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 |
rs50236672 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56696267 | CACCCAAACTCTGTA[C/T]TCTGCTTTAGCCTCC | 21787 |
rs50253898 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tfg | GRCm38.p3 | 16:56692875 | ATCCATAAATAGCTA[C/T]AACTAAGCCTAAGAT | 21787 |
rs50447922 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695980 | ATAATTAATACCACT[C/G]CAAAGAGAATGCATC | 21787 |
rs50474049 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695987 | ATACCACTGCAAAGA[A/G]AATGCATCAGTAGTA | 21787 |
rs50477924 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56698867 | ATCCCACCAATGAAC[G/T]GATAGCTGGTGGGCT | 21787 |
rs50499479 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56717838 | TCATTCAGGATTGAG[C/T]GCCTACGCTTTGCCG | 21787 |
rs50557165 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695997 | AAAGAGAATGCATCA[A/G]TAGTAGTAATGTGAA | 21787 |
rs50752091 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690176 | ATATACCTTTATCGC[C/T]GTAAGGAAAAATCAT | 21787 |
rs51026177 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56716462 | AGTTCTTCTCTGCGG[A/C]GTACTTTCTGCACAT | 21787 |
rs51030041 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56696326 | AGTTTGTTTTAGCTC[C/T]GGCTCTTGTATTTTT | 21787 |
rs51165932 | snp | A/G | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56703059 | GTTCAGAATAAGCAA[A/G]CTGCTTTCATCTGTA | 21787 |
rs51198458 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tfg | GRCm38.p3 | 16:56702416 | GTAAAACAACATAAA[C/T]CTTGTCTAAATTTAG | 21787 |
rs51219572 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56691780 | AACAAATCATATTGT[C/T]CCACTTAATCAACAT | 21787 |
rs51226228 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tfg | GRCm38.p3 | 16:56715936 | TGCATTTTCTGATGC[A/G]TCTCGTTGCTGTCTT | 21787 |
rs51398327 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | GRCm38.p3 | 16:56695018 | ATGTTGGAGCCACCT[C/T]AGTTTATATAAACAT | 21787 |
rs51437920 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56696014 | AGTAGTAATGTGAAG[C/T]GGCTGGAAAGAGGTG | 21787 |
rs51473547 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56693161 | TAACACACTCAAATG[A/G]CATTTCCTTTAAAAT | 21787 |
rs51537352 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56702437 | CTAAATTTAGGAACT[C/G]AACTCTTATGTTTTG | 21787 |
rs51596316 | snp | A/T | 0.32 | 0.24 | intron-variant | Tfg | GRCm38.p3 | 16:56703282 | ACCTAACCATATTTT[A/T]AAAAAGTGTCTACAA | 21787 |
rs51641294 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56704244 | TCAATTAAAGTACTG[A/T]AGTGCAAGTTTACAG | 21787 |
rs51651645 | snp | C/T | 0.231111 | 0.249285 | intron-variant, missense | Tfg | GRCm38.p3 | 16:56704514 | TATTTCGAAGTTCTA[C/T]CAGTTCTCGACGAAG | 21787 |
rs52009659 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tfg | Mm_Celera | 16:56692750 | AGCAATACTGCTCTA[C/T]TAGGTCTATTTGTCT | 21787 |
rs52015206 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tfg | GRCm38.p3 | 16:56694072 | AAATTGTTGATATAC[C/G]TACAAATACTAAGAG | 21787 |
rs52042622 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56716768 | CTTTCTATGTCTTCC[A/T]TGATTCACCCTCCAC | 21787 |
rs52125217 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tfg | Mm_Celera | 16:56700572 | GATTAGGATCCTCTC[C/T]GTCCCCACCAAGAAA | 21787 |
rs52505908 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tfg | Mm_Celera | 16:56700829 | CTGCTTTAAAAAAAA[A/T]AATCTGAAAATACTT | 21787 |
rs107742027 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56702302 | GACCCTACATCAAGT[A/G]CTTCATCAACTGAGC | 21787 |
rs107931517 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56696011 | AGTAGTAGTAATGTG[A/C]AGCTGCTGGAAAGAG | 21787 |
rs108125235 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702009 | CAGCACAGCATGAAC[C/T]CTAGCTCATTCAGGT | 21787 |
rs108341310 | snp | A/G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702121 | TATGCTTTCTGAGAG[A/G/T]GTCTCTCAAAGGCCT | 21787 |
rs108486307 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56702013 | ACAGCATGAACCCTA[A/G]CTCATTCAGGTGTGC | 21787 |
rs108909627 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702248 | ACACACACCATCATA[C/T]CAGACATTTTTTCAC | 21787 |
rs212011181 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714666 | TCCTAATTCTGAACC[C/T]TAAGACTTTTAGTAA | 21787 |
rs212016305 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56697900 | GTGCTGCTTTATTAA[C/G]CAGGTCTCTAATGTC | 21787 |
rs212018100 | in-del | -/TAACA | | | intron-variant | Tfg | Mm_Celera | 16:56703073 | AGCTGCTTTCATCTG[-/TAACA]TATAAATAAGTCTTC | 21787 |
rs212064160 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56692768 | GGTCTATTTGTCTCC[A/G]TTTCTACACCCTCCT | 21787 |
rs212075261 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712605 | CTTAATACCTTAAAA[G/T]CTTACCTTCATCCTT | 21787 |
rs212158611 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56701816 | TAATACAAGCAGGCC[A/G]GGCAACCATAAGCAG | 21787 |
rs212182014 | in-del | -/CAGG | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717828 | ATTCATTCATTCATT[-/CAGG]ATTGAGTGCCTACGC | 21787 |
rs212221936 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56704108 | CTTATTATTCAGTAC[-/G]GGGGACTGAGTACAG | 21787 |
rs212251935 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56697136 | TACCTAAAATTATGT[A/T]TCATCATCTTGATAT | 21787 |
rs212297906 | snp | A/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719527 | CTCAGCTCTTACTGA[A/T]TTTTTATTAGGTATT | 21787 |
rs212344257 | snp | G/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718745 | AGAGGTTGTAGATTT[G/T]GTAGCAGTGCTCAGA | 21787 |
rs212476856 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715806 | CAGGCACCACCGTTA[C/T]TTCCTGTCCCAAGAG | 21787 |
rs212592236 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56710572 | CATATGGAAAATCAT[-/G]GGGGTATCCAAGGCA | 21787 |
rs212601187 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56716007 | CCTTCATCCAAGAAA[-/T]TTCCTGGTAACTGGG | 21787 |
rs212668906 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56702254 | CCATCATACCAGACA[-/T]TTTTTTCACATGGGT | 21787 |
rs212708034 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56708820 | TACAGCAGAGGACTG[A/C]CTGGCCTAGTTTCAG | 21787 |
rs212903864 | in-del | -/TA | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56712814 | GAGTCCAGGATGCTC[-/TA]TATATACAACTCTAG | 21787 |
rs212966867 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56707391 | TCAATAAGGAAGATA[A/C]CCTAAAGTGGGAGCC | 21787 |
rs212998117 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56692435 | TGTGTGTGTTGTGTA[C/G]CTACCCATGAAAGGC | 21787 |
rs213081921 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56699650 | GTGGTAGCTATTTCC[C/T]ACCTTAACCATATCA | 21787 |
rs213109166 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56692918 | AGTCTAGATTGGAGA[A/C]TATAAAACGGTATAA | 21787 |
rs213148538 | in-del | -/CA | | | intron-variant | Tfg | Mm_Celera | 16:56714356 | GGACAGCCAGGGCTG[-/CA]CAGAGAAACCCTGCC | 21787 |
rs213220244 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56707115 | AAAATGTTTTCCTTT[G/T]TAAGAGTTGCTGTGG | 21787 |
rs213271360 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56705542 | AAACACATTTATTAT[A/T]AAAAAATTCATATCT | 21787 |
rs213274353 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56714384 | TGCCTAGGAAAACCA[A/T]AAATAAATAAATAAA | 21787 |
rs213332926 | in-del | -/TCAA | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690235 | TATTTATAGTCTAAG[-/TCAA]TCAAATTTATTATAT | 21787 |
rs213404614 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56715607 | ACTCCCAAGTAAGAC[C/G]AAGTTCCAGCACAAA | 21787 |
rs213482354 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714872 | CCACAGGCTACTCTG[C/T]TTTCATTCCTGAACT | 21787 |
rs213511506 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56692389 | GTCATTAATTTCTCC[C/T]GTCTTCCATACTAAA | 21787 |
rs213745291 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714280 | TAATCTCAGCACTTG[A/G]GAGGAAGAGGCAGGT | 21787 |
rs213966964 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56713881 | TTGAACAACTATCCA[C/T]GATCAAGCAACACAA | 21787 |
rs214061812 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56699591 | CTTATTACTGTTGTC[G/T]ATTCTGTTTTTCTAA | 21787 |
rs214070234 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56706822 | AATATGTTCTCCCCC[A/C]CTCCCCATACACATA | 21787 |
rs214378623 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717651 | CTGCTGGGTGGGCGG[A/G]GCGTAGTCTGCAGGG | 21787 |
rs214412026 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56702551 | GTACTACTTATTAGT[A/T]ATTAAAATACTTGTA | 21787 |
rs214445218 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56698139 | CTAATAAATCTTTGA[A/C]TTATAAATGCTTTAT | 21787 |
rs214465349 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56709524 | ATTTCTATAATAATA[A/G]CAACCATCATGATTT | 21787 |
rs214696687 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56708644 | ACAGAAGCCGGGGAC[A/C]CAGGTGGTGGAATTG | 21787 |
rs214728866 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718584 | TCTTTTCTATAATAC[C/T]GTATGTCCTAGACAT | 21787 |
rs214810194 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709183 | AATAGGAAGAACACA[A/G]TGACTCTCAAAAATT | 21787 |
rs214912305 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56707651 | AGGCAAGAATAGAGT[A/G]TCTTGAGTTAAAATG | 21787 |
rs214912513 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56703479 | AGAAGTTATACATGA[A/C]ATTTTTCCACAGAAA | 21787 |
rs215144559 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56716696 | CCAGGTCTACGCTCC[A/T]ACGTCCAAGCCACTC | 21787 |
rs215182531 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56693039 | CCTCACTGTGGCTAC[A/G]TAACCTGTGATGCCT | 21787 |
rs215246714 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56693620 | TAATAACACAAAACT[A/C]CCAAAATATAATTTT | 21787 |
rs215272534 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56700801 | TCTGGACTTTTTTTT[A/T]AAAATAAAAGTTCTG | 21787 |
rs215272615 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56692594 | CAAAAACTTTCAAAT[G/T]TTAACTTTTTACTTT | 21787 |
rs215313843 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56707180 | AAGACACAGAACGAG[C/T]ATCTCCGTAGGAAAG | 21787 |
rs215325671 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56709361 | ATGACCAGGCTCTGA[C/G]CAATGCTATATGTAC | 21787 |
rs215454573 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56701779 | TGTGTGGGTGGGGCA[A/C]CCCTAGGCTGGTGGT | 21787 |
rs215461375 | in-del | -/GTGG | | | intron-variant | Tfg | Mm_Celera | 16:56692418 | ACTTAAATATTGTGT[-/GTGG]GTGTGTGTGTTGTGT | 21787 |
rs215493999 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56708056 | AGAAAGCAATGGGGG[-/T]GGTGGGGGGGGGAGG | 21787 |
rs215495173 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699816 | CCACAAAAGTTTCCA[A/G]GAAAATCAAAATGAA | 21787 |
rs215628956 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56701488 | AACAAAAGGCTACAA[C/G]AAGAGGATCAAAAGT | 21787 |
rs215679021 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56689903 | AATGTATTACAGAAT[A/G]TTTTTGTGAAACTGT | 21787 |
rs215830259 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711894 | CCACAGTTCAAATCA[C/T]CCTCAGCAACAAAGT | 21787 |
rs215830980 | in-del | -/TAAG | | | intron-variant | Tfg | Mm_Celera | 16:56694311 | TACTGCTTGCCCTCA[-/TAAG]TAAGTAACACTTCCG | 21787 |
rs215883097 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696043 | TGCACGGTTGCTAGA[A/G]CACAGATGGAAGACC | 21787 |
rs215896779 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56702415 | TGTAAAACAACATAA[A/C]TCTTGTCTAAATTTA | 21787 |
rs216079792 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719101 | TAATATTATGGTTTC[A/G]TGGCAAACAAAGTCC | 21787 |
rs216093378 | snp | A/C | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718694 | AATCTACATCTAGAA[A/C]CACAGAGATCTCATT | 21787 |
rs216247237 | in-del | -/AAAA | | | intron-variant | Tfg | Mm_Celera | 16:56701286 | ACCCAAAACCACATT[-/AAAA]AAAAATATATATATA | 21787 |
rs216304741 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56697084 | AGAGGGATAAAAAAA[A/C]CCCACCTCAAATGAA | 21787 |
rs216395994 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56695669 | ATAACTGGCAGTGTC[G/T]ACAATGTATATATTA | 21787 |
rs216488150 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710711 | TAAGCTCAGGTTGAC[C/T]CCACTCCACTGCTGC | 21787 |
rs216501591 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696002 | GAATGCATCAGTAGT[A/G]GTAATGTGAAGCTGC | 21787 |
rs216548116 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56709875 | TAAGCCAGCTTTCCT[A/G]TATTTGGTTGGTGTC | 21787 |
rs216619631 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56710967 | GGTGACTCTTACACA[A/G]TACCAAGTACAGCTG | 21787 |
rs216620393 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56703763 | CATTTTGGTGCCTAA[A/G]CTATATCAGCTTCCA | 21787 |
rs216649496 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56705255 | ATTACTATTTGGGGT[A/T]ACAAAACAAATATAG | 21787 |
rs216713941 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56709253 | GAATTTACACATGTC[A/G]GTAGATGACCAACTT | 21787 |
rs216862029 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711454 | CAAGAGATCTGTTTG[C/T]CTTAGGCTCCTGGGA | 21787 |
rs216934821 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701603 | TATTATTATTTAATA[A/G]TCTCCTTAATAAACA | 21787 |
rs216983143 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714895 | CCTGAACTTTCACTA[C/T]TGCCAGCTTTCTGTC | 21787 |
rs217021009 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56712408 | GAAATCTGAGCAGAA[A/G]AAAAGTATTTGAAAA | 21787 |
rs217238404 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56700792 | AAAAAAAATCTGGAC[-/T]TTTTTTTTTAAAATA | 21787 |
rs217266133 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56694584 | TCCCAATTTAATATG[C/T]AAGCACATTGAATAA | 21787 |
