SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657593 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Usp13 | Mm_Celera | 3:32852299 | ATCTTCTCCACACTC[A/C]GATGTCTCATAGAAG | 72607 |
rs3672584 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp13 | Mm_Celera | 3:32852484 | GCTCAAACTCTAGAG[C/T]GTCTCGGATCCAACT | 72607 |
rs3692404 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp13 | Mm_Celera | 3:32893138 | GCCACCCCTGTTCTC[A/G]CACAGTTTATAGGAC | 72607 |
rs3692438 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp13 | Mm_Celera | 3:32893156 | CAGTTTATAGGACAG[C/T]GTCTGACACACGCTA | 72607 |
rs3711387 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp13 | Mm_Celera | 3:32919401 | CCTAGACAAGCACCC[A/G]CTCAATGGAGCTACA | 72607 |
rs6222284 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp13 | Mm_Celera | 3:32861962 | ACAAACGAGTCAAAG[C/T]AACATCTGATTTTCT | 72607 |
rs6238427 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Usp13 | Mm_Celera | 3:32862582 | GGGACTGTCCACCTG[C/T]AACACCTGCTAAGCA | 72607 |
rs6369960 | snp | A/G | 0.5 | 0 | intron-variant | Usp13 | Mm_Celera | 3:32921447 | CTTGGGCCTCCACAC[A/G]CACCCACACTGCACA | 72607 |
rs6370395 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Usp13 | Mm_Celera | 3:32921491 | AACAAAAAGGGAGAA[A/G]ATGTAATGAGCTGTG | 72607 |
rs6370494 | snp | A/G | 0.5 | 0 | intron-variant | Usp13 | Mm_Celera | 3:32921550 | TGAAACTTCTTAGAA[A/G]TTTTCAAGGGAGAGG | 72607 |
rs6371447 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp13 | Mm_Celera | 3:32921697 | CTGTTTTGTAGGGTG[C/T]CATTATAGTTACATT | 72607 |
rs13477047 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Usp13 | GRCm38.p3 | 3:32850753 | GCCATTGAAACAGCC[A/G]TGGAGCTGGGTTGCT | 72607 |
rs29836515 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp13 | Mm_Celera | 3:32831748 | ATGTCAAGGAAGGGT[C/T]ATAAATGAATGTTAC | 72607 |
rs29836518 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp13 | Mm_Celera | 3:32831840 | CAGTGTTCTAGAAGA[C/T]ACTGTGTGCCCTTGT | 72607 |
rs29836521 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32831959 | TATTATGGTAGTGAC[C/T]GTTTGTTTTCCACAG | 72607 |
rs29836644 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32821139 | TATCTTTTTATGTCC[C/T]CTATATCTTTTTATA | 72607 |
rs29836647 | snp | A/C | 0.18 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32821405 | GAGAGAGAGAGAGAG[A/C]GCTGGACCCACATGA | 72607 |
rs29836650 | snp | A/G | 0.42 | 0.183303 | intron-variant | Usp13 | Mm_Celera | 3:32821446 | ATTGTTGAGCTAAGA[A/G]GACAACTTGCAAACA | 72607 |
rs29836653 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp13 | Mm_Celera | 3:32822066 | GTGCAGCAGTCATCT[C/T]CTTGTCTAATACTGC | 72607 |
rs29837114 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Usp13 | Mm_Celera | 3:32836446 | TAACTTGAAGTGGCC[C/G]ATAGAAGCAGTTATT | 72607 |
rs29837117 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Usp13 | GRCm38.p3 | 3:32837322 | CCAGTTCCATTGTTG[C/T]GGTCTCTGGTGAGGC | 72607 |
rs29837120 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837353 | AGAATGTTGTGGTAG[G/T]GCTGTGTGTGGCAGG | 72607 |
rs29837123 | snp | C/T | 0.5 | 0 | intron-variant | Usp13 | GRCm38.p3 | 3:32837394 | TCACCCCACTGCATT[C/T]AGGAAACAGAGACTG | 72607 |
rs29837306 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32826530 | CTGAGGCTTTATGGT[A/G]GGCTTCAGTGAACGT | 72607 |
rs29837309 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32826531 | TGAGGCTTTATGGTG[A/G]GCTTCAGTGAACGTG | 72607 |
