16:91786942 | ATACAACCAAGTTCC[A/G]AGGTCTCATTTGTGA | 16443 |
rs33602707 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91786902 | GCCTGCCTTCCAGAG[C/T]CCACTGACTTTTGCT | 16443 |
rs33602708 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91786579 | CTCAGAATAACGTCC[A/G]AGTCCCATGCTGGAC | 16443 |
rs33602709 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91786446 | GCACAGTTCCTAAGT[A/G]CCAACATTACATAAA | 16443 |
rs33602710 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91785680 | TTGTCACAAATAGGA[A/G]TTTGGCCACAATCTC | 16443 |
rs33602711 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91785246 | TTTCTGTCGCCTCCT[A/G]CAGTTCTGTTTTTCC | 16443 |
rs33602712 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91785244 | GATTTCTGTCGCCTC[A/C]TGCAGTTCTGTTTTT | 16443 |
rs33602713 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91785201 | GCATAGCCACCTCTT[A/G]AATAATGATGTGGTT | 16443 |
rs33602874 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916248 | CTGGAGAAGAGACTC[A/G]CAAACTGAAGATGGG | 16443 |
rs33602875 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915480 | CGGACCTGGCCTGAT[C/T]CCTAGGAAGAAGCCA | 16443 |
rs33602876 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915171 | TGCCTGTTATCTTCA[C/T]TCAGTGCCAACGTGT | 16443 |
rs33602877 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914867 | TGCCCTCGATGGAAC[A/G]GAGAGCCTTCTAGAT | 16443 |
rs33602878 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914469 | CTCAGATGTCTGCTT[C/T]GTAAATGCTTGCCCA | 16443 |
rs33602879 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914441 | TAGGTCCTTGCCAAC[A/G]AGGAATCTGAGGCTC | 16443 |
rs33602880 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914382 | GATTCTCTCCTCCTT[C/G]ACTCTACTTTTTTGA | 16443 |
rs33602881 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914348 | TGACCCATGGGTGAC[A/G]CACAGAGTCTCAAAC | 16443 |
rs33602882 | snp | A/G | 0.18 | 0.24 | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914343 | TATTGTGACCCATGG[A/G]TGACACACAGAGTCT | 16443 |
rs33603044 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91865250 | TGTAAGGCCTATGCC[A/G]AGTGAGGAAGGAGGA | 16443 |
rs33603045 | snp | A/G | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91864884 | GCTGTCTGCTTTTAT[A/G]TACAAGAGAAGCATA | 16443 |
rs33603046 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Itsn1 | Mm_Celera | 16:91864656 | GATACACACGTAGGA[A/G]CATAAGAGACTGGCC | 16443 |
rs33603047 | snp | A/C | 0.375 | 0.216506 | intron-variant | Itsn1 | Mm_Celera | 16:91864576 | TGATGTTACTTGAGA[A/C]GATGAGACCTGAACT | 16443 |
rs33603048 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863780 | ACATCACTCATTCAC[A/G]GTTCTGACACCTCCT | 16443 |
rs33603049 | snp | A/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91863688 | GAGGTGTTTGGGACA[A/T]GCTGACATGGCAGGT | 16443 |
rs33603050 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863563 | GAACGTGTATCCAGT[C/T]GTCCGACAAGCTCAG | 16443 |
rs33603051 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863452 | AAGGAACAGCATTGC[A/C]CTGCACAGTACAAAG | 16443 |
rs33603052 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91862823 | ATGTTAGTGGGAGAC[G/T]GTCCTAAGCCGTGTG | 16443 |
rs33603053 | snp | C/T | 0.5 | 0 | intron-variant | Itsn1 | Mm_Celera | 16:91862797 | GAATAGGAGGCCTGG[C/T]TGATTTGGCTATGTT | 16443 |
rs33603074 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91761909 | CAGCCTTGCACTTGC[C/T]GCTGAATTCTTCTGT | 16443 |
rs33603075 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91761634 | CGAGTTGCTTTGCAG[A/G]TAAGTTAGATATATT | 16443 |
rs33603076 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Itsn1 | GRCm38.p3 | 16:91761453 | GTAAAGAAGACAGCT[C/G]TGCCCTTCATGAGAT | 16443 |
rs33603077 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91760212 | AGTGCTTGGGTGTAA[C/T]GGCTCGGCACTTGTG | 16443 |
rs33603078 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91760152 | GCCAGGCTTGTCAGT[A/G]TGATCTGAGTTTGTG | 16443 |
rs33603079 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91760046 | TTGACTCTTTCACAC[C/G]TGTACTAATTTGAAG | 16443 |
rs33603080 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | Mm_Celera | 16:91759518 | TTTTGAAGTTTCGAG[A/G]ATTCCTGTATTTTAC | 16443 |
rs33603081 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91759369 | TCTGTATCTGTTGTA[C/T]GAAGAGGCCTGGTAG | 16443 |
rs33603082 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Itsn1 | GRCm38.p3 | 16:91759145 | TGTCATTGTTGTTGT[A/T]TTCTTTGGAAGCAGT | 16443 |
rs33603083 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | GRCm38.p3 | 16:91758332 | GTTTTCTTTAAAAAT[G/T]TACCAACTATAGATA | 16443 |
rs33603504 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91819465 | TCACAGTATATCTGA[A/G]AGCTTGCTTCGTGAG | 16443 |
rs33603505 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91819023 | TTAAAAAATGTTTTG[A/G]TGGAGTTGGAGAGAT | 16443 |
rs33603506 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91818901 | GGGGTGACTTTGGTG[C/T]CAGACCCGGATAGTG | 16443 |
rs33603507 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91818428 | TTTGAAGATAAGAAG[A/C]GGGAGAACTTCGAGC | 16443 |
rs33603508 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91818198 | TTAGCTTTGGGATTG[C/T]CTTTTTCTGTAAAGA | 16443 |
rs33603509 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91817465 | AGTGTCACCGGCTGC[C/G]GTTTCTGTGCTTCCC | 16443 |
rs33603510 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91817113 | TGTGATGCACCTGTA[G/T]TCCATCCTTGAAGTG | 16443 |