rs217318871 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690082 | CAATGCTACAGTATT[C/T]TGTATTTTCAAACAA | 21787 |
rs217318957 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56698617 | ACCTCAAGTTTACTT[G/T]GAAGGGTTATGAGTT | 21787 |
rs217410759 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56692849 | AAAATAGGTAATAGA[C/T]ATTTTTTAAAATCCA | 21787 |
rs217540216 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56706907 | GAAGTGTGCTACCAT[-/G]GGGGCAAGCTTTGAG | 21787 |
rs217697782 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56694609 | GAATAATAATTATAA[-/T]TTTTGTATTATTTAA | 21787 |
rs217705350 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56705560 | AAATTCATATCTAAT[-/A]AGCATTTCAGTCCAA | 21787 |
rs217835194 | in-del | -/CT | | | intron-variant | Tfg | Mm_Celera | 16:56702889 | CAAAGCTAGACTAGC[-/CT]CTACTTGGGGAGGTT | 21787 |
rs217914332 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711796 | AACGGCAAAAAGCAG[C/T]CACATTCTTCACCAA | 21787 |
rs217923534 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56713168 | GTTCTGGTAATCCAT[C/G]CAATTTGGCATCTTC | 21787 |
rs217926621 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718649 | ATACAATGCCTATAG[A/G]TGTAATTTGAGCATA | 21787 |
rs218072498 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56704585 | TTAACTAAAAAAAAA[A/G]CATTAATTTGCTTAA | 21787 |
rs218133046 | in-del | -/GCTA | | | intron-variant | Tfg | Mm_Celera | 16:56694736 | GATGTAACTCCAGTG[-/GCTA]GCTACCACTTTATAA | 21787 |
rs218178436 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714764 | GGCCAAGTAATTCCT[G/T]AACATGCTTATCTAT | 21787 |
rs218248108 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56715739 | GCCCAGTTTCATTTC[C/T]AGTTTCCTCCCTGCA | 21787 |
rs218257718 | snp | A/C | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717686 | GTTTGCTACGAGAGC[A/C]TGGGGGAAGTGGGGC | 21787 |
rs218260860 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56710666 | CAAAGGGCTGGTATC[A/G]GTTCTCCAGCTCTGT | 21787 |
rs218303771 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714111 | AAAGTAGTACTGCTG[C/T]TAATAGCTTGGCCAT | 21787 |
rs218427571 | snp | C/G | | | synonymous-codon | Tfg | Mm_Celera | 16:56701136 | TTCATCTTGGTTTTT[C/G]AGAGGATCAAAAGCT | 21787 |
rs218560609 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56694794 | TATGCCATCAGGTAA[A/G]TAATCAGAGAAAAGG | 21787 |
rs218619529 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56699208 | TCTCATAACTGTAAT[C/T]TTGCTAGTTACGAAT | 21787 |
rs218821984 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56697022 | AATCAGTGAAAAAAA[-/T]ATCAAAACTCAGATA | 21787 |
rs218884779 | in-del | -/TTAT | | | intron-variant | Tfg | Mm_Celera | 16:56696566 | TTAGGTACTGTGGAC[-/TTAT]TTATTATGATTGTGA | 21787 |
rs218962609 | in-del | -/TAT | | | intron-variant | Tfg | Mm_Celera | 16:56698696 | GCTTAATTCAACCAC[-/TAT]TATTAGCAGGCTCTC | 21787 |
rs219031317 | in-del | -/CTACAG | | | intron-variant | Tfg | Mm_Celera | 16:56693561 | TCTATAGCTAGCCAT[-/CTACAG]CTATCTATCTGCAAT | 21787 |
rs219092601 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56705568 | TATCTAATAGCATTT[C/G]AGTCCAAAAATAAAT | 21787 |
rs219133396 | in-del | -/CAAGAATAC | | | intron-variant | Tfg | Mm_Celera | 16:56712027 | TGGTCAGGCCTATCA[-/CAAGAATAC]CCCAGTCCCTGGTAC | 21787 |
rs219143834 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707752 | AATGGATGGATGGAT[A/G]GATGGATTAGAAACA | 21787 |
rs219152559 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56697667 | GCACAATTTAAAGTT[-/C]AGGTTATTGACAATC | 21787 |
rs219221750 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56707009 | TTTCAGCTCCTCCTA[C/T]AGCACCATGTCTGCC | 21787 |
rs219223491 | snp | C/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56717609 | GCACTTCCGGTTTTC[C/T]GGGCAGCCAGTCTTT | 21787 |
rs219331643 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714076 | CCTCTGATTTGAAAA[C/T]TGAACTCGGGTCCTC | 21787 |
rs219368264 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56705479 | CGCAAATATTTTAAA[C/G]TATTATGTAACTCTG | 21787 |
rs219519370 | snp | C/T | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690289 | AATTCTGTAAAATGA[C/T]TATTTTCTTTATGTC | 21787 |
rs219525086 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56713717 | AATTATTAACTTGCA[A/G]CTCTAATGTTAACCT | 21787 |
rs219811851 | in-del | -/AAGA | | | intron-variant | Tfg | Mm_Celera | 16:56693709 | CTCTGATGAAACTAG[-/AAGA]AATACCTAAATTATA | 21787 |
rs219828269 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56706299 | AAAATGAAACCCTAA[-/T]TTTTTTTCAGTTAAT | 21787 |
rs219880948 | in-del | -/CT | | | intron-variant | Tfg | Mm_Celera | 16:56698059 | ATCATAATTTCTTCA[-/CT]CTCTCTATGATTAAC | 21787 |
rs219913041 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56708108 | TGGGAGAGGGGAGGG[-/A]AAAAAGGGAATGAGA | 21787 |
rs219925949 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56713036 | CTACCCCAAAGTTGC[C/T]TCTCCTAAGGCTTTC | 21787 |
rs220133513 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716724 | CTCCCGGGGATCAGG[C/T]ACAAACGCTTTGGGC | 21787 |
rs220145130 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708937 | AGAATGGAAACGGGG[A/G]TGGGGGCGGGGAGGA | 21787 |
rs220181685 | in-del | -/TT | | | intron-variant | Tfg | Mm_Celera | 16:56704163 | CCTACCACTGAGTTA[-/TT]TTCCCCCGTCCTAGA | 21787 |
rs220249181 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56702352 | CCAATGACCTACAAA[-/T]ACAGGTAAAATGCCC | 21787 |
rs220269772 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695785 | GAACTAGAGCTAGTT[C/T]AAACTGGGACATAAC | 21787 |
rs220338403 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56711273 | TTTCCAACTCCTTCA[A/C]TGCCTAAGCTTGGCT | 21787 |
rs220401547 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710160 | cctaatagagcaacc[C/T]cctgagctaagcata | 21787 |
rs220427924 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56716075 | GGATACCTCAGCCTC[A/G]GGCACCTGTTGCTTA | 21787 |
rs220455128 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715181 | ACAATCTGGATGCCA[C/T]AGTTATCTTAATGTA | 21787 |
rs220549793 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56693869 | TGCAGATTTCTATGT[G/T]TTGAAATCCCCTGGG | 21787 |
rs220562668 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56691577 | AATCCCATTACAGAC[A/C]AGTGCTTTATAAGTG | 21787 |
rs220608984 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717914 | ACATTTAGGAAGATC[C/T]GAGTTTAGAGGGCAC | 21787 |
rs220693893 | in-del | -/CAAT | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718406 | TATAATCTAACACTA[-/CAAT]CTAAGTCTTACAAGT | 21787 |
rs220742347 | in-del | -/AATTTT | | | intron-variant | Tfg | Mm_Celera | 16:56706524 | GAGACTAACTAAACC[-/AATTTT]AAGACTTGTTAAGCC | 21787 |
rs220846326 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56691567 | TACCACATGAAATCC[C/T]ATTACAGACAAGTGC | 21787 |
rs220891469 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718755 | GATTTTGTAGCAGTG[C/T]TCAGAAAGGACTTTA | 21787 |
rs220897588 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714950 | TCCATTTTCACCCCC[A/G]CCCCTTTAATGTGGA | 21787 |
rs220996254 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714901 | CTTTCACTATTGCCA[A/G]CTTTCTGTCTCCTTC | 21787 |
rs221040851 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56715914 | AGAACTACTGTTAAG[A/T]TCACTATGCATTTTC | 21787 |
rs221177351 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56710167 | AGCAACCTCCTGAGC[-/T]TAAGCATATACATCA | 21787 |
rs221288182 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56698414 | TACTGTGAAAGTGGA[C/T]TCTGAAGATGACACA | 21787 |
rs221325881 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56691492 | CACTTTCTAGGAAGA[C/T]GAAAATCATAAAAGC | 21787 |
rs221394233 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714003 | TATTTCTGTGTGCAG[A/G]TGCCCCAGGAGGCCA | 21787 |
rs221420950 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690599 | CATTTTGGTCTTTTT[A/G]TGTCTGTATTCTGGT | 21787 |
rs221421205 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56699099 | CATGACCTGAAATTT[A/C]CCTTAAGTCAGTGGT | 21787 |
rs221462146 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717803 | TTTTCCGCCTTCTTT[C/T]TACACGTTCATTCAT | 21787 |
rs221515694 | in-del | -/GGGAATT | | | intron-variant | Tfg | Mm_Celera | 16:56708870 | AGACTTGAGGCCCCA[-/GGGAATT]GGGAATTGGGAGGTC | 21787 |
rs221607663 | snp | C/T | | | missense | Tfg | Mm_Celera | 16:56697492 | GTGTCTGAGCTCCTG[C/T]ATAGGGAGGTTGCTG | 21787 |
rs221671473 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56717158 | CCTCCTTGAGTCGCC[A/G]CGCGCGCCTCACTCC | 21787 |
rs221680772 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690381 | TACATTTTATACATA[A/C]TGTCTAGTCATCTTC | 21787 |
rs221681020 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56706457 | AAGAAATGATATGGG[A/G]TAGAGGGAACCAGTC | 21787 |
rs221695514 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695355 | AACTAACTTTATAGA[C/G]CAGACCCAGTTGAAC | 21787 |
rs221719754 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695252 | GTTGTTCACACAGGG[C/T]CAAAGTTATTGAATA | 21787 |
rs221797445 | snp | C/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56719050 | AGGGGGTTTCATCTT[C/T]ATTTATTATCACCAA | 21787 |
rs221905274 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56707953 | CCAAAGAAGTACAAA[A/G]AATACTCAGGACACA | 21787 |
rs221942773 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56706325 | TTAATACATGTTCTT[A/C]TGTAAATATATATAT | 21787 |
rs222000109 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56689953 | ACAGACTCATTTCAT[-/G]GGGGAAAAAAAAAGC | 21787 |
rs222032076 | in-del | -/CAAA | | | intron-variant | Tfg | Mm_Celera | 16:56693798 | AGAGATGGTAAAACT[-/CAAA]CAAACTCCTCTGTGT | 21787 |
rs222060279 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56698210 | CACACTGATTGCTAC[A/G]TTGTATAAATGTCTA | 21787 |
rs222064837 | in-del | -/TT | | | intron-variant | Tfg | Mm_Celera | 16:56692280 | TGTGAAAACCCTGTC[-/TT]AAACTTCCCAGAAAA | 21787 |
rs222161840 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56704278 | CTTGACAAATAGTTG[-/T]GGGAATGTTGACATG | 21787 |
rs222303657 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699261 | CAGGATCTCTGATAT[A/G]CAACCTCCAAAAGAG | 21787 |
rs222303936 | in-del | -/TCCT | | | intron-variant | Tfg | Mm_Celera | 16:56711161 | TTCTGGACTCTAAAG[-/TCCT]CCCTCAGAGCCACAA | 21787 |
rs222516494 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56701960 | AAGCCTTTTAATAAA[C/T]CCTTTCCTCAAGTTG | 21787 |
rs222576406 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56696722 | TGTGGTCTTTAGTCA[C/T]GCTCTGATGTCATCT | 21787 |
rs222664908 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697439 | TGCCCTTCCACACAC[A/G]GCTCTGAACGCTGTT | 21787 |
rs222677252 | snp | A/C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704862 | TCAGAACTCAGGTTG[A/C/T]ATGTACTGCAGCAAA | 21787 |
rs222688028 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56694031 | ACAACTTAGTTTTTA[G/T]TAAATTCGCTTCTGC | 21787 |
rs222689115 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56702836 | GGCTAGGTAATACCA[C/T]CCTGTAGTTCCAGCA | 21787 |
rs222745824 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56704707 | GGTGAGTGCTCCCAC[A/G]GAGGCCCAAGGCTGA | 21787 |
rs222802153 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56713336 | ATGCTTAGAACCTTC[C/T]AATGAATTCCCATAG | 21787 |
rs222824497 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56697298 | CAGAAACATACTCAG[C/T]ATATTATTTGGTTCC | 21787 |
rs222832281 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56708929 | CTTCCTGGAGAATGG[-/A]AACGGGGGTGGGGGC | 21787 |
rs222888266 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56705557 | TAAAAAATTCATATC[A/T]AATAGCATTTCAGTC | 21787 |
rs222897296 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711516 | AACTTATCTGGGTGC[A/G]ATCTTGCCCCAAGAT | 21787 |
rs222916729 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696477 | CAAGTGTCATCACAG[A/G]ACAAGAAGATTCTAG | 21787 |
rs223051980 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56704127 | GACTGAGTACAGAGT[A/G]CTGCATATGTCAGGC | 21787 |
rs223059491 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704221 | CTGTCCTCCCAGAGC[G/T]CTATGATTCAATTAA | 21787 |
rs223061569 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56701884 | GCTCTTGCTTCCAGA[G/T]TCTTGCCTCGTTTGA | 21787 |
rs223062302 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56695228 | GAAAGTAGAGAACCA[C/T]TGCTTGATGTTGTTC | 21787 |
rs223122636 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56693377 | TAAATATTTTAGGTG[C/T]TGTGGGCTACACTGC | 21787 |
rs223162447 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712008 | ATTTTTCCAAACAGA[C/T]GCATGGTCAGGCCTA | 21787 |
rs223172734 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695127 | TTTGTAACAGTAAAA[C/T]GTATAGTTATGAAGT | 21787 |
rs223228949 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56694950 | GTAACATTGTATTTC[-/T]TTTTTTTTAAAATGA | 21787 |
rs223231440 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710585 | CATGGGGTATCCAAG[A/G]CAACTTCAGTATTAC | 21787 |
rs223238681 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56706076 | CAAATTACTATATTA[G/T]ACTGAAAAATCTTTC | 21787 |
rs223549456 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56703054 | GCAAGGTTCAGAATA[A/C]GCAAGCTGCTTTCAT | 21787 |
rs223626739 | in-del | -/CTTCCCT | | | intron-variant | Tfg | Mm_Celera | 16:56713087 | TTCAAGAAGGCCTTG[-/CTTCCCT]CTTCTCACACCTCAC | 21787 |
rs223713098 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56709200 | GACTCTCAAAAATTT[C/G]TTTGGCTAATTTCAG | 21787 |
rs223810089 | snp | A/G | | | synonymous-codon | Tfg | Mm_Celera | 16:56701205 | AGAAGAGTCAGAAGC[A/G]GCAGGCTTCTCTTCC | 21787 |
rs223862055 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709948 | CTCTTATAAGGGGCT[A/G]GCTTACAGGTTCAGA | 21787 |
