SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3653619 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tle1 | Mm_Celera | 4:72145961 | TATCCAAAGAAGAAA[C/T]CTTAGCTAGTTGTGA | 21885 |
rs3660580 | snp | A/T | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72161849 | GAATTGTTTTTTTTT[A/T]AAATTAGGACTTCTC | 21885 |
rs3661165 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Tle1 | Mm_Celera | 4:72161937 | AAGACAGGCGGCTTC[A/G]GTTCTTATCTCGGGG | 21885 |
rs3661752 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle1 | Mm_Celera | 4:72162058 | TGAAATCTCCTATTA[C/T]ATGAAAGGCCTCTTT | 21885 |
rs3669227 | snp | A/G | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72156665 | TCTCAAGACAGAAGG[A/G]AAGAAAAAAGACAGG | 21885 |
rs3677725 | snp | A/G | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72141010 | TGAGAGACAAATGAG[A/G]TAAAGGGGAACAGTA | 21885 |
rs3684734 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle1 | Mm_Celera | 4:72156911 | GGTATGCGTGACTCG[A/G]GCTTGTGAAAACATG | 21885 |
rs3684736 | snp | G/T | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72156916 | GCGTGACTCGGGCTT[G/T]TGAAAACATGAAGTC | 21885 |
rs3696858 | snp | A/G | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72161710 | ATTGCTAGACAGCCA[A/G]ACAACAGTTCTGTCA | 21885 |
rs3710492 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle1 | Mm_Celera | 4:72145546 | ACCCTGTTACCTTCC[G/T]AGTCTTAAGGCCCTG | 21885 |
rs6155548 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Tle1 | Mm_Celera | 4:72130558 | TATCCTCCCTCTGTC[C/T]CCCTCTCTAAACACA | 21885 |
rs6156030 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Tle1 | Mm_Celera | 4:72130614 | GTTAATACTTTCAGA[C/T]TGCACTTGATCTGAA | 21885 |
rs6156638 | snp | A/G/T | 0.471655 | 0.115624 | intron-variant | Tle1 | Mm_Celera | 4:72130740 | GCAAAAAACAGTATC[A/G/T]GTTTTCCCTGTAGCT | 21885 |
rs6170390 | snp | A/C | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72130922 | GCCCACTTATTTATT[A/C]AAAAAAAAGTATAGG | 21885 |
rs6222684 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tle1 | Mm_Celera | 4:72140288 | AACCAGCACTTCAGA[A/G]ATAAAGTTCCTGAAG | 21885 |
rs6223864 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tle1 | Mm_Celera | 4:72140496 | AGGGTGTAGAAAACA[A/G]AGTGAGCCAAAACTC | 21885 |
rs6223939 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tle1 | Mm_Celera | 4:72140536 | GCTTAGGATTTGATA[A/G]AATGTTCTCAACAAG | 21885 |
rs6224005 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Tle1 | Mm_Celera | 4:72113710 | atgaagtcagtttca[C/T]cccagggatacagag | 21885 |
rs6237858 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Tle1 | Mm_Celera | 4:72113899 | tcccaaagaatctag[A/G]aatacaggggacata | 21885 |
rs6327644 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Tle1 | Mm_Celera | 4:72125643 | AATGACATTATTTAG[A/T]TATCTAGTTAGGNCA | 21885 |
rs6327678 | snp | A/G | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72125656 | AGNTATCTAGTTAGG[A/G]CAGCCCAGTTCACAG | 21885 |
rs6328072 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Tle1 | Mm_Celera | 4:72125681 | TCACAGTCTGCTGAA[C/G]AACAACATTACAGGT | 21885 |
rs6328137 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tle1 | Mm_Celera | 4:72125718 | ATCATAAGGCTAATA[A/G]GTGCTTCTAAGTTCT | 21885 |
rs6341141 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Tle1 | Mm_Celera | 4:72125781 | TCTTTCTGTTCCAGT[C/T]TTACTACAGCTATGG | 21885 |
rs6342234 | snp | G/T | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72126019 | AAACCACTGCAAACA[G/T]CTCCAAAAANCAGCC | 21885 |
rs6342248 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Tle1 | Mm_Celera | 4:72126029 | AAACANCTCCAAAAA[C/T]CAGCCGATCAACACC | 21885 |
rs6342295 | snp | C/T | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72126058 | CCGGGATTTAACCAG[C/T]GTAGTGGCAGTAACT | 21885 |
rs27839931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72194777 | TTTTCTTTGAGGGGT[A/G]GTCTCAACCCTGGCT | 21885 |
rs27839932 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72194574 | GAATGAGATGGGATG[C/T]AGCTCTGGTAACTCC | 21885 |
rs27839933 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72194568 | CAGCCTGAATGAGAT[A/G]GGATGCAGCTCTGGT | 21885 |
rs27839934 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Tle1 | Mm_Celera | 4:72194373 | ACAAATAGCAAATAA[A/C]TGAAAACCAGCACTG | 21885 |
rs27839935 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Tle1 | Mm_Celera | 4:72194254 | TTGGCTGCCAGTCTC[C/T]AACATATTCCTGCCA | 21885 |
rs27839936 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tle1 | Mm_Celera | 4:72193445 | TTGAACTTATGCTTG[C/T]AAAGGACAAGCCTGG | 21885 |
rs27839937 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72192996 | CAGAGCAGAGATCCC[A/G]TCTACACAACAGCAG | 21885 |
rs27839938 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle1 | Mm_Celera | 4:72192958 | CCAGGTCCAATTCTT[C/T]GTCTGAGGCCAGCTT | 21885 |
rs27839939 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Tle1 | Mm_Celera | 4:72192596 | CAGTAACTAAAGCTA[C/T]CTTTCAAAACCACTC | 21885 |
