SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3024119 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | GRCm38.p3 | 10:39421205 | AATAAATAGCACAGA[A/G]CATGACCTCAAGCTG | 14360 |
rs6156018 | snp | A/G | 0.5 | 0 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39565855 | AGTGTGTCTGGAGAC[A/G]AAGTACAGACAAGAT | 14360 |
rs6253608 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39498483 | TTGGCTTATCAGCCC[A/G]TGGNTAAGAGTGTAG | 14360 |
rs6253610 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39498487 | CTTATCAGCCCNTGG[C/T]TAAGAGTGTAGGTCT | 14360 |
rs6278067 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Fyn | Mm_Celera | 10:39545270 | GTTTAACAGCTTTAG[C/T]CAAAGTACTGGGACA | 14360 |
rs6278972 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fyn | Mm_Celera | 10:39545449 | CGTGTTGTTCTCTCA[A/G]CTGAAGAACAGAAAC | 14360 |
rs6280603 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39545789 | TGGATATGTGCGCCC[C/T]GGAAACCAGGTGGTG | 14360 |
rs6353469 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39443804 | aaatcaagcaaatgg[A/G]gtggcagtgtgccca | 14360 |
rs6353945 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39443864 | TTAAACAATGTCAAC[A/G]CCCTTTCTTAATTCC | 14360 |
rs6354036 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39443913 | GGTCAGATCTTTCCA[C/T]NGCTGTAGCTATGAC | 14360 |
rs6354037 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39443914 | GTCAGATCTTTCCAN[A/G]GCTGTAGCTATGACT | 14360 |
rs6354057 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39509830 | TTCTAGGCTCACATC[C/T]TCTGCTTAAACAAAT | 14360 |
rs6354104 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39443955 | GTGACAGAACTTTCA[G/T]CTCTTAATAGAACTG | 14360 |
rs6354463 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39509862 | AATGAAATCCCCAAG[A/G]AAAAAAGCACTTGGA | 14360 |
rs6354644 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Fyn | Mm_Celera | 10:39444052 | TCTCCACTTTCAGAA[C/T]TCATGATGAGGAATT | 14360 |
rs6355038 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39509969 | AGGTACATACCCATC[C/T]GATGGNGCAGCAGTG | 14360 |
rs6355043 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39509975 | ATACCCATCNGATGG[C/T]GCAGCAGTGGTGGTG | 14360 |
rs6355154 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39444128 | GAGGGTTAAAGGACC[C/T]GCAGTATCATCCTCT | 14360 |
rs6355573 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39510066 | TCGCTGTCCATAAAC[A/G]AGAGAACGCCTTGGA | 14360 |
rs6355686 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39444242 | TTTGGAGAGCTCATG[C/T]TTAGAGAAACAGTGA | 14360 |
rs6355713 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fyn | Mm_Celera | 10:39444260 | AGAGAAACAGTGACT[A/G]AAGGTTCACAGCTCT | 14360 |
rs6356052 | snp | C/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39510171 | AGTAGGCGACTGCCT[C/G]ACAAACATTCNCANT | 14360 |
rs6356067 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39510182 | GCCTNACAAACATTC[C/T]CANTCCCAAGAACTT | 14360 |
rs6356071 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39510185 | TNACAAACATTCNCA[C/T]TCCCAAGAACTTGAA | 14360 |
rs6356107 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39510208 | AACTTGAAGTCAACT[C/T]ACTAAGCATTTGCTG | 14360 |
rs6356145 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39444338 | TCCCTGGCCTTTCTC[G/T]CAAGATGAAGGTTAG | 14360 |
rs6369056 | snp | A/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39444402 | CCCCCAGTCTGTACA[A/T]ACCTCTCAAAGCATA | 14360 |
rs6369140 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39444448 | GGATAGAGCCATCGT[A/G]TGTGTGNCTCTCACG | 14360 |
rs6369157 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39444455 | GCCATCGTNTGTGTG[C/T]CTCTCACGGCCTNTG | 14360 |
rs6369536 | snp | C/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39444468 | TGNCTCTCACGGCCT[C/G]TGCAGGTGGCCTTCA | 14360 |
rs6373632 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39438668 | ATGATCCTTAGAGGT[A/G]ACAGTAGTCTGGCCA | 14360 |
rs6373754 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39438743 | GTAGGGGAAGTTTAA[A/G]AGCTGAGTTTCCAGA | 14360 |
rs6374805 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39438902 | CTCTGGGGGAAATGG[A/G]ACAGTGTGGTGACAG | 14360 |
rs6375313 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39438984 | CTCTGCAGGTGTCTC[C/T]GCCCCTGCAGCCTTC | 14360 |
rs6375390 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Fyn | Mm_Celera | 10:39439031 | TGCCCCTTAGGCCTG[A/T]TGTGTCCCTGCCTCC | 14360 |
rs6375854 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39439101 | AGCCCAGCTGGCTGC[A/G]GAGCTTGCTCCCGCC | 14360 |
rs6379743 | snp | A/C | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39372948 | TGTTTGGTTGCTTTG[A/C]TTTTCATCTTCAGCA | 14360 |
rs6379824 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39372998 | ATTTTGTGATTTCGG[A/G]GGACCACTTATCACG | 14360 |
rs6380891 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39373173 | CGCAGTACCATTTTA[C/T]GTANTTTCCTTAACA | 14360 |
rs6380893 | snp | C/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39373177 | GTACCATTTTANGTA[C/G]TTTCCTTAACAATTA | 14360 |
rs29349686 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39521478 | GTGTGTTTTCTACTG[G/T]TATTTATCTCATAGC | 14360 |
rs45635979 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39395853 | GTGTGATTTCCATCC[A/G]TTCTCAATTCCTTGC | 14360 |
rs45640623 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39404549 | TGATGATCGGGGTCT[A/G]TTTTTATAGATTTTA | 14360 |
rs45653522 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39378755 | CTTAGAATTCTTCCC[A/G]TTTGTCAAGGCCCAA | 14360 |
rs45654047 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39466632 | GACTATCTGATGTGC[A/C]ACCTTGTGGGGTTGA | 14360 |
rs45669697 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39399281 | CTAGTTTGACTACTG[G/T]ATAGCTGGTCCATAG | 14360 |
rs45675779 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39496215 | GTGGCTTTCTGAGGG[C/T]GGTGCCTATGGGCTG | 14360 |
rs45686425 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431127 | CATTTTAAAAGTGAA[A/G]TTTCATGATCGCCTT | 14360 |
rs45690083 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39530558 | ATATCTTCATTGTGT[A/G]CACATTCTTCAGTAA | 14360 |
rs45691100 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431401 | TCTGTGCTCAGAAAT[C/T]ACCTCGCTGTCCCTA | 14360 |
rs45698462 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528362 | AAAGCTGAAGGAGGG[A/T]GCCGATGTGAAGCAC | 14360 |
rs45700820 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39461615 | CCTTGGGGCTGTGAC[C/G]AAACCTTCTCTCGTC | 14360 |
rs45702941 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39403997 | TTCCTCTCTGCCTGG[C/T]TTTCTTCTGTAGTTC | 14360 |
rs45704351 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39521860 | GGCTGAGGCGCCTAA[C/T]ATGGTGACCGGCAGG | 14360 |
rs45708398 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39522267 | ACCTGCAGAAGGTCA[G/T]GTCTTCTTCCTACTT | 14360 |
rs45710927 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39523289 | AAAAGACATAGCTTT[C/T]TGTTCCCCAGGCAGA | 14360 |
rs45720770 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39417951 | AAATGTTTTACTAGT[C/T]AATTGTGAGTCCCAC | 14360 |
rs45722935 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39419527 | TTCAGTAAGGTCATT[C/T]TAATTTAGCTGTGTA | 14360 |
rs45724440 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39471731 | GGGTGCCGGCTGGGA[A/G]TGATTGGTGACATTC | 14360 |
rs45725524 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39457467 | GCTGAGGCCGTGGGC[A/G]GACTGCTGTGGACGA | 14360 |
rs45726043 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39520268 | AATTGCCTCATTAGT[C/G]AGTCAATTCATGATT | 14360 |
rs45727637 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39404619 | AGCTTGGGAAATGAT[C/G]ACTTCAAACCGACAG | 14360 |
rs45732449 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39389204 | TTGCCTGGAGTCGCC[A/G]TTTACACATACATGT | 14360 |
rs45734134 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39491604 | ACAGACATGCACACA[C/G]ATATACATATGCATA | 14360 |
rs45748201 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39471212 | CACACTGTCCTTATG[A/G]TGCCAAGAGCATCCT | 14360 |
rs45750938 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39535425 | CAGTGCAAGACTGTT[C/T]ACTTTTAACTAGACT | 14360 |
rs45774664 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39457252 | AGCACTACGCCTGTC[A/G]GGATCTGGCTGGAAT | 14360 |
rs45778437 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39525585 | GTGGCTCTTGCCTGG[C/T]CCGGGGCCTTCTAGC | 14360 |
rs45781158 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39471312 | CAAGTCCCAAACACC[A/C]TCTTTCCTGCCTTTG | 14360 |
rs45791347 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437152 | GTATGTGATGGAGGA[A/G]ACTGGCTGAGATCCC | 14360 |
rs45797434 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39551666 | AGAACTCAGAATTGC[C/T]GTGACCTGTACACCA | 14360 |
rs45799367 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fyn | Mm_Celera | 10:39452963 | ACCAGCTAAGGGAGG[A/T]TGCTGGACTTGATGC | 14360 |
rs45799439 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39471163 | CAGCAACCCTTCTCA[C/G]CGACATTCAGCTTCA | 14360 |
rs45806696 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39468123 | GTGTGCACACCTTCT[C/G]TGATTTCTTGTTTTG | 14360 |
rs45818110 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39495004 | TGAGCTCTCTTCAGC[A/C]TGTTCCTTTTGGGTG | 14360 |
rs45821983 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39445186 | AACATGCAGTATGAA[A/T]TGTCTGCACCTTGAT | 14360 |
rs45825264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39546845 | ATTGAGTAAGACCTG[C/T]CATGCCTCTTCCCCT | 14360 |
rs45834892 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545432 | TTACACTTGTTCCTC[A/G]ACGTGTTGTTCTCTC | 14360 |
rs45841912 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39507619 | GGTCGCCTCACTCTG[A/C]CTGTGCTCCGCCTCC | 14360 |
rs45845286 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39534003 | CTGATTGATCTTTGC[C/T]TGCACAGCCTTCTCC | 14360 |
rs45847319 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39547868 | CATCCCACTCTCAGA[A/G]CCACACTGTCAGGCC | 14360 |
rs45850111 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39459034 | AGTCAGCATTTTCCA[C/G]GCCTAATTAAAAATG | 14360 |
rs45851761 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39431137 | GTGAAATTTCATGAT[C/T]GCCTTACATAGAAAA | 14360 |
rs45855746 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39405078 | GTACTGGTTCTCTTA[C/G]CCTGTTTCCTGTGGC | 14360 |
rs45857375 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39440557 | GAATCCGTCAAGCCC[C/T]GCAGAGGTGAAAACA | 14360 |
rs45863108 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39477418 | GTTCCACAAAATTTA[C/T]TCTATAGTAGGGCTG | 14360 |
rs45874801 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39439731 | AACCAGGAGGAGGGG[A/G]CTCCAGGGTCTCATT | 14360 |
rs45887993 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39433538 | TCAGCCTGCTTAGAT[A/C]AGTTTCCCCTTCAGT | 14360 |
rs45891401 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39426485 | ACACGCAGCACATTG[A/C]GTTGGTACACTCTTG | 14360 |
rs45891776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378073 | CCGTCCATGGATTCC[C/T]TCATTTTCATATGCT | 14360 |
rs45896917 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39438118 | GAATTATCATTTGTT[A/C]TGCTACAGGATGATA | 14360 |
rs45900416 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39505343 | TCTACACAAGCATCG[A/C]CAGAGCTGATTCCAG | 14360 |
rs45910305 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39471257 | CCTTCTTGCTCCTCT[C/T]AGAAGCGTGATGAGC | 14360 |
rs45916885 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39477343 | ATCCCTGAATCAATG[A/T]CAGTTTTTCATAGTC | 14360 |
rs45919313 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39451487 | ACTCAGGATTGAGAG[A/C]TCCTCCACTCACGGA | 14360 |
rs45932954 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39469275 | ACCATGCCTGTGTCT[C/T]CAAGTGCCTGAGTCT | 14360 |
rs45933865 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, LOC105245135 | Mm_Celera | 10:39527242 | GCCTTCATTGCCATG[C/T]AGAACTGTGAGAGGA | 14360 |
rs45942434 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39519818 | TAGCTCAAGTCAAGA[A/G]TAAGGGTCCTGGGCT | 14360 |
rs45946308 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39394866 | GTAGCAACTGCAGAA[A/G]TTACGTGAATGAGGA | 14360 |
rs45949515 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39538427 | AGATCCCTTCCTTAG[C/T]AAGCCACCACTCTCA | 14360 |
rs45949999 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39544835 | ACTAAGTCAAGACCC[A/G]TTTCTGTCTGAGGCA | 14360 |
rs45951844 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39478067 | AGAGGGGCTAGTGAA[G/T]TAGTAATAGGCTTAG | 14360 |
rs45962351 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39430848 | CAGGACTCAGGTTAC[A/G]ATGCAGTTTGCTAAA | 14360 |
rs45963876 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39386572 | TGTTTATACATATTT[C/T]GAGGTATAGAACTTA | 14360 |
rs45970146 | snp | C/G/T | 0.35503 | 0.226867 | intron-variant | Fyn | GRCm38.p3 | 10:39460078 | AGCCTTCAGAGCCTG[C/G/T]GAAAGACAAGGCTCT | 14360 |
rs45979203 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39560059 | TTTGACAAAGCTGCC[A/G]TTGGTATGTGTCTGT | 14360 |
rs45985303 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39417380 | GGAAAAGAGAGGAGC[C/T]CTTCCAGATGCCTGA | 14360 |
rs45992599 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39460376 | CAGCACAGGAAAATG[A/G]GACCCTTCTCTTTGA | 14360 |
rs45998326 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39473348 | TCCTACTCAATGTGG[A/G]TGCCATTTTGGAGGT | 14360 |
rs46000932 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Fyn | Mm_Celera | 10:39420056 | TAAAGAGGAAGCCAG[C/T]GCAGTCTATCATCTG | 14360 |
rs46004714 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550465 | ATTTCAGTATAATGT[A/G]TGGGCTCTATCCATT | 14360 |
rs46019487 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553531 | GAACTGGGTCCAGCA[A/G]AGTATGTGTATTTAC | 14360 |
rs46023105 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Fyn, LOC105245135 | Mm_Celera | 10:39527072 | GTCAGACAGACAGAT[A/G]GAGTCCGGGGTTCTG | 14360 |
rs46028871 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39484759 | TCGCCTCTCCCTGCC[G/T]GCCACCTCCTTCATG | 14360 |
rs46063458 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39400453 | GAACACAGTCGAGCA[A/G]AAGGCAGTCATTAGC | 14360 |
rs46064321 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39546017 | GTCAAAGAGCAGAAC[C/T]AAGGTGCCAGGTTAA | 14360 |
rs46065046 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39499782 | CATCAGTGAGAACAC[C/T]AGACTCCAGGATATT | 14360 |
rs46067958 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39400683 | ACGCCTGTCTCTCTG[A/C]TGCTGAGTTTAGGGA | 14360 |
rs46068775 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39439676 | CACCTGAGCATCCAC[A/G]GCCAGCACTGACTGG | 14360 |
rs46070819 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39430065 | GGGTGCCTTGTGGAG[A/G]CATTTTTAAAACAAG | 14360 |
rs46071201 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39397600 | CCAGCTCTTGCTTTT[G/T]CTGATGCTTACACGT | 14360 |
rs46079167 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39422432 | GGGATCATCCTTGGC[C/T]TGTGATGGTCAGCCA | 14360 |
rs46083913 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39381936 | TCCTTAATGAGTGTT[C/T]TGAACCCTGGGGACG | 14360 |
rs46088623 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39429399 | ATCCAGTCATCTACA[C/T]GCCCTGCTGCCGAAC | 14360 |
rs46098017 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39429997 | ACTTTTCCTTATGCG[C/G]GAGCAGTAACTTGTC | 14360 |