rs223870895 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56705901 | TAAGCAGGGTGTGGT[A/G]GTACACGGCTTTAAT | 21787 |
rs223884969 | in-del | -/GG | | | intron-variant | Tfg | Mm_Celera | 16:56696040 | GGTGCACGGTTGCTA[-/GG]GAACACAGATGGAAG | 21787 |
rs223895317 | in-del | -/AGCG | | | intron-variant | Tfg | Mm_Celera | 16:56699971 | AGTAAATCAAATCTC[-/AGCG]AACTCCAAAGGGAGT | 21787 |
rs223956138 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699423 | CTATGCTAGGTTATG[A/G]TAATAGGAATGTTGA | 21787 |
rs223977193 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56704931 | TATTTTTACAATGTT[A/G]GAATTTAAATGCATT | 21787 |
rs224017370 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704337 | ATATTAAGGATGACA[C/T]CTGACTCCAAGAAGC | 21787 |
rs224017502 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56712227 | AGGCAGCTAGGGTGA[A/G]GGTCTTAAGCCCATG | 21787 |
rs224111490 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708835 | CCTGGCCTAGTTTCA[A/G]TGATATACCTAACCC | 21787 |
rs224130080 | in-del | -/A | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717962 | ACAAACTTGGATAGT[-/A]AAAACCGAGGCTTCA | 21787 |
rs224158268 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56700240 | AGGAAGGAGGAAAGA[A/G]GAGGAAGATGCAGCA | 21787 |
rs224277038 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708303 | TGAAGTGCTCTACAA[A/T]AGGGAGGGAGAACTT | 21787 |
rs224290463 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56698507 | AATTATTAGATTGCA[C/T]TGCCCGAGCTAACAG | 21787 |
rs224306670 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56710371 | CAATCACTTAACTGT[-/A]ATCCTTAAATCAAGA | 21787 |
rs224336336 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56706648 | CATATGTATAGCATA[C/T]ATGCTTAATAATGCT | 21787 |
rs224381363 | in-del | -/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719003 | CATCCCTTCTCTATT[-/G]GCTGTCTAGTGAGTA | 21787 |
rs224394093 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56713970 | TGTATTCTCCTATTA[-/T]TTTTTTAAGATTTAT | 21787 |
rs224476777 | in-del | -/GGGGGT | | | intron-variant | Tfg | Mm_Celera | 16:56708054 | AGAAGAAAGCAATGG[-/GGGGGT]GGGGGGGGGAGGTGA | 21787 |
rs224571246 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56706911 | GTGTGCTACCATGGG[G/T]CAAGCTTTGAGGTCT | 21787 |
rs224775164 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695424 | CTTTTCAAAATTAAA[C/G]CTAAGGCCTCACATA | 21787 |
rs224782164 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56702631 | ATAAACAGGCATGAT[-/C]CTGACCTAAGGTAAT | 21787 |
rs224836554 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56693824 | CTCTGTGTATAGGAA[C/T]GGACCACCTACAGAA | 21787 |
rs224895852 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56716808 | TGCTCTAGAGGGTGA[A/G]GCACCGAGCAAACGC | 21787 |
rs224953608 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56714750 | TTGTTTTTCTGCAAG[A/G]CCAAGTAATTCCTTA | 21787 |
rs225035878 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56709864 | CTGCCTTTGTTTAAG[A/C]CAGCTTTCCTGTATT | 21787 |
rs225142800 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712526 | GGTAAAATAAAATGG[C/T]TAGGGGAAATGGAGA | 21787 |
rs225217155 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56709984 | ATTCTATTATCATCA[A/C]GGCAGGAACATGGCA | 21787 |
rs225272113 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56713535 | TTCTAGAGGTTTCCC[G/T]AACAATCTAACTTAA | 21787 |
rs225293376 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711758 | AAATCTCCCTACCTT[A/G]GCCTTGGGTATACTC | 21787 |
rs225380175 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702970 | AGAATGAAGGGTGTC[G/T]TCTGAGCTCCATGCT | 21787 |
rs225455939 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56714006 | TTCTGTGTGCAGGTG[-/C]CCCAGGAGGCCAGAG | 21787 |
rs225495123 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56696462 | ACTGAGCAAGCATGC[-/A]AAGTGTCATCACAGG | 21787 |
rs225521072 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713996 | TTTATTTTATTTCTG[A/T]GTGCAGGTGCCCCAG | 21787 |
rs225535593 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56705922 | GGCTTTAATCCAGCA[-/G]GAGGGCAGAAGCAGA | 21787 |
rs225576924 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56689907 | TATTACAGAATGTTT[C/T]TGTGAAACTGTTTAC | 21787 |
rs225790271 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56716128 | AGAAGCTTCTAAAAC[A/G]CCCACCCTCTAAACA | 21787 |
rs226197767 | in-del | -/ACATGGTC | | | intron-variant | Tfg | Mm_Celera | 16:56702156 | CTTACCCAGCAGGCT[-/ACATGGTC]TACCACTGGCTGGCC | 21787 |
rs226346293 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709666 | GTTGTGGACAAATGA[A/G]CCCAAGAGCATTGCA | 21787 |
rs226367513 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56706279 | TTTAGATCACTGACC[A/T]TGCTGAAAATGAAAC | 21787 |
rs226367688 | in-del | -/AA | | | intron-variant | Tfg | Mm_Celera | 16:56700775 | TGCAATTTACAAAAT[-/AA]AAAAAAAAAATCTGG | 21787 |
rs226458074 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56716926 | CTTGGGGTATCAGCG[A/G]GGCCAAACGCCCTCC | 21787 |
rs226502196 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714041 | ATCATCAGGAGCTGG[A/G]ACCATGGGTGGTTGT | 21787 |
rs226555111 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56692801 | CACTCCTAAAATGAG[G/T]AACGTTAGGTGGAAA | 21787 |
rs226625053 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714676 | GAACCTTAAGACTTT[C/T]AGTAATTCAAATTAC | 21787 |
rs226657432 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56714285 | TCAGCACTTGAGAGG[A/C]AGAGGCAGGTGGATT | 21787 |
rs226697485 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708139 | TCAGGTATTGGAGGA[A/G]AGGAGGAAAAACAGG | 21787 |
rs226709461 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56698635 | AGGGTTATGAGTTAA[A/G]CAAAGCTTACAGCAA | 21787 |
rs226742267 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708662 | GGTGGTGGAATTGAG[A/G]AAAAGCTGGAAGAAG | 21787 |
rs227110969 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712069 | CTTCTGCCTTAGGGT[C/T]TGACTGCTGTGAACA | 21787 |
rs227478932 | in-del | -/GATAACATTTCTT | | | intron-variant | Tfg | Mm_Celera | 16:56709473 | AGCCACAGGATGCTA[-/GATAACATTTCTT]GATTTTCTTGCATGT | 21787 |
rs227549733 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690626 | TGGTAAATTATATTT[A/T]CAATTAACAGCAACA | 21787 |
rs227662869 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56689845 | GTGAGAAGCTATTGT[C/T]TTATAGGATATATGA | 21787 |
rs227679721 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711653 | TCTAAGCTTGCTACT[C/T]TTGTTCAAAATGCTC | 21787 |
rs227779572 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718384 | TAAATAAAGCAAAGT[A/G]GAGTGGTATAATCTA | 21787 |
rs227817163 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56715414 | TTGATAGTCTGACAG[A/G]AATGAAGATCTTACA | 21787 |
rs227914990 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56710965 | CGGGTGACTCTTACA[A/C]AATACCAAGTACAGC | 21787 |
rs227942444 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716393 | AAAATCTGTATGACA[C/T]GCAGTGTATATGGCA | 21787 |
rs227963360 | snp | A/G | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717357 | AGCCTAGCGACAGCC[A/G]CGGTCCCGTACGTGG | 21787 |
rs228155141 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701515 | AAGTTCTAGGCCAAC[A/G]TGAGCTATAGAGCAA | 21787 |
rs228167518 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56694235 | TGTAGAATCATCTCT[A/G]TAATTACGTTGAATT | 21787 |
rs228190889 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718585 | CTTTTCTATAATACC[A/G]TATGTCCTAGACATG | 21787 |
rs228220890 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56693589 | AATTTGCTGATCTAT[A/G]CTCCTATTCTTTAGT | 21787 |
rs228252477 | snp | G/T | | | missense | Tfg | Mm_Celera | 16:56694477 | TGCTGCTGGTACTGC[G/T]GGTACATCTGACCTA | 21787 |
rs228269555 | snp | A/C | | | synonymous-codon, downstream-variant-500B | Tfg | Mm_Celera | 16:56690990 | TGGTTGGGTAGTATA[A/C]GTTTGTGGAGGGTAA | 21787 |
rs228428787 | in-del | -/GAA | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718361 | CAAGAAGAAGAAGAA[-/GAA]AAATAAATAAATAAA | 21787 |
rs228581303 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708307 | GTGCTCTACAATAGG[A/G]AGGGAGAACTTGTAG | 21787 |
rs228626764 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701357 | TAGAACTGTGTTCAT[A/G]CTTCAGGGAAAATGA | 21787 |
rs228636719 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56713679 | TTGTACATAGTAGTT[A/C]TTCAAATGGACAATG | 21787 |
rs228759887 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710314 | ATAGCACTCTCAACA[A/G]TGTTAACAGTCCAAA | 21787 |
rs228798046 | in-del | -/CT | | | intron-variant | Tfg | Mm_Celera | 16:56710518 | GGGTGGTTTCACTCC[-/CT]GCTAGCAGCATTCCT | 21787 |
rs228817113 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56709047 | ATAATAAAAATTTTT[A/T]AAAATTAAAAATTGA | 21787 |
rs228873013 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56707124 | TCCTTTTTAAGAGTT[A/G]CTGTGGTCATGGTGT | 21787 |
rs228988916 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56697683 | AGGTTATTGACAATC[C/G]AAATAAAATCACTAT | 21787 |
rs229070132 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714115 | TAGTACTGCTGCTAA[C/T]AGCTTGGCCATCTAT | 21787 |
rs229070659 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56696950 | TGTGCCACCACTGCC[C/T]GGCAAGAGTTATTTT | 21787 |
rs229078152 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719062 | CTTCATTTATTATCA[C/T]CAAGGTCCAGAAAGT | 21787 |
rs229120554 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56696826 | GTTTTGGTTTTTTTT[G/T]GGTTTTTTTGGGGGG | 21787 |
rs229278329 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695805 | TGGGACATAACGTAT[A/G]GTGTTTAAAGTGTTC | 21787 |
rs229332712 | in-del | -/A | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718673 | AGCATACTTTTTATT[-/A]AAAAAAATCTACATC | 21787 |
rs229522959 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56693641 | ATATAATTTTGTTAA[A/G]ATTCAATTTATAGAA | 21787 |
rs229604998 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56703191 | ATCAGAAAATATTTA[C/T]TTAGCTTTTATCATC | 21787 |
rs229607437 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56716283 | CTGAGTGCACCACCA[A/C]CAACTGGCTCCTTTT | 21787 |
rs229660652 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56703583 | TTGTATAGTTTTAAG[C/T]ATTTGAAAATTATGA | 21787 |
rs229691362 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56702609 | AATAATATACAAGGC[A/G]ACAAAGTATAAACAG | 21787 |
rs229778031 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709610 | GTAATTCTATGTTTG[A/G]TGAAATATTTGTTAA | 21787 |
rs229822300 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707805 | AATGGACTGAGGAAC[A/G]AAATATAAAGAAATA | 21787 |
rs229879384 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56710347 | TCAAGGTCTCTTCTG[C/T]GATTCATCCAATCAC | 21787 |
rs229894358 | in-del | -/TGAAGAATGAAGGGTGTCTTC | | | intron-variant | Tfg | Mm_Celera | 16:56702952 | TAGGTGGAAGGCACA[-/TGAAGAATGAAGGGTGTCTTC]TGAGCTCCATGCTGC | 21787 |
rs229938261 | snp | C/T | | | synonymous-codon | Tfg | GRCm38.p3 | 16:56712654 | ATCATTACTCAGAAG[C/T]TTTCCTCTGAATACT | 21787 |
rs229991247 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56698450 | TACGGCTTTAAGTTA[C/T]GCTAGCAACACAGAA | 21787 |
rs229991742 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711298 | TTGGCTGTCCTGGAA[C/T]TTGCTCCATAAACTG | 21787 |
rs230036637 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56714549 | TTAAATGGTAAAAGT[A/G]GCTATTTGATACTGG | 21787 |
rs230107748 | in-del | -/AAA | | | intron-variant | Tfg | Mm_Celera | 16:56707857 | AATGGATGGAACTAG[-/AAA]AAAAAAATCATCCCG | 21787 |
rs230182994 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56705287 | ACTTAAGACATTAAT[A/C]TTCCCAAACATAAAT | 21787 |
rs230316755 | in-del | -/GA | | | intron-variant | Tfg | Mm_Celera | 16:56695456 | CTTAGGTATATGCTT[-/GA]GCCTGAGCCTTCCAA | 21787 |
rs230349009 | in-del | -/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719526 | CTCAGCTCTTACTGA[-/T]TTTTTTATTAGGTAT | 21787 |
rs230518057 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56692771 | CTATTTGTCTCCATT[C/T]CTACACCCTCCTAAC | 21787 |
rs230561742 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695879 | AGCAAAATCCACCAA[C/T]CTCTTTCTAAATCGA | 21787 |
rs230584938 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56696999 | CCAATTTTCGTATTA[-/T]TTTTTTAAATCAGTG | 21787 |
rs230590229 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56697146 | TATGTATCATCATCT[C/T]GATATAAATTCTTTT | 21787 |
rs230621019 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56705437 | TCTAAGACATAAAGT[C/T]CCAAGTAATTCAAAG | 21787 |
rs230654926 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56691756 | TTAGCATGGCATAAT[-/A]AAACAAAAAACAAAT | 21787 |
rs230660991 | in-del | -/AAC | | | intron-variant | Tfg | Mm_Celera | 16:56700207 | ACCAAAAAAAAAAAA[-/AAC]ATAAATAAATAAAAA | 21787 |
rs230828041 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56704382 | CTCCCCACAAAAATG[-/A]AAAAAAAGAATTCAT | 21787 |
rs230888789 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56701292 | AAACCACATTAAAAA[A/T]ATATATATATATATA | 21787 |
rs230987388 | snp | A/G | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718761 | GTAGCAGTGCTCAGA[A/G]AGGACTTTAGTACTG | 21787 |
rs231003079 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56700390 | CTGCTGGAAGCGCAA[G/T]AACAAAAAAATAAAA | 21787 |
rs231039473 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56699609 | TCTGTTTTTCTAAGA[C/T]TTCATTCTCTTCACT | 21787 |
rs231129219 | in-del | -/AAAAC | | | intron-variant | Tfg | Mm_Celera | 16:56693737 | ATTATAACCACAGTT[-/AAAAC]AAAAGAAATTTATCA | 21787 |
rs231147450 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56707037 | GCCTGCACGCCACCA[G/T]GTGCATATTTCCTGC | 21787 |
rs231337285 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711916 | CAACAAAGTCTTCCA[C/T]ATTCCTACCAGGATG | 21787 |