rs33603511 | snp | C/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91816987 | GAGCTGAGTAGCTGA[C/G]GGAGATTTCTAGCAC | 16443 |
rs33603512 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Itsn1 | Mm_Celera | 16:91816872 | CGGCAGTGGGATGTC[C/T]GTCATAAGCTCTTCT | 16443 |
rs33603513 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91816796 | CCCTTCCTTCTGCCC[A/G]GTGCGGTGCTGCCCA | 16443 |
rs33603774 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91785087 | TCACCTTGTTAAACC[A/G]CAGCTTAAAGTGGAC | 16443 |
rs33603775 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784980 | TTTTAAAATCTCGAC[C/T]CTTCTCAGTAGCATC | 16443 |
rs33603776 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784914 | ATCAGGTATTAAAAC[A/G]GAAAGCTTGGTTTTG | 16443 |
rs33603777 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784693 | CATCTGGGCTTCCCT[A/G]GAGGTGCTTTTTATT | 16443 |
rs33603778 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91784664 | CAGCTCACCAGTTCC[A/G]GACAGAAAGAGGGCA | 16443 |
rs33603779 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784652 | GCTGTTTAGTCACAG[C/T]TCACCAGTTCCGGAC | 16443 |
rs33603780 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784314 | AAACCTTTGTTTGTC[A/G]TCATCATGGTGTGTG | 16443 |
rs33603781 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91784056 | TCTTCTTGCCTTTGG[A/G]CTGCAGGTAGCCTGG | 16443 |
rs33603782 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91783843 | TTTTTGCCTGTGACA[C/T]TTTAGGCACCTGAAA | 16443 |
rs33603783 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91783003 | CTAACAGGCAATCTC[A/G]TCGGGGTAGGGACAC | 16443 |
rs33603894 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91860890 | ATGTATTCTGTCTGG[A/G]CGGCAGACTCAGATG | 16443 |
rs33603895 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91860598 | CCCTGTCCTGGCTCC[C/T]GTGGTCTCGGCTGGC | 16443 |
rs33603896 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | Mm_Celera | 16:91860565 | TAAGCCACTTTGTCC[C/T]ACAGAGTGCATGCTG | 16443 |
rs33603897 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91860254 | CTCATCGCTGTTCTT[C/T]ATTTGATATGCAGAC | 16443 |
rs33603898 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91860193 | GCTCTCTTCTGTGCA[C/T]GGAGCCTTGGGAATC | 16443 |
rs33603899 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91859869 | CTGACCTATGAGCTG[C/T]TGCTTACCATAGCCT | 16443 |
rs33603900 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91859482 | GGCTCCATTAAGATC[A/G]TGACAATGACATTTC | 16443 |
rs33603901 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91859263 | TCACTCCAGGAATGA[C/T]TTCTAAAACAATTTA | 16443 |
rs33603902 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91859174 | GTGCACATTGGCTTC[A/G]GTAGGCCCTGTAGCC | 16443 |
rs33603903 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91859136 | GTGGCCAGGCACTCG[C/T]TGTCATTTAAATGCC | 16443 |
rs33603994 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91757324 | TCTGAAAGGATTTTT[A/G]AAGGGTAGTCAACGA | 16443 |
rs33603995 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91757156 | GCTCTCCATGCTTTT[C/T]TTGCCTTTCTCCGCA | 16443 |
rs33603996 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91756544 | TGTGTTGTTGCTTTG[G/T]TCTTTAGTAAGCTGT | 16443 |
rs33603997 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91756495 | TTGTGTGCCTAACCA[C/T]GCTGCCCTAGGCTGC | 16443 |
rs33603998 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91756449 | CACATCTGTGTACCT[A/G]TATAATGTAGATATA | 16443 |
rs33603999 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Itsn1 | GRCm38.p3 | 16:91756344 | TATTTCTGAATTGCA[A/G]TCTAGAGTTTTATCC | 16443 |
rs33604000 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Itsn1 | GRCm38.p3 | 16:91755432 | ATATAAAAGAGAGCA[C/T]TAGAGCATTTTTAAT | 16443 |
rs33604001 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91755155 | TTTACCACTCCTTCC[G/T]GTAGATGCCAGTCTG | 16443 |
rs33604002 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91754999 | TGCATTGGCTGAAAC[G/T]TCTCCAGAACATCTC | 16443 |
rs33604003 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91754948 | CTTGTGTCAGCCAAA[A/T]GGCCTTTGTCTCTGG | 16443 |
rs33604454 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91816152 | TCTGCTTCGCGTGGC[A/G]CTGGGAGCAAAATGC | 16443 |
rs33604455 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91815501 | TGGTCAGCCACTGCC[A/G]CCCGTCCTGCCTCCA | 16443 |
rs33604456 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | GRCm38.p3 | 16:91815353 | TGGTGAATAGTAAGA[C/T]CTCTGCATTTTTTGT | 16443 |
rs33604457 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91814676 | TTTGAAAACCATTCC[A/G]TCTGACTTACCCTAA | 16443 |
rs33604458 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91814575 | GCTATTAGAATGATA[A/T]AATTTTTTTTCCACA | 16443 |
rs33604459 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Itsn1 | Mm_Celera | 16:91814547 | CCTGATTTCATTGAT[A/G]ATTCAAGGCATCGCT | 16443 |
rs33604664 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Itsn1 | Mm_Celera | 16:91782954 | ACTGGGTACACCTCA[A/G]CCCAGACTCTGTAAC | 16443 |
rs33604665 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91782930 | CCCAGCTGAGCACGC[C/T]AGGCAAGCACTGGGT | 16443 |
rs33604666 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | Mm_Celera | 16:91782753 | CCGCATGTTGCTTGC[A/T]TGGGCTTGATGGATC | 16443 |
rs33604667 | snp | G/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91782036 | CCTTTCATTGTGACT[G/T]TCACTTGCAGGTGTG | 16443 |