rs46102747 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39458951 | CTGTCCACAGCCTTT[C/T]GTGGCCTCATTGCTC | 14360 |
rs46106998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39540413 | TGATAAGTTGACCCT[A/G]TAGACACATACAGCC | 14360 |
rs46108256 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39440100 | GTAGAGGCAGGCAGA[C/T]GTCTTCAGTTGAAGG | 14360 |
rs46116203 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39520864 | GCACGAATGGTAGCT[A/G]AGAGAGATGTTCACT | 14360 |
rs46139436 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39433430 | CAGTGGCCTTGTGCT[A/G]ACCCCAGGAGGAGAA | 14360 |
rs46142852 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39543912 | GCTCCCTCCTCCTGG[C/T]GACCCTGGAGTGCCC | 14360 |
rs46148546 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39521881 | GACCGGCAGGCCTGT[C/T]TCCCTGGCCCTCATA | 14360 |
rs46152325 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39384798 | TTGAGTCAGGTGGAG[G/T]TAGCGTGGTTTCTCA | 14360 |
rs46152520 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39403798 | TATCAGAAAACCATA[A/G]ATGCCATGCTGTGTG | 14360 |
rs46153498 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39423781 | TCATGTTGTCACCAC[C/T]TTAAATGGAGCTGGG | 14360 |
rs46156546 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39378810 | CTTACATTGAGCATC[C/T]ATCTCTCTTGTAACG | 14360 |
rs46166960 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Fyn | GRCm38.p3 | 10:39506429 | GCCCCATCCCGTAAC[A/G/T]AGGCATTCATCTTCT | 14360 |
rs46172635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39499764 | AGTTGAAGCCTCATC[A/G]CCCATCAGTGAGAAC | 14360 |
rs46176064 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39501818 | CCTCACTTCAGACTT[A/G]CAATGCAGATGGCGG | 14360 |
rs46182254 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553652 | CGATGAACAAGATGT[G/T]TCGTCCTGCCTGTCA | 14360 |
rs46192530 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418402 | TTCTGTCTCCTTCCT[C/T]TGGCCACAGGGGTTG | 14360 |
rs46197494 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39424608 | AGGGGCTGAAAGAAT[A/G]AATTGATATTCCTCT | 14360 |
rs46200930 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39535386 | TTCCGTCTGTGTGTG[A/G]GAAAGTCTCCGTGGC | 14360 |
rs46215121 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39482141 | TAGGAAGAACACAGA[A/G]CCATGCAGAGAGAGG | 14360 |
rs46220264 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39515182 | CGACTCGATGTCCCC[A/G]AGCCACAGAACAAGT | 14360 |
rs46222457 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39531590 | CAGTTGAAAGCCTAC[A/T]CCAAGCATCCTTGGT | 14360 |
rs46222484 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39390971 | AAGGATGATTGCAAA[C/T]TGACAAGCAGAGAAT | 14360 |
rs46223156 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39420824 | TGTAGGAGAACTGAG[A/G]AGGCAAAAGAGACTT | 14360 |
rs46224123 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39442090 | CAATTTCATTGGCCC[A/G]TATCCTCAACACACA | 14360 |
rs46231928 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39541174 | CAGGCCGCCCGCCGC[C/T]GTTCCAGCTCAAGGA | 14360 |
rs46233508 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560349 | TTGTCACATGTACTA[C/T]GTCCAAGTCTTGGGT | 14360 |
rs46235947 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39435867 | TCCAAGCTTTCCCCA[C/T]GGAGAAGACACTGTA | 14360 |
rs46237284 | snp | C/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39565489 | CGGGCCACTGTGCAG[C/T]GATTTCCAAACGACA | 14360 |
rs46243397 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39520182 | TCTGAACAACTGTTA[C/G]ATTCTAATGTGTGTA | 14360 |
rs46243803 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39390774 | ACTGCCCCTTGTCAC[C/T]GCTGCTCTCAGTCAT | 14360 |
rs46247596 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39384779 | CTTGTTGATCAGTGT[C/T]CCATTGAGTCAGGTG | 14360 |
rs46252365 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39476160 | AAAGTTCTTGCTGAA[A/T]ATGTGTGAGGCCCAG | 14360 |
rs46256013 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39510922 | TAATGTGGCACAGTG[G/T]GTCCCAAGCTGAAGG | 14360 |
rs46259371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39422689 | CCAGCCATTTCTTGA[C/T]GTGATTAGTGGGGAC | 14360 |
rs46266634 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39438876 | AAGTCACTGAATGGT[A/G]TTAGCGTATGCTCTG | 14360 |
rs46269401 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39493813 | TAACATGCCAGGGTT[C/T]TCAGAATTCTGCCTG | 14360 |
rs46275485 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39425727 | ACTCATGAAAATGGC[A/G]GTGGGGCACCCACAT | 14360 |
rs46283721 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545201 | TGAGTAAGTCACTGC[C/T]CAAGTGGGCCTTTGT | 14360 |
rs46293194 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39464159 | TGGTACCCAGCTTTT[A/G]TATGGTCGTGGGGGA | 14360 |
rs46297392 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39461628 | ACGAAACCTTCTCTC[A/G]TCTGGTTGTGTCTGG | 14360 |
rs46297521 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39507101 | ACTAAGGCTGTCTGC[A/G/T]GCTCAGCCCCCAAGG | 14360 |
rs46299460 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39463026 | CCTGAGCCTTCCAGC[C/T]GCCATGCTCCCTCCA | 14360 |
rs46300746 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39473967 | AAAGATGCAGGGACT[A/G]GAATTTCTACATGTG | 14360 |
rs46301512 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39455183 | TAGTGTAAAATGGTG[C/T]CACCGAGAGGTGCCC | 14360 |
rs46311829 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39494656 | TAGGCTTTTATCATA[A/T]TAACCCATGTTGTCA | 14360 |
rs46336069 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39383697 | TAGGCCTGTTTTTAA[A/G]AACATGTGTTGGTTG | 14360 |
rs46343387 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39457910 | CAGAATACACAGGCC[C/T]GAGATGGCTCTCAAG | 14360 |
rs46352631 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39482839 | TCACAGATAATGAAA[G/T]GCTTTTGAAAATGAA | 14360 |
rs46368204 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39456319 | GCTGTACAGAGTGCT[C/G]ATATTAAAGCCACAT | 14360 |
rs46368705 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39488669 | CATAGTGCTTAGACA[A/G]TATATTTTTGTAAAT | 14360 |
rs46369708 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453520 | TAGCAGGCAGGAATC[C/T]ACTCTCCATTTTCCT | 14360 |
rs46377329 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39396655 | ACGGTTGGGTGCTCA[A/G]AGACATCCCAGGGCT | 14360 |
rs46384425 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39433780 | TGCAAACTCAGCTTA[A/G]TAGTGACAAACTCTG | 14360 |
rs46384663 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39395349 | TTCCTAAGTAAAATG[G/T]AACGGCTGAGGGATG | 14360 |
rs46399640 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39423938 | ACTTGGCTAGGTGGT[A/G]CTGACATATCTCTAC | 14360 |
rs46403830 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39550539 | CCTCATAAGACCAAT[A/T]TGTGACTTTATATAC | 14360 |
rs46405475 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545656 | AAAGATGGCATTTCA[A/G]ACAAGCCGATACAAC | 14360 |
rs46407373 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39541437 | TTCCTTGCTAAAGAA[C/G]TGAACCCATCTTTTA | 14360 |
rs46411282 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39537792 | CTGTCACCTACGCCT[C/T]TCCTAGAACTCTACT | 14360 |
rs46414169 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39405628 | TTCCTGCTGTTCTAC[A/G]GGTGCTGTGAACTAT | 14360 |
rs46425654 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550551 | AATTTGTGACTTTAT[A/C]TACCTCAGGACACAG | 14360 |
rs46429022 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489274 | CTCTCATCTGAAGCC[A/G]GGGTTCCTCTGATGG | 14360 |
rs46429412 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, LOC105245135 | Mm_Celera | 10:39533428 | TGGTTTTACTAACTC[A/C]TTTCTCACTGCTTAT | 14360 |
rs46434482 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39508079 | GTTGCAGAGAAAGGC[A/G]TTTGCCAGCATGCCC | 14360 |
rs46440296 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39484876 | AACTTTTAAAAGCAC[A/G]GTATCAGGCCTATAA | 14360 |
rs46443194 | snp | A/G | 0.18 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554706 | CTGCTGCAGCCCTGT[A/G]GGCTAAAAATGGGGT | 14360 |
rs46447695 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39436243 | TTAACAAAGACTGGG[C/G]ACCAGATAGTTACAG | 14360 |
rs46458502 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39404757 | CTCTTACACTTGTTT[C/T]CATAAAAGTCTCGGC | 14360 |
rs46469294 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39469702 | ACAGCCTCACCACGT[A/G]CCACAGAGGCTTCTT | 14360 |
rs46470188 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39471400 | TTCTGAACTTGAATT[A/T]AAAAAAGTATGTAGA | 14360 |
rs46471280 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39513190 | TGCTCTGACAACCTA[G/T]CATGGCTTTTTACCC | 14360 |
rs46476388 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39383373 | TAAAAGTTCTGCCTA[A/G]TTCTCTCTGCTTCAG | 14360 |
rs46477817 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39535599 | ACTGTGGCCTCAGGC[A/G]GCTGGCACCTCTCAT | 14360 |
rs46478070 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39477847 | CACCAGAACTATTTA[C/T]TGTCTAGGTATCTCT | 14360 |
rs46490848 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39427719 | ACCAAGGGATTCATG[A/C]GCATAGTATTCCTTT | 14360 |
rs46492057 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39490570 | AGAGACAGATGTCAG[A/C/T]ATGAAAGATGGAGAG | 14360 |
rs46497140 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39446080 | GCACCTGCAGTGAAC[A/G]AGAAGACTGCCTGTG | 14360 |
rs46501381 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39429226 | TCCCACAGAACCCAA[A/G]GATGCATTGTCTGTC | 14360 |
rs46503169 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39426404 | ATAGGTTATAGGTGA[C/T]TGCAGATCTGTACGA | 14360 |
rs46509885 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Fyn | Mm_Celera | 10:39471902 | CCTTCAGAAGCCTGA[A/C]TGCAGCCTGGGCTCC | 14360 |
rs46519350 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39435273 | ACCCTTGTTCCTCAG[C/G]CTCAGAAGGTGAGCC | 14360 |
rs46519896 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39441344 | TCAGTGTAGGCAGGG[C/T]GGTGAGCTATAAAGA | 14360 |
rs46521177 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39534882 | CAAGCTGAGCAGTAG[C/T]GGGGATGGATTACAG | 14360 |
rs46525834 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39458836 | CCCCTGCCATGGGTC[A/G]CACCAGAACATCATT | 14360 |
rs46529173 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39543462 | TTGTATAGGATAATT[C/T]GCACAGTCTGTGGCT | 14360 |
rs46534530 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Fyn | Mm_Celera | 10:39551469 | TGACGTATGGTCTTT[C/T]GGAATCTTACTCACA | 14360 |
rs46537580 | snp | C/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559211 | GTTAACAAAAGGAGG[C/T]GCTGAGGCTGGAGCA | 14360 |
rs46538452 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39485974 | CTAAGACAAAGGGAG[C/T]GTGTGCCCTAATTTA | 14360 |
rs46540306 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39510287 | CGAGCGCAGTGCTTA[A/G]GAACTGCCACCAGCA | 14360 |
rs46542517 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39478823 | CACACAGCAGCACGG[G/T]TCCTGTTTTAAAATA | 14360 |
rs46542911 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39510592 | CAGTAACATTAGAAA[A/G]TGCAGGACAGTATGG | 14360 |
rs46544197 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378984 | TGAGAGTTCTGTCTT[C/T]CCAAAGAGATTGTTG | 14360 |
rs46548930 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39479302 | ACTTGCTGAGAATGG[C/T]ATGCGGCTCCTAGCT | 14360 |
rs46552086 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561902 | TCTACTTAAACACAG[C/T]CAAAGGAATGCTAAA | 14360 |
rs46552908 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39543911 | GGCTCCCTCCTCCTG[A/G]CGACCCTGGAGTGCC | 14360 |
rs46563448 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39520396 | TTGATTTAACTAGAA[C/G]TAACTTGATGAAGGT | 14360 |
rs46570052 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561944 | CCAGAAATTATAAGT[A/C]CAGAGAATAAAAGAG | 14360 |
rs46572997 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39505380 | GGAATGCGCCTCTTT[C/T]CTGCTGTGCCATGGT | 14360 |
rs46577203 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39439590 | GGAGCTGGAGTTCAG[A/G]AGGCTCCGAAATAAA | 14360 |
rs46582329 | snp | A/G | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Fyn | Mm_Celera | 10:39420247 | CCAGACCCTCTGGAG[A/G]CGACACCAAGGGTGA | 14360 |
rs46584721 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | GRCm38.p3 | 10:39405237 | GCTCCCTAGCATTCG[C/T]TCCCAGTATCAGCCT | 14360 |
rs46584795 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39492964 | ACTTGTTCTGAGTGG[C/T]TATCCATGTGGTCAC | 14360 |
rs46587666 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39434454 | AAGGCACTTCCACTG[C/G]TTAGCTTTCTGTCCC | 14360 |
rs46589071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39377104 | AACGCCATGTAAGCC[C/T]TTGGCAAATCAGGGG | 14360 |
rs46591895 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39483077 | ATGATTATTATTGTC[C/G]CTTGCAGTTGTTGCT | 14360 |
rs46594320 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39395220 | GGGTTACAGGCATGG[C/T]CCTGCCAAGCCTCAT | 14360 |
rs46596967 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553163 | AACCTAGGTTTACAA[A/G]TCTGAGTGGATGCCT | 14360 |
rs46601277 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39538027 | GGTCTTTTTCCTCAT[C/T]CCTCAAGCAGCTGAG | 14360 |
rs46601731 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39482261 | AGAAGGTCCTACAGA[C/T]GTGGAGACAGGAATT | 14360 |
rs46603221 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39399239 | AATAGTTACATTTTT[G/T]AATGGAAGGCCACAT | 14360 |
rs46607084 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39507601 | CAGGAGCCTCTCTCC[A/T]AAGGTCGCCTCACTC | 14360 |
rs46615709 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39452912 | TTCTATACTATGCAC[A/G]ACCCTGGGAGATGGA | 14360 |
rs46629468 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39463131 | TCTAACCCAATGTAT[A/G]CCCAAAATGTTGTGT | 14360 |
rs46629671 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39547288 | AGAGACAAGAGACCA[A/G]ATAAGTTACCCATAG | 14360 |
rs46635041 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559420 | GACCCAAAGGATAAG[A/G]GAAAGAAAACATGGG | 14360 |
rs46641753 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39478199 | GGTGGCTTCAAGCAT[C/T]TCTTCTAAGTGAAAC | 14360 |
rs46646374 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561494 | GGCAGAGTCACAGGT[C/T]TACATGAAAACTCCA | 14360 |
rs46646897 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Fyn | Mm_Celera | 10:39551391 | CCATTCTGCAGGTGC[A/G]AAGTTTCCCATTAAG | 14360 |
rs46649586 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39459129 | GCAGAGACATGCAGA[A/C]AAAGCTCTGCAGCCC | 14360 |
rs46654416 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489990 | GTGTGCATATGTATA[C/T]GGTAGCCAGAGGTAG | 14360 |
rs46663312 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39422944 | AGCACTGTAGATTTC[A/G]GGTTGTTGATTATAG | 14360 |
rs46663358 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39430116 | AAGGACCCTAGTTCC[C/T]GACTGAGGTCTGCTG | 14360 |
rs46673959 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39543805 | ATCTCCTCCATGGCC[A/C]GAGCCATCATCTTCG | 14360 |
rs46675669 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39493442 | TCAGCTTTGCAGGTT[C/T]CCAGATTCTAGCTGA | 14360 |
rs46678019 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39429174 | TTCTTTGGATCTGCA[A/G]AGCAGCTGTAGCCCT | 14360 |
