SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6262977 | snp | C/T | 0.463757 | 0.129645 | intron-variant | Usp43 | GRCm38.p3 | 11:67892416 | TGGGGCCTTTAAACA[C/T]GGCCTTCTAAACTGG | 216835 |
rs6358583 | snp | A/G | 0.5 | 0 | intron-variant | Usp43 | Mm_Celera | 11:67891960 | ACATCTGCTTCCCAC[A/G]GCTCACTGACTGGGC | 216835 |
rs6359150 | snp | C/T | 0.5 | 0 | intron-variant | Usp43 | GRCm38.p3 | 11:67892112 | CATTTGTAAATTAGG[C/T]ACAGTGGGAGAATAG | 216835 |
rs28201408 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp43 | Mm_Celera | 11:67913662 | CAGGTGTACACAGTG[A/G]CTGGAAGACACAGGA | 216835 |
rs28201409 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67912456 | GAAGCTGATGATACA[A/G]ACATGAAAGCTAGTC | 216835 |
rs28201410 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67911217 | CTTGGATGTCTAATC[A/G]GGCTGCTGTAGTCTT | 216835 |
rs28201411 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67909674 | GATTGGCAGGCCCTC[A/G]TGGCTTAAACAAACT | 216835 |
rs28201412 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Usp43 | GRCm38.p3 | 11:67889904 | CAAAAAAACATCAGC[A/G]GCAACAGCATTGTGG | 216835 |
rs28201413 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67889897 | CCTATTTCAAAAAAA[C/T]ATCAGCGGCAACAGC | 216835 |
rs28201414 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67888854 | AAGAGCTAGGTTTTC[C/T]GTAACTAAGGTGAAT | 216835 |
rs28201415 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp43 | Mm_Celera | 11:67888823 | CTTACCATGAGAGGT[A/G]TTATCTCATCTGAGC | 216835 |
rs28201416 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Usp43 | GRCm38.p3 | 11:67888631 | CCTGGATAAAGAGCC[A/G]GCTTTCTGTTTTATC | 216835 |
rs28201417 | snp | C/T | 0.18 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67888629 | TCCCTGGATAAAGAG[C/T]CGGCTTTCTGTTTTA | 216835 |
rs28201418 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Usp43 | GRCm38.p3 | 11:67888385 | CAGCTGATCAACCTA[A/G]TCCTGTGCTGTGCAG | 216835 |
rs28201419 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67888297 | GTTGAATCGATGTTG[C/G]TAAAGCTAGGCACAA | 216835 |
rs28201420 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67888191 | AATGTCCAGCTGTAG[A/G]CTTGTCAGTGAGCAC | 216835 |
rs28201421 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Usp43 | GRCm38.p3 | 11:67888132 | TGTGTCCTGTCTCAG[A/G]AATATTCTCATTACT | 216835 |
rs28201422 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67888036 | CAGTGCAGACTATTC[C/T]AAGAGATGAGCTTCC | 216835 |
rs28201423 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67887922 | CAAGAGTCATGGATG[C/T]AGGATTCGCTCTGGT | 216835 |
rs28201424 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Usp43 | Mm_Celera | 11:67887849 | TTCCCGAATCAAGAA[C/T]GGTGGTCCAAACCTG | 216835 |
rs28201425 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67887621 | TACAAGCCACAAAAG[A/G]GTAACTGTTTGCACA | 216835 |
rs28201426 | snp | A/G/T | 0.277778 | 0.248452 | intron-variant | Usp43 | GRCm38.p3 | 11:67887444 | ATCAAGCATCTTCAA[A/G/T]TTTTTACCTAGATGT | 216835 |
rs28201427 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67886868 | ATGCCAGAGCAGTTC[C/T]TGACACGGAAGCTGT | 216835 |
rs28201428 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67886825 | CCGAGAGACTACTGA[G/T]GCAACCTTACAGATC | 216835 |
rs28201429 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67886812 | AACAGTTTCTAAACC[A/G]AGAGACTACTGAGGC | 216835 |
rs28201430 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67886805 | CTTTTTAAACAGTTT[C/T]TAAACCGAGAGACTA | 216835 |
rs28201431 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67886719 | AATGTATAGGGCTGT[C/G]TGTGAGTAGGAATAG | 216835 |
rs28201432 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67886614 | TAATTCAGGCTCCTC[A/G]GTGCAGTGAACAAAT | 216835 |
rs28201433 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67886587 | TGACCTACTTGTGGG[A/G]AAGCTCACTTCTAAT | 216835 |
rs28201434 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67886565 | CTGCCACTGTTACTA[A/G]GGAGCCTGACCTACT | 216835 |
rs28201435 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67886442 | AAATGCACACAACAA[A/G]GAAAGGAACAGGAGC | 216835 |
rs28201436 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67886351 | GGCTGCGGCTTCCTG[C/T]ATTGGAATCCCGCTA | 216835 |
rs28201437 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Usp43 | GRCm38.p3 | 11:67886256 | TTTAAAACCAGTATG[A/G]GTTAAGTAGGAGGGC | 216835 |