rs231524772 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56702567 | TTAAAATACTTGTAG[-/A]AAAAAATATATTTAG | 21787 |
rs231635759 | in-del | -/CTCACAC | | | intron-variant | Tfg | Mm_Celera | 16:56713097 | CCTTGCTTCCCTCTT[-/CTCACAC]CTCACATCTAAAGTG | 21787 |
rs231787089 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56706777 | TTTACTTGAATCCCA[C/T]ATCAGTAACAGAATG | 21787 |
rs231798093 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714875 | CAGGCTACTCTGCTT[C/T]CATTCCTGAACTTTC | 21787 |
rs231819540 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714254 | CACCGGGCCGTGGTG[A/G]CGCACACCTTTAATC | 21787 |
rs231828684 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704745 | TGTTTCCTCTACCCC[G/T]TTTTTAACCTTACTC | 21787 |
rs231906001 | in-del | -/AACAACAAAACAAC | | | intron-variant | Tfg | Mm_Celera | 16:56700285 | TAAAAACATAAACAA[-/AACAACAAAACAAC]AACAACAACAACAAA | 21787 |
rs231945191 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715718 | CCTTAACATCTACCA[C/T]GGGTGGCCCAGTTTC | 21787 |
rs231945289 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707756 | GATGGATGGATAGAT[A/G]GATTAGAAACAAAGA | 21787 |
rs231982114 | in-del | -/TAATA | | | intron-variant | Tfg | Mm_Celera | 16:56703885 | TGTTAAAATAAACTT[-/TAATA]TAATACTTATAGTAC | 21787 |
rs232068843 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56709341 | CTGCAGCTCAGCGAA[C/G]CCACATGACCAGGCT | 21787 |
rs232293236 | snp | A/T | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690319 | CTTAAATAATTAGGC[A/T]ACAAGACCACAGTTG | 21787 |
rs232300503 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56706865 | TGGTTCATAGGGAGT[A/G]GCACTATTAGTTGTG | 21787 |
rs232318981 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714620 | TATCTCATTTCAGGT[G/T]ATTCAATATGATTGT | 21787 |
rs232397757 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56705803 | ATCAGCGAAGAAAGA[-/T]TTTTTTTAGAACAAC | 21787 |
rs232485370 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56698232 | AAATGTCTACAGAGG[-/C]CCCACTTTGATTTTC | 21787 |
rs232588375 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56702056 | GTGTTCACCTGTGTA[A/C]ATAGAGATCAGAAGA | 21787 |
rs232672691 | snp | A/G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714413 | AATAATTGATCGATC[A/G/T]ATCAGTCCAGGCTAC | 21787 |
rs232674767 | in-del | -/CACACACACACACACACA | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719296 | TACTTGCCTCTACTG[-/CACACACACACACACACA]CACACACACACACAC | 21787 |
rs232728048 | snp | C/T | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690164 | GCCAATATGTAAATA[C/T]ACCTTTATCGCCGTA | 21787 |
rs232730080 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56708509 | GGGGAGGTTCAGGGC[C/T]CTGATACTGTTACTG | 21787 |
rs232777751 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56696107 | ATCATTTTGCAATTT[-/A]AAAAAAGCTCTCAAA | 21787 |
rs232888698 | snp | A/G/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56718122 | CAAAGGAGCAAACAC[A/G/T]GCTTGGACTCACCCT | 21787 |
rs232984048 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56698098 | TCACATACTTAAATG[A/G]CCTTCTTTAAAACCT | 21787 |
rs233048102 | in-del | -/AG | | | intron-variant | Tfg | Mm_Celera | 16:56700002 | TACCCCTGTAGACAC[-/AG]AGTGAACTAAGAATT | 21787 |
rs233137982 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56713112 | CTCACACCTCACATC[G/T]AAAGTGTCAGCAAAC | 21787 |
rs233173350 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56701426 | CTCTAACAGTCACTG[C/T]CCCTTTTAGAATTAC | 21787 |
rs233207759 | in-del | -/ATACAA | | | intron-variant | Tfg | Mm_Celera | 16:56694107 | CTAGAAATATGAGTG[-/ATACAA]ATAGAAGAAAATCTT | 21787 |
rs233246483 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56692921 | CTAGATTGGAGACTA[A/T]AAAACGGTATAAAGA | 21787 |
rs233277614 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708949 | GGGGTGGGGGCGGGG[A/G]GGAGGGTAGGTATGG | 21787 |
rs233354100 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56713921 | CCTGTCAACCCACAT[G/T]ACCTCCAATCAAAAT | 21787 |
rs233378904 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56693878 | CTATGTGTTGAAATC[C/T]CCTGGGTTTTCAACT | 21787 |
rs233526873 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56709042 | AAAGAATAATAAAAA[A/T]TTTTTAAAATTAAAA | 21787 |
rs233544633 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56705069 | AACAATATCCAAGAC[C/T]CATCATTGTTAGTTT | 21787 |
rs233584939 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710433 | ATCTCCATGCCTGAT[A/G]TCAAAGGTGGTCTTC | 21787 |
rs233616715 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56714407 | TAAATAAATAATTGA[A/T]CGATCGATCAGTCCA | 21787 |
rs233815366 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56712371 | AGTATCAGAATCCCT[G/T]TCAAATCTGAACATA | 21787 |
rs233839389 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Tfg | Mm_Celera | 16:56717523 | TCGGGTGAGCGGCCC[C/G]GCTTCCTCACTGGAT | 21787 |
rs234036863 | in-del | -/CT | | | intron-variant | Tfg | Mm_Celera | 16:56693931 | TTAAAACACTGAATA[-/CT]CTTAGTTGCCTGAAT | 21787 |
rs234058192 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701658 | TAGTGCCTTGAGCTG[A/G]CTAGTTTTTCTGTAA | 21787 |
rs234094850 | snp | C/T | | | missense | Tfg | Mm_Celera | 16:56701166 | TGACATACTTGCTGC[C/T]ATAACCTGAGTTGAC | 21787 |
rs234194143 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56715340 | TACATAACATCTACT[A/C]TACCCCAGGCTCTAA | 21787 |
rs234196147 | in-del | -/AT | | | intron-variant | Tfg | Mm_Celera | 16:56702531 | CTGCTCCTCTTTTAA[-/AT]ATATGTACTACTTAT | 21787 |
rs234445628 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695581 | CAAATTATTAATTTC[A/G]TAAGAGATGTTAAAC | 21787 |
rs234548640 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717678 | AGGGCTGGGTTTGCT[A/G]CGAGAGCCTGGGGGA | 21787 |
rs234746542 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56712185 | TGGCAGCACTAGGCA[A/G]GCATGGTGCAGGAGG | 21787 |
rs234779739 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56705744 | ATCAGTAATAAACTG[C/T]CATAAAAAATGTAAA | 21787 |
rs234783718 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716706 | GCTCCAACGTCCAAG[C/T]CACTCCCGGGGATCA | 21787 |
rs234947482 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56710805 | ACTAGGCTTCACCAA[-/C]TGCCAAGCCTCAAAT | 21787 |
rs234967776 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711825 | AAAATATCAAGAAAA[C/T]AGTCTCTGGTTCATG | 21787 |
rs234975306 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56700058 | TTCATGGTTAGACAA[A/G]GAGCTGGAAATGAAG | 21787 |
rs235051094 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710869 | ACTGCAACTGAGGCT[A/G]CACCTTTACCAATGG | 21787 |
rs235114121 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56709878 | GCCAGCTTTCCTGTA[C/T]TTGGTTGGTGTCTTA | 21787 |
rs235143546 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56692630 | TTGGGGGAATACTTT[C/T]ATATTGAAAATGACT | 21787 |
rs235249317 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56705793 | CTCCCATAAGTATCA[A/G]CGAAGAAAGATTTTT | 21787 |
rs235306309 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56703955 | TTACTACAGAAAATC[A/G]ATTTCTAAGATTCAT | 21787 |
rs235326214 | in-del | -/TTT | | | intron-variant | Tfg | Mm_Celera | 16:56693122 | ATTTGTACCATATAC[-/TTT]TTTTTTTTTTTTGCT | 21787 |
rs235355222 | in-del | -/TTTCAA | | | downstream-variant-500B, cds-indel | Abi3bp, Tfg | Mm_Celera | 16:56690624 | TCTGGTAAATTATAT[-/TTTCAA]TTAACAGCAACAATG | 21787 |
rs235546645 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56694847 | TTAGCAATACCTCTC[A/T]GACGATTCATAGCAC | 21787 |
rs235587418 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56699664 | CCACCTTAACCATAT[A/C]ACACCTTTAGAATTA | 21787 |
rs235665895 | in-del | -/TG | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56719298 | CTTGCCTCTACTGCA[-/TG]CACACACACACACAC | 21787 |
rs235789109 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56706153 | TCCCATAGTTCAAAT[C/T]CTTATTTTTAATAGA | 21787 |
rs235959393 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56706876 | GAGTAGCACTATTAG[G/T]TGTGGCCTTGGTGGA | 21787 |
rs236080725 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716792 | CCTCCACCTTCCAAG[C/T]TGCTCTAGAGGGTGA | 21787 |
rs236085536 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56710997 | CTGCAGGAGTTACAA[-/C]CCTTGGCTATCTCTG | 21787 |
rs236133993 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56712560 | AGTCTACTGGGGGGT[G/T]GGGGAATGGGTGAAA | 21787 |
rs236168129 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56707100 | AAGCCAGCCCCAATT[-/A]AAATGTTTTCCTTTT | 21787 |
rs236325078 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56714243 | ATCAGTCCAGGCACC[A/G]GGCCGTGGTGGCGCA | 21787 |
rs236343582 | in-del | -/TTTT | | | intron-variant | Tfg | Mm_Celera | 16:56705016 | AAATTCCCTACTTCC[-/TTTT]TTTTTTATCTCCCTC | 21787 |
rs236366407 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56703773 | CCTAAACTATATCAG[C/T]TTCCAATATGTCAGT | 21787 |
rs236483754 | in-del | -/AT | | | intron-variant | Tfg | Mm_Celera | 16:56704132 | AGTACAGAGTGCTGC[-/AT]ATGTCAGGCAAGCAC | 21787 |
rs236508528 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Tfg | GRCm38.p3 | 16:56690849 | AGGGTTAGCCCCACT[A/G]GAAGGAGGGGTCATG | 21787 |
rs236575852 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56700985 | TATGTAAAAAAATAA[C/T]TGGCTGAACCCTTAA | 21787 |
rs236739498 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56704777 | TGGAATGAGGGCTTT[-/C]ACTGAACCAGCTTTT | 21787 |
rs236768565 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56704082 | CTCCTTATGCAGCCA[G/T]CTGCACATTTACTTA | 21787 |
rs236806534 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56711626 | TGAACCATATGTTTT[A/C]TATTTTTCCTTTCTA | 21787 |
rs237020833 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56701294 | ACCACATTAAAAATA[A/T]ATATATATATATACA | 21787 |
rs237023223 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56693188 | AAATCAATTCATCTG[G/T]TTTTTGCAATCAGAT | 21787 |
rs237066102 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56698171 | CCTTAGTGAATTTAT[C/T]TATGGCTTACTTTTT | 21787 |
rs237087279 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56715846 | TCCACACAGCTGTCA[A/G]CTCTGGTCCTGCCTT | 21787 |
rs237087334 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56691576 | AAATCCCATTACAGA[C/T]AAGTGCTTTATAAGT | 21787 |
rs237105837 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56708938 | GAATGGAAACGGGGG[G/T]GGGGGCGGGGAGGAG | 21787 |
rs237181449 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56701938 | TGGACTATGATTCAG[G/T]ATATGTAAGCCTTTT | 21787 |
rs237191131 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56694264 | TTTGCTCACTAAAAA[-/T]AGAAAATGCTGATTT | 21787 |
rs237197574 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690002 | TGGGAGGGAGCCAAG[A/G]AAATTATTGCTTGCC | 21787 |
rs237281803 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56689940 | AAGCTGTAACAAAAC[A/G]GACTCATTTCATGGG | 21787 |
rs237405958 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710221 | AGCTTGTTCAAACAC[A/G]TGAATCTATGGAGGC | 21787 |
rs237415260 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56712568 | GGGGGGTGGGGGAAT[A/G]GGTGAAAGAACATGT | 21787 |
rs237421680 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56708162 | AAAACAGGACTGAAG[C/T]CCTGAGGGCCATCAG | 21787 |
rs237490903 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708830 | GACTGCCTGGCCTAG[C/T]TTCAGTGATATACCT | 21787 |
rs237652969 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56694959 | GTATTTCTTTTTTTT[-/A]AAATGACTTTCAACC | 21787 |
rs237863024 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56704982 | GTAACAAAAATCAAA[C/T]AAGATACACAGTTGA | 21787 |
rs237910468 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56711475 | GCTCCTGGGATTAAA[-/G]GCTTGTGCTACCATG | 21787 |
rs237929899 | snp | A/C | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717234 | GGCCGCTGCGGGCTC[A/C]CTCGGTGTCGCAGAG | 21787 |
rs237954405 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56705513 | CATTAAGAGGAAAAA[G/T]CCAAAGCAAATAAAA | 21787 |
rs238010570 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56707029 | CCATGTCTGCCTGCA[C/T]GCCACCATGTGCATA | 21787 |
rs238043057 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711071 | TTTCACCTCAGTGAT[G/T]CTGGTCTCTTCTTAA | 21787 |
rs238096143 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56706458 | AGAAATGATATGGGG[C/T]AGAGGGAACCAGTCA | 21787 |
rs238097956 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714458 | GGACATTGATCTGTG[A/G]TACAGTGCTTGCTTA | 21787 |
rs238388476 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714910 | TTGCCAGCTTTCTGT[C/T]TCCTTCCCTAAAACT | 21787 |
rs238457542 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56705917 | GTACACGGCTTTAAT[C/T]CAGCAGAGGGCAGAA | 21787 |
rs238521455 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718916 | TTGTCTTGCTTATTC[C/T]TTTATAATGTCTTGT | 21787 |
rs238602548 | in-del | -/A | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717408 | GGGAGCGAAGGGGAG[-/A]AAAAAAAAAACTGCC | 21787 |
rs238669586 | in-del | -/AAAC | | | intron-variant | Tfg | Mm_Celera | 16:56705134 | ATATGCTAAGCCTTA[-/AAAC]AAACAAACAAACAAA | 21787 |
rs238831030 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56693444 | AGTGCCAAAGTGCAG[C/T]AGCAACAGGGACAAC | 21787 |
rs239033398 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56700802 | CTGGACTTTTTTTTT[A/T]AAATAAAAGTTCTGC | 21787 |
rs239082430 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56714518 | ACTTGGTACCACGTT[-/A]AAAAAATGTATTTTT | 21787 |
rs239146254 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56691349 | TTTTTAAATTCTATA[A/G]CCTAAAATTCAAGTC | 21787 |
rs239275239 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709338 | CATCTGCAGCTCAGC[A/G]AAGCCACATGACCAG | 21787 |
rs239303881 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56696580 | CTTATTTATTATGAT[G/T]GTGATCAACCCGTTG | 21787 |