rs33604668 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91781971 | ACCTGTGACAGCCCC[C/T]GAGCTTCCATATTGT | 16443 |
rs33604669 | snp | A/C | 0.32 | 0.24 | intron-variant | Itsn1 | Mm_Celera | 16:91781924 | GTATCACATACAACA[A/C]CGGAGATTAAATAGC | 16443 |
rs33604670 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91781836 | TACGCCTGCACAGTG[C/T]GCCCCTGATATTCAG | 16443 |
rs33604671 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91781804 | ATGCACAGGGCTGTG[A/C]GTGACTAGAAGAGCT | 16443 |
rs33604672 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91780737 | TCTTAGGCACCTACT[A/C/G]CCATATCTGACTGAA | 16443 |
rs33604673 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91780690 | CCTTGAATTCATGAT[C/T]CTCCTGCTTCCTCTT | 16443 |
rs33604694 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91858901 | TGAGGTGGTGCAATC[A/G/T]TAATGAAATGGTTGG | 16443 |
rs33604695 | snp | C/T | 0.260355 | 0.249785 | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91858728 | TGTAAATGAAGGTGT[C/T]CTGGTGATACTGACC | 16443 |
rs33604696 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91858501 | TATGGTGGTAACTAA[C/T]GTGGCCTGCAGCTGT | 16443 |
rs33604697 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Itsn1 | GRCm38.p3 | 16:91857994 | GTGCAGTGCGCTTGC[C/T]GTGAGGTCCTGGAGC | 16443 |
rs33604698 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91857707 | TGGCACTGTATGTTT[C/G]AAGTGTCACTGGGGC | 16443 |
rs33604699 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91857607 | GTACCTGCTTGTGCA[A/G]CCTGGGTGACAGCAG | 16443 |
rs33604700 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91857569 | ATAGGTTAGGGAGAT[A/G]TTACTCTTGTCATTA | 16443 |
rs33604701 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91857336 | AAACCAGTGTCTCTT[C/T]CTGTAAGTCTTTTGT | 16443 |
rs33604702 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Itsn1 | GRCm38.p3 | 16:91857303 | CTTAAAATACACAGA[A/G]GCCTGACAAAATGGA | 16443 |
rs33604703 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91856960 | TGTGTACTTATTTCA[A/G]TTTTCATTAGAACAA | 16443 |
rs33604704 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91754916 | TGGCTTCTCTCTGCA[G/T]CCCCTTGTCTACTTT | 16443 |
rs33604705 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Itsn1 | GRCm38.p3 | 16:91754668 | CTCACACTGTGTCAA[C/T]GCTACCATGCATGTA | 16443 |
rs33604706 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91753837 | AGGAGGTCGACGTGG[C/G]TTTACTTAAGTTTAA | 16443 |
rs33604707 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Itsn1 | Mm_Celera | 16:91753713 | TTTAAAAATATTAAT[C/T]CTTATGATACATGCT | 16443 |
rs33604708 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91753524 | TCCACTGAGATCCAG[C/T]GCCCTGACTCTTGAG | 16443 |
rs33604709 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Itsn1 | GRCm38.p3 | 16:91753474 | GCGCCATTTCCCTCC[C/T]GTAGTCCATTTCCGA | 16443 |
rs33604710 | snp | C/T | 0.375 | 0.216506 | intron-variant | Itsn1 | GRCm38.p3 | 16:91753337 | TCTAAACACACTGTA[C/T]GTCTTGGCAGTACTT | 16443 |
rs33604711 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Itsn1 | Mm_Celera | 16:91753271 | AAGAAGGGCTGTATG[C/T]GCAGTGTTGAAAGGA | 16443 |
rs33604712 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91752874 | CCGGAGCAAGGCCTG[C/T]GGATTGAACAGGTGC | 16443 |
rs33604713 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Itsn1 | GRCm38.p3 | 16:91752588 | ACATAGCTCTGTAGC[C/T]AGTGTCTGAGGAAGC | 16443 |
rs33605474 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91855516 | TTATTATATGAACTC[C/T]TATAATGATCACCTT | 16443 |
rs33605475 | snp | A/G | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91854205 | TTTGGGAAAGTAATG[A/G]ATGGATTTGGAAGAA | 16443 |
rs33605534 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Itsn1 | Mm_Celera | 16:91752231 | CAAGCATGCACATCT[A/G]TCTCAGTTGCTCATC | 16443 |
rs33605535 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | GRCm38.p3 | 16:91751831 | AGAAACAGTATCTGC[C/T]GTAGGGTGATCCCTG | 16443 |
rs33605536 | snp | C/T | 0.32 | 0.24 | intron-variant | Itsn1 | GRCm38.p3 | 16:91751701 | AAACAAAAGAAAAAC[C/T]GTGGTGCTAGATGGG | 16443 |
rs33605537 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Itsn1 | Mm_Celera | 16:91751644 | GGTGTGCGCCACCAG[A/T]CTTAGCCACCAGGCT | 16443 |
rs33605538 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Itsn1 | Mm_Celera | 16:91751252 | TGTGTATAGGAAATA[C/T]GGCAAAGTGGATTTC | 16443 |
rs33605539 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Itsn1 | Mm_Celera | 16:91749176 | TTGTTGGTTTGGGTA[A/G]CTGATGAGAGCACAT | 16443 |
rs33605540 | snp | G/T | 0.260355 | 0.249785 | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747935 | CGTCAGTCAGACCTC[G/T]TGCTCTGGTGCTTCT | 16443 |
rs33605541 | snp | C/T | 0.165289 | 0.235211 | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747654 | GTTGAGTAGCTCAAC[C/T]TCACTGTAGAGGCTG | 16443 |
rs33605584 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91780439 | GTGGACCAAATGGCT[A/G]AGTCAGAAGTCTGGT | 16443 |
rs33605585 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Itsn1 | Mm_Celera | 16:91780058 | TTCTATTTCCCTGTT[C/T]GTGTTGGGACCATCC | 16443 |
rs33605586 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Itsn1 | GRCm38.p3 | 16:91779912 | AACGAATTCCCATAG[A/G]GCACGCATGGTCCAT | 16443 |
rs33605587 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Itsn1 | Mm_Celera | 16:91779761 | ACGTGCAGGTACGCC[G/T]GGAAGAGAGGGCCGC | 16443 |