rs29837312 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32826543 | GTGGGCTTCAGTGAA[C/T]GTGAATTTTCTCTCC | 72607 |
rs29837396 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp13 | GRCm38.p3 | 3:32845323 | AGCTCCTCAGGCTCA[A/G]CATGCCAGGCTGTGT | 72607 |
rs29837399 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp13 | GRCm38.p3 | 3:32845642 | TTGGCTCACAACTGG[G/T]ACATAGAGCCTTTTC | 72607 |
rs29837402 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Usp13 | Mm_Celera | 3:32846443 | CTTAGATTTCTCTTA[A/G]TACTTCCCATAACCC | 72607 |
rs29837414 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Usp13 | GRCm38.p3 | 3:32856454 | TCTGTGATCTTCTCA[A/G]AGTCAGTGTCAAGAC | 72607 |
rs29837417 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32856487 | GTCTTGCTTTTCCTG[C/T]GGGAACTGGTGCTGG | 72607 |
rs29837420 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Usp13 | Mm_Celera | 3:32856571 | TCCCCTGATTCCCCT[G/T]TGGCCTCCAGTCCTC | 72607 |
rs29837423 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Usp13 | GRCm38.p3 | 3:32856634 | ACCTGTTTCCTATAG[C/T]TGGCTCCCAGAAGGC | 72607 |
rs29837454 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Usp13 | Mm_Celera | 3:32832002 | GCGTCCCCAGCTTCC[C/T]GAGTTGTCATCCACA | 72607 |
rs29837457 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp13 | Mm_Celera | 3:32832153 | GCTCACTTGTGTCTT[G/T]GAGACTTGTGCCCTT | 72607 |
rs29837460 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32832185 | ACCTTTGGATGGGAA[A/T]CTTCTGTCACTGTTT | 72607 |
rs29837463 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32832234 | GAAGAAGTCACTTTG[C/T]CCCGATGGTACTCAC | 72607 |
rs29837576 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Usp13 | Mm_Celera | 3:32822096 | CTTTCCCCTGGTGAG[C/T]GTTTATCAAGGATCC | 72607 |
rs29837579 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32822247 | ATCCCTTTAATTCTT[A/G]CTTTTGAAGCATTTA | 72607 |
rs29837582 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp13 | Mm_Celera | 3:32822339 | GACTGCAGAATGAGC[C/T]GCTTGTCTAGCCCTT | 72607 |
rs29838135 | snp | G/T | 0.5 | 0 | intron-variant | Usp13 | GRCm38.p3 | 3:32837520 | AGGTCTCTCCCCTTA[G/T]CGATTTCTCCCGGAA | 72607 |
rs29838138 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837531 | CTTATCGATTTCTCC[C/T]GGAAACTCACATGAA | 72607 |
rs29838141 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837558 | TGAACCCAGAAGTTC[C/T]ACTCAAACTGAAAAC | 72607 |
rs29838175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32826558 | CGTGAATTTTCTCTC[C/T]GTTTGGACCCTGGAC | 72607 |
rs29838178 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32826566 | TTCTCTCCGTTTGGA[C/T]CCTGGACATAGCAGA | 72607 |
rs29838181 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32826590 | TAGCAGATGAGGGCA[C/T]AAAGACCGAGGGGAT | 72607 |
rs29838276 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Usp13 | Mm_Celera | 3:32856725 | CCATCAGAGTCAAAG[C/G]GAGGCCTGCGGGTCC | 72607 |
rs29838279 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Usp13 | Mm_Celera | 3:32856726 | CATCAGAGTCAAAGC[C/G]AGGCCTGCGGGTCCC | 72607 |
rs29838282 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp13 | GRCm38.p3 | 3:32856865 | ACGTACCCTATCTTC[A/G]TATTTATTGCATAGC | 72607 |
rs29838386 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp13 | Mm_Celera | 3:32832250 | CCCGATGGTACTCAC[A/G]AATGCACGCAGGGTA | 72607 |