rs239362082 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56705351 | TTAAAACTATACTAC[A/T]CTTACTAGAGATTCC | 21787 |
rs239470216 | snp | A/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56719087 | GAAAGTCTCAGTTAT[A/T]ATATTATGGTTTCAT | 21787 |
rs239605680 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56695233 | TAGAGAACCATTGCT[C/T]GATGTTGTTCACACA | 21787 |
rs239693684 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56693324 | TAGCAATCAGCAACT[A/G]TCTGGACCAATAAAA | 21787 |
rs239810226 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714022 | CCCAGGAGGCCAGAG[C/T]TGGATCATCAGGAGC | 21787 |
rs239870798 | in-del | -/GCCAAATA | | | intron-variant | Tfg | Mm_Celera | 16:56696740 | TCTGATGTCATCTGT[-/GCCAAATA]GCCCTTTTAAATACT | 21787 |
rs240034219 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56712200 | GGCATGGTGCAGGAG[A/G]AGCTGACTTCCAGGC | 21787 |
rs240061821 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56713741 | TTAACCTGGGAGAGG[A/G]AGCATGTATGAACAT | 21787 |
rs240084649 | in-del | -/TA | | | intron-variant | Tfg | Mm_Celera | 16:56707270 | ATTAAACAGTTTTTT[-/TA]AAAAATACCATAAAA | 21787 |
rs240095285 | in-del | -/TCA | | | intron-variant | Tfg | Mm_Celera | 16:56711835 | AAAATAGTCTCTGGT[-/TCA]TCATGTATTAAAATT | 21787 |
rs240197686 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56705992 | TCTACTAGGGTTACA[A/C]AGAGAAACCCTGTCT | 21787 |
rs240221352 | in-del | -/TCT | | | intron-variant | Tfg | Mm_Celera | 16:56713276 | CCCACTTTCACTGAA[-/TCT]TCAACAAACCAGACG | 21787 |
rs240364769 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56694201 | CTTTGTAGTAAAACA[-/T]ATTTATACTGTAGAT | 21787 |
rs240438901 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714771 | TAATTCCTTAACATG[C/T]TTATCTATAGACACA | 21787 |
rs240511096 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56700135 | ATTATAAACTCTAAC[C/T]AAATCCTTAGCCACT | 21787 |
rs240570386 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701785 | GGTGGGGCACCCCTA[A/G]GCTGGTGGTCCTGGG | 21787 |
rs240620539 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56709474 | AGCCACAGGATGCTA[C/G]ATTTTCTTGCATGTT | 21787 |
rs240638524 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707493 | TCAAAAATGACGGTT[A/G]TATGACAGAATTCTA | 21787 |
rs240794834 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718821 | CATTCACTACTTAAC[C/T]GGGGTACTATTTTGT | 21787 |
rs240796686 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56705375 | GATTCCTAAGTTACA[-/C]CTCATCTCAAAACCA | 21787 |
rs240833519 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56693936 | ACACTGAATACTCTT[A/C]GTTGCCTGAATTCAA | 21787 |
rs240837532 | in-del | -/A | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717773 | TCTGTCACATCTCGG[-/A]AAAAAACGAACCCCT | 21787 |
rs240879335 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56706711 | TTATAGAAATTAACA[C/T]ACTGATGCAAAAATA | 21787 |
rs241193978 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715049 | AATATTAAATATAAA[C/T]CTCCCAGTAGTCCTC | 21787 |
rs241404309 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714645 | GATTGTCCTATGAAT[G/T]TATAATCCTAATTCT | 21787 |
rs241435417 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707550 | ATTTTCTGACACTTC[A/G]CAGATTGCTGACACT | 21787 |
rs241500643 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690611 | TTTGTGTCTGTATTC[C/T]GGTAAATTATATTTT | 21787 |
rs241539915 | in-del | -/CCCAC | | | intron-variant | Tfg | Mm_Celera | 16:56716048 | TGTCCAAGGACATAG[-/CCCAC]CCCCTGCACTAGGAT | 21787 |
rs241541057 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56698438 | TGACACATGGCTTAC[A/G]GCTTTAAGTTACGCT | 21787 |
rs241544201 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56707974 | TCAGGACACAACCCA[C/T]AGGATTCAAGAGGTC | 21787 |
rs241579545 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56699851 | TCAAATAAATTCTCT[A/T]TTTTAAACTGCTAAA | 21787 |
rs241613207 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56691574 | TGAAATCCCATTACA[A/G]ACAAGTGCTTTATAA | 21787 |
rs241696840 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56708828 | AGGACTGCCTGGCCT[A/C]GTTTCAGTGATATAC | 21787 |
rs241725421 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56712267 | ACACACCTATTCCAA[C/T]AAGGCCACATCTCCT | 21787 |
rs242033196 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56707412 | AGTGGGAGCCACAAA[-/C]CACACCCAACAGAAC | 21787 |
rs242264444 | snp | A/G | | | synonymous-codon | Tfg | Mm_Celera | 16:56697583 | GCGGTCTTCTGTAGG[A/G]GCACTGGGTGGGCCT | 21787 |
rs242356665 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56692458 | TGAAAGGCAGAAGAG[A/G]GAGGGCATGGACATG | 21787 |
rs242374364 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56698228 | GTATAAATGTCTACA[C/G]AGGCCCCACTTTGAT | 21787 |
rs242387886 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56710140 | CCTATTCTAACAAGG[-/C]CACACCTAATAGAGC | 21787 |
rs242414792 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714401 | AATAAATAAATAAAT[A/G]ATTGATCGATCGATC | 21787 |
rs242494479 | snp | C/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717936 | AGAGGGCACACCCAC[C/G]GGTGCAAAAGACAAA | 21787 |
rs242526101 | snp | C/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718226 | TTTATTAAGAGCCAT[C/G]CCTTGTGTCTAAAGT | 21787 |
rs242640780 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56694048 | AAATTCGCTTCTGCA[C/T]GTGTGGGGAAATTGT | 21787 |
rs242642267 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56702861 | CCAGCAATAGCAAGA[C/T]GGAAGGCAGAAACAA | 21787 |
rs242742970 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56700195 | AGAGGTCTCAGAACC[-/A]AAAAAAAAAAAAACA | 21787 |
rs242743102 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695243 | TTGCTTGATGTTGTT[C/T]ACACAGGGTCAAAGT | 21787 |
rs242795702 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56712009 | TTTTTCCAAACAGAT[A/G]CATGGTCAGGCCTAT | 21787 |
rs242856203 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710602 | AACTTCAGTATTACA[G/T]GTTCTTGTTTCAATG | 21787 |
rs242981889 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56704398 | AAAAAAAGAATTCAT[G/T]ACAATAAAATAAAAT | 21787 |
rs243028101 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56695261 | ACAGGGTCAAAGTTA[A/T]TGAATAACATTTCTC | 21787 |
rs243270824 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56713338 | GCTTAGAACCTTCCA[A/G]TGAATTCCCATAGAA | 21787 |
rs243293855 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56701601 | ATTATTATTATTTAA[C/T]AATCTCCTTAATAAA | 21787 |
rs243295776 | in-del | -/AAC | | | intron-variant | Tfg | Mm_Celera | 16:56700293 | TAAACAAAACAACAA[-/AAC]AACAACAACAACAAC | 21787 |
rs243299621 | snp | C/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717692 | TACGAGAGCCTGGGG[C/G]AAGTGGGGCATCTGT | 21787 |
rs243367263 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56703000 | TGCCCTTGTATGGAC[A/G]TCCACCCATATGCAA | 21787 |
rs243425814 | in-del | -/GGG | | | intron-variant | Tfg | Mm_Celera | 16:56696825 | GTTTTGGTTTTTTTT[-/GGG]GGGTTTTTTTGGGGG | 21787 |
rs243447443 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702157 | TTACCCAGCAGGCTA[C/T]ATGGTCTACCACTGG | 21787 |
rs243514307 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714046 | CAGGAGCTGGAACCA[C/T]GGGTGGTTGTGAGAC | 21787 |
rs243639790 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56706861 | AAATTGGTTCATAGG[A/G]AGTAGCACTATTAGT | 21787 |
rs243641144 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714720 | CATATTTAGGATCAA[G/T]TAATGGGTTAATATT | 21787 |
rs243683301 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56698473 | ACACAGAAGGGTGAT[A/G]TGAAGAGTTCCTGGA | 21787 |
rs243760673 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56695394 | ACAGAGATTGGCTGG[C/T]CTCTCGTTTTTTCAC | 21787 |
rs243818523 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56707044 | CGCCACCATGTGCAT[A/G]TTTCCTGCTGTGGTG | 21787 |
rs243823346 | in-del | -/AAA | | | intron-variant | Tfg | Mm_Celera | 16:56691824 | TTACTAGAATATAAT[-/AAA]AAATAAAATCTGCTT | 21787 |
rs243936256 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704340 | TTAAGGATGACACCT[G/T]ACTCCAAGAAGCAAT | 21787 |
rs244002655 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56693406 | GCTTCTCTCACTTTC[A/C]AACTACTCACTCTAC | 21787 |
rs244013937 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56703630 | TCATTTTACCTGAAA[A/G]TTAAGAATATTAAAC | 21787 |
rs244070276 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716457 | GCTCAAGTTCTTCTC[C/T]GCGGCGTACTTTCTG | 21787 |
rs244087916 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715532 | TCAGTTCCTGAACCA[C/T]AGAACCATCTCACAG | 21787 |
rs244096957 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56696866 | GACATGGTTTCTCTG[-/A]TAGATCAGGCTGACC | 21787 |
rs244238257 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711232 | AATATGGCTCCCTTG[C/T]TCTATTACATTATCA | 21787 |
rs244311039 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56714755 | TTTCTGCAAGGCCAA[A/G]TAATTCCTTAACATG | 21787 |
rs244396684 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56704886 | CAGCAAACCGACCAA[C/G]TGGGCCATCATCTCC | 21787 |
rs244397930 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56691604 | AGTGAAACAGTGCTA[C/T]AAACACTCTTCATAT | 21787 |
rs244421663 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56713557 | CTAACTTAAAATGCA[C/G]CTCATCACTGTCTTC | 21787 |
rs244500486 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56712528 | TAAAATAAAATGGCT[A/G]GGGGAAATGGAGAAT | 21787 |
rs244523756 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56705896 | AAAGTTAAGCAGGGT[A/G]TGGTGGTACACGGCT | 21787 |
rs244556744 | in-del | -/ATCGATCGATCT | | | intron-variant | Tfg | Mm_Celera | 16:56714413 | ATAATTGATCGATCG[-/ATCGATCGATCT]ATCAGTCCAGGCTAC | 21787 |
rs244743784 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718440 | AACTTCTGGCAGACT[A/G]TTCACATGGTTTAGG | 21787 |
rs244839771 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56713357 | ATTCCCATAGAAAAA[C/T]GTACAAATGACCCAA | 21787 |
rs244846037 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56716126 | TCAGAAGCTTCTAAA[A/G]CGCCCACCCTCTAAA | 21787 |
rs244945848 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717630 | GCCAGTCTTTCCTAA[A/G]TCTGGCTGCTGGGTG | 21787 |
rs245021964 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56693593 | TGCTGATCTATACTC[C/T]TATTCTTTAGTTAAT | 21787 |
rs245112752 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695378 | AGTTGAACTCATATA[C/T]ACAGAGATTGGCTGG | 21787 |
rs245159385 | in-del | -/GAGT | | | intron-variant | Tfg | Mm_Celera | 16:56693002 | AAGCCACTTATAAAA[-/GAGT]GAGTAGAACAACATC | 21787 |
rs245351591 | snp | G/T | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717359 | CCTAGCGACAGCCAC[G/T]GTCCCGTACGTGGCA | 21787 |
rs245361696 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56692508 | ATCATTATGGATGCT[-/A]AAAATCTGAGCCCAG | 21787 |
rs245556683 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56702307 | TACATCAAGTGCTTC[A/C]TCAACTGAGCTATTT | 21787 |
rs245580808 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711684 | TTCATGAGACTTAAC[C/T]AGAGAACAAAGTCTC | 21787 |
rs245583821 | in-del | -/AAA | | | intron-variant | Tfg | Mm_Celera | 16:56705747 | GTAATAAACTGTCAT[-/AAA]AAAAAATGTAAAATT | 21787 |
rs245653669 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56714617 | TATTATCTCATTTCA[A/G]GTTATTCAATATGAT | 21787 |
rs245708482 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712595 | ATGTATAGTACTTAA[G/T]ACCTTAAAAGCTTAC | 21787 |
rs245833832 | snp | A/C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704170 | ACTGAGTTATTCCCC[A/C/T]GTCCTAGAGAGTACT | 21787 |
rs245972178 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56692335 | CACTCATGGTAGTTC[C/T]TGAATACTGAATTAA | 21787 |
rs245991638 | snp | A/G | | | synonymous-codon | Tfg | Mm_Celera | 16:56701223 | AGGCTTCTCTTCCCT[A/G]CCATCCACAGTATCT | 21787 |
rs245993053 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56702076 | AGATCAGAAGACAAT[C/T]TCCAGTGACATTTCT | 21787 |
rs246119184 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56697001 | CAATTTTCGTATTAT[C/T]TTTTAAATCAGTGAA | 21787 |
rs246177728 | in-del | -/AA | | | intron-variant | Tfg | Mm_Celera | 16:56691983 | CCCTGCATTTAGAAG[-/AA]AAAAAAAAAGGATTG | 21787 |
rs246260177 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56700820 | TAAAAGTTCTGCTTT[-/A]AAAAAAAATAATCTG | 21787 |
rs246262634 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56697700 | AATAAAATCACTATG[A/T]AACAGCCATGTCACC | 21787 |
rs246379649 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56708638 | CAATGGACAGAAGCC[-/G]GGGACCCAGGTGGTG | 21787 |
rs246381650 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711780 | GGTATACTCTTCAGA[C/T]AACGGCAAAAAGCAG | 21787 |
rs246467644 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710066 | TGAAGGCTGCTAACA[G/T]AATACTGATTTCCAG | 21787 |
rs246543052 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56713664 | ATTGCAGAAGAAGCC[-/T]TGTACATAGTAGTTA | 21787 |
rs246548038 | in-del | -/A | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690183 | TTTATCGCCGTAAGG[-/A]AAAATCATAAAATGA | 21787 |
rs246549460 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56698082 | TGATTAACTGCAACA[C/G]TCACATACTTAAATG | 21787 |
rs246549521 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56706707 | CATTTTATAGAAATT[A/G]ACACACTGATGCAAA | 21787 |
rs246597812 | in-del | -/CCCT | | | intron-variant | Tfg | Mm_Celera | 16:56716973 | GGCGCCCTCTCCTCC[-/CCCT]CCCTCCCTCCCTCCC | 21787 |
rs246624815 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699373 | TCATTTTAGGCTTAC[A/G]GCTTGTCCATTAACA | 21787 |
rs246627764 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56705932 | CCAGCAGAGGGCAGA[A/G]GCAGAGGCAGAGGCA | 21787 |