rs45662612 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790171 | AGAGTCACATGCAAC[A/G]GTTGCTTGCTGGGTT | 16443 |
rs45692950 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795646 | AGGTGTGCGCCACCA[C/T]GCCCGGCTGCATGTT | 16443 |
rs45715894 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810921 | GGCCCTCAGCAGCCG[A/G]GCCTGCAGCATCTTG | 16443 |
rs45751468 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811451 | CTCCCGAGTGCTTGG[A/G]TTAAAGGCGTGCGCC | 16443 |
rs45839950 | snp | A/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802453 | AGTCTAATACGCCTC[A/T]TCTGTCTGTCCGTTG | 16443 |
rs45843891 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795643 | CAAAGGTGTGCGCCA[C/T]CACGCCCGGCTGCAT | 16443 |
rs45924087 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899799 | GGGCTCTCTCCCGCT[C/T]GTTAATACAACTGAT | 16443 |
rs45960269 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897076 | CATACACACACATGT[A/G]CACACAAACTGCACA | 16443 |
rs46000458 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749928 | ACAAGAGCTTCATCC[C/T]TCTACCCTATGTGTG | 16443 |
rs46002875 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860502 | ATTTCAATTGAAATA[C/T]TTAATTTACTACAAG | 16443 |
rs46060239 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810734 | ACTTTTCTGCCAATA[C/T]GTTATATGTAAATAA | 16443 |
rs46093955 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898464 | GCATGTGTCCTGTCT[A/C]AGTTAGGACTTTGCT | 16443 |
rs46137264 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797716 | GCATTTTCAAGGTTA[C/T]TTTCCTGTTTTTTTA | 16443 |
rs46219642 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899069 | CAGGGCGCCTGGCTC[A/G]TCCTCCTGCTCTCTG | 16443 |
rs46250197 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898124 | CCTGATAAGGGATAT[A/G]CTGTGGCATTTGGCT | 16443 |
rs46327619 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789621 | AGTCAGTCCATACGA[A/G]TGCGGTTGCTGGTTC | 16443 |
rs46339498 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91837660 | GTTTGGCTGTTTGTG[C/T]CTGTTTTGTACCTTT | 16443 |
rs46357821 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895547 | TTTGCTGATGGGAGA[C/G]AAGGATTTTTTTTTT | 16443 |
rs46382132 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900456 | TCGGGGCAGCATATT[C/T]GCCTCCACATAGCAC | 16443 |
rs46400534 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789507 | CATCCACACTAGGTT[A/G]TTTCCGTGTACTGTG | 16443 |
rs46403257 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91897393 | GTATCTAAGGAAAGA[A/C]CCGAGGGCGGGCAAC | 16443 |
rs46462628 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781628 | TTGCACTGTTGGGTG[A/G]TGAGCGCTTTTAGCC | 16443 |
rs46686429 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749785 | AAGAGAGCTTCATCC[C/T]TCTACCCTATGTGTG | 16443 |
rs46733597 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780946 | TGGCAGAGGGGAGGA[A/G]CGGTGGCTGGCACAG | 16443 |
rs46768291 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774024 | TGTTTTTTGAGAAAT[A/G]GTTTCTCTGCCTGGT | 16443 |
rs46792264 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869529 | CCATCTATCTCATTT[C/T]CCCCCGTTCTGAAGG | 16443 |
rs46828508 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781503 | TTATTACTGTGTGCA[C/T]ACGGGCAGAGTGTGT | 16443 |
rs46960264 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91770038 | TGCTGAGCCATCTCG[A/C]CAGCTCAGTTGGCTC | 16443 |
rs46985038 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91796450 | CTCCTTCTCTAGCAC[A/G]GTGTCTGTCACGCTT | 16443 |
rs46989001 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883063 | ATATTATTTCAGCTG[C/T]GGGCCAATTTTAGTT | 16443 |
rs47034501 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91843613 | TAGCAATAAATGGCC[A/G]CTCTTCTGATGTGGA | 16443 |
rs47058745 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781675 | TGCCTGTCCCTCACA[A/G]TCCTCATGAAGCAGT | 16443 |
rs47062534 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806015 | GTCAACACCGCCAAC[C/T]TTAGACAGACATGTT | 16443 |
rs47123371 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797580 | AAATAAGTCTTAAAC[A/T]TTTTTCTTTTTGGAG | 16443 |
rs47216964 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796211 | GTGTGGTAAAGGCAC[A/G]TGGACTCCGAGATTT | 16443 |
rs47239411 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860486 | TTAAACCCTTTGTCT[C/T]ATTTCAATTGAAATA | 16443 |
rs47242858 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750497 | TGGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT | 16443 |
rs47337318 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844537 | TGGCTCGTTGGTTAA[A/G]ACTACTGGCTGTTCT | 16443 |
rs47364129 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795726 | ATCCATTTTTTAATA[A/G]AGATGTCCCGATTCT | 16443 |
rs47414365 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895472 | GGCCAAGGGCTGATG[A/G]TTTGGATGTCAGAAC | 16443 |
rs47426937 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91773959 | AGTTATGTTGTGGAC[A/T]CGCTTGTGAGCTAGA | 16443 |
rs47452185 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760344 | CTGCGGCAGCTTTCC[A/G]GAACTTTGAAAGCTA | 16443 |
rs47489139 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904455 | TGAGTGGTGGGAGAG[A/G]GCCATGCCCTTCAGG | 16443 |
rs47510254 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777829 | GATTGCCCAGGCATT[A/G]GAAGATGTGCGGGAG | 16443 |
rs47569226 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91888524 | GCCCAAAGAATTTCA[A/G]AGGAGCCTCTGCCCC | 16443 |