rs28201438 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp43 | GRCm38.p3 | 11:67885990 | TATTAAAAGGATTAA[A/G]GCTGGGGGCTGGTGA | 216835 |
rs28201439 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67885864 | GGTAAGCCAATTCAT[C/T]TTAGAACCTTCAGTG | 216835 |
rs28201440 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp43 | Mm_Celera | 11:67885363 | TTCTCCAACTCTCCC[A/G]TCATACCTGAGCTGT | 216835 |
rs28201441 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp43 | GRCm38.p3 | 11:67885325 | GTTATTGGGGCATCC[C/T]TAAAGGAACTCCAAA | 216835 |
rs28201442 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Usp43 | GRCm38.p3 | 11:67885296 | GGAGGTAGGGTCTTA[C/G]GAGAGATGCTTAGGT | 216835 |
rs28201443 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67885016 | GGCATGAGAAATATG[C/T]CAGATTCCGTCTGGC | 216835 |
rs28201444 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp43 | GRCm38.p3 | 11:67884891 | AAATGAAGAAATAGA[A/G]TTTTTAAAGCTGTCA | 216835 |
rs28201445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67884596 | TTGGGAGAGCTTTAT[C/T]GCATGCAAGACCCTG | 216835 |
rs28201446 | snp | G/T | 0.42 | 0.183303 | intron-variant | Usp43 | Mm_Celera | 11:67883753 | CACTTCTGAAGCAAG[G/T]CTCACAGAGATACAC | 216835 |
rs28201447 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67883692 | CATCGCCACAAATAA[A/G]ACAGCTATGTACAAA | 216835 |
rs28201448 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67883529 | CCATGCTTGATCTAG[C/T]GAACACAACCCCACA | 216835 |
rs28201449 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67883483 | GCTTCATTGTTTTGA[A/G]GATCCAGTCTTTTAA | 216835 |
rs28201450 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67883344 | GGCAACAGTTTATCA[C/T]GCAGTCCATTTTGCA | 216835 |
rs28201451 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp43 | GRCm38.p3 | 11:67883315 | TCCCCAGGTCCTTCC[A/G]TGACAAAACCAGAGG | 216835 |
rs28201452 | snp | C/T | 0.489796 | 0.070696 | missense | Usp43 | Mm_Celera | 11:67883309 | ACAGAGTCCCCAGGT[C/T]CTTCCATGACAAAAC | 216835 |
rs28201453 | snp | C/T | 0.32 | 0.24 | missense | Usp43 | Mm_Celera | 11:67883236 | TGGCAAAGGGGCCGG[C/T]TGTCCTTTGGAGATA | 216835 |
rs28201454 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67883199 | CACAAGCTGTCTCTT[C/T]CCTTACCTGTCAACT | 216835 |
rs28201455 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67882777 | GACAAGCTATTGAAC[A/G]GACATGTGGAGCATC | 216835 |
rs28201456 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67882609 | CATTCCAGACAAGCA[G/T]TTCAAGCTGACCAAG | 216835 |
rs28201457 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67882450 | CCTGTCATCTCCAAT[A/G]CCAAATGCCACAAGG | 216835 |
rs28201458 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67882164 | GAAGAACAGTAGTGG[C/T]CAAGTTCATGCCCAA | 216835 |
rs28201459 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67881520 | TTCTAGCTACTATGA[C/G]TCAATGAACTGCTTT | 216835 |
rs28201460 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67881495 | CTCAGGAGATGGGAG[C/T]TCTAAAGCCTTCTAG | 216835 |
rs28201461 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67881342 | CACAGTTCTCAGGGC[A/T]CATCAGCCAGCTTTC | 216835 |
rs28201462 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Usp43 | Mm_Celera | 11:67881223 | CTCTGTGACAGAGCT[A/G]TCCCATTCCACAGCC | 216835 |
rs28201463 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67880714 | GAAGCAGTACTTGCT[A/G]GATTGAAGCATGCCC | 216835 |
rs28201464 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67879423 | TCTAAATGACCCAGA[A/T]GAACAGAAATTAAAA | 216835 |
rs28201465 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67879126 | CAAGGGCCTTGTTTC[C/G]CTCTTTCTCTCCAAG | 216835 |
rs28201466 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp43 | GRCm38.p3 | 11:67879116 | TGTTCGCTCGCAAGG[A/G]CCTTGTTTCCCTCTT | 216835 |
rs28201467 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Usp43 | GRCm38.p3 | 11:67879057 | ACCTGGCGCCCACTG[C/T]AGTCTTCATATGGTC | 216835 |
rs28201468 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Usp43 | GRCm38.p3 | 11:67878991 | CTGTCGCCTGGAGCA[A/G]GACAGCTGTGCAGAA | 216835 |
rs28201469 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Usp43 | Mm_Celera | 11:67878873 | CTCCCAAGATGTACA[C/T]ACACATAGGTTTCAA | 216835 |
rs28201470 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp43 | GRCm38.p3 | 11:67877387 | TGTGCTTAAAAATGA[A/G]TGGCAGAGTGAAGCT | 216835 |
rs28201471 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp43 | GRCm38.p3 | 11:67877279 | AGCAAAAGAATGAGT[A/G]TGTGTGCCCTAATCC | 216835 |