rs29838389 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32832257 | GTACTCACAAATGCA[C/T]GCAGGGTAATACAGA | 72607 |
rs29838392 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32832468 | TTTCCATCCACAGTT[A/C]CTGTTGTTTGTCCCA | 72607 |
rs29838415 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp13 | GRCm38.p3 | 3:32846472 | CCATTGTGCTTTCTG[C/T]CTGCACTTGGTTGCC | 72607 |
rs29838418 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp13 | GRCm38.p3 | 3:32846480 | CTTTCTGTCTGCACT[C/T]GGTTGCCCTCTGTGT | 72607 |
rs29838421 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Usp13 | GRCm38.p3 | 3:32846543 | TGTTTGATTGGTCAC[A/C]CACTGAACCTGACAA | 72607 |
rs29838755 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32822717 | CACCCTGGCCTTATC[C/T]TGGATCACTGCAAAG | 72607 |
rs29838758 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32822987 | ACCCTCACTTACCAG[A/C]TCAGCATTTGTTCTG | 72607 |
rs29838761 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Usp13 | Mm_Celera | 3:32823204 | CTATCGGAGAAGGGC[C/T]TGGTAGTCAGGCCTG | 72607 |
rs29839124 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32826650 | CTTCCATGCAGCTCA[A/G]TCCATGGGGTCTTGG | 72607 |
rs29839127 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32826685 | TGGCTGAATAGAACA[A/C]GTTCAGCCAGGAGTG | 72607 |
rs29839130 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32826740 | TTCTTCTCTCTACAG[A/G]AAAGCCTGACAGAAT | 72607 |
rs29839133 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Usp13 | Mm_Celera | 3:32826768 | AATGCCTGGCACAGG[A/C/T]ACCTCTCTGGAATCC | 72607 |
rs29839184 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837600 | TCACGACATGCAACC[A/G]TTCCTAGCTCCTGAC | 72607 |
rs29839187 | snp | A/G | 0.5 | 0 | intron-variant | Usp13 | GRCm38.p3 | 3:32837620 | TAGCTCCTGACACAC[A/G]TAGCATCTCACCTGG | 72607 |
rs29839190 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Usp13 | Mm_Celera | 3:32837644 | CACCTGGACTGAAAG[C/T]AGCCTGACTCAATAA | 72607 |
rs29839193 | snp | A/G | 0.5 | 0 | intron-variant | Usp13 | GRCm38.p3 | 3:32837707 | TCTTCGGTTCTGGCA[A/G]ATACCTATGAGAGTC | 72607 |
rs29839215 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32857093 | CTTATGCCAGCCAGC[C/T]CTTAACCTCAAGTGT | 72607 |
rs29839218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp13 | GRCm38.p3 | 3:32857306 | TGATAATTCTTATTT[C/T]TCTGTAAATCTGGTT | 72607 |
rs29839221 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp13 | Mm_Celera | 3:32857628 | AAATAACCTTTTATT[C/T]AGAGTACAAAAGATG | 72607 |
rs29839404 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Usp13 | GRCm38.p3 | 3:32846568 | TGACAAATGGGCATG[G/T]TGCTATTTGCTAAGA | 72607 |
rs29839407 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp13 | GRCm38.p3 | 3:32846594 | TAAGAAAGGAGTTTC[C/T]GTGCTTGAACCCTGC | 72607 |
rs29839410 | snp | A/C | 0.42 | 0.183303 | intron-variant | Usp13 | GRCm38.p3 | 3:32846623 | GCATTGCCAAAAGTG[A/C]AAAGGCAATGTTCTG | 72607 |
rs29839413 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Usp13 | GRCm38.p3 | 3:32846673 | TTTTTCCCCCTGTAG[A/G]GCGTATTTTAATCTG | 72607 |
rs29839425 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Usp13 | GRCm38.p3 | 3:32832525 | GGGAAGGTGGGTACT[A/T]ATGCATGCAGCTGAT | 72607 |
rs29839428 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32832558 | AGTGAATTTTTTGGA[A/T]GAAGAGGACCTTTAA | 72607 |