rs47653744 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891132 | GGAGCATCTAAGAGA[A/G]GTGGGGTGACTTCCC | 16443 |
rs47688951 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789445 | CATAGCTCCTGTCAT[A/G]GTAGCAGGCGTGCCT | 16443 |
rs47936895 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831839 | GTTACACCTCATTTT[A/G]CAGAAAATCAGGTTT | 16443 |
rs48075607 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898208 | ACGTATTTGGGGGCT[A/G]GGGAGGTGGCTTGGC | 16443 |
rs48146374 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789879 | TCACCATCACACTGG[G/T]GAAACAGGAAGGCCA | 16443 |
rs48182858 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869530 | CATCTATCTCATTTT[C/T]CCCCGTTCTGAAGGG | 16443 |
rs48194435 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782241 | TTTTCAAGGTTTCTT[A/T]CTTAATATAAGTTGG | 16443 |
rs48215122 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896602 | AAAAGACTAATAAAA[C/T]ACAGCCTTCAGATGG | 16443 |
rs48241586 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91904497 | TAACGGGGTTCGATT[A/C]AGCATGCACTGTTGT | 16443 |
rs48288150 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797850 | CCATCAAGATAAACC[C/T]GATACACATTGATAT | 16443 |
rs48329388 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904644 | AGCACCGACGACTAC[C/T]GAGTCTTGTGGGGAC | 16443 |
rs48392996 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750214 | AAGAGAGCTTCATCC[C/T]TCTACCCTATGTGTG | 16443 |
rs48453198 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898713 | CCACGCCCACTGTGA[C/T]ACACCTACTCCAACA | 16443 |
rs48456411 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745961 | AATACTGGACACAGT[A/G]CTTGCAAGTCAACAT | 16443 |
rs48483823 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817435 | GAGGCTCTCTGTTCT[A/G]ACTACGTCCTTGCCA | 16443 |
rs48552834 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759046 | GCTGGAATTACAGGC[A/G]TGTGCCACCACTGCC | 16443 |
rs48573741 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781719 | TAGTGGGCACGGCTG[C/T]GGCGTTTGTTGCCCT | 16443 |
rs48674174 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898263 | ACCTATGTAAAAAAG[C/T]AGACATGGTGGTCTA | 16443 |
rs48703131 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810739 | TCTGCCAATACGTTA[C/T]ATGTAAATAACAGTT | 16443 |
rs48734461 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789478 | ATGGTTCTACGTGCC[A/G]TAGTGCTTCTGCCCA | 16443 |
rs48759978 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811227 | AGCTACTCTGTGCCA[A/G]GAATAAAGATGCTCA | 16443 |
rs48825031 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91761494 | GGTCAGGGCGCGCCT[A/G]TCTCTTACACAGGAG | 16443 |
rs48917556 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898351 | AGCCCTGCGTGCCAT[C/T]AAAACATTCTGTCTC | 16443 |
rs48935284 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898302 | CTGGACAGCAGAGAT[C/G]GAGGGAATCCTAGCT | 16443 |
rs49075110 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797915 | TGTGTGGTACCAGGC[A/G]TTGATGGTGGGTGTG | 16443 |
rs49103313 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810486 | ACAGTCCCATGGTAA[C/T]GAGCTGTGCAGCAGT | 16443 |
rs49165492 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789679 | CCACTTGGGGTTGTA[A/G]TTTCCCCACCAACAG | 16443 |
rs49354152 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904495 | AGTAACGGGGTTCGA[G/T]TAAGCATGCACTGTT | 16443 |
rs49492218 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810614 | GAGGAGAAGGAAAGA[G/T]GCGCTTCTTGCATTC | 16443 |
rs49513579 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860224 | GTCCCACGCTTATGT[A/G]CATGCAAGCACTCTC | 16443 |
rs49571821 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797845 | TACAGCCATCAAGAT[A/T]AACCTGATACACATT | 16443 |
rs49607604 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781843 | GCACAGTGCGCCCCT[G/T]ATATTCAGTGCTCAG | 16443 |
rs49634467 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860421 | AGCAATAATAATAAA[A/G]TGCATTCCACTGCAC | 16443 |
rs49715383 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781755 | AATCACTCCCCTCTT[A/T]GTTGTTTTCCCTTTG | 16443 |
rs49847645 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895079 | ATGACTGTGCCTCAG[A/G]CTTTTGGGGGTGGCC | 16443 |
rs49899484 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896068 | GGAAGAAATTCTGAA[A/G]TCAGAATGTCCTTTC | 16443 |
rs50014078 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898779 | AAGCAAATACAAACC[A/G]TCGCATGCTCTCACA | 16443 |
rs50043358 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789880 | CACCATCACACTGGG[A/G]AAACAGGAAGGCCAG | 16443 |
rs50063511 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896710 | CAGAATTTGGAGCAA[C/T]ACACGCACACACAAA | 16443 |
rs50077130 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91796259 | GGTCTGGTGGTTTCA[A/G]TAGAAATGCCCCCAT | 16443 |
rs50083177 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91896715 | TTTGGAGCAACACAC[A/G]CACACACAAAGAGAG | 16443 |
rs50083667 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91805244 | GGGTTCCATTCCCAG[A/G]ACCCATGGGGCAAAC | 16443 |
rs50084930 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896607 | ACTAATAAAATACAG[C/T]CTTCAGATGGCAACC | 16443 |
rs50119322 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790147 | AACCTGATTCCAGCA[C/G]CAGCTTCCAGAGTCA | 16443 |
rs50252145 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796101 | TAGTAGCCTTGAATG[C/T]GTTGTCTTAGGGAGG | 16443 |
