SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4188874 | snp | A/C | 0.476371 | 0.106096 | intron-variant | Tfg | Mm_Celera | 16:56691566 | GTACCACATGAAATC[A/C]CATTACAGACAAGTG | 21787 |
rs4188875 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Tfg | Mm_Celera | 16:56693562 | TCTATAGCTAGCCAT[C/T]TATCTATCTGCAATT | 21787 |
rs4188876 | snp | C/T | 0.4992 | 0.019984 | intron-variant | Tfg | Mm_Celera | 16:56693860 | CTCAGGCGATGCAGA[C/T]TTCTATGTGTTGAAA | 21787 |
rs4188877 | snp | C/G | 0.4992 | 0.019984 | intron-variant | Tfg | Mm_Celera | 16:56693906 | ACTGTGCCACTTCAC[C/G]TCAGCACAGTTAAAA | 21787 |
rs4188878 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tfg | Mm_Celera | 16:56695680 | TGTCTACAATGTATA[C/T]ATTATATATCAAGAG | 21787 |
rs4188879 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tfg | GRCm38.p3 | 16:56695696 | ATTATATATCAAGAG[A/G]TATTCACTAAAGCAG | 21787 |
rs4188880 | snp | C/T | 0.5 | 0 | intron-variant | Tfg | GRCm38.p3 | 16:56703934 | TTTACATTTGAAACA[C/T]AGTTTTTACTACAGA | 21787 |
rs4231231 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56691331 | TAGAATTTAAAAAGT[A/G]TCTGGAAAAATTTTG | 21787 |
rs4231232 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56691224 | TTTTGGTCCATAGCA[A/G]TAAGACTAAGTCTCT | 21787 |
rs4231233 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56691214 | TAGCAATAAGACTAA[A/G]TCTCTGGAAAACTTT | 21787 |
rs4231234 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56691192 | GAAAACTTTCACCAA[A/G]AAACCCAAAACATTT | 21787 |
rs4231235 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56691171 | CAAAACATTTGTTAT[A/G]TATTTTGCTTTTTTC | 21787 |
rs13475551 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Tfg | GRCm38.p3 | 16:56701184 | TGACTCTTCTGGGAA[A/G]CAGTCAACTCAGGTT | 21787 |
rs45689701 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Tfg | Mm_Celera | 16:56693552 | CTATAGTCTATCTAT[A/C]GCTAGCCATCTATCT | 21787 |
rs45720976 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56705082 | ACCCATCATTGTTAG[C/T]TTTTACTCCCTGAAA | 21787 |
rs45731254 | snp | C/T | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56696746 | GTCATCTGTGCCAAA[C/T]AGCCCTTTTAAATAC | 21787 |
rs45765073 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56693179 | TTTCCTTTAAAATCA[A/C]TTCATCTGTTTTTTG | 21787 |
rs45774011 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56695658 | AGTCAATCTAAATAA[C/T]TGGCAGTGTCTACAA | 21787 |
rs45965124 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Tfg | Mm_Celera | 16:56697022 | AATCAGTGAAAAAAA[A/T]ATCAAAACTCAGATA | 21787 |
rs46046760 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56695996 | CAAAGAGAATGCATC[A/C]GTAGTAGTAATGTGA | 21787 |
rs46097124 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56696003 | AATGCATCAGTAGTA[G/T]TAATGTGAAGCTGCT | 21787 |
rs46128132 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56692396 | ATTTCTCCCGTCTTC[C/T]ATACTAAACTTAAAT | 21787 |
rs46235667 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tfg | Mm_Celera | 16:56712395 | GAACATACATGTGGA[A/T]ATCTGAGCAGAAGAA | 21787 |
rs46362641 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696014 | GTAGTAATGTGAAGT[G/T]GCTGGAAAGAGGTGC | 21787 |
rs46388011 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56695815 | CGTATGGTGTTTAAA[A/G]TGTTCCAAATCACTG | 21787 |
rs46466240 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56692907 | CTGACCACTCAAGTC[C/T]AGATTGGAGACTATA | 21787 |
rs46492212 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56698485 | GATGTGAAGAGTTCC[C/T]GGAGCTAATTATTAG | 21787 |
rs46528311 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tfg | Mm_Celera | 16:56694243 | CATCTCTATAATTAC[A/G]TTGAATTTGCTCACT | 21787 |
rs46533767 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tfg | GRCm38.p3 | 16:56707221 | TGCCATCTCATGTAG[C/T]TGCTAACAGACTATG | 21787 |
rs46551187 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56704017 | AAAAGTGTTTGAAAA[C/T]TGGCCTACTGTACAG | 21787 |
rs46555295 | snp | A/G | 0.18 | 0.24 | intron-variant | Tfg | Mm_Celera | 16:56716099 | TTGCTTAACCTGAGA[A/G]GAGGCCCTCTTTCAG | 21787 |
rs46652252 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56692681 | AATAAAACTATCTTT[C/T]CATCCTACACCTGAA | 21787 |
rs46746244 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tfg | Mm_Celera | 16:56706203 | GGGAAGAGTTTCATA[A/T]ATTAGTAGCATGAGC | 21787 |