rs46682055 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39543887 | CAGCTTTAGAACATT[C/T]CTACAGGAGGCTCCC | 14360 |
rs46682901 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39406887 | CTTCCAAATGTAGAC[C/G]TGGGGACCGGTAGCT | 14360 |
rs46687284 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39492210 | TCAAAGAACAGCAAG[A/G]CAAAGGGTGTACAAA | 14360 |
rs46688166 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39472383 | TGCTGGTGGCAGGAG[C/T]GACTTGGTGACTTTC | 14360 |
rs46703206 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39436830 | CTCTGCCAGGAGTCA[A/G]TGTTACACATTACTT | 14360 |
rs46705896 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39425813 | CTGCTGTAGCTCCTG[C/T]CTCACTAGGACACTT | 14360 |
rs46706939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39551715 | GCTGGTATAAATGTT[C/T]CAGTTCCCACAGGTC | 14360 |
rs46715906 | snp | C/T | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39560134 | GAGGTCTGGAGAGAG[C/T]ACCTGGAAAAATAAA | 14360 |
rs46728427 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39395258 | TAAGAGAGAAGCTGA[C/T]TTAGAGGTAAAATTG | 14360 |
rs46734106 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39439520 | ACCCCACCCAGGGTA[C/T]AGATGGCAAGCTCTG | 14360 |
rs46740982 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39378322 | GGAATCCAAGCTGGC[A/G]GATCAGCAAACTCTC | 14360 |
rs46749036 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39392677 | TATCCTACAGTCAGG[C/G]TTCGATATAGATAAA | 14360 |
rs46751848 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39517956 | GTGCACACTCCCGAC[A/G]TAGGCCTGTTTTGAG | 14360 |
rs46753637 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39422567 | CCTCTGTTCACTCTG[G/T]TAGGAGCGTGTCATA | 14360 |
rs46756846 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39520420 | TGAAGGTTAGCATGC[A/G]TTAGGAGACAAGCCT | 14360 |
rs46766154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39449645 | GTTACTGTGCTCAAA[A/G]GATGCCAGCTCTACA | 14360 |
rs46776100 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39549980 | CCCTAACATGAAAAC[A/G]CAGGCTGCTAGGTCC | 14360 |
rs46784432 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39487646 | TAAAACCAGATCCCA[G/T]AGAGTCTACCACCAA | 14360 |
rs46786570 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39422367 | TGTGTGTGGAGCTGA[C/G]AGATGGAGACCATCA | 14360 |
rs46790820 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39457392 | TCTGAGAATGGAGAA[A/T]GGAGGGCAGCGTAGC | 14360 |
rs46791759 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39488603 | AGAAGCAGAGTGGTG[A/G]TCCTCTGCAGGAGTG | 14360 |
rs46815490 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39498957 | TCCTTGCTCCTAGAG[G/T]CATCCCCTTCCTCTC | 14360 |
rs46821124 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39462171 | GCAGCTGGAAGTCTG[A/G]GTCTGGGCGTGCCCT | 14360 |
rs46827742 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39378522 | GGAGCTGATGTTGAC[C/G]CTGGTTCCTCCTGTG | 14360 |
rs46831157 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39460762 | GGATTAACACAGCCT[A/G]CTGACAGAGATCTGT | 14360 |
rs46832357 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39451828 | AAGTTTATTGTTGAC[A/T]CGGTCACTGGCAAGA | 14360 |
rs46834339 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453676 | GGATTCCTAAAAATG[G/T]CATTTACTTTAGATT | 14360 |
rs46841553 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39433697 | ATCTCAGGACAAGAA[C/G]GTAAATGTCATTGGC | 14360 |
rs46844183 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39403727 | TGGCAGAAAGGGCAC[A/G]GCGATCGAGGGTCCT | 14360 |
rs46844236 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39477904 | TGAATCACAGGGAAA[A/T]CGTTCTGACTCAGGC | 14360 |
rs46846020 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39495816 | TGGGAATGAACATAA[A/G]GAGGAGGCTGTCTGG | 14360 |
rs46847894 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39477619 | TGTTCTCCTCAGACC[A/G]TTGGAATTATTTGGC | 14360 |
rs46851927 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554316 | AAAGTGCTCTGGCTC[A/G]TAAGTGACAGTGAAA | 14360 |
rs46853124 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560541 | AGTAGTTAATTGAAT[C/T]CTGTGGTGCTGTGCT | 14360 |
rs46854598 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39512005 | GGGACAGGTAAGCCA[C/T]TGTCAATCAGGATGG | 14360 |
rs46857486 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418441 | TCACAAACACACTAC[A/G]ATTAGTTTTGTAATG | 14360 |
rs46865980 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | GRCm38.p3 | 10:39471227 | GTGCCAAGAGCATCC[C/T]GTAAGTGAGGAGCGC | 14360 |
rs46868798 | snp | C/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557009 | AGGTGTGAGTGTTCT[C/G]CTAACGTGTGTGCAG | 14360 |
rs46876813 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39450449 | AGACAGGAAGTAGCA[A/G]GAGCTCCCGTGAGAC | 14360 |
rs46889962 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39498696 | GAATAAAGTACAGAT[A/C]CTCGGTAGAATCAAC | 14360 |
rs46904953 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39547781 | CTTAGACATACCCTT[C/G]TCAGTCTCAGGTTTT | 14360 |
rs46908944 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378847 | TACATGATGCCATGC[C/T]GTGTTACTTAAAAGC | 14360 |
rs46909508 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39542377 | GAGGGACAGGCAGAG[A/C]ACATGCACACTGCCT | 14360 |
rs46910583 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39470398 | AAGCTTGTCTTAACC[A/G]CAAGCAGTGGAGGAA | 14360 |
rs46913080 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39481472 | TTGCCTCATTTAAAT[C/T]TGAAAGAGAGCTGCA | 14360 |
rs46915994 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39399529 | GGACAAGGAAGACCT[C/T]TCCCAGCCTTCTGAG | 14360 |
rs46921794 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39433459 | AAGCTGAAACTGGGT[G/T]CCCGAGTGGAACAGA | 14360 |
rs46925203 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39417804 | AAAGCATTCTAATGA[A/G]ATCATTGGGCGTGTT | 14360 |
rs46941460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39536605 | CAGTTGTGAGTTTCC[C/T]ATCTCAAGGTGCTCT | 14360 |
rs46946319 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39474150 | GATCTGGGTGAGGTG[C/T]TTGGTGAAGACCAGG | 14360 |
rs46951761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39539091 | GCCAGATAGGTGGAT[A/G]ATTGATTGATTGACT | 14360 |
rs46952684 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39502190 | ATCTTCGTGACTAGT[A/G]CTACTGAATTAAAGG | 14360 |
rs46958962 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39458792 | TGTGCTTTACATGGG[A/G]CAAGTGTCTGTATGG | 14360 |
rs46960013 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39497412 | AATGACTGGGAATGA[G/T]GAATCCAGAGGGGCA | 14360 |
rs46975930 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39472041 | TGTTTCTTGATGTCT[C/G]CCTGCCCTGCGCGCT | 14360 |
rs46980775 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39441402 | CCAGTATCAAGGTAA[C/G]AGTGTTACAATATCA | 14360 |
rs46982632 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39450719 | GAGGCAGATAGCAGC[A/G]TCTCACTGCCTGACA | 14360 |
rs46989103 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39537247 | AGAACATTAAACTCA[C/T]GCAGCAAAGCCCAGC | 14360 |
rs46989976 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39399036 | CCTGTCCAAAGGGCA[C/T]GGTGGCCTTCCACAG | 14360 |
rs46992111 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39404014 | TTCTTCTGTAGTTCT[C/T]TGTCAGGATTCAGTG | 14360 |
rs46993389 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39406581 | CACAGGAGCATGCAA[A/C]TATTTGTCCAGTTAC | 14360 |
rs47008600 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39473334 | TTATGACACCTGTCT[C/T]CTACTCAATGTGGAT | 14360 |
rs47029473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437529 | TCAAGCAAAAACATA[C/T]CTGGTGAGAAACCTA | 14360 |
rs47032389 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39381749 | CCAGGAAGATGCTGA[A/T]GCAGAGGTAACTCTT | 14360 |
rs47032883 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39424118 | AGGAATACTCTGAAA[A/G]TGATAGAATTCTTCA | 14360 |
rs47035155 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39382535 | CCAGGTCTGAAACTC[C/T]TGTCCCCTCTTGGTA | 14360 |
rs47039960 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39478249 | AGACTTTATTACCAC[A/G]GTCTCAACTCCTTCA | 14360 |
rs47042639 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39399190 | TTTACAGTGGAACTA[C/T]TAGTCTTGTGGGAAG | 14360 |
rs47046480 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39493262 | CAGTCTTTCAGGCAT[G/T]GTTCAGCACCTAACT | 14360 |
rs47053093 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39417321 | GTTCTCTTCAGGGTC[G/T]CCTCTGGTTCTCATA | 14360 |
rs47056085 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39446205 | GCTTTCCTTTTATGG[G/T]TAAACTAAAATATTT | 14360 |
rs47056620 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39382492 | TGGAAGGAAACCACC[A/G]TGAAGTAGTGGTTAT | 14360 |
rs47057836 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39421802 | AAGCCCCTTCCTACT[G/T]GATTGATGCCGCACC | 14360 |
rs47061813 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fyn | Mm_Celera | 10:39448522 | CAGACTAGATTGCAG[A/G]TCCTAGAAACAGCCT | 14360 |
rs47077063 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39522934 | GACACAGCACAGGAG[C/G]GAGAAGACCTTTCCC | 14360 |
rs47080707 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39498320 | GTGGTTTGTCCGGCT[C/T]ACGGAGTTGCATCTC | 14360 |
rs47081190 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39400937 | ATGACTTGCATAGAC[G/T]TCTTGTCTGCAGAAA | 14360 |
rs47091587 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | GRCm38.p3 | 10:39480858 | ATTGGATGGATGCAT[A/G]ACGAGACAGGTGAGA | 14360 |
rs47095351 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39406657 | CATTCCTATTCGGCA[C/T]ACTTACTTACACATT | 14360 |
rs47095912 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39462702 | AGGAGGGGCCTGGCT[A/G]CGGACAGCACTCGTG | 14360 |
rs47096521 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39486062 | GACAGCCAATGGTTT[C/T]GTTGGGACTCATACA | 14360 |
rs47102576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39404587 | AGAGTAAGATTGTTT[A/G]GAGGAAAAAAATAAA | 14360 |
rs47105900 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39473001 | ACACAGAAAGTCAGG[A/G]TTATTTGTAAGCCTC | 14360 |
rs47119546 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39382195 | TTATTTAAGAGGCAG[A/G]CTTTCTTAGAAGGAA | 14360 |
rs47120276 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39419250 | AGCAGGATCATGTTA[C/T]GGTACAGCATCCCAG | 14360 |
rs47133446 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39471676 | CCTATGTAATTACTC[C/T]TAAGAAGGTGTATGA | 14360 |
rs47143249 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39465026 | TGGCGAAGGCTTTGG[A/G]CAGATAAATCTGACT | 14360 |
rs47147099 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39466147 | CCAGAGGAGGGTGTG[C/T]GAGGGCTGATCTGTC | 14360 |
rs47151353 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39480104 | GGATTTCGTACACAC[A/C]GCTTTACCATACCTT | 14360 |
rs47168492 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39511588 | AGAAATTGGTGGCCA[A/G]CTTTGGGCAGTGGTT | 14360 |
rs47168944 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39396855 | TCTGTAAGGCCTTAA[A/G]CTAATTACTGTCCCT | 14360 |
rs47178711 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39423564 | GGTAATACAGCAACG[A/G]GCTTCTGTAGCAGTG | 14360 |
rs47180131 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39432276 | ACTGTTAACAGAACT[C/T]GGCAGTTACCTGTAG | 14360 |
rs47182743 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39525530 | GAGAGGGCAAAACTG[A/G]TGTGCTGTTCAGATC | 14360 |
rs47190263 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39434473 | GCTTTCTGTCCCGTC[G/T]AGACTTGCTGGCTTT | 14360 |
rs47198402 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39430549 | ACCAGCCTGACATCA[A/G]AAGGAGTCACAAACC | 14360 |
rs47202720 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39524210 | TTCTCACATAGCTGG[C/T]GTCGTATCCTTTACA | 14360 |
rs47204206 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39524129 | CCTCTTGTTCTGCAG[A/G]CCTTCCTCTCACCAG | 14360 |
rs47213748 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39504088 | TCTCCTCTGCTTACC[A/G]TTCTGTCGTAGACAT | 14360 |
rs47225745 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39534272 | AGAAATCAGGTGACA[C/T]TCCAAGTCAGACAAG | 14360 |
rs47227792 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39442155 | AAATCCTGTTTCTAA[A/G]GAGTTTTTCTTACCC | 14360 |
rs47228715 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39503960 | CTGTCACGCGCCTGC[A/G]GTGATTCAGCCTGTC | 14360 |
rs47242627 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39452011 | CCCTGCTCTTAAGGC[A/G]CGGTGGCTGGGGAAG | 14360 |
rs47251113 | snp | G/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418360 | GTAGCCAGTCTCTTG[G/T]CTGTCTCCCTGTGAG | 14360 |
rs47262527 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453113 | ATGAAGATCCACTCT[C/T]TAAAAAGAAGAGAAC | 14360 |
rs47265951 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500048 | TCCGGGCAGGTGTTT[C/T]AGTTCTGTTAAGCCG | 14360 |
rs47266436 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550308 | GGCTGGTAGGAGAAA[A/G]ATAGGAGGAAAGCAG | 14360 |
rs47282319 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39436049 | TTATAAGGGAACTGA[A/G]GACTCCTGAAGCAGT | 14360 |
rs47292013 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39399574 | CTGGATGGAGTAACA[A/G]GACCATGCTTGTCTT | 14360 |
rs47292402 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39457402 | GAGAAAGGAGGGCAG[A/C]GTAGCAAATCCACCT | 14360 |
rs47292961 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559264 | TACAGAGTCTGGAAG[C/T]GACATCTGTTCGGCG | 14360 |
rs47295757 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39493582 | AGGGACTGGTTGGCT[C/T]CAGCAGCACACTGCT | 14360 |
rs47301762 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39435225 | GGGTGGCGGTAGACA[G/T]CTGGATGGAAAAGGG | 14360 |
rs47311425 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39464526 | TACCTGCAGTGCATT[C/T]TCTGAGGTCATGCAG | 14360 |
rs47322930 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39395463 | CACCCCCGACGGCTA[A/T]TGCTCACTGTGCCCA | 14360 |
rs47322979 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39463504 | CTGGAAATGCTGGCG[C/T]GTGCTAGAGCATAGC | 14360 |
rs47345466 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39503655 | GGTTTGACATCAGTG[C/T]CTCTGCTTCCCTTGC | 14360 |
rs47348021 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39491391 | AGGGAAAACCTTATC[A/T]GTGTTGCCTCAAGAG | 14360 |
rs47362246 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528197 | AGAAAACCTCCTTGC[A/G]CTTCAGTGATATACA | 14360 |
rs47364171 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39468180 | AATTATTGTTATTAG[C/T]TTGTCTCACTACGTA | 14360 |
rs47365627 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39457989 | GAATTCAGACAGACA[A/G]ATCCTTCTGAATGAT | 14360 |
rs47366102 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39417520 | GAGGTCCAGTGGTGA[C/G]AGCTCACGGTGATGC | 14360 |
rs47367845 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39436532 | GAAGTCAGTAACTGT[A/G]TCCACTGCAGTATTC | 14360 |
rs47372517 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39495930 | AGGAGCCACTGTCAC[A/C]CAGTTAACCTGAACC | 14360 |
rs47379108 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Fyn | GRCm38.p3 | 10:39501684 | ATCCTAAATCACTGC[A/C/T]GGATGCAGAGGCTGC | 14360 |
rs47381789 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39424687 | TTCTGTAAGGCAGCC[C/T]GGTCCTCACAGGCCT | 14360 |
rs47385931 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39390793 | GCTCTCAGTCATCAG[C/T]GGTGATGGCACAACA | 14360 |