rs50305556 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796181 | CAGGAAGGTGTACAC[G/T]GTGTTAGGGAGGAAG | 16443 |
rs50340293 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91796030 | CCAGTGTTTTCTGCT[A/G]TTTGTAGGACCACTC | 16443 |
rs50359051 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837821 | GCAAACTATAAACTG[A/G]GTAATTGCAGTTACA | 16443 |
rs50422293 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761764 | AAGTTTATCATTTAC[C/T]CTAGCCTGTGACAAC | 16443 |
rs50431247 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781722 | TGGGCACGGCTGTGG[C/T]GTTTGTTGCCCTGTT | 16443 |
rs50440743 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886389 | GTAAAAAAAAAAAAA[A/G]GGGGGGGGACCAGCC | 16443 |
rs50489516 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895535 | AGGACCCCACTCTTT[A/G]CTGATGGGAGAGAAG | 16443 |
rs50512181 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898910 | CGTGGCGTAGGGCAC[C/T]TGTCCTGCTCACCCA | 16443 |
rs50512456 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781844 | CACAGTGCGCCCCTG[A/G]TATTCAGTGCTCAGT | 16443 |
rs50557857 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894067 | TTTCCACTAGTGGCC[C/T]CCAGGGATGGATGGA | 16443 |
rs50594217 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749970 | TGGACAAGAGAGCTT[C/T]ATCCCTCTACCCTAT | 16443 |
rs50626069 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843299 | TTGCTTTTAGAATCT[C/T]TTTGCTTTTAAACCG | 16443 |
rs50640956 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896995 | AGAAACTTAGCTGTG[A/G]GTGCAGATATGCTCA | 16443 |
rs50646940 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91761816 | TGAGAGAAAAAAGTA[C/T]CTGAGATCTGCAAGT | 16443 |
rs50756697 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810319 | TCATTTCACAATGCC[A/G]TAATAACTTGAGACT | 16443 |
rs50778674 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823798 | GGGTCCATTCCTGAC[C/T]AAGCACACTTAGTCA | 16443 |
rs50854724 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900437 | CCACCTGGCGGTCAC[A/G]GGGTCGGGGCAGCAT | 16443 |
rs50865136 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894324 | ACACACCAGAAGAGG[A/G]CATCAGGTCCCATTA | 16443 |
rs50917744 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898433 | CCTCCACTCATGGGC[C/G]CACACACTTACATAC | 16443 |
rs50933536 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860192 | TGCTCTCTTCTGTGC[A/G]CGGAGCCTTGGGAAT | 16443 |
rs50961262 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91773997 | TAAAAGAATTTTTGC[C/T]TATTTGTTTTATGTT | 16443 |
rs50970807 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895000 | GGGCGTGAACTCTGG[C/G]CTTTCCATTGGATTC | 16443 |
rs51038199 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811326 | TCTTTTTTTGTTTTG[G/T]TTTGGTTTTTGGTTT | 16443 |
rs51065041 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779093 | ACTTAATAGTAGCTA[A/G]CACGTTACTGTAATT | 16443 |
rs51137615 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770036 | CCTGCTGAGCCATCT[C/G/T]GCCAGCTCAGTTGGC | 16443 |
rs51150800 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91779029 | TCTTTTTTTTTTTAA[A/G]AAAGCACGCTTGTCT | 16443 |
rs51220034 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894383 | CTGAGAATTGAATCA[A/G]GACCTCTGGAAGAGC | 16443 |
rs51239059 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91797579 | TAAATAAGTCTTAAA[A/C]ATTTTTCTTTTTGGA | 16443 |
rs51275982 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810890 | AGGCCTGGGAGGGAG[C/G]AGCTCCCCTGCCCCA | 16443 |
rs51331029 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781584 | TCCACCTTTATGCAG[A/G]TGCGGGCATCAAGCT | 16443 |
rs51339157 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811232 | CTCTGTGCCAAGAAT[A/G]AAGATGCTCATTATC | 16443 |
rs51345778 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807072 | CGACTCTGGCATGAT[A/G]CCAGTCAGAAAGGTG | 16443 |
rs51365995 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810717 | CGTGTACATTAATGT[A/G]CACTTTTCTGCCAAT | 16443 |
rs51397809 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91769960 | CAGATGGTTGTGAGC[A/C]CCAATGTGGTTGCTG | 16443 |
rs51441823 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91778459 | CAGTGGTGACATACT[C/T]CTTCAATCCCAGCAC | 16443 |
rs51474200 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904635 | CTTTCCAGAAGCACC[A/G]ACGACTACCGAGTCT | 16443 |
rs51507614 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91789620 | GAGTCAGTCCATACG[A/C]GTGCGGTTGCTGGTT | 16443 |
rs51540358 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895478 | GGGCTGATGGTTTGG[A/G]TGTCAGAACTCCAGA | 16443 |
rs51575362 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796413 | CACCTGCTGCCTTCC[A/G]ATCAAGATTTAGAAC | 16443 |
rs51613859 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91734187 | GGTCACCCTGAAGAG[G/T]AGTCAGCCTCTCCAG | 16443 |
rs51686953 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798104 | AGCATGCATGTGGCC[C/T]AGGATTCATTCCACA | 16443 |
rs51714436 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845898 | GTAATAGCACCTCCC[C/T]GGGAACCAAGTTGGA | 16443 |
rs51725712 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779099 | TAGTAGCTAGCACGT[C/T]ACTGTAATTCAGTGG | 16443 |
rs51729075 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898307 | CAGCAGAGATGGAGG[A/G]AATCCTAGCTACCCT | 16443 |
rs51782145 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91882849 | GCTGGTCAAGTATGT[C/G]CATGACGGTTTAGGG | 16443 |
