SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8158708 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78175388 | TTGTTAGAATAAGCT[C/G]CAGATTAGTTTTAAT | 287622 |
rs8163889 | snp | A/G | | | utr-variant-3-prime | Tom1l1 | Rn_Celera | 10:78174376 | CAATGTTTTCTAATA[A/G]GGTCTTAAAGTAACC | 287622 |
rs64621569 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191335 | ACACTGAAATGCTAA[A/G]TGGAAATCTAGACCA | 287622 |
rs64623079 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191324 | GACAATGTGGGACAC[A/T]GAAATGCTAAATGGA | 287622 |
rs65190285 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191334 | GACACTGAAATGCTA[A/G]ATGGAAATCTAGACC | 287622 |
rs65367642 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191352 | GGAAATCTAGACCAG[C/T]CCTGTTTAACAACTG | 287622 |
rs65692079 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191349 | AATGGAAATCTAGAC[C/G]AGTCCTGTTTAACAA | 287622 |
rs104897380 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187809 | AAACAGCCACCAAAC[C/T]CTTCCTTATAGTAAA | 287622 |
rs104940936 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187404 | CCTTGCTTACTTAGA[A/G]GGCTTTAGAGGAAAC | 287622 |
rs104959808 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78189570 | TGGAAAAAAGAGGCC[G/T]AGGGCCAGGGAAAGC | 287622 |
rs104982678 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78180180 | AATGAATGCCTCAGC[A/T]CTGGGGACCATCAGA | 287622 |
rs104998021 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78219256 | CCACTTCAAGCCAAA[A/G]GCCACTCGGATCGTT | 287622 |
rs105028769 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78189875 | TTTCCTAGAAGCTCC[A/G]TGTCTCTACCTTGGG | 287622 |
rs105049683 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78221754 | AGAAGGCACAGCCAC[A/G]TTGAGGTCAGAAAAG | 287622 |
rs105053210 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78178628 | AATAGTGCCTCCCCA[A/C]CCCCCAAGCTAAAGA | 287622 |
rs105062115 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78175505 | TTTTTTTGTTTGTTT[G/T]TTTTTTTTGTTTTGT | 287622 |
rs105071122 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187792 | CAGTCCCCCACACCA[C/T]GAAACAGCCACCAAA | 287622 |
rs105073956 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187346 | GCAAACTTCAGCCAC[A/C]AGGCCACCGTAGCAT | 287622 |
rs105142281 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177101 | CCTGGGGAAGTGCCA[G/T]CATCCTGGTTAGGAA | 287622 |
rs105172891 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78178246 | GCTGACATGCATGCA[C/G]GCAAATAGAACACAT | 287622 |
rs105211991 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78208442 | CAATGAAATGTCATG[C/T]CCTCTGAGAGGGAGA | 287622 |
rs105234995 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78193409 | TTACATTTCTGACAC[C/T]GACTGTAGTCGCCCT | 287622 |
rs105238374 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188859 | TACCATAGACAGCAG[A/C]CATGGAACCGGCTTG | 287622 |
rs105285812 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78178976 | TAACACTTTAGGTGG[A/G]GAGAAAAAAAAAAAA | 287622 |
rs105305247 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177580 | TGAGCATTTTTAACC[A/G]GGATGAGAGGGTCAG | 287622 |
rs105380847 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78206321 | CAGTGCAGATCCAAG[A/T]CAGAAAAGAGTGAGC | 287622 |
rs105476571 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78206732 | AGAGAGAGAGAGAGG[A/G]GAGAGAGAGAGGAGA | 287622 |
rs105477877 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187456 | GGTTGTCAATGTGTG[C/T]GACAACCTAAAGAGC | 287622 |
rs105527298 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78201108 | ATATCATATATATTA[C/G]ATTCTATTAACAAGT | 287622 |
rs105561048 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188903 | GCTACAGAAACTTAC[G/T]GTATTCCCATTAAGA | 287622 |
rs105624452 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78221069 | AGCAGCCTGATCTCT[G/T]TTCCATGTTTAGAGT | 287622 |
rs105641874 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78189350 | TAGCTCAGAGGCTAC[C/G]ACAGGCTAGAGGACA | 287622 |
rs105657932 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177441 | TAATTTTTAAAACGT[A/T]CACTTTAAATTCTGC | 287622 |
rs105730372 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78179004 | AAAGACCAGTAAGTA[A/C]ACAATGTGCTTGTGA | 287622 |