rs47388510 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39381395 | GTGACCAGATGGATC[A/G]TAGCATCTGTGGTCT | 14360 |
rs47395942 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39402004 | GCCTCCTACTGAATA[A/C]GAGAAGGCCCAGGGT | 14360 |
rs47397613 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561813 | AGAAAAAGGTACTCC[C/T]ACACTGGCCTCAGCA | 14360 |
rs47408269 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550030 | TTTCTAACTCTGAGA[A/C]AAGCAGGGTGGGCTG | 14360 |
rs47408472 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39523008 | GTCTGCGCAGTACAC[C/T]GTTATTCACTTCGTG | 14360 |
rs47411080 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39394035 | CTCCATGCATTCTCA[G/T]ACACTCTCATCCTTC | 14360 |
rs47413502 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431655 | TATACCTAGAAGACA[C/T]TGTGCCTTTGTGTGC | 14360 |
rs47413842 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39531684 | ATCTAAGGGACAGCT[A/G]TTGGATACTCAGGCC | 14360 |
rs47427045 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39500711 | GATGAGGGGCAGTGT[A/G]CCACACCCCTTCTCC | 14360 |
rs47429763 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39512449 | CAGTGTCCACTGTGG[C/T]CTGTCAGCCAAGGGC | 14360 |
rs47429826 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39470702 | CAGCATACGTGTTGA[C/T]GCGGTCCCACATACA | 14360 |
rs47434711 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39546661 | GTGAGTGGAAGAAAA[C/T]TGGACATTGGAGACG | 14360 |
rs47442306 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39457188 | CCATGAAGCTCTTAG[C/G]AGAGGCTCCTGCCTT | 14360 |
rs47444586 | snp | C/G | | | intron-variant | Fyn | Mm_Celera | 10:39458542 | CTTACGAAAGCTCTG[C/G]TGTGATGTTCTTTCG | 14360 |
rs47450767 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381718 | CTCATCTAAGGAAAC[C/T]CAGAGATAGAAGGTT | 14360 |
rs47455580 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557056 | AAGACTTGACTTCGG[A/G]TGTCTCTGCTGTCTC | 14360 |
rs47460683 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39403941 | TACTTCCCAGCTTTA[A/C]TGGGTAGGAGATTTA | 14360 |
rs47464591 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39476367 | CTAAATCATCAGAGA[A/G]TCAGTTGTTGCACGT | 14360 |
rs47465945 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39548918 | AGAGTGAAAGCCACA[C/G]GTTACCACATCTGTA | 14360 |
rs47483141 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545395 | GCAGCCAGTCTCCTT[C/T]CACACATCCCGTTTC | 14360 |
rs47484568 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39481570 | ATAGTAGTGGAACAG[G/T]GAGGAGTGAGGGAGA | 14360 |
rs47486240 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39444710 | GTTATTCCCAAAACC[A/T]ACGTCCACAACTCCC | 14360 |
rs47491819 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39543075 | TTCCTTTATATTTAT[C/T]CTCAAAACATGACGC | 14360 |
rs47494030 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39535658 | GGCCCTCTCAGCCTG[A/G]CCATGCAGCCTTCCT | 14360 |
rs47501916 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39493091 | ACAGAAAAATGTGAG[C/G]ACTGAAAGTTATATA | 14360 |
rs47503524 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39459710 | GCTTTAATCTGTAGC[A/G]ACGTGTAGAAGCCCC | 14360 |
rs47504634 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39525064 | TCAGAAATCAAGGGT[C/T]GTACAGCTGAGCTAT | 14360 |
rs47504847 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39457842 | TGTTTTGAGAGTTTA[G/T]ATTTTACAATACTTT | 14360 |
rs47508630 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500998 | CTTTCAGGCCTACTG[C/T]GAGCAGAATTCTCCA | 14360 |
rs47511970 | snp | C/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559452 | ACATATGACAGTCTG[C/T]GTGGCAACTGCACAA | 14360 |
rs47513522 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39551578 | TTTAACTTCATTTTA[C/T]AGGAGTCTTGCCCAG | 14360 |
rs47516287 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39544962 | CTCTAACCGGACATC[G/T]CGTCTTCACTTAAAG | 14360 |
rs47516985 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39465905 | GCACCAGAAGGTGAA[A/G]AGCACGCCACCATTT | 14360 |
rs47524505 | snp | C/T | | | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528191 | TGGAGCAGAAAACCT[C/T]CTTGCACTTCAGTGA | 14360 |
rs47533396 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39524891 | TAGAGCTGAGTTCCC[A/G]TCTTCAGAATTCCTG | 14360 |
rs47539795 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39479994 | AGACCTGATGCTGAG[C/T]TCCATGAAGATCCAC | 14360 |
rs47545906 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39398079 | GTAGGGTTACGTTGT[A/G]AGGAAACAGTGTCAT | 14360 |
rs47550990 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39401772 | TGTCAACAGCCAGGT[A/G]GGATCAGCTTAGGGC | 14360 |
rs47558602 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39522212 | GTAACATCCTGTTGA[A/G]AGTGTCTGAGGAAAT | 14360 |
rs47562150 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39540462 | CACAGATAGTACCCA[C/G]GAGCCATGCTGTACA | 14360 |
rs47565417 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39395640 | AAAGTGTGATGGAAT[A/G]ACACTGGAGCAGATC | 14360 |
rs47567970 | snp | A/G | 0.18 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39472962 | TATTTTTACTAAACT[A/G]ATAGCTGATTCAGAC | 14360 |
rs47570801 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39497253 | TAGTTGCAAAATCCT[A/G]ACAAAGTAAGAAAAC | 14360 |
rs47576504 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39427953 | GCCAGCCTCCTTTGA[C/T]CCGCTGTTACGTTAT | 14360 |
rs47591350 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559933 | GCAAAGGTTCACTGC[A/G]GAAGTGGCAGGTTTG | 14360 |
rs47608771 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39507175 | GCTTAGGACCTCCAC[C/G]AGTGCTTATGCAACC | 14360 |
rs47640945 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39422393 | CATCAATGGTGAATA[C/T]ACTTGGATAAATACG | 14360 |
rs47643700 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39462811 | TTCCTTCGTGTGTGA[A/G]AACTCCACCCTTCTC | 14360 |
rs47647877 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39458691 | GGGACTCTTTGTTGT[C/G]AGTTCTTGTCTTTAA | 14360 |
rs47660517 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39422232 | ATGCAAGCATTTTCT[A/C]TTCGATTGAAAGAGA | 14360 |
rs47662357 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39476413 | AGAGACCCTGTCTCC[A/G]ATGACGTAGAAGATA | 14360 |
rs47667345 | snp | C/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559994 | TTTGGTTGGTTGGAA[C/G]ACAGCTATTCTGTTG | 14360 |
rs47669952 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39511432 | GGAGTGTCTGGTAAA[C/T]AGTCCTGGGGCTGCA | 14360 |
rs47671709 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489524 | GCTGATAAAAGAAAC[A/G]CTGAGCAGTAGGGTG | 14360 |
rs47672011 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Fyn | GRCm38.p3 | 10:39545856 | GCTACAGAAGCTGCC[A/C/G]TTTACAAGGATTAAT | 14360 |
rs47672746 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39464544 | TGAGGTCATGCAGCA[A/G]CTGAAGGAAGAGTGG | 14360 |
rs47697700 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437244 | GATAATTCAATGGCT[A/G]CTTTTATAGGTACCA | 14360 |
rs47705572 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39416974 | CTTGCGACTTGATAG[A/G]AATAAGATAGGAACA | 14360 |
rs47706165 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39519305 | TTACCAGGTACGAGT[G/T]AATTAAAAAGCTGAA | 14360 |
rs47709093 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39546613 | GTGGAGAGAAGAGTC[A/G]GGAACACTGAAGCCC | 14360 |
rs47712575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39427700 | AGGCTCCTTCCCGAT[A/G]TCCACCAAGGGATTC | 14360 |
rs47713043 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39502416 | GTGTGTTTGCTTGTG[C/T]CTATGCCAGGTGACA | 14360 |
rs47717941 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39435556 | ACAAAAAGAGAAACC[A/G]AGTATTGGACTGTAA | 14360 |
rs47732874 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39379555 | GGCAGAGGAAGCAGA[A/G]CCTCACCTACAGTGG | 14360 |
rs47733561 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39532414 | CTGCACAGTTAAAAC[A/G]TCCATCTTTCTATCC | 14360 |
rs47733895 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381540 | AGTTTAGTATTGATT[C/T]GACTAGTCAAGCGAT | 14360 |
rs47738514 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39503985 | CCTGTCCCCCTAAAG[C/T]GCATCGCAGGCATCC | 14360 |
rs47738943 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Fyn | Mm_Celera | 10:39540703 | TTGTTACTGGTTTAT[A/G]TATTAAGTAGAACAA | 14360 |
rs47741052 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545485 | CGTGTGTCAGATGTG[C/G/T]GGCACACAGAGCTAG | 14360 |
rs47741905 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500160 | TCTTGTTCAGGTGTC[A/G]TAATTCATGGTTGTT | 14360 |
rs47743780 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39393018 | GTGCTTATGGCTGTA[A/G]ATTCATAGACTCGTT | 14360 |
rs47745646 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39398470 | ATGTGGAGATAAGAT[A/G]GCCATTCTTTGGCTT | 14360 |
rs47747744 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39487790 | GTCAGTTAGGTGAGC[A/C]GAAACATCCCTGTCT | 14360 |
rs47749167 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39540781 | AATAGATTATTGTCT[A/G]GAGTAAAATTCACTT | 14360 |
rs47752088 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39448813 | AAGATATGAACTTAT[A/G]TTGGTAATGGTATTG | 14360 |
rs47763498 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Fyn | Mm_Celera | 10:39477575 | TGTATTTCTCATGAT[A/T]TGCTTTCCATGTGGG | 14360 |
rs47765674 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39462734 | GGTCCAGCCTGCTTT[A/C]TCTAGAGTTGCGCTG | 14360 |
rs47779972 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39543238 | GTTTTCCTCTGCCAA[A/G]TTTGACCGGGTTTGA | 14360 |
rs47781236 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39501616 | AAGCTGAGTGTGTTT[C/T]CCAACTGCCTGGTTT | 14360 |
rs47786473 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39517732 | AGGGGCGTTTGCCTT[C/T]GATCTCTTCCCGTTT | 14360 |
rs47788168 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39502637 | AGTGAGAAGTGATGT[A/C]TCCAGCAGACCTTAG | 14360 |
rs47793217 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39536712 | TCTGTTACAGGTCTT[C/T]CATGTGTCTTTGTCT | 14360 |
rs47796402 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559019 | ACATTTATTTACACC[A/G]TGCAGTTGTCCCGAT | 14360 |
rs47814180 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39382347 | AGTGCTTACAGAGAT[C/T]TGGAGAAGCCTAGAC | 14360 |
rs47817827 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39517784 | GAGTCTCAGATGAGC[A/G]CTGCTTGTCAGAGTC | 14360 |
rs47823381 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | GRCm38.p3 | 10:39472082 | GTTTTGCATAGCACA[C/T]ATTCAGCTTGTTGTT | 14360 |
rs47835590 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453550 | TTTACTGGGGCATTT[C/T]CTTTATTATGTAATA | 14360 |
rs47839118 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39460164 | CACAAGTGGAGCCAG[A/T]TGCACACTCATGATT | 14360 |
rs47840263 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39424240 | TGACGGACTGGGAGG[A/C]GATTGCTGCTGAAGC | 14360 |
rs47840556 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39544596 | GTATCTGCAGAGCCT[A/G]ATTTCTACATGACCA | 14360 |
rs47868681 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381876 | CCCTTGGTTCAAGCA[C/T]TTATAAATATTTTGA | 14360 |
rs47874199 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39433052 | GAAAGGGACTAATTC[A/G]GGGAGTGAGAGAGAT | 14360 |
rs47875556 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39536893 | GTAATGGCCTGGACA[C/T]TTCAAAATAAGAACT | 14360 |
rs47875824 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, LOC105245135 | Mm_Celera | 10:39533584 | ATACAGCCACTATTG[A/G]GAATCTTTGCCTCTC | 14360 |
rs47886464 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39491712 | ATCTTCAATACTGTG[A/G]TCTTCCTGCACCCCT | 14360 |
rs47888975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39434719 | GGATTAGATGTTAAG[A/G]GTCCCTCCGACTTGC | 14360 |
rs47890530 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39507447 | TCTAGCAGTTATGTG[A/C]GGAAAACTCCTAATC | 14360 |
rs47893122 | snp | C/G | | | intron-variant | Fyn | Mm_Celera | 10:39507330 | AGGAACAACCCATTG[C/G]GCAGGATGGAAAGGT | 14360 |
rs47911265 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437766 | AGCAGATTCAGGTTA[A/G]ATGATGACAACCAAA | 14360 |
rs47923234 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39454975 | GGTGCCCCAATCGAT[A/C/T]GATCGGTAGGTGAAG | 14360 |
rs47926760 | snp | A/T | | | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528534 | TCTCAGAAACAGATT[A/T]AAAAAAAAAAAAAAA | 14360 |
rs47930027 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39421497 | AGCCTGGTGGCAGAG[A/C]CCAGTCGCTTCCAGT | 14360 |
rs47930577 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39501636 | CTGCCTGGTTTATCA[A/G]CATTCACACCAATCT | 14360 |
rs47931845 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39438292 | TAAGGTGTCTGTACG[C/G]TTACAGTGGGAGTCA | 14360 |
rs47932167 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39397857 | CAGTCGTCGGTTGAC[C/T]GGTGTGCCCTGTGCA | 14360 |
rs47934623 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39478431 | TTAAGGCAAGCTCTC[A/G]GGGAAATATCCTGTT | 14360 |
rs47941732 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39482988 | GCTGCTGCAATCTAA[G/T]CACCTAAGACTTGAG | 14360 |
rs47951854 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39492714 | CACCCTTAGTGGATG[A/G]CATCTCCTATGTTGA | 14360 |
rs47954153 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553670 | GTCCTGCCTGTCACC[C/T]GGAAAAGCTGCAGAG | 14360 |
rs47965248 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39458313 | GATTGCTAAGCACTT[C/T]TGTAGCCCAATATGG | 14360 |
rs47970431 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39430776 | ACCTGTAATATAAAT[C/T]CTTGGACCTTAATGT | 14360 |
rs47973273 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39477748 | AAAGGAAAACCATAT[C/T]GTCATAGTGCTTATA | 14360 |
rs47994837 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Fyn | Mm_Celera | 10:39520086 | GCCTTATAATGTGTG[A/G]CTGTTTGTCATTTGT | 14360 |
rs47997869 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39490209 | AGGCCCCATTAGGGT[C/T]TTACCTCACACAGGT | 14360 |
rs48001852 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39396564 | TGCACTTTGGTTTGA[A/T]GTCAGGAGTTGAAAG | 14360 |
rs48003243 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39547347 | AGCTGGACAGCTAAC[A/G]CACTGCCCAGCTCTG | 14360 |
rs48007711 | snp | A/G | 0.152778 | 0.230321 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39558028 | GGGCCAAAGCACTGC[A/G]GTACACTGTGTTCCT | 14360 |
rs48009936 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39530782 | TCTTAAGCCATTACA[A/T]AAGCACCAGGGTGTT | 14360 |
rs48010281 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39495612 | CAGTATCTGCCCCAC[A/G]TAGGCATCTTGCCAA | 14360 |
rs48010539 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39490719 | ATGGAGAGGACCCAA[A/G]CACAGTGTAATACAG | 14360 |
rs48018262 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39380315 | AAGGTTGTATTAAAC[C/T]ACAGCAAGCTGTGCA | 14360 |
rs48027026 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39492247 | AGGATTGTGGGAGCC[A/G]AGGCAAATCTGATAA | 14360 |
rs48030823 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39492678 | TGTGATTGTTTCACT[A/G]GCCGTTTTCCAATCA | 14360 |
rs48031266 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39499687 | CTGTGGGCTCCATGG[G/T]TTTGTTTGAATCTAT | 14360 |
rs48032420 | snp | C/T | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557582 | CCAAGCCGTGGCCCT[C/T]GACTGAACACCTGCT | 14360 |