rs28201472 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Usp43 | GRCm38.p3 | 11:67877042 | GGCCAACTTTTAGTG[A/G]TTGGCCAGACCAGCA | 216835 |
rs28201473 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Usp43 | GRCm38.p3 | 11:67876886 | GAGAAAAGTGAGTCT[C/T]CTGGTTGCCTCTTCC | 216835 |
rs28201474 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67876749 | TGCACGCTGTCATCT[C/T]GTCCAGCACAGTCTC | 216835 |
rs28201475 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Usp43 | Mm_Celera | 11:67876738 | TGGAAGGTGAGTGCA[C/G]GCTGTCATCTCGTCC | 216835 |
rs28201476 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67876718 | TCTTAGCCAGGATTG[A/C]TCACTGGAAGGTGAG | 216835 |
rs28201477 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67876713 | GGTTATCTTAGCCAG[C/G]ATTGCTCACTGGAAG | 216835 |
rs28201478 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Usp43 | GRCm38.p3 | 11:67876351 | TGAGCTGTGCCCCTT[C/G]TGAGCTAGCTGTGGC | 216835 |
rs28201479 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67876091 | GCAGGCTTGAGATAG[C/T]TTTGATCCAAACCCA | 216835 |
rs28201480 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67876058 | CCTCTCTCAGTGTCT[A/G]CCTTCTATAAATGGA | 216835 |
rs28201481 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67875787 | CCATAGTCAGAGTGA[C/T]AGCATTTGCCCCCTG | 216835 |
rs28201482 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67875619 | GGCCAGAGGGGAACC[C/T]TTGGAACCATGATGT | 216835 |
rs28201483 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp43 | Mm_Celera | 11:67875489 | GAGCCTGCAGGAAGG[C/T]GGAGAGTTGTTCTAC | 216835 |
rs28201484 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67875443 | CTGCAGAAGAAGCAA[A/G]AGAGAGAGCTGGATC | 216835 |
rs28201485 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Usp43 | Mm_Celera | 11:67875233 | ATGAAAAGCAGGGGG[A/G]AAAAAAAGACAGTCA | 216835 |
rs28201486 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67875232 | AATGAAAAGCAGGGG[A/G]AAAAAAAAGACAGTC | 216835 |
rs28201487 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Usp43 | Mm_Celera | 11:67874788 | GGATGCACAGTGGTT[C/G]CTCAGAGCTCATGAA | 216835 |
rs28201488 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp43 | Mm_Celera | 11:67874710 | TGTCCCTGCTTTAAA[C/T]TGCATTGCTGTGTTA | 216835 |
rs28201489 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67874672 | GCCTCTGCTAGCTCC[A/G]TCCCATTTCACCTCT | 216835 |
rs28201490 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67874647 | GTCAGGGCTCCCTGT[A/G]TACTCCCCAGCCTCT | 216835 |
rs28201491 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67874576 | AGTCTTCTGCATGAG[C/T]ATCAATCCTCTTCCC | 216835 |
rs28201492 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp43 | Mm_Celera | 11:67873897 | AGTAGACTTTTAAAA[C/T]GCAAACCAGGGTGGG | 216835 |
rs28201493 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp43 | Mm_Celera | 11:67873771 | CCATCTGACCATGCA[A/G]GAAGACCTCGACACA | 216835 |
rs28201494 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp43 | Mm_Celera | 11:67873767 | TCTACCATCTGACCA[C/T]GCAAGAAGACCTCGA | 216835 |
rs28201495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67873313 | GTCCTGAACACAGTT[A/G]GCCCTTTTCCAGCAC | 216835 |
rs28201496 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp43 | Mm_Celera | 11:67873279 | GCCCTTCAGCCAGAC[A/T]GGTGCTCCACATCCC | 216835 |
rs28201497 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67873167 | ACTGGCCTTTAACCA[C/T]GTCACATGATGAAAC | 216835 |
rs28201498 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Usp43 | Mm_Celera | 11:67873126 | CAGACACTGCTCTGA[G/T]CCTGGCTTCTTATGC | 216835 |
rs28201499 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67873102 | GTCAGCTCTTTCAGC[A/C]CAGGAAAACAGACAC | 216835 |
rs28201500 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp43 | Mm_Celera | 11:67872975 | CTTTGCCCAAAGAGA[C/T]ACACATACACAGACG | 216835 |
rs28201501 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Usp43 | Mm_Celera | 11:67865843 | AGATAGGTATGAGGG[A/C]GTAAGGACTCCAGAG | 216835 |
rs28201502 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp43 | Mm_Celera | 11:67865620 | ACGCCATATGGCTTC[A/T]CAGGTAAAATTCATC | 216835 |
rs28201503 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp43 | Mm_Celera | 11:67865557 | ATGCACACCAGGTGC[A/G]CCTCCCAAGAACAGT | 216835 |
rs28201504 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp43 | Mm_Celera | 11:67865445 | CCCTGTCTTTGCTTT[G/T]AGCCTTTCTCGCTAA | 216835 |