rs51900818 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91895623 | AATACAGTTGGTAAA[A/C]GTGGTTGGGAAGCTG | 16443 |
rs51935091 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904812 | TTTTTTTTTTTTTTT[G/T]GGTTTTTTGAAACAG | 16443 |
rs52113615 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807551 | ACAGACACACACACA[C/T]ACACACACATACATA | 16443 |
rs52124849 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860279 | GCAGACTGTGAAAAT[A/G]ACAAGAACATTAATA | 16443 |
rs52125130 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807561 | ACACATACACACACA[C/T]ACATACATACACACA | 16443 |
rs52154966 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789017 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGGTGGT | 16443 |
rs52184954 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91805371 | CTCTCTCTCTCTCTC[A/T]CACACACACACACCC | 16443 |
rs52211569 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807565 | ATACACACACATACA[C/T]ACATACACACACACA | 16443 |
rs52277538 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807524 | CACACACACACACAC[A/G]CACACACACACACAG | 16443 |
rs52297183 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783155 | ATCGGCTGTTTTGTG[C/T]GATTTGCATTTTTTT | 16443 |
rs52332673 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807550 | CACAGACACACACAC[A/G]TACACACACATACAT | 16443 |
rs52345322 | snp | C/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807539 | ACACACACACACACA[C/G/T]ACACACACACATACA | 16443 |
rs52355053 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807533 | ACACACACACACACA[C/T]ACACAGACACACACA | 16443 |
rs52363584 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807420 | GATAGATGCACACGT[C/T]CATCTAACACTAATC | 16443 |
rs52373000 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91783143 | CTTTTCCAGGTCATC[A/G]GCTGTTTTGTGTGAT | 16443 |
rs52375056 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807521 | ACACACACACACACA[C/T]ACACACACACACACA | 16443 |
rs52412130 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769618 | CTCAGGGAAGCCACA[C/T]AGGTCACCAGATCCC | 16443 |
rs52435345 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769603 | GTCTGTGCACACGTG[C/T]TCAGGGAAGCCACAT | 16443 |
rs52499217 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900016 | CTCTCCCTCCTCCTC[C/T]TCCTCTAACACACTT | 16443 |
rs52509135 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807505 | ATAAATACACACACA[C/T]ACACACACACACACA | 16443 |
rs52512857 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894288 | ATTTAATGTATATGA[A/G]TACACTGTAGCTGTC | 16443 |
rs52556608 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895646 | GGAAGCTGGGTGGTT[A/G]GGAGGATGATTCGGG | 16443 |
rs52574278 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807569 | ACACACATACATACA[C/T]ACACACACACACACA | 16443 |
rs52582865 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807657 | ACACACAGACACACA[C/T]ACATACATACACACA | 16443 |
rs52584772 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860360 | AATTTTACTTTAAGC[C/T]TTCCTCTTCTCTAAT | 16443 |
rs108083528 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897017 | ATATGCTCATGGCTA[C/T]TCTGGCATGTGACTG | 16443 |
rs108142323 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778554 | GTCTAGAAAAACAAA[A/G]ACAAAAACGAGAGAG | 16443 |
rs108291892 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807665 | ACACACACACATACA[C/T]ACACACACACACACA | 16443 |
rs108323780 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91835219 | GCTTTGAGAGTCAGT[C/T]TACACACACACACAC | 16443 |
rs108362983 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91758875 | TTCTTTTCTTGGGAA[A/G]CCATCTTTTTTGACT | 16443 |
rs108631655 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807661 | ACAGACACACACACA[C/T]ACATACACACACACA | 16443 |
rs108759985 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811331 | TTTTGTTTTGGTTTG[G/T]TTTTTGGTTTTTTGA | 16443 |
rs108887845 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896986 | ATGGTGTTCAGAAAC[C/T]TAGCTGTGGGTGCAG | 16443 |
rs211713222 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844921 | TCCCCGTCCTCTAGG[A/C]CCCTGCCTTAGAGAA | 16443 |
rs211716863 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742925 | GCTCTGGAGTCCACA[G/T]GACACACTTTGAGAA | 16443 |
rs211717427 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837296 | GTGTGTGGGCAAACA[A/G]ACGCATTTAAATCTC | 16443 |
rs211727576 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885190 | CAGGGACTGAATATG[C/T]CTTCCACAGCTCAAG | 16443 |
rs211730181 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794951 | GTGGCTTGTGAGTGC[C/T]ATAGTTGAGCAGGAC | 16443 |
rs211731085 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788129 | AGAAAAACAGGGAGA[A/G]CCAGAGTTTTAAGGC | 16443 |
rs211737169 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891429 | TCAAGCAGGGCAGGA[A/G]CCTGGAGGCAGGGAG | 16443 |
rs211745892 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832369 | ACAGTCTCCTGAAAG[-/T]TTTTTTTTTCATCCT | 16443 |
rs211776169 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890661 | AGATCCTTCTGAGTC[C/T]GCCTCCCGAGTACTG | 16443 |
rs211786965 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890727 | TGTTCTTTTATAACA[A/G]CTTGCTCTAAACAGA | 16443 |
rs211789322 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794585 | CTACAGGAGATGGCT[A/G]TCTTAGGACTAGACT | 16443 |
rs211810248 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895629 | GTTGGTAAAAGTGGT[C/T]GGGAAGCTGGGTGGT | 16443 |