rs46748049 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716691 | TAACTCCAGGTCTAC[G/T]CTCCAACGTCCAAGC | 21787 |
rs46786590 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718658 | CTATAGATGTAATTT[A/G]AGCATACTTTTTATT | 21787 |
rs46816358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56698910 | GAGGAAGAAAGAGGA[A/G]TGGGCTCTTGAGAGC | 21787 |
rs46819057 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tfg | Mm_Celera | 16:56705569 | ATCTAATAGCATTTC[A/C]GTCCAAAAATAAATA | 21787 |
rs47053490 | snp | G/T | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56701401 | AACAGTTTTCCAAAA[G/T]AATTATTGTCTCTAA | 21787 |
rs47062538 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56700087 | AGGATGAAGCTCCCT[A/G]TCAGTGAAGGCCTAG | 21787 |
rs47112020 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56698820 | CTGACAAGAAGTGTT[C/T]GAAACGAGTGCTTGG | 21787 |
rs47235825 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56716544 | TACAATTCTCCCTAC[C/T]GTGCCCAGAGACGGC | 21787 |
rs47252583 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tfg | GRCm38.p3 | 16:56697104 | CCTCAAATGAATTGA[C/T]CCAAATCTACATTCT | 21787 |
rs47374639 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716463 | GTTCTTCTCTGCGGC[A/G]TACTTTCTGCACATG | 21787 |
rs47438255 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56692170 | TCTCCATGCAGAGTA[A/G]TTAGTTATCTATTTC | 21787 |
rs47482130 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tfg | GRCm38.p3 | 16:56697344 | ACCATGTCAGTAAGA[C/T]AGACTATTTTCCATC | 21787 |
rs47492664 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tfg | GRCm38.p3 | 16:56694884 | CATTACAAGTCATTT[A/G]GATTTTAGCAACTAT | 21787 |
rs47554104 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56698977 | TCACTTCCTTGTTTA[C/T]TTGCCTTCTGACCAC | 21787 |
rs47626905 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718739 | GAAAGAAGAGGTTGT[A/G]GATTTTGTAGCAGTG | 21787 |
rs47632052 | snp | A/C | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56698084 | ATTAACTGCAACAGT[A/C]ACATACTTAAATGGC | 21787 |
rs47634203 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Tfg | GRCm38.p3 | 16:56692981 | CTGAATATCTGCATG[C/G]CTTGAAAAGCCACTT | 21787 |
rs47804468 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718993 | AGTCTAGAACACATC[C/T]CTTCTCTATTGCTGT | 21787 |
rs47834089 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56703332 | CCCTGAGTCTGATAC[G/T]CAAAGGCAGAGATTG | 21787 |
rs47916312 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695786 | AACTAGAGCTAGTTC[A/G]AACTGGGACATAACG | 21787 |
rs47989070 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tfg | Mm_Celera | 16:56706055 | CTCAGAGATGTAACA[A/G]TATCACAAATTACTA | 21787 |
rs48040497 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56692965 | CTGTTCAGCCTCCTC[A/G]CTGAATATCTGCATG | 21787 |
rs48049231 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716698 | AGGTCTACGCTCCAA[C/T]GTCCAAGCCACTCCC | 21787 |
rs48061034 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tfg | Mm_Celera | 16:56692842 | TTGCAACAAAATAGG[C/T]AATAGATATTTTTTA | 21787 |
rs48066510 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tfg | Mm_Celera | 16:56695454 | AAGCTTAGGTATATG[C/T]TTGCCTGAGCCTTCC | 21787 |
rs48087395 | snp | G/T | 0.231111 | 0.249285 | intron-variant, synonymous-codon | Tfg | GRCm38.p3 | 16:56704443 | ATTTTCAGGAATACT[G/T]GTGGAAGGTCCTGGT | 21787 |
rs48184276 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56689895 | CATGAATGAATGTAT[C/T]ACAGAATGTTTTTGT | 21787 |
rs48257217 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718780 | ACTTTAGTACTGTTG[C/T]TTGTCTGCTTTCAGG | 21787 |
rs48470946 | snp | A/G | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56704351 | ACCTGACTCCAAGAA[A/G]CAATCAAATAATCCT | 21787 |
rs48543884 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tfg | Mm_Celera | 16:56706080 | TTACTATATTAGACT[A/G]AAAAATCTTTCCATT | 21787 |
rs48558331 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56717612 | CTTCCGGTTTTCCGG[C/G]CAGCCAGTCTTTCCT | 21787 |
rs48741213 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696049 | GTTGCTAGAACACAG[A/G]TGGAAGACCATTTTC | 21787 |
rs48759912 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56697801 | TAGAAATGCTTCCCT[A/G]CAAATGTGTGAAATG | 21787 |