rs246695458 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56698610 | AATTCTGACCTCAAG[G/T]TTACTTTGAAGGGTT | 21787 |
rs246991425 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697449 | CACACGGCTCTGAAC[A/G]CTGTTTTACCTTCAA | 21787 |
rs247279018 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714255 | ACCGGGCCGTGGTGG[C/T]GCACACCTTTAATCT | 21787 |
rs247321407 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56705559 | AAAAATTCATATCTA[A/T]TAGCATTTCAGTCCA | 21787 |
rs247331831 | in-del | -/ATACATAT | | | intron-variant | Tfg | Mm_Celera | 16:56706629 | TGTATAAGCAGGCCC[-/ATACATAT]ATACATATGTATAGC | 21787 |
rs247363010 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714197 | TGGACAGGATCAGGA[A/G]CTCAGGCCAGCCTCA | 21787 |
rs247519066 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56714420 | GATCGATCGATCAGT[A/C]CAGGCTACCAGACTC | 21787 |
rs247847526 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707787 | AGGGTGGGTGGATGG[A/G]TGAATGGACTGAGGA | 21787 |
rs247947910 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56700069 | ACAAGGAGCTGGAAA[C/T]GAAGGATGAAGCTCC | 21787 |
rs247948269 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56708759 | TCAGACACTGAGCCA[A/C]CAGCCAGGAAGCATA | 21787 |
rs247960457 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Tfg | GRCm38.p3 | 16:56717469 | GTCAGGACGCATGCG[C/T]AGTGGGTGAGGGGCG | 21787 |
rs247975676 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56692791 | ACCCTCCTAACACTC[A/C]TAAAATGAGTAACGT | 21787 |
rs248310444 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56696845 | TTTTTTGGGGGGATT[A/T]TTTTGAGACATGGTT | 21787 |
rs248386026 | in-del | -/G | | | intron-variant | Tfg | Mm_Celera | 16:56696816 | GTTTGTTTGGGTTTT[-/G]GTTTTTTTTGGGTTT | 21787 |
rs248405202 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56717131 | CTGCGGCCCTCCCGG[G/T]TCCCCCGACCTCCTC | 21787 |
rs248424722 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56707176 | AACTAAGACACAGAA[C/T]GAGTATCTCCGTAGG | 21787 |
rs248426369 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56712095 | GAACAGATACCATGA[A/C]CAAGGCAATTCTTAT | 21787 |
rs248455240 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717582 | CGGACACGCATGCGC[A/G]GGGAATTACCAGCAC | 21787 |
rs248598241 | in-del | -/AAGAAAAGTATTTGAAA | | | intron-variant | Tfg | Mm_Celera | 16:56712406 | TGGAAATCTGAGCAG[-/AAGAAAAGTATTTGAAA]AACACATGTGAAAAT | 21787 |
rs248601207 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711605 | TCTTGGTACCCCTTT[A/T]ATACCTGAACCATAT | 21787 |
rs248736386 | snp | A/G/T | | | intron-variant | Tfg | Mm_Celera | 16:56708069 | GGGGGTGGGGGGGGG[A/G/T]GGTGAGGAAAGGAGG | 21787 |
rs248750755 | snp | A/C/T | | | intron-variant | Tfg | Mm_Celera | 16:56704079 | GCACTCCTTATGCAG[A/C/T]CATCTGCACATTTAC | 21787 |
rs248751649 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56709816 | CCTGCCAAAGGAAGA[A/C]GAAAAAAAGAATAAA | 21787 |
rs248815619 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56707894 | AGGTAACTAAGACCC[A/C]AAAGGACATGCATGG | 21787 |
rs248841735 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56700587 | CGTCCCCACCAAGAA[A/G]AACAGGTACAACGCT | 21787 |
rs248921680 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56716495 | GAAGGGAGCCTAACA[A/C]GCTACTTTGGTAGAA | 21787 |
rs248925382 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56699732 | AACTAAGTAAACATA[G/T]CCACATGAAAAGGTA | 21787 |
rs248947736 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56700335 | CACAGATACCAGCTA[A/C]TACTCTCTCTGGTAA | 21787 |
rs248991216 | in-del | -/AA | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717407 | GGGAGCGAAGGGGAG[-/AA]AAAAAAAAAAACTGC | 21787 |
rs249071869 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56700474 | GAAAACCTGCAAGAT[A/G]GATAGAAACAAGAAA | 21787 |
rs249108607 | in-del | -/CT | | | intron-variant | Tfg | Mm_Celera | 16:56715514 | TTAGAAAGCTGAACA[-/CT]CTCAGTTCCTGAACC | 21787 |
rs249129756 | in-del | -/AAAATGGCTAGGG | | | intron-variant | Tfg | Mm_Celera | 16:56712519 | AATAGTAGGTAAAAT[-/AAAATGGCTAGGG]GAAATGGAGAATTAG | 21787 |
rs249165484 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56709252 | AGAATTTACACATGT[C/T]AGTAGATGACCAACT | 21787 |
rs249224649 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56701061 | GAGGGAAAAAGGAAC[C/G]GACTTACCTGAAACC | 21787 |
rs249238342 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708375 | GGGATGAGGTTGCCA[C/T]CCCACAGTCAAAAGC | 21787 |
rs249369646 | in-del | -/CTG | | | cds-indel | Tfg | Mm_Celera | 16:56697515 | GTTGCTGCGGCTGAA[-/CTG]CTGCTGGGTGTGCTG | 21787 |
rs249499367 | in-del | -/AC | | | intron-variant | Tfg | Mm_Celera | 16:56692943 | TATAAAGACAAGAGA[-/AC]ACCATTCTGTTCAGC | 21787 |
rs249676858 | in-del | -/TG | | | intron-variant | Tfg | Mm_Celera | 16:56692414 | ACTAAACTTAAATAT[-/TG]TGTGTGTGTGTGTTG | 21787 |
rs249740032 | in-del | -/AAC | | | intron-variant | Tfg | Mm_Celera | 16:56705813 | GAAAGATTTTTTTAG[-/AAC]AACTAAATCAACTTT | 21787 |
rs249863928 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56705560 | AAAATTCATATCTAA[A/T]AGCATTTCAGTCCAA | 21787 |
rs249904414 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56713137 | GCAAACCTGGTGTCA[C/G]CACCACCTTTAAAGT | 21787 |
rs249932828 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714579 | GCTTGCTACAGAATT[C/T]TCCCCTCATGGGTTT | 21787 |
rs250098387 | in-del | -/TCC | | | intron-variant | Tfg | Mm_Celera | 16:56706151 | TTCCCATAGTTCAAA[-/TCC]TCCTTATTTTTAATA | 21787 |
rs250274030 | in-del | -/TATA | | | intron-variant | Tfg | Mm_Celera | 16:56701292 | AAACCACATTAAAAA[-/TATA]TATATATATATACAT | 21787 |
rs250274033 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56701944 | ATGATTCAGGATATG[G/T]AAGCCTTTTAATAAA | 21787 |
rs250274139 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56710359 | CTGCGATTCATCCAA[C/T]CACTTAACTGTAATC | 21787 |
rs250313326 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56709649 | TATCTCCATAAAAAA[C/T]AGTTGTGGACAAATG | 21787 |
rs250315309 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56699290 | AGCTACCCCACAGCC[-/T]TGAGACCACTACCCT | 21787 |
rs250320630 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710516 | TAGGGTGGTTTCACT[C/T]CCTGCTAGCAGCATT | 21787 |
rs250398563 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56702789 | TTCAAGAGGACCTGA[G/T]TTCTAAACCTCCAGA | 21787 |
rs250454070 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56703365 | GACACAAACAAGCAC[A/G]TAGGAATGGAGGGAA | 21787 |
rs250468617 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56689957 | ACTCATTTCATGGGG[A/G]AAAAAAAAAGCATTG | 21787 |
rs250535996 | snp | A/C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56713220 | TCCCTACTTTGTCTG[A/C/G]TTTATTTCAAAATGT | 21787 |
rs250598414 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711480 | TGGGATTAAAGGCTT[A/G]TGCTACCATGCCTGG | 21787 |
rs250633210 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711937 | TACCAGGATGGCCCA[G/T]TAAGCCCCACTTAAA | 21787 |
rs250767514 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56715233 | TTGATCAGTCTCACA[A/G]GTGACTTCTAATGGC | 21787 |
rs250796565 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717878 | TAGGATGAGTCAGTT[C/T]CCCAGCTAAGCTCTA | 21787 |
rs250823122 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56701474 | CAATAATCCTGGCAA[A/T]CAAAAGGCTACAACA | 21787 |
rs250829291 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56714083 | TTTGAAAACTGAACT[A/C]GGGTCCTCTTCAAAA | 21787 |
rs251085893 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56708888 | GAATTGGGAGGTCAG[A/G]TGGGGTTGGGGGTGA | 21787 |
rs251086028 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56716714 | GTCCAAGCCACTCCC[C/G]GGGATCAGGCACAAA | 21787 |
rs251120771 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56716038 | ATACACTGATGTGTC[C/T]AAGGACATAGCCCCT | 21787 |
rs251303944 | in-del | -/TATGGTATT | | | intron-variant | Tfg | Mm_Celera | 16:56695524 | TACTTCGGGGGAAAA[-/TATGGTATT]TATGGTATTCAATTA | 21787 |
rs251336912 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56717153 | GACCTCCTCCTTGAG[C/T]CGCCACGCGCGCCTC | 21787 |
rs251356211 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56708973 | GGTATGGTATGAGGA[G/T]CGGTTGGAAGGCAGA | 21787 |
rs251363262 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56692749 | CAGCAATACTGCTCT[A/T]TTAGGTCTATTTGTC | 21787 |
rs251383403 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56703278 | TAAAACCTAACCATA[-/T]TTTTAAAAAGTGTCT | 21787 |
rs251412863 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717791 | AAAACGAACCCCTTT[C/T]CCGCCTTCTTTCTAC | 21787 |
rs251514671 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56697106 | TCAAATGAATTGATC[C/T]AAATCTACATTCTTT | 21787 |
rs251565466 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719503 | TGACTCAGCCTCCTT[A/G]GAAAACAGCTCAGCT | 21787 |
rs251741766 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56714862 | CCTGAACCTCCCACA[A/G]GCTACTCTGCTTTCA | 21787 |
rs251777426 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710331 | GTTAACAGTCCAAAG[A/T]TCAAGGTCTCTTCTG | 21787 |
rs251815223 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695485 | AACCAAAGAAGATAT[C/T]TGAATTACAATCAGT | 21787 |
rs251975842 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56697417 | CCTCAATAAACACTT[C/G]TGCACATGCCCTTCC | 21787 |
rs252104761 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712349 | AAATTCCTTTTCCAT[C/T]CAATATAGTATCAGA | 21787 |
rs252116892 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56711889 | GGCTTCCACAGTTCA[A/G]ATCACCCTCAGCAAC | 21787 |
rs252383010 | in-del | -/ACAG | | | intron-variant | Tfg | Mm_Celera | 16:56707227 | CTCATGTAGCTGCTA[-/ACAG]ACTATGAAACAACAA | 21787 |
rs252579043 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697172 | CTTTTTAAGTGACAG[A/G]AAAATGTAGTGTTTG | 21787 |
rs252648696 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695249 | GATGTTGTTCACACA[A/G]GGTCAAAGTTATTGA | 21787 |
rs252662614 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56704655 | TTACTTTCATCCATG[A/C]ATTTTAACCTGTTTA | 21787 |
rs252714078 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56701037 | AAAAAAGGGAAAGAT[-/A]AAAGATGAGAGGGAA | 21787 |
rs252737870 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56705464 | AAAGTCTCACCTGAA[C/T]GCAAATATTTTAAAC | 21787 |
rs252739387 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696327 | GTTTGTTTTAGCTCC[A/G]GCTCTTGTATTTTTG | 21787 |
rs252778064 | in-del | -/GGG | | | intron-variant | Tfg | Mm_Celera | 16:56708052 | GGAGAAGAAAGCAAT[-/GGG]GGGGTGGGGGGGGGA | 21787 |
rs252783373 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695687 | AATGTATATATTATA[C/T]ATCAAGAGATATTCA | 21787 |
rs252807373 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56711204 | GCCGAGTTCTGCTGC[-/T]TGCTGGAGCTAGAAT | 21787 |
rs252829962 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695163 | CAACAAGAATATTAC[A/G]GTTGGGGTCACTACA | 21787 |
rs252990883 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699585 | ATGTAGCTTATTACT[A/G]TTGTCTATTCTGTTT | 21787 |
rs252999175 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701742 | AGGCAAGCCTCTAAG[A/G]CACTTTCTTTAATTA | 21787 |
rs253001098 | snp | A/G | | | missense, downstream-variant-500B | Tfg | GRCm38.p3 | 16:56690946 | CCAGGCTGAGAGCCA[A/G]GGGGAACAGTATAGT | 21787 |
rs253031152 | in-del | -/GTT | | | cds-indel, downstream-variant-500B | Tfg | Mm_Celera | 16:56691043 | GTGGTTGAGCAGGCA[-/GTT]GTTGTGGCTGGCCAG | 21787 |
rs253082585 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56707134 | GAGTTGCTGTGGTCA[C/T]GGTGTCTGCACAGGA | 21787 |
rs253318888 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56706880 | AGCACTATTAGTTGT[A/G]GCCTTGGTGGAGGAA | 21787 |
rs253621288 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56707030 | CATGTCTGCCTGCAC[A/G]CCACCATGTGCATAT | 21787 |
rs253775855 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56712885 | GAAATTGTGCCCCTT[-/A]AAAAATAGTGCCTCT | 21787 |
rs253806671 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56713639 | AGCTGTGCTTTTGTT[A/C]TCTTTCTAGATTGCA | 21787 |
rs253870171 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56706459 | GAAATGATATGGGGT[A/C]GAGGGAACCAGTCAG | 21787 |
rs253912876 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690063 | CAACATGCTTCAGTT[C/T]TATCAATGCTACAGT | 21787 |
rs253938507 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56713018 | AAAATAAATTCCTGA[C/G]TTCTACCCCAAAGTT | 21787 |
rs254109375 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719023 | TCTAGTGAGTACCGG[A/G]TGGTTGGGGGTAGGG | 21787 |
rs254182934 | in-del | -/CAAGTGTC | | | intron-variant | Tfg | Mm_Celera | 16:56696462 | CACTGAGCAAGCATG[-/CAAGTGTC]ATCACAGGACAAGAA | 21787 |
rs254236151 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | Tfg | Mm_Celera | 16:56717472 | GGACGCATGCGCAGT[-/G]GGGTGAGGGGCGGGG | 21787 |
rs254586807 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56706246 | TATGGGACTGCTTTA[A/G]TAAACCATGGTGAAA | 21787 |
rs254853072 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56709492 | TTTCTTGCATGTTGA[A/G]CCACTGAGAATGTAA | 21787 |
rs254946874 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56705894 | CCAAAGTTAAGCAGG[A/G]TGTGGTGGTACACGG | 21787 |
rs255012514 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56704008 | CCGTGAATCAAAAGT[C/G]TTTGAAAACTGGCCT | 21787 |
rs255055161 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715343 | ATAACATCTACTCTA[C/T]CCCAGGCTCTAAAAC | 21787 |
rs255305740 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56692548 | AAGACAGCAAGTGCT[A/C]GCAATTTCTGAGCCA | 21787 |
rs255527650 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56698936 | AGAGCATGTACTTTA[A/T]GAATGCATCTTGTCG | 21787 |
rs255565249 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56708643 | GACAGAAGCCGGGGA[A/C]CCAGGTGGTGGAATT | 21787 |