rs211820613 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844229 | ACCAGCTACCTAGTC[A/G]TTTGTCTGAAAGCTG | 16443 |
rs211841759 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748602 | GGGGGCATTTTCTTG[A/G]TTGCTAATCAATGTA | 16443 |
rs211855285 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802447 | AGGAGGAGTCTAATA[A/C]GCCTCATCTGTCTGT | 16443 |
rs211868231 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91749341 | GTTTTAACCACCAGG[A/G]CCTTTGAGTGACCCT | 16443 |
rs211886210 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851953 | CTTGAAGGGGTTGGA[A/G]GTGAGGTCAGTCCAG | 16443 |
rs211917873 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802043 | ATAGAATTCCACAGT[A/G]AGGAAAACCGAGCAG | 16443 |
rs211923355 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757123 | CTCCAGAGCACAGGA[C/T]GGCATGGCCTCTCAT | 16443 |
rs211924572 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91757937 | TTTATTTTATGTATA[C/T]GAGTACACTATTGCT | 16443 |
rs211931937 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765545 | TGTACCAGTCTGCTT[G/T]GGCATAGACTGGACA | 16443 |
rs211947462 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810570 | AACAGAAGCATTAGA[A/G]GTTGACTCTCCTCAC | 16443 |
rs211955872 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91858997 | TAACAGAAACATAAG[A/G]CAAGCCCACAGGAAT | 16443 |
rs211964613 | in-del | -/AGGC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831655 | GAGTGCTGGAATTTA[-/AGGC]ATTCACCACACCAGT | 16443 |
rs211968395 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764857 | CCTCTATGTAGAAAG[C/T]GGCTTGGCTGGTGCC | 16443 |
rs211973077 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91809858 | CAGTGTAGGCTCGTC[A/G]GCCACTCACGAGTCC | 16443 |
rs211975796 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816718 | ACACGTGCGCACATG[C/G]GCCAGCACTGAGCTG | 16443 |
rs211983846 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816248 | TAAAAGAATGTGAGA[A/G]TTTTTTGCTTCTCTT | 16443 |
rs211995210 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859976 | TTAAATGTAAGGGCA[A/C]AGTCCTATCAAACTT | 16443 |
rs212006377 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905037 | AATAAATGAAAGGGG[A/G]AGACATACCACATCC | 16443 |
rs212040619 | in-del | -/GGGGGGC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890793 | GTGGGGGGGGGGGGG[-/GGGGGGC]GATGTGTCTCAAGTA | 16443 |
rs212043520 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912085 | GTGGTCAGCCTCAGA[A/G]CAACGGGGATGAAGC | 16443 |
rs212047749 | in-del | -/ACTGAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91788831 | TGGATTGGCTTGACC[-/ACTGAA]ACAAAGCTCCCGCCC | 16443 |
rs212054352 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868351 | CTTCTAGCTATTTAT[A/G]TTGGGATTTGGACCA | 16443 |
rs212059516 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91772291 | GACACGTGCTCTTTA[C/T]CACTGACCCATAACC | 16443 |
rs212060693 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822703 | GTTGAGTTCCTTACA[C/G]GTTTTCCTATCAGCA | 16443 |
rs212078927 | in-del | -/TG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912867 | CTGTGCTTGAAAGAC[-/TG]TTGTGAGAAGTAACA | 16443 |
rs212104986 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918196 | GTGGACAGAGACCCT[C/T]CTCAGCTTCCCTGCC | 16443 |
rs212105661 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869126 | GCGCTGGCTTAACTT[A/C]CCCCTGAGGCAGGAG | 16443 |
rs212125398 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905678 | CTAAGATAAGGCAAG[A/G]GGAGGAGCTGGGTTA | 16443 |
rs212142168 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779521 | GTCTGCAGTCTCTGG[A/G]CACGAAGGGGTTAAT | 16443 |
rs212146802 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876767 | GGGAAAGTGACAGGT[A/G]GGGTGGACATGGCGA | 16443 |
rs212152702 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91732704 | CCACAGGGTCCTATA[A/C]ATTACAGATTTTATG | 16443 |
rs212152726 | in-del | -/AAGCCCTACC | | | intron-variant | Itsn1 | Mm_Celera | 16:91790099 | GGACATTTATCATAT[-/AAGCCCTACC]CTGTGTCTGACACCT | 16443 |
rs212160561 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875991 | ATTGCCCCAGCACCC[C/T]GCTGCCTGCACCCAG | 16443 |
rs212162719 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884081 | CTTCCCGATGTACTA[C/T]GAGGATGACATTAAC | 16443 |
rs212173525 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912649 | AGGGTGATTCCGTTC[C/T]GATTCTGGGTGAGCT | 16443 |
rs212203613 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835618 | GGACTCTTTGCTTCC[A/G]GCAGGAGAGAATGAA | 16443 |
rs212230254 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91883808 | TTGTACCCAGAGGAG[A/C]CTCCAGAATCCCAAA | 16443 |
rs212235243 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829465 | TTCTCGCTTGCTCTC[A/G]CTGTAACTTACTGCT | 16443 |
rs212260783 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91842777 | TACCACAGAGTTGTA[C/T]TGAAAAGAAAAGTCT | 16443 |
rs212273625 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889672 | CATGTATGCCTCGTA[C/T]CTGTTTAGTCTGCAG | 16443 |
rs212285709 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911498 | ATATATTATCTATAT[C/T]TATATGTATGTGTGT | 16443 |
rs212300093 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740592 | ATCCTGCCTGCTGGC[C/T]GGGCCTTCTGCCGCT | 16443 |
rs212325476 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894518 | GAGTCCACCTCTTCA[A/T]GTAGCATCAACGTTG | 16443 |
rs212328351 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780132 | GAGAATCAAAGGGCC[A/G]CTATGTGACTACACG | 16443 |