rs105731865 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176470 | GACTTGGCAACAATT[A/G]GCAAGGCTGCCTCCT | 287622 |
rs105755209 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78182288 | GGACAACGTGGACTG[A/T]TACGAGATGAAAGTC | 287622 |
rs105773727 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177667 | GTCTGGATATAAACG[A/G]CTTACTGCGCATGTG | 287622 |
rs105876486 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78191843 | AGTGTTTCTGAAGTA[A/C]CCTGACACTGGAAAT | 287622 |
rs106001676 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78189377 | GACAACTGGGGGACT[A/G]AAGAACACAACAGGA | 287622 |
rs106018761 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176507 | CCCCTCTAGCCTTCA[C/T]TTATGTTACTCCTGT | 287622 |
rs106024228 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78184378 | GGGTGGTTCATGACC[A/G]TGAGCCCTGCTCTTG | 287622 |
rs106031990 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176733 | GAATATATGTCCCAC[G/T]AGGACAAAAAGAAAA | 287622 |
rs106064252 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78180128 | ATATGGGAGGAGAGA[A/G]GCTGAGGTAGAGTGG | 287622 |
rs106064818 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176803 | CCAGAATTTCCAAGA[A/G]TCTATGCTTTTTCTT | 287622 |
rs106071205 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188860 | ACCATAGACAGCAGA[C/T]ATGGAACCGGCTTGC | 287622 |
rs106121836 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78185144 | GGATGCTGAAGGGGA[A/G]GCGACACAATGGGAT | 287622 |
rs106215902 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176502 | TGACTCCCCTCTAGC[C/T]TTCATTTATGTTACT | 287622 |
rs106256485 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78220676 | ATAGTGGGTTAACCC[C/T]CCCCCCCCCCCGGAA | 287622 |
rs106270275 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78195667 | GCCTCTCAAGCCTCC[A/C]TCTCCATTCAGGCAA | 287622 |
rs106338747 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78212995 | GCTTGACAGGCTAGA[C/T]TGACATAAGGGGAGA | 287622 |
rs106359628 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78206731 | GAGAGAGAGAGAGAG[A/G]AGAGAGAGAGAGGAG | 287622 |
rs106363799 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78182280 | GGCTCCAGGGACAAC[A/G]TGGACTGATACGAGA | 287622 |
rs106370149 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78213095 | TGTCCAAGTGAAGGT[A/G]GAGGACATGATGGAC | 287622 |
rs106477216 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78202239 | GAAGTCACAGGATAG[C/T]GTTTGGTGTCTGGTT | 287622 |
rs106485043 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188773 | TTTTGTCTGCTAAAC[A/G]GGAAGAGCCTTTGAG | 287622 |
rs106500825 | snp | C/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176184 | TTAACATTTGTGTTC[C/G]TATTCACTTTCACTA | 287622 |
rs106532815 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78193830 | ACTGCTGTTCTAACT[C/T]CCTTTGTCCACAGGT | 287622 |
rs106618980 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177889 | TGTATATAAGTCGAG[C/T]GACTTTGCTGCTCGG | 287622 |
rs106635512 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78175586 | AATTAAGTCTGCCTT[A/C]TTTAACATTGTATTA | 287622 |
rs106637474 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78183436 | TTTTCACCTGGATGA[G/T]GGGATTGGGCTTCAA | 287622 |
rs106692698 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78183971 | GCGTTTTCAAGTTCG[A/C]TGTGTGACGTCAGCC | 287622 |
rs106704047 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176280 | ATGTCCATATATCAT[C/T]CAGTTTTCGGTTCTT | 287622 |
rs106803590 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78201899 | TTAATGCAAAGATAT[A/T]AATGAGCATTGTTAA | 287622 |
rs106923521 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78198105 | TCATACTCCTGGAAC[C/T]CCAGAATGTGGAAGG | 287622 |
rs106951732 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Tom1l1, LOC100363423 | Rn_Celera | 10:78217261 | GCCATCCTCACACAG[C/T]AGGAGGCGCTCAGAA | 287622 |
rs106963942 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78176273 | ATCCTCTATGTCCAT[A/G]TATCATCCAGTTTTC | 287622 |
rs106972853 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188597 | TCCTAAAGCGAAGAC[C/T]GTCCTTTTACACTGT | 287622 |
rs106990065 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78197891 | TGATTTTTCTTTTAT[A/T]GTCCTATACTAGTAG | 287622 |