rs255602282 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56699094 | TGGATCATGACCTGA[A/C]ATTTACCTTAAGTCA | 21787 |
rs255683012 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56691479 | GGTGAAATAATTACA[A/C]TTTCTAGGAAGACGA | 21787 |
rs255808517 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56693123 | ATTTGTACCATATAC[-/T]TTTTTTTTTTTGCTT | 21787 |
rs255846405 | snp | C/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56719199 | TAGATAGGAACTGTA[C/T]CAAACTATACAGATA | 21787 |
rs255882889 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Tfg | Mm_Celera | 16:56690652 | CAACAATGATATCAT[-/A]AAAAAATGCTCTGCT | 21787 |
rs255925017 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697828 | AATGCTAAATTCCTG[A/G]GTCCTAACCTCCCCA | 21787 |
rs255928502 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710537 | TAGCAGCATTCCTCA[A/G]CAGGTATTCTATGGC | 21787 |
rs256288907 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56704908 | ATCATCTCCCTATTC[C/T]CCAGTAGTATTTTTA | 21787 |
rs256484643 | in-del | -/AAG | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718347 | GTAATCTCCTTTAAC[-/AAG]AAGAAGAAGAAGAAA | 21787 |
rs256522880 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56693141 | TTTTTTTTTGCTTAA[A/T]AGAATAACACACTCA | 21787 |
rs256542295 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695917 | ATATTTATATAGACA[C/T]ACTTGGCTGATTATC | 21787 |
rs256768923 | snp | A/G | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717314 | AGCTGCAGGCTGCGC[A/G]GAGCTGGCCAATCGC | 21787 |
rs256785316 | in-del | -/CAGTC | | | intron-variant | Tfg | Mm_Celera | 16:56710102 | TAGGGTGAGGGTCTT[-/CAGTC]CATGCCTACAATGAC | 21787 |
rs256799405 | in-del | -/GG | | | intron-variant | Tfg | Mm_Celera | 16:56696042 | TGCACGGTTGCTAGA[-/GG]ACACAGATGGAAGAC | 21787 |
rs256801776 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711784 | TACTCTTCAGATAAC[A/G]GCAAAAAGCAGCCAC | 21787 |
rs256864899 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56707544 | GTATTTATTTTCTGA[C/G]ACTTCACAGATTGCT | 21787 |
rs256935267 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56700521 | AATACTGGAAAGCAG[C/T]CAGTAAAAACATGAA | 21787 |
rs256938579 | snp | C/G/T | | | intron-variant | Tfg | Mm_Celera | 16:56708944 | AAACGGGGGTGGGGG[C/G/T]GGGGAGGAGGGTAGG | 21787 |
rs256982601 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56710271 | ATGCAAAATACATTT[A/C]GTCCAACTTCCAAAG | 21787 |
rs257043026 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708848 | CAGTGATATACCTAA[C/G]CCTCCAGAGACTTGA | 21787 |
rs257115293 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711161 | TTCTGGACTCTAAAG[C/T]CCTCCCTCAGAGCCA | 21787 |
rs257117050 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710951 | CATGCTTCAAAAAGC[A/G]GGTGACTCTTACACA | 21787 |
rs257285526 | in-del | -/AA | | | intron-variant | Tfg | Mm_Celera | 16:56702810 | ACCTCCAGAATTCAC[-/AA]AAAAAAAGCTGGCTA | 21787 |
rs257315960 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56699914 | CCCCAAGTAGCAAAA[A/G]CTTGAACAAAGTAGA | 21787 |
rs257353005 | in-del | -/AG | | | intron-variant | Tfg | Mm_Celera | 16:56693684 | TTGACTATACATGGT[-/AG]AGAGAGACACTCTGA | 21787 |
rs257544923 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56703244 | GGGCATGAAAGAAAT[A/G]ATAGAAAATAGTTCT | 21787 |
rs257654740 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56710906 | ATGGCCTCTCACAAT[C/G]CTGAGCTTAGCTGCT | 21787 |
rs257685556 | in-del | -/A | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717712 | GGGGCATCTGTCCAG[-/A]AAGGTTTGGGTCTTG | 21787 |
rs257711810 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56715158 | AGAACAAAGTGGAAC[A/T]ATGTTCCACAATCTG | 21787 |
rs257763244 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714057 | ACCATGGGTGGTTGT[G/T]AGACCTCTGATTTGA | 21787 |
rs257787430 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56695732 | CCTACATCACTATCT[C/T]CAGCTATATATTATA | 21787 |
rs258071627 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56713384 | CCAACCTCCGGCATT[C/T]TCTACTTCTCTGCCT | 21787 |
rs258097645 | in-del | -/AAA | | | intron-variant | Tfg | Mm_Celera | 16:56691982 | CCCTGCATTTAGAAG[-/AAA]AAAAAAAAAAAGGAT | 21787 |
rs258118237 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56704334 | AAGATATTAAGGATG[A/C]CACCTGACTCCAAGA | 21787 |
rs258118353 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56712213 | AGGAGCTGACTTCCA[A/G]GCAGCTAGGGTGAGG | 21787 |
rs258152649 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711763 | TCCCTACCTTGGCCT[C/T]GGGTATACTCTTCAG | 21787 |
rs258185974 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696676 | ACTTGGGGGTGGAGG[A/G]AGCCATGTTAAGGGT | 21787 |
rs258451048 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56706821 | AAATATGTTCTCCCC[C/G]ACTCCCCATACACAT | 21787 |
rs258490938 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56695844 | TGTCTCATTTCTAAT[A/G]TATAAAATCCAATAA | 21787 |
rs258528077 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56702862 | CAGCAATAGCAAGAT[C/G]GAAGGCAGAAACAAA | 21787 |
rs258541111 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56705030 | CCTTTTTTATCTCCC[C/T]CACAGAAACCCTGGC | 21787 |
rs258598795 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56709953 | ATAAGGGGCTGGCTT[A/T]CAGGTTCAGAGGTTC | 21787 |
rs258610660 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56697084 | GAGGGATAAAAAAAA[-/C]CCCACCTCAAATGAA | 21787 |
rs258614514 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56714291 | CTTGAGAGGAAGAGG[A/C]AGGTGGATTTCTGAG | 21787 |
rs258681107 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56712121 | CTTATAAGAATTGGG[A/G]CTGGCTTACAGGTTC | 21787 |
rs258853476 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713748 | GGGAGAGGAAGCATG[G/T]ATGAACATGAAATTA | 21787 |
rs258884235 | snp | G/T | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718822 | ATTCACTACTTAACT[G/T]GGGTACTATTTTGTT | 21787 |
rs258893743 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718272 | TTTTACGCTGAACAC[A/G]TTTCAATCTGCTTGC | 21787 |
rs259049624 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56695789 | TAGAGCTAGTTCAAA[C/G]TGGGACATAACGTAT | 21787 |
rs259057702 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56701381 | AAATGAGTAAAAGAT[-/A]AAAGAACAGTTTTCC | 21787 |
rs259062839 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695320 | TTTTTGAGACTCACT[A/G]TGAAGCCCTGGCTAG | 21787 |
rs259093240 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56704126 | GGACTGAGTACAGAG[C/T]GCTGCATATGTCAGG | 21787 |
rs259285569 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56693566 | TAGCTAGCCATCTAT[A/C]TATCTGCAATTTGCT | 21787 |
rs259320055 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56701410 | CCAAAATAATTATTG[C/T]CTCTAACAGTCACTG | 21787 |
rs259348509 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56713701 | TGGACAATGGCTACA[A/G]AATTATTAACTTGCA | 21787 |
rs259407992 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56693194 | ATTCATCTGTTTTTT[A/G]CAATCAGATCTAACA | 21787 |
rs259423271 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56703095 | TAAATAAGTCTTCAT[C/T]ATAAAGTGTCTAAGA | 21787 |
rs259475184 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56691621 | AACACTCTTCATATA[A/C]ATTGTTTTATATAAA | 21787 |
rs259506028 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56706024 | GAAAATGTTTCATAC[A/G]CATTAACTTTTAGTA | 21787 |
rs259541671 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56700182 | GGGGATAAATCCAAG[A/C]GGTCTCAGAACCAAA | 21787 |
rs259541819 | snp | A/T | | | intron-variant | Tfg | Mm_Celera | 16:56691785 | ATCATATTGTCCCAC[A/T]TAATCAACATCTATA | 21787 |
rs259612907 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56698132 | TATAATTCTAATAAA[C/T]CTTTGAATTATAAAT | 21787 |
rs259830016 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56699531 | CTGTACTATTAATCC[G/T]AAAAATACTCAGTGC | 21787 |
rs259934687 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56702592 | TTTAGAATTTGCTTC[-/A]AAATAATATACAAGG | 21787 |
rs260012321 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56704580 | GGCCATTAACTAAAA[A/C]AAAAGCATTAATTTG | 21787 |
rs260157440 | in-del | -/GTATTTATA | | | intron-variant | Tfg | Mm_Celera | 16:56695528 | TCGGGGGAAAATATG[-/GTATTTATA]GTATTCAATTAATAA | 21787 |
rs260440216 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56705743 | CATCAGTAATAAACT[A/G]TCATAAAAAATGTAA | 21787 |
rs260441568 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56696897 | CCAAACTCAGAAATG[C/T]GTCTGCCTCTGCCTC | 21787 |
rs260469821 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56704994 | AAATAAGATACACAG[C/T]TGATGCTAAATTCCC | 21787 |
rs260550538 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56711637 | TTTTCTATTTTTCCT[G/T]TCTAAGCTTGCTACT | 21787 |
rs260570656 | snp | A/C | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718770 | CTCAGAAAGGACTTT[A/C]GTACTGTTGCTTGTC | 21787 |
rs260777229 | in-del | -/TTCA | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717809 | CCTTCTTTCTACACG[-/TTCA]TTCATTCATTCATTC | 21787 |
rs260860610 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56715905 | TGAGTTCCTAGAACT[A/G]CTGTTAAGATCACTA | 21787 |
rs260867534 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56714534 | AAAAAATGTATTTTT[G/T]TAAATGGTAAAAGTA | 21787 |
rs260922386 | snp | C/T | | | downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56690321 | TAAATAATTAGGCAA[C/T]AAGACCACAGTTGGA | 21787 |
rs260991669 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56698205 | TAAGCCACACTGATT[G/T]CTACGTTGTATAAAT | 21787 |
rs261077566 | in-del | -/CAGT | | | intron-variant | Tfg | Mm_Celera | 16:56706740 | TAGTGAAACTTTCTG[-/CAGT]CAGTCTTAATCTTGT | 21787 |
rs261104121 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714404 | AAATAAATAAATAAT[C/T]GATCGATCGATCAGT | 21787 |
rs261125500 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56699564 | GGCTCTTCTTTTCTC[C/T]CTTATATGTAGCTTA | 21787 |
rs261227306 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56699401 | ACAGTCAAGTACTAA[C/T]GAGAAGCTATGCTAG | 21787 |
rs261313647 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56691608 | AAACAGTGCTACAAA[C/T]ACTCTTCATATACAT | 21787 |
rs261362365 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56693819 | AACTCCTCTGTGTAT[A/G]GGAACGGACCACCTA | 21787 |
rs261481955 | snp | A/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56717681 | GCTGGGTTTGCTACG[A/G]GAGCCTGGGGGAAGT | 21787 |
rs261489884 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697607 | TGGGCCTGGGTGGTC[A/G]TGAAAAGTCAGTTAA | 21787 |
rs261722422 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697452 | ACGGCTCTGAACGCT[A/G]TTTTACCTTCAATCT | 21787 |
rs261808759 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56702478 | TATTAATAAGCCAAG[A/G]CAGCCAGAATTCCTA | 21787 |
rs261921234 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56705985 | AGCCTGGTCTACTAG[A/G]GTTACACAGAGAAAC | 21787 |
rs261991179 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56715257 | TAATGGCTGTGATGA[C/T]GTGACACCTCTATAG | 21787 |
rs262072243 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710090 | TTTCCAGGCAGCTAG[A/G]GTGAGGGTCTTCAGT | 21787 |
rs262158219 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56699219 | TAATCTTGCTAGTTA[C/T]GAATCATAATATAAA | 21787 |
rs262292463 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56700356 | TCTCTGGTAATTTAC[A/G]TCCACACAGACTAAG | 21787 |
rs262319712 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56704220 | CCTGTCCTCCCAGAG[A/C]TCTATGATTCAATTA | 21787 |
rs262361039 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56696242 | TGACATGGCTATTGG[A/G]ATCTTTGTCCACCCA | 21787 |
rs262453692 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708418 | TTGCTCCTGTCTGAA[A/G]GAACTGTAAGAACAA | 21787 |
rs262545873 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56694959 | GTATTTCTTTTTTTT[A/T]AAATGACTTTCAACC | 21787 |
rs262801874 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56694336 | CTTCCGACAGTGTGA[A/G]CATTACAGATCAAGT | 21787 |
rs262819140 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56702110 | AAGCTGCCCTGTATG[A/C]TTTCTGAGAGGGTCT | 21787 |
rs262833142 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711354 | TGTGTCTTCTAAACA[C/T]TGGGATTAAAGGTGT | 21787 |
rs262833367 | in-del | -/TTT | | | intron-variant | Tfg | Mm_Celera | 16:56705017 | AAATTCCCTACTTCC[-/TTT]TTTATCTCCCTCACA | 21787 |
rs262908543 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708090 | GGAAAGGAGGGACCT[A/G]AGTGGGAGAGGGGAG | 21787 |
rs262923979 | in-del | -/CATTTCTCACTAGT | | | intron-variant | Tfg | Mm_Celera | 16:56697959 | GTTCAGAGATCCAAA[-/CATTTCTCACTAGT]CTTCTCACATGTTCT | 21787 |
rs262985649 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714848 | ACCATTTAAGCTGTC[C/T]TGAACCTCCCACAGG | 21787 |
rs263214643 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56706999 | GATGTAGAACTTTCA[A/G]CTCCTCCTATAGCAC | 21787 |
rs263224241 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56709005 | TGGGAAGGGGATGAA[A/G]TCTGGACTGTATAAA | 21787 |
rs263356085 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710416 | GACAAAGTCCAAACT[A/G]CATCTCCATGCCTGA | 21787 |
rs263394511 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56706456 | TAAGAAATGATATGG[G/T]GTAGAGGGAACCAGT | 21787 |
rs263449237 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56692413 | TACTAAACTTAAATA[G/T]TGTGTGTGTGTGTGT | 21787 |
rs263449905 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56698449 | TTACGGCTTTAAGTT[A/C]CGCTAGCAACACAGA | 21787 |
rs263478854 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714454 | AAAAGGACATTGATC[G/T]GTGGTACAGTGCTTG | 21787 |
rs263655976 | snp | C/G | | | intron-variant | Tfg | Mm_Celera | 16:56714034 | GAGTTGGATCATCAG[C/G]AGCTGGAACCATGGG | 21787 |