rs48040548 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39464847 | CTTGTTCATCTCACA[A/G]TGTCTTTTTAGTGGC | 14360 |
rs48041245 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39545721 | CTACAGGAGCGAAAC[A/G]CAAACTAACCTGGAT | 14360 |
rs48043866 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39382323 | ACATCTTTGCCTGGG[C/T]TAGTGAGAAGTGCTT | 14360 |
rs48049256 | snp | A/T | | | intron-variant | Fyn | Mm_Celera | 10:39439591 | GAGCTGGAGTTCAGG[A/T]GGCTCCGAAATAAAG | 14360 |
rs48059882 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39461879 | ATAACCTAGTGTCTC[A/C]TGGCCTCCTTGCATG | 14360 |
rs48061872 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39480776 | TATGTTCCCTTTATC[A/C]AAAGCAGCTTAGGGG | 14360 |
rs48064085 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39435375 | CAGCAGCGTGAGTCA[C/T]GTGTGGATTGCCAGA | 14360 |
rs48066856 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39399674 | ACACATGTATTCGGG[A/G]CTGCCCCATCCAGGG | 14360 |
rs48072127 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39390626 | GGTTAATTGTATATA[A/G]GTTCAGTTTGTGGGG | 14360 |
rs48076558 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Fyn | Mm_Celera | 10:39476522 | CAGATTTTATGTAGG[C/T]GTTTTACATTTGTAA | 14360 |
rs48079732 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39507972 | AGAGCTAAGTCTAGA[G/T]CTGTCACTTCTCCAT | 14360 |
rs48090496 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453010 | CCATACTTATCACGT[A/T]TGCCCATGTAGGCAT | 14360 |
rs48096344 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39483270 | AAGAAACTCTCAACC[A/G]TATTTGGATCAACTG | 14360 |
rs48098371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39546445 | GAACAATAAATTAAG[C/T]TTACAGTTGCTGTAT | 14360 |
rs48106721 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39523632 | AAAGGAGTCACTGTC[A/G]GTTGCTCACGGCCTG | 14360 |
rs48107458 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39538338 | CTCTAGTCCACAATC[A/G]GCCCCAGAGAGGGCT | 14360 |
rs48114242 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39400709 | AGGGATTGTTTTATT[A/G]TATTTTCATCTCAGC | 14360 |
rs48114487 | snp | C/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554574 | GAAACTGAACAAGGC[C/T]TTGAAGCCGTAGAGG | 14360 |
rs48123835 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39475968 | TGTGTATGTCCCTTT[G/T]ACTGTACTTTACTCA | 14360 |
rs48134152 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39442771 | ACATGGAAATTAAGT[C/T]ATGATGAGAAGTTGT | 14360 |
rs48135493 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39504464 | CAATAGTGTTCCCTC[A/G]TTTCCTGCCTAGTTG | 14360 |
rs48159012 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39504284 | CACAGTACTGTAGGA[A/G]CAAACTCATTTCAAG | 14360 |
rs48163420 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39404297 | TTGTGGTAGTGGCCC[A/G]CTTTGAGCTGTGAGT | 14360 |
rs48171225 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39384072 | AAACCGTCACTTATC[C/T]TGAATATTTGTGCAT | 14360 |
rs48174190 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39378017 | AGGGTCTGTACATCC[A/G]TGACAGCCTGTCCCG | 14360 |
rs48184713 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39429815 | AGTATCCCTCTGTTG[A/T]TGTATGTCTAAAACT | 14360 |
rs48200415 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39438592 | GATGTGATCAGGTCT[C/T]TCTTTAAGCCATGCA | 14360 |
rs48207885 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545945 | TGAAGGCTAGGTACC[A/G]AGGCAGGAGGACTCA | 14360 |
rs48210069 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39438989 | CAGGTGTCTCCGCCC[C/G]TGCAGCCTTCGCTTC | 14360 |
rs48220346 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39433207 | TGGTGATGGCCTTCT[C/T]ACCATCGTCTGCTAA | 14360 |
rs48220436 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39525695 | GAGGCGCCTCCAGAA[A/G]CAGAGGCCAGGCTTC | 14360 |
rs48228561 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39439812 | AGAATCTGAACTTGT[A/G]AAAACGGGTACTTTG | 14360 |
rs48229022 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39422954 | ATTTCGGGTTGTTGA[A/T]TATAGTTTTATATCA | 14360 |
rs48231482 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545960 | GAGGCAGGAGGACTC[A/G]GCGGGACTGGTGACT | 14360 |
rs48232782 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39470830 | TATCCAGAAACTGCT[A/C/G]CCTACCTATTTGACT | 14360 |
rs48235590 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39465069 | GACCTGGAGCCTGTC[C/T]CTGAATCTCTCTAGG | 14360 |
rs48255674 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39377926 | ATGGAAAATTTAAAA[C/T]GAGCCAGTTTTTCTT | 14360 |
rs48260066 | snp | A/T | 0.18 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39491782 | GTGTGTGTTTGTATG[A/T]GCATGCACACATACA | 14360 |
rs48264386 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39461640 | CTCGTCTGGTTGTGT[C/G]TGGTGTCTGCATGAG | 14360 |
rs48265499 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Fyn | GRCm38.p3 | 10:39379426 | CACTGCAGAGGGACG[A/C/G]GCAAGACCAGGGAGG | 14360 |
rs48267994 | snp | A/G | 0.142012 | 0.225474 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557439 | TGCCCGGTTATCCTC[A/G]CATATGGCCAACACG | 14360 |
rs48278661 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39420954 | CTAGTTCAAAAGTCC[C/G]GCCTGAGGCTGAGAG | 14360 |
rs48279156 | snp | C/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554690 | GCAACGCACAGCTCG[C/T]CTGCTGCAGCCCTGT | 14360 |
rs48279277 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Fyn | Mm_Celera | 10:39511983 | TGGGACCCTACGCAC[A/G]AGAGGAGGGACAGGT | 14360 |
rs48280658 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39417407 | CTGAGATTGTGATTG[C/T]TGTCCCAGGAGAAAG | 14360 |
rs48283725 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39421352 | CATCAAGGCCCAGAG[A/T]CGTGTCCCATTGCTG | 14360 |
rs48284937 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39454878 | TCTTATTAGTGTACG[C/T]TAAGATAATTCATAA | 14360 |
rs48289646 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554144 | AGTCCAGGTCTCTGT[G/T]TATCAGATGCTTCCA | 14360 |
rs48293178 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39430336 | GACACACTGTGCACT[A/G]CTGGGTTTACTGTAT | 14360 |
rs48304439 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39488968 | TACCACCTGGACTCG[A/C]TCTACTGAGAAGAAC | 14360 |
rs48308192 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39501866 | GGCTGTTTCCACAAC[C/T]GTGCTTCCGAGCAAA | 14360 |
rs48311772 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39458773 | GAGAGGCTGTAAAAG[A/G]CACTGTGCTTTACAT | 14360 |
rs48318956 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39532305 | TCCACTCTGCTCACT[C/T]AGGATAACACTTAGA | 14360 |
rs48322382 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39533769 | GACTCTCAAGGTGTT[G/T]TGGTGTAACAGCTGT | 14360 |
rs48324160 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39502402 | GCCGCTTTGTTCTAG[C/T]GTGTTTGCTTGTGCC | 14360 |
rs48331782 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Fyn | GRCm38.p3 | 10:39418207 | CCCCAGCCTTTAGGA[C/T]GTCTTAATACTGAGG | 14360 |
rs48337487 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381364 | TGTGCTGTGACCACA[C/T]GGATCCTGGGCAGCT | 14360 |
rs48340575 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550345 | AGTGCAGAATGAAAA[C/T]GTCCCAGGAATAAAG | 14360 |
rs48345077 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39427574 | AGGTCCTTGAGCATG[A/G]TCTCTGGACATCAAA | 14360 |
rs48347556 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39466446 | TTTCTGTAGCTGTCT[A/G]TCCAAATTACCCTTG | 14360 |
rs48350246 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39457816 | GAGCCAGTAAAAATA[C/G]TGAAAGTGCCTGTTT | 14360 |
rs48356041 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39450349 | TCTAGGCTATAAATC[C/T]TTCCCAGATGACAGG | 14360 |
rs48361756 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39380957 | GGTGAGGGGTGCCTG[A/G]GAAGCAGCTGAGACC | 14360 |
rs48374735 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon | Fyn | Mm_Celera | 10:39551460 | AATCAAGTCTGACGT[A/G]TGGTCTTTTGGAATC | 14360 |
rs48378508 | snp | G/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, LOC105245135 | Mm_Celera | 10:39533534 | TGATGCAATTATCCT[G/T]TTCATCTCCCTTTTA | 14360 |
rs48379188 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545460 | CTCAGCTGAAGAACA[A/G]AAACGTCTGCGTGTG | 14360 |
rs48389224 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39432797 | CTGTACTGTTGCTGC[A/G]CTGCCTTCACAAGAC | 14360 |
rs48389360 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39482960 | TCATTAAAGAACTCT[C/T]GAGCTCTTCCATGCT | 14360 |
rs48390867 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39505822 | AAGGAAACTTTCCGC[G/T]ACCGCCTCCCTCGTG | 14360 |
rs48392291 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39439114 | GCAGAGCTTGCTCCC[A/G]CCTGTCTTTCCTGCC | 14360 |
rs48402394 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39471524 | TTAGGCTTAGCCCTG[C/T]CTCCAGCAGCTGATG | 14360 |
rs48405371 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39562173 | TGTTGAATATTATGT[C/G]GATTCCTTACTAGTG | 14360 |
rs48405710 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39545333 | CTGCGCTGTGCTCGG[A/C]GCTACACTCAGCAGC | 14360 |
rs48406648 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39514468 | CACTGGGAAATGTGC[C/T]GAAATTAAAACAAGA | 14360 |
rs48408857 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39459111 | TTTAAATGGTGTGGA[A/G]AAGCAGAGACATGCA | 14360 |
rs48410179 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39495252 | GAGCCTTGGAGTGGC[A/G]TGATCCCCACCTGAC | 14360 |
rs48413634 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39423291 | TGAACAAAAATTACA[C/G]AAGTATCCAACATAC | 14360 |
rs48416570 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39449082 | GTCTTCCTAGTGCTC[A/G]AAATAAAAGGAGCAG | 14360 |
rs48417821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39401980 | TGCAGCTAATGTAAA[A/G]AGAGCCTAGCCTCCT | 14360 |
rs48436927 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39380017 | GGACAGCTGCAGAAG[C/T]AAAGGGAGTGTGCCT | 14360 |
rs48440395 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39423652 | TTAAGTTTTAATTTT[A/T]TTTCTCCTAAAGAGA | 14360 |
rs48448758 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39485913 | AGTTGACATCTTTCT[C/T]TTAAGACCCATTTTC | 14360 |
rs48455305 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489793 | TGGAAAAGAAGCAAT[C/T]ACTGGTTTCTAGTTT | 14360 |
rs48460374 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378768 | CCGTTTGTCAAGGCC[C/G]AATTAGAATCCCAGT | 14360 |
rs48464382 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560937 | CCCATGGGAGCAAAT[A/G]CACATTGGAATCAGA | 14360 |
rs48472099 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39379891 | CTAAGAGTCTTCTGA[A/G]CCACCTGTGAGCTGC | 14360 |
rs48475567 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39419299 | AATCTCTGCCTTATG[C/T]ACCTTATGCTGTAGC | 14360 |
rs48477050 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39472376 | GTTTGGCTGCTGGTG[G/T]CAGGAGTGACTTGGT | 14360 |
rs48480751 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39503633 | GTGATCACCCATTGC[A/G]TCCTCAGGTTTGACA | 14360 |
rs48485430 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39507437 | TAAATGAGGCTCTAG[C/T]AGTTATGTGCGGAAA | 14360 |
rs48487786 | snp | C/T | 0.152778 | 0.230321 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559795 | AGAGGAGAGCTGAGA[C/T]CAAACTGGGTAACGG | 14360 |
rs48496406 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39515228 | CTACCTTGTGCTAGG[A/G]ATGGAAGAGTGATCC | 14360 |
rs48497197 | snp | A/C/T | 0.336735 | 0.234472 | intron-variant | Fyn | GRCm38.p3 | 10:39383803 | GCCCATCTCAATCCG[A/C/T]AATGTTTTCCCTTAT | 14360 |
rs48504961 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39426603 | GTATCTATCTAATCT[C/T]GAGGCACTAATAGTG | 14360 |
rs48526260 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39500720 | CAGTGTGCCACACCC[C/T]TTCTCCTGGCCTCTT | 14360 |
rs48526661 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39510560 | TATGTCTGAGTTCTC[A/G]CTTCTCACCTACATA | 14360 |
rs48530751 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39531820 | GGGAAAAGTTAGTGA[A/G]TTATTAAACAGCTGT | 14360 |
rs48542993 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39494801 | GGTTAGCTCTGCCAG[A/C]AAGAGAACACTTCAG | 14360 |
rs48547175 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39464338 | TTAGACCATAATCAC[A/G]GTGTGGAGAGGAGGC | 14360 |
rs48562451 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39544133 | TCTTTCCAGCTTTTG[A/G]AAGTTTCGAAGGGCA | 14360 |
rs48563114 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39558872 | TTTAAGAGAGCTTAT[A/G]CAGGGAAGCAAGGGG | 14360 |
rs48567755 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39552563 | CTCTAAGGGAGGAAG[A/G]TTGGCACTGAGGCAG | 14360 |
rs48574603 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39551193 | TTTGAAGAAAGATTT[A/C]AAGTTATTTGCTTAA | 14360 |
rs48580154 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39458202 | GCTGAGAGAGGGGAC[A/G]GGTCTCGGTACAGTT | 14360 |
rs48588800 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39421209 | TTGAGGTCATGTTCT[C/G]TGCTATTTATTTGCA | 14360 |
rs48590562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39397586 | TCAAGCACCGTGTAC[C/T]AGCTCTTGCTTTTGC | 14360 |
rs48596987 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453391 | CCAAACTAGGAAGAT[C/G]AATGAAACAATGGAA | 14360 |
rs48600082 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39397412 | TAGAGGTAGGAAATA[A/C]CTTTGTAGATGTCAA | 14360 |
rs48612273 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39505688 | TCTACCACAAGTACA[C/T]ACGTCTTTTGTGTTT | 14360 |
rs48619337 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431204 | AAAATAAGAGACATC[A/G]TGGAAATGAGAGAAG | 14360 |
rs48629972 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39437794 | AAACATGTGGCTGCT[A/C]TCAGGAAGGCTGTCT | 14360 |
rs48632882 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39445901 | ATGACCCACGTTGTA[C/T]GTCAGAACTCATTCA | 14360 |
rs48640831 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39472125 | GAGCCTTGCTTATGG[A/C]TCTCTGTCCTTGTTC | 14360 |
rs48645200 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39536928 | CTTGTTTAGTCATAA[A/G]CTCTGCACTAAATTC | 14360 |
rs48646660 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39399338 | AGTTTCAGCAAAGGA[C/T]TTTCTAAGCTCGGAT | 14360 |
rs48650632 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39541124 | AATGCAGTTCCTGTC[C/T]TTCCTTTGTTCTGAT | 14360 |
rs48656078 | snp | A/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39552977 | TTTGCATTTCCGTGA[A/T]GCTTTCTCTTACAGT | 14360 |
rs48663865 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39406553 | TGGCCTCTAAGAAAA[C/T]TTTCACAACAGCCAC | 14360 |
rs48668394 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39382405 | AGGGATTCTTCTAAG[A/G]GGCCATTCAAGATCT | 14360 |
rs48670704 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39508724 | AATAGTTAGTACACT[C/T]ACTCCATGTTGGTGG | 14360 |
rs48672331 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489106 | ACTTTTCCACTCACT[C/G]TGCCCTGCTCCTTCT | 14360 |
rs48675842 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39564728 | CTTTTTTCAGGTCCC[A/G]GGGCCTAGTCACGAG | 14360 |
rs48682264 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39387802 | TTTCCAGTCAGGCTT[A/G]TACGCCACACTCTGC | 14360 |
rs48688553 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Fyn | GRCm38.p3 | 10:39476342 | TTGACCAGGAAGTGT[A/G/T]ACTTGGAAACTAAAT | 14360 |
rs48693761 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39400893 | TACTGTCTGATTTCT[C/G]TGTGATAGAGGTTGG | 14360 |