rs48801532 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56698970 | GCCCCTTTCACTTCC[A/T]TGTTTATTTGCCTTC | 21787 |
rs48850140 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56693931 | TTAAAACACTGAATA[C/T]TCTTAGTTGCCTGAA | 21787 |
rs48980547 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Tfg | GRCm38.p3 | 16:56690969 | AGTATAGTTGGCAGG[C/T]TGAGATGGTTGGGTA | 21787 |
rs49021427 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56693711 | CTGATGAAACTAGAA[A/G]AAATACCTAAATTAT | 21787 |
rs49052699 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718921 | TTGCTTATTCCTTTA[C/T]AATGTCTTGTGATCT | 21787 |
rs49139517 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56704608 | TTGCTTAAACTTAGG[A/G]AATGATGCCATTAAA | 21787 |
rs49193740 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tfg | Mm_Celera | 16:56692788 | TACACCCTCCTAACA[C/G]TCCTAAAATGAGTAA | 21787 |
rs49194518 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56695507 | ACAATCAGTAGCAAA[A/C]CATACTTCGGGGGAA | 21787 |
rs49213756 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Tfg | Mm_Celera | 16:56695400 | ATTGGCTGGTCTCTC[C/G]TTTTTTCACTTTTCA | 21787 |
rs49222015 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56690191 | CGTAAGGAAAAATCA[G/T]AAAATGAAGAGCTAC | 21787 |
rs49230681 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tfg | GRCm38.p3 | 16:56692929 | GAGACTATAAAACGG[C/T]ATAAAGACAAGAGAA | 21787 |
rs49368973 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tfg | GRCm38.p3 | 16:56698001 | AATGATCCACTTCAT[A/G]GTTTCATAGGATGTC | 21787 |
rs49542158 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tfg | GRCm38.p3 | 16:56709707 | TGACAATGTATATTA[A/G]CATAATGAACACCAA | 21787 |
rs49546902 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718661 | TAGATGTAATTTGAG[C/T]ATACTTTTTATTAAA | 21787 |
rs49547648 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716646 | TGTACGACCGAATGG[A/G]GCTCCTTTCTGTGTC | 21787 |
rs49551515 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tfg | Mm_Celera | 16:56693104 | AATGTCTATATGTTA[C/T]ACAATTTGTACCATA | 21787 |
rs49554164 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56700027 | AGAATTTCAAGACAA[C/T]CATCATGGTAACAAT | 21787 |
rs49618972 | snp | C/T | 0.231111 | 0.249285 | intron-variant, synonymous-codon | Tfg | GRCm38.p3 | 16:56704470 | TGGTTCTCCAGGTGG[C/T]TCTAAGCTATCCAAT | 21787 |
rs49657926 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718979 | TCATCTAAACTCCCA[A/G]TCTAGAACACATCCC | 21787 |
rs49665366 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718893 | TGGCCTGAAATTCAG[A/G]GTTTTCCTTGTCTTG | 21787 |
rs49671924 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tfg | Mm_Celera | 16:56707488 | ACTCATCAAAAATGA[C/T]GGTTGTATGACAGAA | 21787 |
rs49720676 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718603 | TGTCCTAGACATGGA[C/T]ACAGTTCCCTATAGT | 21787 |
rs49730130 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tfg | Mm_Celera | 16:56692926 | TTGGAGACTATAAAA[C/T]GGTATAAAGACAAGA | 21787 |
rs49732444 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56693013 | TAAAAGAGTAGAACA[A/T]CATCAGTGGTCCTCA | 21787 |
rs49752601 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56698259 | TTTCCTTAAGACTGT[A/G]AGAACTTTGGCCATA | 21787 |
rs49774320 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690404 | TCATCTTCTCAGAGG[C/G]CTCTATTTTTAGTAC | 21787 |
rs49775485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56701331 | TAAATACTGTCAGGA[C/T]TTTGTGAATATAGAA | 21787 |
rs49945457 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tfg | GRCm38.p3 | 16:56694995 | ACTCACTGTGTAATA[A/C]CCTAGTGATGTTGGA | 21787 |
rs50009659 | snp | A/G | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56699505 | CGCACACAGTTTCCC[A/G]AGAGAAGATACTGTA | 21787 |
rs50058533 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716472 | TGCGGCGTACTTTCT[G/T]CACATGCGAAGGGAG | 21787 |
rs50159047 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56705376 | GATTCCTAAGTTACA[C/T]TCATCTCAAAACCAA | 21787 |
rs50172536 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56699642 | ACATTACTGTGGTAG[C/G]TATTTCCCACCTTAA | 21787 |
rs50189923 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56691538 | TAGGTTTAAAGGGAA[A/G]TCCTATTTAACAGTA | 21787 |
rs50231035 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56695717 | ACTAAAGCAGCTTAT[C/T]CTACATCACTATCTC | 21787 |