rs107015252 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78199922 | GGAGACCTGACTTTT[A/T]CCCTAACTGCCTCTT | 287622 |
rs107017830 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78203046 | ATGGTAGGCTGTCAC[A/G]TAACAGGCCTTATTA | 287622 |
rs107030381 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78185103 | ATTTAAAACGTCCAT[C/T]TTGGAGGGAGGTTCC | 287622 |
rs107054596 | snp | A/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78185108 | AAACGTCCATCTTGG[A/T]GGGAGGTTCCTTAAA | 287622 |
rs107055132 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78178176 | TCGAGGTGTTACAGC[A/G]GCCTATAAGGAATCT | 287622 |
rs107114874 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78197876 | ACAAAGTCCAATAAT[C/T]GATTTTTCTTTTATT | 287622 |
rs107145245 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78187998 | TACTTGGAGATAGTA[C/T]TTTGCTATGCAGGAC | 287622 |
rs107151962 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78181152 | GATGAACAGCTTCGG[A/G]ATCTTGGCAAATGTA | 287622 |
rs107156228 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78199962 | AGATTAAACAGAAAC[A/G]TCCACCTGACTGTTT | 287622 |
rs107247249 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78177799 | AGGTGATTCATTCTC[C/T]GCCAATCCCTGGAGG | 287622 |
rs107250055 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78189384 | GGGGGACTGAAGAAC[A/G]CAACAGGAATGAAGT | 287622 |
rs107265666 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78201889 | GGATAGCCTTTTAAT[A/G]CAAAGATATTAATGA | 287622 |
rs107305001 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78206938 | CAAAAGGAAGAGTAT[G/T]AAGAGTTACTATTAT | 287622 |
rs107348195 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78207701 | AATGGTCTTAGGCGA[C/T]CCCTAAGAAAGGGTT | 287622 |
rs107388620 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78184945 | AGTATTCTTAGAGGA[A/G]AGTGACAACTCACAC | 287622 |
rs107415503 | snp | A/G | 0 | 0 | intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78215166 | GAAGGAAGGTATAAA[A/G]GAAGGGAGGCATCTC | 287622 |
rs107510883 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78184034 | GGAGCTGACAGATTA[A/G]ACGTAACTAAACACC | 287622 |
rs107568238 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78183554 | GAATGAGGAAGAGCC[A/G]GAGGGCAGTTATTGA | 287622 |
rs107583969 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188391 | GTGCATATATGTGTA[C/T]TTGTGTGTGCGCACA | 287622 |
rs197070312 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78183247 | TGAAAATAAATATGA[A/G]CAAGTAAGCCCCCCA | 287622 |
rs197144542 | snp | G/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78208296 | GAACCAAGCAGCGCG[G/T]AAGTGGGCGACTCAA | 287622 |
rs197165558 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78200172 | TAGGTCAGTACAGAT[A/G]TTGAAAAACATGTGG | 287622 |
rs197174954 | snp | A/G | 0 | 0 | intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78215010 | GAGATATTTCCATAA[A/G]AGCTCACATCCGTAC | 287622 |
rs197262955 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78190902 | GAAAGAATGTTCTTG[C/T]GGGCTCTCTGGAAGG | 287622 |
rs197392438 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78178116 | GCTCAGCGGTTAACA[C/T]TGGCTGCTTTTCAGA | 287622 |
rs197398983 | snp | A/G | 0 | 0 | intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78215273 | TTTTTAACCACAAAC[A/G]CGAAGACCTTGACCA | 287622 |
rs197429362 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Tom1l1, LOC100363423 | Rn_Celera | 10:78215722 | TTTGATCGCGATTCC[A/G]CGGGAGCTGGGCCAC | 287622 |
rs197462050 | snp | A/C | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78184536 | CCTGTTCTCTCAGAA[A/C]TCTGAAAAGCACTGC | 287622 |
rs197479735 | snp | C/T | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78185567 | TTTGAGTCATTTCTG[C/T]TCCTGTAAATTACCC | 287622 |
rs197536755 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78186550 | TGTTCATTTTGTAGC[A/G]TAAGAAAACCTGTTG | 287622 |
rs197585251 | snp | A/G | 0 | 0 | intron-variant | Tom1l1 | Rn_Celera | 10:78188193 | CAATACCTATGAAGT[A/G]TTTTCATAAAAATCA | 287622 |
rs197593402 | snp | C/T | 0 | 0 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Tom1l1, LOC100363423 | Rn_Celera | 10:78219909 | GCCGCCGAGAGGCGC[C/T]AGGCTGCGAGCAGGG | 287622 |