rs48694516 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39443664 | CCTTCTGCAAACCCA[A/G]CAATTACTTTAGCTC | 14360 |
rs48699678 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39417574 | ACATGTCTTAAATCA[A/G]ATCTCTTTCCATTTT | 14360 |
rs48700915 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39377140 | GGGGTGATTTGAGAG[A/G]GTGACACACAGCATT | 14360 |
rs48705091 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39453286 | ACTGATTGATTCAGA[C/T]AGTATTGATGACTGC | 14360 |
rs48711044 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39458178 | AGTGATTCTGGGGGA[G/T]GAAGGTGTGCTGAGA | 14360 |
rs48711133 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39544935 | GGCTTGGAGTGGCCC[A/G]TCCTGATGTGACTCT | 14360 |
rs48713384 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39422777 | TTGTAATCCAAAAAG[C/T]ACTGAAAAATCGAGA | 14360 |
rs48713472 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39432278 | TGTTAACAGAACTCG[A/G]CAGTTACCTGTAGCA | 14360 |
rs48715279 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39542654 | AGTGTGGCCTGGCGT[C/T]GCCCAGGTCCCTCTG | 14360 |
rs48720250 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39487688 | AACTTTGAATCACAG[C/T]GGACACTCAGTCACA | 14360 |
rs48721316 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39488744 | CTTTGTCCCTAAACT[C/T]GACTCTGGTAGAATG | 14360 |
rs48726768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39389107 | CGAAGCATGAGAGAC[C/T]GCTGGCCATCTTTGC | 14360 |
rs48728867 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39411288 | GCCAGTTCACGCAAC[A/G]TAGCAGGACCCTATC | 14360 |
rs48729444 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39444957 | ATGCTGGAAGGACAT[C/T]TTGAGTGTTTTCTGT | 14360 |
rs48734133 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39423399 | TTAAATTGACTTCCC[C/G]ATCACCTAGGTCCTT | 14360 |
rs48740646 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39547613 | CAAAGTCTTTAAGCA[A/C]GTAGCACTCAGGCCA | 14360 |
rs48741102 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39458143 | CTGGGCTGGTCCTTC[A/G]TTTTGAGTCAAGGAT | 14360 |
rs48742087 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39421285 | GTAGACAGTGCTGGG[A/G]AAGAAGGCACATGAC | 14360 |
rs48743900 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39398247 | TCTGTGCTAAACCTG[A/T]TGCCTAAATCATAGC | 14360 |
rs48752392 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39512368 | AATGCCTGGCTTCTC[A/G]GGAGCAGGAGACCTC | 14360 |
rs48760091 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Fyn | GRCm38.p3 | 10:39462829 | CTCCACCCTTCTCCC[A/C/G]GTTAACAGATTAACC | 14360 |
rs48762257 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378127 | TACTGACAAGGGTAA[A/T]ATTTGGTTCTTGTTT | 14360 |
rs48766147 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557265 | GTTCTGATTCCCAGC[A/C]GTGTCTGCCCACAGT | 14360 |
rs48766345 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39434760 | TAGAGTGCAGCCATA[C/T]ACTGGGGCAGTGGGA | 14360 |
rs48766491 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39507141 | TGCACAATGCAAACC[C/T]GGCTGGATCTTTCCT | 14360 |
rs48777717 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39429273 | GCCTTCAATTCTAGA[C/T]TCCTTGTAGAGCAAT | 14360 |
rs48778272 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39395622 | GGGACCCACTTAGGC[A/G]ATAAAGTGTGATGGA | 14360 |
rs48784801 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39397697 | GAGGAAAGCCACTGC[C/T]GGCCTGGTGTTTGCT | 14360 |
rs48785358 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39503798 | CTATTGTGCCTTCCA[C/G]AAGTTGCCTCTTAAT | 14360 |
rs48802095 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39507431 | GCTGCCTAAATGAGG[C/T]TCTAGCAGTTATGTG | 14360 |
rs48804873 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39422722 | CACTTAGAGAACAGG[A/G]CCACTGACAACCAAG | 14360 |
rs48809481 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39379080 | CAGGTCAGAGGATGC[C/T]GCTTTGGACAGACCC | 14360 |
rs48822966 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381188 | TCTTGGCCCTGCCCC[G/T]TCAACAGTTGTTTTT | 14360 |
rs48823614 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39519142 | CTCCAAAGTATCTGG[A/C]CTTCCAGCACCTGAA | 14360 |
rs48839425 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39515423 | AGACCACATTATAAA[A/G]CCAGCCATGTGACTA | 14360 |
rs48841264 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39396801 | ATATGGAGCTTAAGA[A/G]GAGTTGAGGGAAGGG | 14360 |
rs48842680 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39474459 | TCATACTGAAGTTTT[C/T]CATACTTGGCAGTTT | 14360 |
rs48849329 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39472838 | TTTCACATTTTATAT[C/T]TTGTGAAAGCTCGTC | 14360 |
rs48851727 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39435716 | TGGCCTCATGTTCTG[A/G]TTTTACTCAGTGATA | 14360 |
rs48853542 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561782 | TTGAGCTCGTTGGCT[C/G]CAGGGAACACCCAAC | 14360 |
rs48853792 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39394328 | GAGCCTACAGAGGGA[A/G]GCACTGACTCTTGGG | 14360 |
rs48860188 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39424975 | TGGCAATGGCAGCAT[C/T]GACATCTTTGGGAAC | 14360 |
rs48861754 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39381441 | CTTGGAGGGTTTCTG[C/T]GGTTCCCCTTAGGGC | 14360 |
rs48869766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39459765 | TATTTTCAGAGTCAG[A/G]AGCTGTCATGTATGT | 14360 |
rs48879101 | snp | A/G | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554463 | TAGAGGCGTGGCCAG[A/G]TGAAGGGCAACCTAG | 14360 |
rs48880012 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39477846 | CCACCAGAACTATTT[A/G]CTGTCTAGGTATCTC | 14360 |
rs48884671 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39460145 | GGGCTAGGTGAGCAA[C/T]GAACACAAGTGGAGC | 14360 |
rs48889152 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39536947 | TGCACTAAATTCTGT[C/T]CATCTGGAGTCGCTT | 14360 |
rs48890003 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39484734 | TGTTCTGTTTGTTCA[G/T]GCTTGGTCTTCGCCT | 14360 |
rs48896335 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39425384 | ATTCATAAACTCTAA[A/G]CCTCTTTTATGAAAG | 14360 |
rs48916705 | snp | G/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418202 | TCAGTCCCCAGCCTT[G/T]AGGACGTCTTAATAC | 14360 |
rs48924891 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39514559 | AAAATTAACAGCTTA[A/C]ACAGCACATACATTT | 14360 |
rs48933139 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39552824 | GGATGAAAATATACC[A/G]TCTCCAGGTTTTAAA | 14360 |
rs48937978 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39452871 | TTCCAAGTGCTGCTA[A/T]CTGGCCTGGCCAACA | 14360 |
rs48946415 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39462860 | ACTCTAGGCGCAGAG[C/G]CGCAGCTCCCTGCCA | 14360 |
rs48951528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39377097 | CTTTTACAACGCCAT[A/G]TAAGCCTTTGGCAAA | 14360 |
rs48964513 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39481843 | TACTGGATAATATTG[C/T]TTAAGCCCGTTTTTT | 14360 |
rs48965388 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39549432 | CAAAATGACTGCTCA[A/G]AGAATCCCAGATCAT | 14360 |
rs48978057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39472933 | CACCATTGTGCAGTA[C/T]GCTCAGATAACCTTA | 14360 |
rs48978135 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437171 | GGCTGAGATCCCAAA[G/T]GTTTGACAGGTCATA | 14360 |
rs48979611 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418234 | GAGGTAGCACTCAAA[C/T]ATGTTTTGATTTTGC | 14360 |
rs48987665 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39465019 | AAGGACATGGCGAAG[A/G]CTTTGGGCAGATAAA | 14360 |
rs48993767 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39520772 | TGGGCTCCTGGCCTT[C/G]TGTGCACTAGGCAGG | 14360 |
rs48994991 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39425751 | CCCACATGGGCTAGG[G/T]TGAGAAATGAGGGCT | 14360 |
rs48999472 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39447057 | AAATAAATAAATCCC[A/G]CTGGCTCCAGCTCTC | 14360 |
rs48999977 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39394274 | GGGTCATCTTGGGGC[A/T]AGCATGCAGCAGACC | 14360 |
rs49013403 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39399371 | TTAGCAATGATGGTA[C/T]GGCTCATCCAGAGGT | 14360 |
rs49015594 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39511066 | AAGAGTGAAGTAAAC[A/G]GAGCAGCCCTGAGGA | 14360 |
rs49020212 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39406193 | AACTTTGAAGAGGAG[A/G]GAGAAGTCTGGGGAG | 14360 |
rs49021593 | snp | G/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39558651 | ACCCTCTGGTCAGTA[G/T]CCCTCTGCTCCACAT | 14360 |
rs49022116 | snp | G/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39418346 | TGTTTTGCCATTTTG[G/T]AGCCAGTCTCTTGGC | 14360 |
rs49026054 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39400821 | AGGCCTCAGCTACTT[A/G]GGTCTATCTGTTTTG | 14360 |
rs49030210 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39517314 | TTTTACCACAAATTT[A/C]AAGGACAGAATTTAC | 14360 |
rs49036628 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39459331 | GGCTCTGTAGAAGGT[C/T]GGAGGCACGGAACGG | 14360 |
rs49036868 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fyn | Mm_Celera | 10:39451239 | TCCATGTGACTTCTC[A/T]GGAAGGCAACCAGTG | 14360 |
rs49044730 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39560024 | GCACTCGTCACTCAG[C/T]CAGTTGCAGTGTCTA | 14360 |
rs49050087 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39466360 | TAGCAGAAGATGAGC[A/G]CATGCTGAGCCTGCA | 14360 |
rs49052662 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39537522 | AAAGAGCCAATTACC[A/G]TTCAGGGTTAAAAAA | 14360 |
rs49052747 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39376542 | TGTTGTGGGCCTTTA[C/T]GCTCCTCACCATTTT | 14360 |
rs49057773 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39532657 | CATGCATGTGTTGAC[A/G]CACACGTGAGCATGC | 14360 |
rs49061642 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39500933 | GCTGCCTTGGCCTCT[A/G]GAGTGCTGGGATCAG | 14360 |
rs49075756 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39386216 | CCAGGCCTGGTGGGT[C/T]GGTGGCACCGTAACA | 14360 |
rs49078450 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528190 | ATGGAGCAGAAAACC[A/T]CCTTGCACTTCAGTG | 14360 |
rs49084986 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39528703 | CTTACTCTCTGTTGG[C/T]GTTTAGTCAGTCTCC | 14360 |
rs49085469 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39379303 | TTGCCTTTCGCTGAA[A/C]ATTTCGGATGGTCAA | 14360 |
rs49096134 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39445594 | GGTGTTCTTAAATAA[G/T]AAAGGTTGGGCTTTA | 14360 |
rs49099103 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39564806 | CTTAGGAGTGAGCAT[G/T]TTAAGCAAAAAGCAG | 14360 |
rs49100163 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39441543 | ATGTAAACAGCCGTT[C/T]ACTACACTCTTACTA | 14360 |
rs49114968 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, LOC105245135 | Mm_Celera | 10:39527350 | GGAAGCACATTCTTG[C/T]ACTCTGTAGAAGAAA | 14360 |
rs49116078 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561200 | AGAGCTGGGCAGATA[C/T]CTACCATCTATGCTA | 14360 |
rs49144300 | snp | A/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39493724 | AAGGAGCCACGGAAG[A/T]ATTCAAAGATGACTG | 14360 |
rs49150001 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Fyn | Mm_Celera | 10:39526695 | GGTTTGTAATAATTA[G/T]TAATCAGAATAGTCA | 14360 |
rs49164525 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39507498 | GGATTCACTGTCTGC[C/T]GAGAATCTAGTAAAG | 14360 |
rs49165528 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39429923 | CCACACACATCAGTT[A/T]CTGCTGGACACAACT | 14360 |
rs49173999 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39406433 | GTGGGCATGCCCAGT[C/T]CTCTCCTCACCAGGT | 14360 |
rs49186048 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39450899 | TGGGAATCAAAATGA[C/T]ACTGAAGCCACATGT | 14360 |
rs49188514 | snp | G/T | 0.18 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39477510 | ATCCTTATTAATCTA[G/T]CAGGTTCTAAAGGAG | 14360 |
rs49189006 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39496324 | CAGATTCATGTCTAG[G/T]AGTAGAATGGCCACA | 14360 |
rs49191823 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39427931 | ACGAGGCCCCATGTC[A/G]AGCCTTGCCAGCCTC | 14360 |
rs49195227 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39473992 | CATGTGACTCTGGTA[A/G]TGAGTAGAGTTTGGA | 14360 |
rs49195411 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39537084 | TCCTCTGGGGACTGA[A/G]GAGGGAAGATCTCAT | 14360 |
rs49204153 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Fyn | Mm_Celera | 10:39470646 | TTATGTAAGACTCCA[C/T]GTGATGTCTTTCCAC | 14360 |
rs49209250 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39518311 | TTTGTACAGCAAAAC[A/G]ATATCCTGGAGTCAA | 14360 |
rs49224430 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39505371 | CAGGTGCCGGGAATG[C/T]GCCTCTTTTCTGCTG | 14360 |
rs49227324 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39494747 | GCCTGTCTCAAGGGG[C/T]CAGGAAGTCTCTGGG | 14360 |
rs49238685 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437540 | CATACCTGGTGAGAA[A/G]CCTAAGAGTTTTACA | 14360 |
rs49246160 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39440776 | GGTCAGGTGCAGAGG[A/G]CCAGTGTCAGCCCTG | 14360 |
rs49246178 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39377632 | ATAAAGCAAGCAGAG[G/T]TCCAGCTCTTGTGAT | 14360 |
rs49252258 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39489494 | TTGAGTCAAGTTTTT[G/T]ACCCCAAACTTGAGG | 14360 |
rs49252847 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39536865 | AAGCAACTAGAATCA[C/T]TTGGGGTTCCTTGTA | 14360 |
rs49254425 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39422895 | GCTAGAACTCTGTAC[A/G]TTCGTTTACGACCTA | 14360 |
rs49261541 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39488647 | GGAATAAGTGACCAT[C/T]GATTCACATAGTGCT | 14360 |
rs49265515 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39480291 | ACTAGACTGTAAGAA[A/G]TCCACTGAGTCTTCC | 14360 |
rs49266853 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39494062 | TTCAACACAAGAGTT[A/G]TAATAAAATATAAGC | 14360 |
rs49270621 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39421541 | GCACTCACGCCTCTG[A/G]GGTTATTCTATACTG | 14360 |
rs49273919 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39470087 | GGATGCTACGGGTGA[C/T]ATTCTAGGTGTAGAA | 14360 |
rs49277754 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39381488 | GTAGCTGTGCTTTTG[G/T]CCTTGGAATGGAAAA | 14360 |
rs49284330 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39405544 | TCATGATCTTGTTTC[A/T]GTTCGGCATGGTCTC | 14360 |
rs49285302 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39381274 | GAGATGTTGGTGAGG[A/T]AGGAAGAGGTGGCAT | 14360 |
rs49287677 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39427807 | ACACAGTCATTTCTA[C/T]TTACTGTTGTTCTCT | 14360 |
rs49294606 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39481278 | GGAGTATTTCACACG[C/T]GCTATACCATCTCCA | 14360 |
rs49295526 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39457368 | TGCAGGTGGTCTGTT[C/T]TGTGGGCTTCTGAGA | 14360 |
rs49301225 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39379561 | GGAAGCAGAGCCTCA[C/T]CTACAGTGGACCTGC | 14360 |
rs49301832 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39384736 | TTTCCAAACGGTTTT[A/G]AGCAAAATACCCCTC | 14360 |
rs49304822 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39396694 | AACCGTGGTGCTGCC[C/T]AGGCCGTGGGCTCGC | 14360 |
rs49304910 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39533981 | GGCACTTCCAGGGCA[A/G]TGGCTCCTGATTGAT | 14360 |
