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 |