rs263794525 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56712021 | GATGCATGGTCAGGC[C/T]TATCACAAGAATACC | 21787 |
rs263796942 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56704164 | CCTACCACTGAGTTA[-/T]TCCCCCGTCCTAGAG | 21787 |
rs263814984 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56704766 | AACCTTACTCTTGGA[A/G]TGAGGGCTTTCACTG | 21787 |
rs264145199 | in-del | -/ACACACAG | | | intron-variant | Tfg | Mm_Celera | 16:56703679 | TTTAAACACACACAC[-/ACACACAG]ACAGATACACACACA | 21787 |
rs264213910 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56713864 | AGTATTCTCCTGGGC[-/T]TTTGAACAACTATCC | 21787 |
rs264220364 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56714917 | CTTTCTGTCTCCTTC[C/T]CTAAAACTTACTGAA | 21787 |
rs264372230 | in-del | -/TGAGTTCCTAG | | | intron-variant | Tfg | Mm_Celera | 16:56715889 | AGAGATTAACATGAA[-/TGAGTTCCTAG]TGAGTTCCTAGAACT | 21787 |
rs264464224 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56706846 | ACACATATGTTTGAA[A/T]AATTGGTTCATAGGG | 21787 |
rs264470874 | snp | G/T | | | missense, downstream-variant-500B | Tfg | Mm_Celera | 16:56690977 | TGGCAGGCTGAGATG[G/T]TTGGGTAGTATACGT | 21787 |
rs264536821 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56695407 | GGTCTCTCGTTTTTT[C/T]ACTTTTCAAAATTAA | 21787 |
rs264595520 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690448 | TAAATAGCCAAGTGT[A/G]ATGGCTATACCTTAG | 21787 |
rs264716377 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56696769 | TTAAATACTGAGCTT[C/T]CAATTTCATTCAGGA | 21787 |
rs264850929 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56694005 | GAGTATTTTAAACAG[C/T]CTTAAATAAAACAAC | 21787 |
rs264997947 | snp | G/T | | | intron-variant | Tfg | Mm_Celera | 16:56693361 | TTAAAGGGCCAGATA[G/T]TAAATATTTTAGGTG | 21787 |
rs265061362 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56701252 | CTATAATAAAGAATA[A/G]ACAAGTTTACTTTAT | 21787 |
rs265061513 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56700925 | CAAACAAATCTCCTT[G/T]GGGGTGCTGAAATCA | 21787 |
rs265130581 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56706949 | TCAAGCTATGCCCAG[G/T]ATGGAACAGTCTCCT | 21787 |
rs265130944 | in-del | -/GCAAA | | | intron-variant | Tfg | Mm_Celera | 16:56710176 | CTGAGCTAAGCATAT[-/GCAAA]ACATCACATTCCACT | 21787 |
rs265233260 | in-del | -/CACACACACACACA | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56719297 | TACTTGCCTCTACTG[-/CACACACACACACA]CACACACACACACAC | 21787 |
rs265299229 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56703005 | TTGTATGGACATCCA[C/T]CCATATGCAAGTATG | 21787 |
rs265576757 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56711732 | ACTTCCTTTGTCAAT[A/G]CAATTAATATAAATC | 21787 |
rs265613178 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56715383 | TTAGAAAGATAGTAA[A/C]TATCTCATACTTTCA | 21787 |
rs265622267 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56697705 | AATCACTATGAAACA[A/G]CCATGTCACCGAGGA | 21787 |
rs265632297 | snp | A/C | | | intron-variant | Tfg | Mm_Celera | 16:56705873 | TACATTCATGAGAAA[A/C]TGTAGCCAAAGTTAA | 21787 |
rs265651841 | in-del | -/GCCACA | | | intron-variant | Tfg | Mm_Celera | 16:56698561 | ACTGAATCCTTCTGT[-/GCCACA]GCTTCTCCACTTATG | 21787 |
rs265652425 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56716239 | GACCAGGCTGGCCCC[A/G]AACTCAGAAATCCAC | 21787 |
rs265789181 | snp | C/T | | | intron-variant | Tfg | Mm_Celera | 16:56711721 | GCTTTTTTGAGACTT[C/T]CTTTGTCAATGCAAT | 21787 |
rs266006054 | snp | C/G | | | upstream-variant-2KB | Tfg | Mm_Celera | 16:56718054 | TTTTGCTTTGGATGT[C/G]TTTAAATGGATGGAA | 21787 |
rs266031735 | snp | A/G | | | intron-variant | Tfg | Mm_Celera | 16:56710740 | GCTGCTGCTCTTGGT[A/G]AGCATCCCATGGTAC | 21787 |
rs266146305 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | Mm_Celera | 16:56690627 | GGTAAATTATATTTT[A/C]AATTAACAGCAACAA | 21787 |
rs266151319 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56701821 | AAGCAGGCCAGGCAA[-/T]CCATAAGCAGTAACC | 21787 |
rs266197754 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56700975 | GAAGCTTAAATATGT[-/A]AAAAAATAACTGGCT | 21787 |
rs386909353 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | Abi3bp, Tfg | Mm_Celera | 16:56689957 | ACTCATTTCATGGGG[-/G]AAAAAAAAAGCATTG | 21787 |
rs387040719 | in-del | -/AGAATGAAGGGTGTCTTCTGA | | | intron-variant | Tfg | Mm_Celera | 16:56702955 | GTGGAAGGCACATGA[-/AGAATGAAGGGTGTCTTCTGA]GCTCCATGCTGCCCT | 21787 |
rs387064216 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56694958 | GTATTTCTTTTTTTT[-/T]AAAATGACTTTCAAC | 21787 |
rs387219801 | in-del | -/TATT | | | intron-variant | Tfg | Mm_Celera | 16:56696571 | TACTGTGGACTTATT[-/TATT]ATGATTGTGATCAAC | 21787 |
rs387342778 | in-del | -/A | | | intron-variant | Tfg | Mm_Celera | 16:56692512 | TTATGGATGCTAAAA[-/A]TCTGAGCCCAGTTAC | 21787 |
rs387400137 | in-del | -/T | | | intron-variant | Tfg | Mm_Celera | 16:56713867 | ATTCTCCTGGGCTTT[-/T]GAACAACTATCCATG | 21787 |
rs387705841 | in-del | -/AA | | | utr-variant-5-prime | Tfg | Mm_Celera | 16:56717418 | GGAGAAAAAAAAAAA[-/AA]CTGCCCTGGCGCCCC | 21787 |
rs387756272 | snp | A/G | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56719268 | GATAAGCATTGGATC[A/G]TGTCACTCTGCCCTA | 21787 |
rs387759629 | in-del | -/C | | | intron-variant | Tfg | Mm_Celera | 16:56702632 | TAAACAGGCATGATC[-/C]TGACCTAAGGTAATT | 21787 |
rs387760981 | snp | C/T | | | utr-variant-5-prime | Tfg | GRCm38.p3 | 16:56717364 | CGACAGCCACGGTCC[C/T]GTACGTGGCAGGTGG | 21787 |
rs387827107 | in-del | -/TT | | | intron-variant | Tfg | Mm_Celera | 16:56693134 | TACTTTTTTTTTTTT[-/TT]GCTTAATAGAATAAC | 21787 |
rs578283408 | snp | A/G | | | downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56690177 | TATACCTTTATCGCC[A/G]TAAGGAAAAATCATA | 21787 |
rs578631219 | snp | A/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56717757 | TCGTGACTACGCGCT[A/T]GTCTGTCACATCTCG | 21787 |
rs578707284 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711157 | TCTATTCTGGACTCT[A/G]AAGTCCTCCCTCAGA | 21787 |
rs578862537 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696670 | CAGTTAACTTGGGGG[G/T]GGAGGGAGCCATGTT | 21787 |
rs579223954 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56710506 | TTCCTTCTCCTAGGG[C/T]GGTTTCACTCCCTGC | 21787 |
rs579267162 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704094 | CCATCTGCACATTTA[C/T]TTATTATTCAGTACG | 21787 |
rs579585077 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56697947 | TCTCCCTGGTTGTGT[A/T]CAGAGATCCAAACTT | 21787 |
rs579601102 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708065 | ATGGGGGGGTGGGGG[G/T]GGGAGGTGAGGAAAG | 21787 |
rs579908017 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56692950 | GACAAGAGAACCATT[C/T]TGTTCAGCCTCCTCG | 21787 |
rs580088241 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56699273 | TATGCAACCTCCAAA[A/G]GAGCTACCCCACAGC | 21787 |
rs580188057 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711955 | AGCCCCACTTAAAGC[A/G]TTCTACTGCTTTCCA | 21787 |
rs580748181 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56702522 | TAACACAATTCTGCT[C/T]CTCTTTTAAATATGT | 21787 |
rs580991929 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708864 | CCTCCAGAGACTTGA[A/G]GCCCCAGGGAATTGG | 21787 |
rs581079407 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696032 | CTGGAAAGAGGTGCA[C/T]GGTTGCTAGAACACA | 21787 |
rs581270199 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708983 | GAGGATCGGTTGGAA[G/T]GCAGACTGGGAAGGG | 21787 |
rs581293379 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713650 | TGTTATCTTTCTAGA[C/T]TGCAGAAGAAGCCTT | 21787 |
rs581352815 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56703276 | TTTAAAACCTAACCA[C/T]ATTTTTAAAAAGTGT | 21787 |
rs581462024 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713677 | CCTTGTACATAGTAG[C/T]TATTCAAATGGACAA | 21787 |
rs581781218 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56701835 | AACCATAAGCAGTAA[A/C]CTCGAGCAGCACTCC | 21787 |
rs581827271 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56711006 | GTTACAACCTTGGCT[A/G]TCTCTGGAACACAGC | 21787 |
rs581855459 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696817 | TTTGTTTGGGTTTTG[G/T]TTTTTTTTGGGTTTT | 21787 |
rs581911697 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Tfg | GRCm38.p3 | 16:56717479 | ATGCGCAGTGGGTGA[C/G]GGGCGGGGCGGGCGA | 21787 |
rs581953106 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56704392 | AAATGAAAAAAAAGA[A/G]TTCATGACAATAAAA | 21787 |
rs582402007 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56711218 | GCTGCTGGAGCTAGA[A/C]TATGGCTCCCTTGCT | 21787 |
rs582489521 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56704118 | CAGTACGGGGACTGA[A/G]TACAGAGTGCTGCAT | 21787 |
rs582554564 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56712891 | TGTGCCCCTTAAAAA[A/T]AGTGCCTCTCATTGA | 21787 |
rs582614338 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696733 | GTCACGCTCTGATGT[C/T]ATCTGTGCCAAATAG | 21787 |
rs582671940 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56694265 | TTGCTCACTAAAAAT[A/G]GAAAATGCTGATTTG | 21787 |
rs582991813 | snp | G/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708752 | AGATCTCTCAGACAC[G/T]GAGCCAACAGCCAGG | 21787 |
rs583076831 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56698554 | GCATGCTACTGAATC[C/T]TTCTGTGCCACAGCT | 21787 |
rs583219210 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56691837 | ATAAAAAATAAAATC[C/T]GCTTCACTGAAAACT | 21787 |
rs583546851 | snp | C/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56713288 | TGAATCAACAAACCA[C/G]ACGTTTGTTCTTAAG | 21787 |
rs583649293 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56692991 | GCATGGCTTGAAAAG[C/T]CACTTATAAAAGAGT | 21787 |
rs583649898 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56705756 | CTGTCATAAAAAATG[C/T]AAAATTACAGAGAAT | 21787 |
rs583950211 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56694211 | AAAACAATTTATACT[A/G]TAGATTACTGTAGAA | 21787 |
rs584131632 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56695449 | CACATAAGCTTAGGT[A/G]TATGCTTGCCTGAGC | 21787 |
rs584225771 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56702794 | GAGGACCTGATTTCT[A/G]AACCTCCAGAATTCA | 21787 |
rs584233769 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56711016 | TGGCTATCTCTGGAA[C/T]ACAGCTTCTTTGTGC | 21787 |
rs584550849 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56696459 | ATTCACTGAGCAAGC[A/G]TGCAAGTGTCATCAC | 21787 |
rs584727549 | snp | C/T | | | upstream-variant-2KB | Tfg | GRCm38.p3 | 16:56717724 | CAGAAAGGTTTGGGT[C/T]TTGTTGCTTTGTGGC | 21787 |
rs584736505 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56713656 | CTTTCTAGATTGCAG[A/C]AGAAGCCTTGTACAT | 21787 |
rs584926136 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708915 | GTGAGTGGGGATATC[C/T]TCCTGGAGAATGGAA | 21787 |
rs584958892 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56710173 | CCTCCTGAGCTAAGC[A/G]TATACATCACATTCC | 21787 |
rs585026815 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56703287 | ACCATATTTTTAAAA[A/G]GTGTCTACAACTCAG | 21787 |
rs585244548 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56714505 | GGGTTCCATAAATAC[C/T]TGGTACCACGTTAAA | 21787 |
rs585254590 | snp | C/T | | | downstream-variant-500B | Abi3bp, Tfg | GRCm38.p3 | 16:56690173 | TAAATATACCTTTAT[C/T]GCCGTAAGGAAAAAT | 21787 |
rs585268967 | snp | C/T | | | synonymous-codon | Tfg | GRCm38.p3 | 16:56697508 | ATAGGGAGGTTGCTG[C/T]GGCTGAACTGCTGGG | 21787 |
rs585682238 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56692399 | TCTCCCGTCTTCCAT[A/G]CTAAACTTAAATATT | 21787 |
rs585745249 | snp | A/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56694202 | CTTTGTAGTAAAACA[A/T]TTTATACTGTAGATT | 21787 |
rs585777932 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56698573 | TGTGCCACAGCTTCT[C/T]CACTTATGCAAAGGG | 21787 |
rs586032954 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56712435 | AAAAACACATGTGAA[A/G]ATGTCAGACACTCCC | 21787 |
rs586300256 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696736 | ACGCTCTGATGTCAT[C/T]TGTGCCAAATAGCCC | 21787 |
rs586353112 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56704149 | ATGTCAGGCAAGCAC[C/T]CTACCACTGAGTTAT | 21787 |
rs586508402 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713204 | CAATATTGAAACCAA[C/T]TCCCTACTTTGTCTG | 21787 |
rs586686134 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56693016 | AAGAGTAGAACAACA[C/T]CAGTGGTCCTCACTG | 21787 |
rs586884600 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713290 | AATCAACAAACCAGA[C/T]GTTTGTTCTTAAGTA | 21787 |
rs586972607 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56708862 | ACCCTCCAGAGACTT[A/G]AGGCCCCAGGGAATT | 21787 |
rs587140514 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56713671 | AAGAAGCCTTGTACA[C/T]AGTAGTTATTCAAAT | 21787 |
rs587310121 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56708926 | TATCTTCCTGGAGAA[C/T]GGAAACGGGGGTGGG | 21787 |
rs587374422 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56696030 | TGCTGGAAAGAGGTG[C/T]ACGGTTGCTAGAACA | 21787 |
rs587502022 | snp | A/G | | | intron-variant | Tfg | GRCm38.p3 | 16:56706626 | GAACTGTATAAGCAG[A/G]CCCATACATATGTAT | 21787 |
rs587522893 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56701815 | GTAATACAAGCAGGC[A/C]AGGCAACCATAAGCA | 21787 |
rs587546249 | snp | A/C | | | intron-variant | Tfg | GRCm38.p3 | 16:56700204 | AGAACCAAAAAAAAA[A/C]AAAACATAAATAAAT | 21787 |
rs587571973 | snp | C/T | | | intron-variant | Tfg | GRCm38.p3 | 16:56694257 | CGTTGAATTTGCTCA[C/T]TAAAAATAGAAAATG | 21787 |
rs864273229 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Abi3bp, Tfg | GRCm38.p3 | 16:56690352 | TTCAATCACCTTTAT[C/T]AGCCTATCAATGTTA | 21787 |