rs49305267 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39542104 | TTTGTGCTCACAGGG[A/G]CATCGTCCTCTCCTC | 14360 |
rs49309251 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39386648 | AGAGCAGTTTTATAC[A/G]GAATCTGAGATTGCT | 14360 |
rs49309328 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39452905 | TTCACCATTCTATAC[A/T]ATGCACGACCCTGGG | 14360 |
rs49314279 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39402370 | CCCCCCCTTTTACTG[G/T]GTATTTGTTATTTAT | 14360 |
rs49315310 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39490532 | ACTTTGGGGGCATTG[A/T]TGCAGAGACTCTGAA | 14360 |
rs49315768 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39542558 | CCCTCCTCTTGGGAC[A/G]TTTTTTCTAGACTCA | 14360 |
rs49317706 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39505536 | GCTTTGATTTGATGC[A/G]TAGCAGGTCCAGTCT | 14360 |
rs49321304 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39490822 | TTTGGCTTGAGCTGT[C/T]GCTTAAATCAGTGCC | 14360 |
rs49321720 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39501839 | CAGATGGCGGCTGGC[A/G]GATTCTGCTGTGGCT | 14360 |
rs49323369 | snp | C/T | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39565621 | TAGTGTATCCCGCAC[C/T]GTCTCTCGCTGGAAT | 14360 |
rs49328927 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39509182 | TTCTCTCGTTACTCC[C/T]GATTCTTCCTCTAAA | 14360 |
rs49334014 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39492903 | CCTGTGTGTCCTCTT[C/T]ACTGGCCTCAGGAGG | 14360 |
rs49343142 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545010 | GGTAGGCTGAGAAAA[A/G]CCATCATCTCTTACA | 14360 |
rs49346763 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39476350 | GAAGTGTGACTTGGA[A/G]ACTAAATCATCAGAG | 14360 |
rs49349764 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39427021 | GGGAGTGAAATAATT[C/T]TGCTGTGTAAGCATA | 14360 |
rs49349963 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39495532 | GGTAAGCATTGTGTG[C/T]TCTCCCTGATGCCAT | 14360 |
rs49351744 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39472477 | ACACTGGTAGACCTG[C/G]GTCCAGCATAGCTGT | 14360 |
rs49351795 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39425648 | TTTGAGTGTGTTGTA[A/G]GATTCCCTCTTTGTT | 14360 |
rs49356093 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39458222 | TCGGTACAGTTGATT[C/G]AGATCAAGTATTTTG | 14360 |
rs49362218 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39551185 | TCCAACTCTTTGAAG[A/G]AAGATTTAAAGTTAT | 14360 |
rs49370094 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39501957 | TCATGTTTTGTTTTG[G/T]TTTTTTTTTTTTTTA | 14360 |
rs49385322 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39493111 | AAAGTTATATAGTCA[A/G]AGCTTTTTCATTTAA | 14360 |
rs49387241 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431293 | AGTACTACAGGCATG[A/G]TGGCTGCAGGCATGA | 14360 |
rs49389301 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39478765 | AAGGTCCATGGGGGT[C/T]CAAGCTGAAGATAAG | 14360 |
rs49392680 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39462570 | TTCAAGCTGTCCTGT[A/G]TTTGCCCATTTTGTG | 14360 |
rs49394363 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39550275 | TGTCTAGTAGTGTTA[C/T]TCACTTGAACCCTCT | 14360 |
rs49403529 | snp | A/G | 0.165289 | 0.235211 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553940 | TGACAGAAACTCTAA[A/G]GGAGGAGCTCCTGCA | 14360 |
rs49417765 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39447948 | CAGTGCCCTTAGCAC[A/G]CTGGGCCTGGCAGAT | 14360 |
rs49419072 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39417894 | TGGAAGGTTCAGACA[A/T]TTGTGTATGGGATTT | 14360 |
rs49425132 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39395726 | AGACTACTCCTCCGC[G/T]CTCTCTGCAAGAGTG | 14360 |
rs49431594 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39464272 | GCAGTAGAAAGGTCA[C/G]CTTCTGTTTCTGTCA | 14360 |
rs49433602 | snp | A/G | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559127 | TGAGAAGCCACACAA[A/G]TGGGAAGCAGTAAAG | 14360 |
rs49433782 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39401132 | GGTTATTACTGCCCA[C/T]CTTTAACCCACAACC | 14360 |
rs49439412 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39489387 | AAGTCACCAAGGGGA[A/G]AAAGAAGTCTGGCAG | 14360 |
rs49444577 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39422888 | TCATGGGGCTAGAAC[G/T]CTGTACGTTCGTTTA | 14360 |
rs49445264 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39452521 | GGTTACTGATGCTCA[C/T]TGGAGGAAATCATTA | 14360 |
rs49454448 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39497068 | TCTGGTACCACAAAG[A/G]GAAGATAAAATTTTA | 14360 |
rs49459103 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39417001 | AACAAGAGTTCTCAG[A/C]TGAAGTGCCAGCAGG | 14360 |
rs49470729 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39481108 | TTGCATACATTTGAG[A/G]AGACGGTACTGTGGG | 14360 |
rs49475053 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39430270 | TTGGGGAAAGGGATA[A/T]GCAGGCATGCGTGAT | 14360 |
rs49477352 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39471540 | CTCCAGCAGCTGATG[A/G]TGCGAACACATGTTC | 14360 |
rs49478478 | snp | C/T | 0.345679 | 0.230967 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39565301 | TTTGTTAATGATTTA[C/T]TTGTGAGTTTACATT | 14360 |
rs49481770 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39448939 | AATTTCAGAGCCACA[A/G]TCTCAGGAATCTACA | 14360 |
rs49482521 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39417637 | ATACTTACATGAGAG[C/T]CTCAGCTCTTTGTGA | 14360 |
rs49485814 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39384778 | TCTTGTTGATCAGTG[G/T]TCCATTGAGTCAGGT | 14360 |
rs49487595 | snp | A/G | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39554046 | CGCTGTGGCCCAGTC[A/G]GCCAGCCTGTGCTGA | 14360 |
rs49492028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39432863 | TGTAGAGGACTCTGA[C/T]CTCAACCATAGTGCA | 14360 |
rs49493021 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39425405 | TTTATGAAAGTTTAC[C/T]CAACAGTTAGGTTTT | 14360 |
rs49498250 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39501222 | ACAAGGTCAGGCTTC[A/T]GTCATGCCTTCAGTG | 14360 |
rs49507791 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39531773 | TTCACAATTATATGC[A/G]TAAGCCATAAAAAGA | 14360 |
rs49512302 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39439136 | TTTCCTGCCCTTAGC[C/T]TCATTTTCAACCCAG | 14360 |
rs49512876 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561100 | TTTAATCCCAGTCCA[A/G]TGTTTCTAGCCACTT | 14360 |
rs49527229 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Fyn | Mm_Celera | 10:39467509 | GACATTAGAGCCTCT[A/G]TGGTTTCTGTCCAGC | 14360 |
rs49528385 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39509211 | AATCAGTCAAGAATA[A/G]AGCGAGATCCGAGTA | 14360 |
rs49532964 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39402545 | GTCCAGGGTTTCCCT[C/G]TGAGTGGCTGTCTAG | 14360 |
rs49533017 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39405732 | ATTTCTCAGTGGTTA[C/G]AGTACTCTCCTAGTA | 14360 |
rs49535517 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39499999 | CATGAATGTAGTAAC[C/G]TGGACTCAGACCGAA | 14360 |
rs49536529 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39445209 | ACCTTGATAATCATC[G/T]TAAGTGAATAAAACC | 14360 |
rs49539136 | snp | A/G/T | 0.260355 | 0.249785 | intron-variant | Fyn | GRCm38.p3 | 10:39423511 | TTTCTTTCTTGTTCC[A/G/T]GCCCTGTAGTTGGCA | 14360 |
rs49539326 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39484350 | CAAATGAGAGCAATA[C/T]GAAGTGAGAACAGTT | 14360 |
rs49540979 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39551611 | GCCTTTCTAAGCCCT[C/G]TGCTCAGCCTTCTGC | 14360 |
rs49549052 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39388006 | ACAAGCCTCGCTTAC[A/G]TTCCTAATAAGTCTC | 14360 |
rs49552056 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39421328 | GGGAACTAGTGAGCA[A/G]TTCTGCAGCATCAAG | 14360 |
rs49561532 | snp | A/G | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39453642 | AATTAAGGACATCCT[A/G]AAATACGACTTCATT | 14360 |
rs49578881 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39524240 | AGCAGCTATTGCTAC[A/C/G]CTGGGATTGTGGAGA | 14360 |
rs49588015 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39417101 | TCCACATGGGAGAAG[A/G]AAGAAAGTCTAGAGA | 14360 |
rs49592271 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fyn | Mm_Celera | 10:39449473 | GTTCACTAGCAAACC[A/G]TCCTGGCTCTGGCGG | 14360 |
rs49594371 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39446127 | TCACCGGCCTTTCCT[G/T]GTGCCTGTCCTGGTT | 14360 |
rs49596964 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39450873 | CTCCACAACTATACA[C/T]AACTCCTACATGGGA | 14360 |
rs49598443 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39452483 | TGGTAAATTTCTGCC[C/T]AAACAGTTGGTCACT | 14360 |
rs49608135 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Fyn | GRCm38.p3 | 10:39405117 | AGACCTGCTAGCCCA[A/C/G]CCCTGTGCTCTAACC | 14360 |
rs49626445 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | GRCm38.p3 | 10:39389133 | TTTGCCTGTGCTACC[A/G]GCTAGGCTTTCCTCT | 14360 |
rs49628884 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39389158 | TCCTCTTGATGTCAG[C/T]GTACCACACCATTAT | 14360 |
rs49643546 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39544146 | TGGAAGTTTCGAAGG[G/T]CAGTGATGCTGAGGG | 14360 |
rs49645072 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39426766 | TATTTTAGAGATGAC[A/G]ATCACATGTTACTTG | 14360 |
rs49651711 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559740 | ATCACCTGGGTCCTC[A/G]GAAAGAGTGGAGACA | 14360 |
rs49655827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39427991 | CACTGGTCATGCTGT[A/G]GATTACCCTGTAAGC | 14360 |
rs49656248 | snp | A/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39449385 | GTGAGGCCTTCCCAG[A/T]GTACCCTGTTAGTCA | 14360 |
rs49675163 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39470553 | GGGCCTGCTGCCCAG[C/T]AAGCTTCCTCACTGA | 14360 |
rs49684714 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39543283 | TTGAATCACCACCAA[A/G]TTCCAGGTTGGGTCA | 14360 |
rs49684913 | snp | A/C | | | intron-variant | Fyn | Mm_Celera | 10:39508895 | CTCGAACTCAGAAAT[A/C]TGCCTGCCTCTGCCT | 14360 |
rs49690357 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39542034 | GTGCCAGCACAGGTC[C/T]CTGAGCCGACTCTGA | 14360 |
rs49693571 | snp | C/T | 0.5 | 0 | intron-variant | Fyn | Mm_Celera | 10:39449712 | GGGAAGGGCTCACCA[C/T]CTCTCTCAGACCTTA | 14360 |
rs49695002 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39440531 | CAGCGTTGCCTATCT[A/G]TGTGCATGCAGAATC | 14360 |
rs49698946 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559079 | ACTAGAAAATAAACC[A/G]CAGACTACAGGTACG | 14360 |
rs49700413 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39446242 | TGTTGGCTGTTTCCC[A/G]TGTTTTCCTTCTCAA | 14360 |
rs49706772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39484247 | TTATCCTTTGAAATA[C/T]AAATGTCTCTCAATG | 14360 |
rs49718428 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39450419 | ATATATACAGTAAGG[C/T]GGGAGAGAAGCCAGA | 14360 |
rs49724221 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39439975 | TCTACCACGTCCTGC[C/T]CAGCCTTTCCCCCCC | 14360 |
rs49762396 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39560048 | GTGTCTACTCTTTTG[A/G]CAAAGCTGCCGTTGG | 14360 |
rs49773224 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39537930 | TCCTCAGCATCAGTT[C/G]TTTGCTCCTCTGTCA | 14360 |
rs49774096 | snp | A/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39552857 | TGAGAAGGCACTTTT[A/T]AAAAATTATTATTGT | 14360 |
rs49774572 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39471794 | TGAGAATGGAATCAA[A/G]GGCTGGCATTTCGAA | 14360 |
rs49774812 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39485099 | CCAAGAGTGGTGGGC[A/G]TGTTGGAGTTAACAT | 14360 |
rs49782714 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39507059 | GCAGAACTGCACTGC[A/G]CTGCGCTGACACAGG | 14360 |
rs49783971 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39533023 | TCACTCAGCCTCACA[C/G]GAGTGGCTCTGAAGC | 14360 |
rs49788180 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39439508 | ATGGGTGCGCTGACC[C/T]CACCCAGGGTACAGA | 14360 |
rs49796546 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39530583 | CAGTAACGGCAACTG[C/T]ACTGGGCCCTTGAGA | 14360 |
rs49800062 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39420730 | CAGCCGCCTGTATGT[A/G]GATATTGGACAGGCG | 14360 |
rs49804118 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39378061 | GAAGGCAGGTGACCG[C/T]CCATGGATTCCTTCA | 14360 |
rs49807945 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39480732 | CTCATACAGCTGCCA[A/C]GGGACTGTGTTTTAT | 14360 |
rs49813451 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39376485 | GAAGGGCTTATAGCT[C/T]GGGCCTTACTCCTGC | 14360 |
rs49831793 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500639 | AAATCTCAAGGTGTG[C/G]TCTTCAGCTGTACGG | 14360 |
rs49841114 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39488728 | ATGCCGTACAGGAGA[A/G]CTTTGTCCCTAAACT | 14360 |
rs49846637 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39512528 | CACTCCAGTGTGATG[C/T]ACCCTTCCTGACTTA | 14360 |
rs49862867 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39435730 | GATTTTACTCAGTGA[C/T]ATTTCTGCTTGGCTG | 14360 |
rs49863872 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39381810 | AACCTGTAGACAGTA[A/C]GGACACTAGATGTAA | 14360 |
rs49870519 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39495992 | GAAAGTTACCCTTGC[A/T]TTGACATGTTGCTAT | 14360 |
rs49886338 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39505486 | CAGTGACCACACACA[C/T]GGATGATCCAGACAC | 14360 |
rs49888970 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39440179 | CAGAGTCCCTGTCTG[A/G]AAAAAAACAAACAAT | 14360 |
rs49894452 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39464417 | CACACAGACTGATTT[A/G]TAAAACCTAAGTTTC | 14360 |
rs49895196 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39558506 | GCAGCTCTCCCAACC[A/G]GCATTTCTGATTTTA | 14360 |
rs49912877 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560739 | GGGAGATTCCTGCAG[A/G]CCCAAGCTGTGTAGT | 14360 |
rs49916129 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39540400 | TTAACAAAAGCAGTG[A/T]TAAGTTGACCCTATA | 14360 |
rs49917679 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39431590 | CCATGCTGCTTCCTG[A/G]GAACTCTAGCTCAGC | 14360 |
rs49923254 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39482100 | CTGAGCAGGACCCAG[C/T]GTGCTTCTCAAGCTC | 14360 |
rs49924750 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39380762 | TGCTGTGACTCCCTT[C/G]CTTGCCTTCCTGCAA | 14360 |
rs49941173 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Fyn | Mm_Celera | 10:39419642 | CGTTAACCTGTTTCT[C/T]GGGTCCTTTTCTAAT | 14360 |
rs49943163 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39544640 | GAAGAACATTCTAGC[C/T]CAGCCCACCGTCGGG | 14360 |
rs49948084 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Fyn | Mm_Celera | 10:39470909 | TGACGGAGTTTTCCT[G/T]CTGAGGAGGGAAGGA | 14360 |
rs49949295 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39478266 | TCTCAACTCCTTCAA[C/T]ACGATCACTCTTTTG | 14360 |
rs49952512 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39379461 | ACAGAATGGCCTGCA[A/G]GAGACTGGGAGCATA | 14360 |
rs49958949 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39474209 | GTCCTCCTTTTAAGT[C/T]ACCTCCCATGACCAG | 14360 |
rs49964872 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39552080 | CCTGCAGTTGTTCTG[A/G]GCTGTCAGATGCTCC | 14360 |
rs49985476 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39440387 | TGTCTGGATAGGGAA[A/G]TGGGTATTTCTGGGG | 14360 |