rs29839431 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Usp13 | Mm_Celera | 3:32832661 | TTAGTCTTTATTATT[A/T]TTTTTTTATATATAC | 72607 |
rs29839674 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Usp13 | Mm_Celera | 3:32823249 | GGGAGGCCTGTGAGC[A/C]CATCTACTTGTGGGA | 72607 |
rs29839677 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp13 | Mm_Celera | 3:32823792 | ATGACTCTGCCTCGT[C/T]GCCTCAGTTTACCTG | 72607 |
rs29839680 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp13 | Mm_Celera | 3:32823814 | GTTTACCTGGCTGAC[C/T]CATCTTTCTTGTGTT | 72607 |
rs29839683 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Usp13 | Mm_Celera | 3:32823833 | CTTTCTTGTGTTAGC[G/T]CTCAGGTGCCCTCCA | 72607 |
rs29839931 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Usp13 | Mm_Celera | 3:32815054 | CTAGTTGTCCTTGCT[G/T]CAGTAAGCCTCTTTG | 72607 |
rs29840076 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32826783 | TACCTCTCTGGAATC[C/T]GGTGGCTGTCCCTGT | 72607 |
rs29840079 | snp | A/G | 0.5 | 0 | intron-variant | Usp13 | Mm_Celera | 3:32826855 | TGCTCTTTTTTTTTC[A/G]AGCCCTGGCAGCGAC | 72607 |
rs29840082 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp13 | Mm_Celera | 3:32827034 | CATTTCTGTACATAT[A/G]TGGGAGGTTTGAGTT | 72607 |
rs29840186 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837721 | AAATACCTATGAGAG[C/T]CACTGTAACCCTTTG | 72607 |
rs29840189 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Usp13 | GRCm38.p3 | 3:32837756 | GGCTGACCCTCATCA[C/T]TTACTTCTTCCAGTT | 72607 |
rs29840192 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Usp13 | GRCm38.p3 | 3:32837821 | GTAACTTTGTACCCT[C/G]TCTCTTTCTTCTAGA | 72607 |
rs29840224 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32832920 | GTTGTTGCCTTGTGA[C/T]GTGTCAGCTTTGCTT | 72607 |
rs29840227 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Usp13 | Mm_Celera | 3:32834036 | AGCTCAGCTCCTAGA[C/T]TGGACTGCTTGCTGA | 72607 |
rs29840230 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Usp13 | Mm_Celera | 3:32834048 | AGATTGGACTGCTTG[C/T]TGATTCTTTGCTGAG | 72607 |
rs29840233 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Usp13 | Mm_Celera | 3:32834341 | GTTAAATTTCTAATG[C/T]GTCAAATGCCCCAGA | 72607 |
rs29840244 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32858542 | GGTGGGCTGAGCAGG[C/T]TGGAAGGAAACCTGA | 72607 |
rs29840247 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp13 | Mm_Celera | 3:32858554 | AGGTTGGAAGGAAAC[C/T]TGACTTTGTAACTCT | 72607 |
rs29840250 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp13 | Mm_Celera | 3:32858565 | AAACCTGACTTTGTA[A/T]CTCTGATGCTTGCTG | 72607 |
rs29840253 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp13 | GRCm38.p3 | 3:32858733 | GTAATTCTTCCTTCA[C/T]AGAACAGTTCCCTTT | 72607 |
rs29840256 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Usp13 | GRCm38.p3 | 3:32846780 | TCCTCTTCCATCATG[C/T]AGAAGTAGAGATGGA | 72607 |
rs29840259 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp13 | GRCm38.p3 | 3:32846811 | AGAAGACCACAGATG[C/T]CTGTAGAGAAAAGAG | 72607 |
rs29840262 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Usp13 | GRCm38.p3 | 3:32846976 | AAAAGCTATTGAAAC[A/C/T]GTGTGAAAATAACTA | 72607 |
rs29840705 | snp | A/G | 0.42 | 0.183303 | intron-variant | Usp13 | Mm_Celera | 3:32823863 | AGAGTTAGGAGTTCC[A/G]TACCTCACCTCTGCC | 72607 |
rs29840708 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Usp13 | Mm_Celera | 3:32824087 | TACAGATTGTCCAAA[C/G]CATGGAATATGTAAG | 72607 |