rs49986500 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561680 | TTTCTGTCTGGAGTA[C/T]CTCAGAAGAGAGCTG | 14360 |
rs49988846 | snp | C/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39499744 | ACATCAGCATCACCA[C/G]TTCTAGTTGAAGCCT | 14360 |
rs49991842 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39508092 | GCATTTGCCAGCATG[C/G]CCGGTGTCTCATCCA | 14360 |
rs49994957 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39389435 | CGAGACTTGGGCACA[C/T]GGGCCATCATGGTGG | 14360 |
rs49996713 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39378415 | GTTCTTTGTACACCT[C/T]GGTCTGGTCCATGTC | 14360 |
rs49998450 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39534806 | TGTGGGTTTTAAAGC[C/T]GGAACTCAGGCAGGG | 14360 |
rs49998727 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39471995 | TGCCCACACAGGCCA[C/G]TGCCGCCTTTGTCCC | 14360 |
rs49999032 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39378296 | CCAGCATCTAACTGT[C/T]CTCAGCCGCAGGAAT | 14360 |
rs49999854 | snp | A/T | | | intron-variant | Fyn | Mm_Celera | 10:39417329 | CAGGGTCGCCTCTGG[A/T]TCTCATACAGATCCC | 14360 |
rs50002908 | snp | A/C | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557094 | TTACATCTTGGACAC[A/C]CCAAGGAATTTGTCT | 14360 |
rs50006380 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561913 | ACAGTCAAAGGAATG[A/C]TAAATTTTGTCACCA | 14360 |
rs50007114 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39481153 | TATTCAAAAATCAGA[A/C]ATAATTTGAAAGCTG | 14360 |
rs50007768 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39406157 | GTGGGTCAACAATTG[A/G]CATGCCTATGAGGAA | 14360 |
rs50008107 | snp | A/G | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557622 | GCGGGATCTGGCAGA[A/G]CAGGGCTCTTCTCTT | 14360 |
rs50009993 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | GRCm38.p3 | 10:39495274 | CCACCTGACAGGGAA[A/G]AAGCCACCTTCCTAA | 14360 |
rs50010471 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39421515 | AGTCGCTTCCAGTGG[A/G]AGGTACCTCAGCACT | 14360 |
rs50016565 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39461175 | TGGGTGCCAGGGACA[A/G]AACCCAGGTCCTCTG | 14360 |
rs50016581 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39467791 | CCTCAAGCTGAGCAT[C/T]CTTCTCCATGTCCCA | 14360 |
rs50020450 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39544769 | TCCCTGTGAGCATTT[A/C/G]AAACATTGTCACCAT | 14360 |
rs50021945 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39436519 | AATGAAATCAGTAGA[A/C]GTCAGTAACTGTATC | 14360 |
rs50028627 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39439988 | GCCCAGCCTTTCCCC[C/T]CCACCTTGCCTGTAG | 14360 |
rs50036314 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39395634 | GGCGATAAAGTGTGA[C/T]GGAATGACACTGGAG | 14360 |
rs50036584 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39539782 | TATCACTGCCCTTCT[C/T]CTCGCTCTCTGCAGA | 14360 |
rs50047654 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39383376 | AAGTTCTGCCTAGTT[C/T]TCTCTGCTTCAGTAT | 14360 |
rs50052258 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39545554 | GTCCAGCATTAAATT[A/G]CCACTTCTGATCAGG | 14360 |
rs50054429 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39530293 | CAGGACAGGAACCCA[C/G]TGATGGTGACGCTTT | 14360 |
rs50057982 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Fyn | Mm_Celera | 10:39525485 | TACCTTTCTTATCCG[C/T]GAGAGCGAAACCACC | 14360 |
rs50070425 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Fyn | Mm_Celera | 10:39404384 | TGCTCACTGGAGCAA[A/G]CCCAGGATGCTCACT | 14360 |
rs50075569 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557502 | GTCCCCAGAGTTCTG[A/G]GAAGTTGACCCCACG | 14360 |
rs50076487 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500393 | CCTGAAGGTTAAAGC[C/T]GATGAGTTAGGGTGA | 14360 |
rs50084390 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39438012 | AACCTTTGTGGCTGG[C/T]GTGGAAGATGTGTTG | 14360 |
rs50085956 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39459429 | CTGGCACAGCCTCCA[A/G]GGTTCCCTTTCAGAT | 14360 |
rs50086152 | snp | A/G | 0.152778 | 0.230321 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39556062 | TAACTCCAGAAGGCC[A/G]CACCCTGCACAAGTC | 14360 |
rs50086569 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39484746 | TCATGCTTGGTCTTC[A/G]CCTCTCCCTGCCGGC | 14360 |
rs50088946 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39417975 | GTCCCACCCAGACAC[A/G]TATTTTAACAGTTAC | 14360 |
rs50089646 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39486006 | TGAAGTTTAGCCTCA[C/G]TTGCCTTTAGAGGAT | 14360 |
rs50091550 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fyn | Mm_Celera | 10:39456362 | GGACAAGGACATGGA[C/T]GTGGCCTCAGGAGGT | 14360 |
rs50100349 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39482979 | CTCTTCCATGCTGCT[A/G]CAATCTAAGCACCTA | 14360 |
rs50102486 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553509 | AGAGAGCAGAGGAGT[C/T]AAGTGAGAACTGGGT | 14360 |
rs50103174 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39437450 | GCAGCAGTGGGAATT[A/C]TGTCTTGTTTTAGAA | 14360 |
rs50107148 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39389196 | CTTTGTCTTTGCCTG[A/G]AGTCGCCATTTACAC | 14360 |
rs50117493 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39553796 | GAAGAGCCATTGGAG[C/T]CTGGCAGGTTGACTT | 14360 |
rs50126710 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39510610 | CAGGACAGTATGGTG[A/G]TGCACAGCTTCCAGG | 14360 |
rs50139239 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39424821 | GCAATGCCTGTGGTG[A/T]TTCTTGGAATGCACA | 14360 |
rs50140213 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39391823 | CTCCATCGGGCAGTC[A/C/G]GCCTCCGCACCTCTC | 14360 |
rs50154294 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39513208 | TGGCTTTTTACCCGG[A/G]GAGCTGACGCTGCCG | 14360 |
rs50156298 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39398868 | GGCTGACTTCCTTGT[A/G]CCCTGGATGGCCTTT | 14360 |
rs50156417 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39506069 | CTGGACGTGGTGTCA[A/G]GAGGCGTCCTTCCCT | 14360 |
rs50163949 | snp | C/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39557980 | CTTAGCAGTGCATGA[C/T]GGGTCCTCTGCCTCC | 14360 |
rs50166850 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39461712 | GTTTTTGCTCTCTCT[G/T]GTCTTGAATTCTCTG | 14360 |
rs50172078 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39431283 | GTGACACAGGAGTAC[C/T]ACAGGCATGATGGCT | 14360 |
rs50172686 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39426291 | ATGTTTCTGTCCATG[A/C]GACACAGGCTTGACT | 14360 |
rs50183984 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39499026 | TGACTTGAGGCCAGC[C/T]AGCCCGTGTGTTTGT | 14360 |
rs50190621 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39464452 | GGAAAAGATTGTCTC[A/G]TGTTCTTACCTGGGG | 14360 |
rs50190710 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39402061 | GAACCCCAGTCCAGG[A/G]TCATGGTCATAACAC | 14360 |
rs50193029 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560897 | ACAGGTGGCTGTCTT[G/T]GAGCCCCAGCTTCTC | 14360 |
rs50199591 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39399671 | TTGACACATGTATTC[A/G]GGGCTGCCCCATCCA | 14360 |
rs50199901 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39497754 | CATCCCTGAGCTGCC[G/T]TGAGTTGAGTGCTGC | 14360 |
rs50199971 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39533056 | TGGCTGTCCGAGGCA[C/G]AGGCGTGACTGGCTG | 14360 |
rs50201120 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500027 | GAAGCCTTACAAACT[A/G]CATAATCCGGGCAGG | 14360 |
rs50206444 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Fyn, Gm16364 | Mm_Celera | 10:39559154 | AAAGTATTAATACTT[C/T]TTTGGTGAGACCTTG | 14360 |
rs50211285 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn, LOC105245135 | Mm_Celera | 10:39532546 | TGCTGAGTTAAGTTC[C/T]GTCCCCATCTCAACA | 14360 |
rs50218223 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39468239 | GCCACAGGTTCCACA[A/G]TACGAGGTCTAAGTT | 14360 |
rs50220183 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39463153 | ATGTTGTGTGCCATG[A/T]AACCTTTAGACTACA | 14360 |
rs50225550 | snp | C/T | | | intron-variant | Fyn | Mm_Celera | 10:39417342 | GGTTCTCATACAGAT[C/T]CCACTGGACAGTCCT | 14360 |
rs50227962 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39552486 | TTGTTTCTGGTCATC[A/G]TCAGAGAACAGAGAA | 14360 |
rs50233755 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39478191 | TGCTTAAAGGTGGCT[C/T]CAAGCATTTCTTCTA | 14360 |
rs50240980 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39506872 | AGGTTGGCTACGCCA[A/G]GTGACACAGCCTAAC | 14360 |
rs50242347 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39501156 | TAAATGTATGGTGGC[C/T]CATAAAACACGTGTG | 14360 |
rs50243404 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fyn, LOC105245135 | Mm_Celera | 10:39534128 | CAGTGCTGGTCTAGT[A/G]AGTGGGCGTCTGTTC | 14360 |
rs50246878 | snp | G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39442817 | GATACAGCTGGCTTA[G/T]TCTCCCTGTCCTTCA | 14360 |
rs50252243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39387766 | CACTGCCTGCCTCCA[C/T]GTTGCATTTGTCACC | 14360 |
rs50256803 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39487472 | ATGGGAGCAAGTGTA[C/T]GGTTGCTTCTCAGAC | 14360 |
rs50258539 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39501253 | CGTTAGCAGAGGCGG[C/T]AGCAGCTCCTTCCTC | 14360 |
rs50259262 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39390668 | CTGTACACTTTGCCT[C/T]CCTTCGCCATCCAGT | 14360 |
rs50261504 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39404932 | ACCTGGAGGAAGCCC[C/T]GAGTTCAGGTGCTTC | 14360 |
rs50264476 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39382627 | GTGTAGAGATGCTGG[A/G]AATCCTGGGATCAGA | 14360 |
rs50270102 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39437828 | GAACACTCCAATTCC[A/G]AACTGAGAGAAGCTG | 14360 |
rs50272080 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39543525 | TGGTTTAGAAACCTA[A/G]GCTCTATTGTTGAAG | 14360 |
rs50275107 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39492861 | GGTACATGTGTCCCT[C/T]CAGCAGGTGTGTTGT | 14360 |
rs50302815 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39467742 | AATTCTTTTTAATGG[A/G]AAGCTTATTTGAGAT | 14360 |
rs50304882 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39423706 | TTCTGATGGTCAGGT[G/T]TGAGTTAAAGATAGG | 14360 |
rs50306723 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fyn | Mm_Celera | 10:39390892 | AATGATAACGGTAAC[A/G]TTAAGTGAGTACACA | 14360 |
rs50307132 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39420784 | TTACTTTACTTTTCT[A/G]TAGGATTGTGACTGG | 14360 |
rs50309615 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39560813 | GCAGCAAGGAATTGC[C/T]TGAGAGAATACCAGC | 14360 |
rs50315010 | snp | A/G | | | intron-variant | Fyn | Mm_Celera | 10:39507550 | TTACTCATCCTGTGG[A/G]TGGTGTTGATTTTCT | 14360 |
rs50316913 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39377497 | CCTGCTGGAGTGCAC[A/G]TTCCCAGGCCACATT | 14360 |
rs50317856 | snp | C/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Fyn, Gm16364 | Mm_Celera | 10:39565573 | TGGCTAACTCAGAGT[C/G]GCTAAAGCAAAACTG | 14360 |
rs50322711 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fyn | Mm_Celera | 10:39422072 | TCAGGGCACATGTGC[A/G]TAGATACAGAGTTTC | 14360 |
rs50329149 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39476412 | TAGAGACCCTGTCTC[C/T]GATGACGTAGAAGAT | 14360 |
rs50333684 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39505603 | ACACTCCCCTGTCCC[A/G/T]TGGCCTTCTCACCTG | 14360 |
rs50336028 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39496337 | AGGAGTAGAATGGCC[A/G]CAGGAAAGGCCGACT | 14360 |
rs50339151 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39524801 | AGGTACTTGGTAAAC[A/G]CTCCTCACGAATGCT | 14360 |
rs50341879 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39542311 | TTCTGGCTTCCTTGT[C/T]GTACTCTGCTGGCTG | 14360 |
rs50346995 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39485439 | TTGAACATACATGAA[A/G]TAATCAAACGGTTAC | 14360 |
rs50349412 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39507558 | CCTGTGGATGGTGTT[C/G]ATTTTCTCAGCATCA | 14360 |
rs50359449 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39397938 | TGCCCCAGGTTCTGT[A/G]GTTACAGCAGGAATC | 14360 |
rs50363368 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39403486 | TCCTCCAGGTCCGTG[C/T]GTTCTATAGAGAGCT | 14360 |
rs50366250 | snp | G/T | | | intron-variant | Fyn | Mm_Celera | 10:39381031 | TCCTGGAAAAGGAAA[G/T]AGTGCAGCTCACTTA | 14360 |
rs50373916 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39376434 | GAGCACCTATTTCCT[A/G]TAAGCTTTTGGGAGA | 14360 |
rs50381371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn, Gm16364 | Mm_Celera | 10:39561595 | GCTCTGTTATTCTGC[C/T]GAGTGCCATTTCCTG | 14360 |
rs50381706 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39398731 | CACATGAATTTTGGG[C/T]GAAAATGTCTTTTTT | 14360 |
rs50392561 | snp | A/C | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39492101 | TTACAACATCCATCC[A/C]CTGAGTGCTTTGTGG | 14360 |
rs50398611 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39500035 | ACAAACTACATAATC[C/T]GGGCAGGTGTTTTAG | 14360 |
rs50399579 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39431347 | AGGGAAGGAAGCTCT[C/T]ATGTTGTGGTCATAG | 14360 |
rs50402934 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39482405 | CCTATAATCCACATG[C/T]GTTTCCATGTGTAGA | 14360 |
rs50420559 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fyn | Mm_Celera | 10:39393784 | GACATCTTTGAAACA[A/G]TGATGATCCTGTTAT | 14360 |
rs50427252 | snp | G/T | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Fyn | Mm_Celera | 10:39467940 | CAGCTCAGGGAGCCG[G/T]AACGAAAGGCCTGAG | 14360 |
rs50430118 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39508036 | CTCTGCTAAGATGGC[A/G]GCTACTCATTGGCTC | 14360 |
rs50434795 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fyn | Mm_Celera | 10:39386226 | TGGGTCGGTGGCACC[A/G]TAACAGGTGGCTGTT | 14360 |
rs50437330 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fyn | Mm_Celera | 10:39485919 | CATCTTTCTCTTAAG[A/G]CCCATTTTCCATCTG | 14360 |
rs50446122 | snp | A/G | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39491311 | ACCTCTCTTTATGAT[A/G]TCTGGTCTTAAGCCA | 14360 |
rs50447214 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fyn | Mm_Celera | 10:39460843 | GCCAGCTTGAATGAG[C/T]ATGCACCAGATTCGT | 14360 |
rs50447311 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39538523 | GCTTCTCACAGCAGA[A/C]TGATATTTCACTGAG | 14360 |
rs50447375 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39396372 | ATCCGCAACATTGAT[C/T]TAGAGCACTCACAAG | 14360 |
rs50466010 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39541457 | CCCATCTTTTAAGAA[A/C]AGCAAACCTCTTCCC | 14360 |
rs50476544 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fyn | Mm_Celera | 10:39400532 | AAAGGGATGTTCACC[C/T]TTACTTACTGTAATC | 14360 |
rs50495459 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Fyn, LOC105245135 | Mm_Celera | 10:39526945 | GGTAACCCCAGTGCC[A/G]TCACCGTCACCGTCA | 14360 |
rs50498059 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fyn | Mm_Celera | 10:39510726 | TTGTTGATGAAAGTC[A/G]CTGGCAGAAAGGTTG | 14360 |
rs50499162 | snp | C/T | 0.32 | 0.24 | intron-variant | Fyn | Mm_Celera | 10:39544086 | TGGAATTCTCGGTGG[C/T]TGATGGATGAGTGTG | 14360 |
rs50499912 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fyn | Mm_Celera | 10:39433958 | TTGGTGGAGTCCTTT[G/T]GCTAGTGGGTGGCTG | 14360 |
rs50501648 | snp | C/G/T | 0.391111 | 0.206368 | intron-variant | Fyn | GRCm38.p3 | 10:39380964 | GGTGCCTGGGAAGCA[C/G/T]CTGAGACCATGATAG | 14360 |