rs27839940 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72192520 | TTTAATTCACTTCTA[G/T]AAACCACAGTAGGAA | 21885 |
rs27839941 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Tle1 | Mm_Celera | 4:72192151 | CCTACCCTTAGCCTC[C/T]TAACACACATACCCC | 21885 |
rs27839942 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72191582 | ACAGAATAGCATGGC[C/T]GTGTACACATTAGCA | 21885 |
rs27839943 | snp | C/T | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72191355 | ATAACTTCATCCCTA[C/T]ATGCAAAATGTCCAG | 21885 |
rs27839944 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Tle1 | Mm_Celera | 4:72191154 | TATAGAAGGAGACGA[C/G]TGACAGGCAGAATGG | 21885 |
rs27839945 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Tle1 | Mm_Celera | 4:72191071 | TTTGTCTGGATTAAG[A/T]GAGCTGCAGGACAGA | 21885 |
rs27839946 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72190744 | CTGAAGACAAGAGCT[A/G]GAATAATAAACAAGG | 21885 |
rs27839947 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle1 | Mm_Celera | 4:72190457 | CTACTCTTAAGTCAG[A/G]ATTTTAACCTGGGTC | 21885 |
rs27839948 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Tle1 | Mm_Celera | 4:72189359 | ACTCTTTCTTCAATC[A/G]GGTAAGCCAAGCTCT | 21885 |
rs27839949 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Tle1 | Mm_Celera | 4:72188470 | GCTCCTGAAGAGCCA[A/G]TCTGCTGTCTGGGAA | 21885 |
rs27839950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72188359 | GTTTCTTCTATAATC[A/G]AGCGTGTCAAGACGC | 21885 |
rs27839951 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Tle1 | Mm_Celera | 4:72188051 | TACTAAGATGCTTAT[C/T]AGTGCTAAGACACCC | 21885 |
rs27839952 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72187590 | TATTAAGTAATGAAA[C/T]AAGAACCTTTGATAA | 21885 |
rs27839953 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Tle1 | GRCm38.p3 | 4:72187277 | AGAAACAAGATGGAA[A/C/G]TATAAATGGAGCAAG | 21885 |
rs27839954 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tle1 | Mm_Celera | 4:72187177 | TTATGATCTAAAGAG[A/G]AAATCAATAAGACTT | 21885 |
rs27839955 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Tle1 | Mm_Celera | 4:72187174 | TGCTTATGATCTAAA[G/T]AGGAAATCAATAAGA | 21885 |
rs27839956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72186299 | TGATTTTGGCGTTTG[A/G]CAAGCTAAAATGTAT | 21885 |
rs27839957 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72186264 | ACTAGTTAGCATTTC[C/T]CCTCTTGAATCTAGC | 21885 |
rs27839958 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72186237 | AAGGAACAGGTTTCT[C/T]ACCAGATTCTTACTA | 21885 |
rs27839959 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72186123 | TGAATACAACTGTAA[A/C]AACCAGCAGGAAAAC | 21885 |
rs27839960 | snp | A/G | 0.42 | 0.183303 | intron-variant | Tle1 | Mm_Celera | 4:72185580 | ACGTTGGCTAACCCT[A/G]CAAATCATTTGAGTA | 21885 |
rs27839961 | snp | A/G | 0.42 | 0.183303 | intron-variant | Tle1 | Mm_Celera | 4:72185084 | TATGCCAAAATTTCA[A/G]TTGTGCATACAGACA | 21885 |
rs27839962 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle1 | Mm_Celera | 4:72185043 | AGGAAACTTAGCAAA[C/T]ACAAATATGTACCTT | 21885 |
rs27839963 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle1 | Mm_Celera | 4:72184917 | GAACCAGTTAAACAA[C/T]GTAATAATAAGGGGA | 21885 |
rs27839964 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle1 | Mm_Celera | 4:72184504 | TCACTAACCGTGTGG[G/T]TTCCAGGACATGCCA | 21885 |
rs27839965 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tle1 | Mm_Celera | 4:72183985 | CAGTCCGCACAATGG[C/T]GTGGGTATATACAGA | 21885 |
rs27839966 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tle1 | Mm_Celera | 4:72183975 | ACTTAGAAGACAGTC[C/T]GCACAATGGTGTGGG | 21885 |
rs27839967 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72183621 | TTCCCAGGCTGAGCT[A/C]CCAGACAGGAATAGT | 21885 |
rs27839968 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle1 | Mm_Celera | 4:72183545 | GAGTGGTAGTGCATG[G/T]GACACGTATATGTTT | 21885 |
rs27839969 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Tle1 | Mm_Celera | 4:72183428 | TAACTAAATTACCTG[G/T]ACAGACATGGTAGCA | 21885 |
rs27839970 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72183385 | ACTGTGGGCCAGCGA[C/T]TCCCTAACTTTATAA | 21885 |
rs27839971 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Tle1 | Mm_Celera | 4:72182900 | TGTTCACAAGAAATC[A/C]TATTGACTTGTTACA | 21885 |
rs27839972 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Tle1 | Mm_Celera | 4:72182801 | TAAAGCTGCATCTTT[C/G]ACAAAAGCATCACAG | 21885 |
rs27839973 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle1 | Mm_Celera | 4:72182730 | AATTAATGATTTAAA[A/T]GTTTTGACCCAACTG | 21885 |
rs27839974 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72182381 | CAGAATGCAGAAAAC[A/T]CTGCCATCAATTCAG | 21885 |
rs27839975 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72181139 | AGGACTGTGCAAGAG[A/T]AATTGCCCAAGGGTC | 21885 |
rs27839976 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tle1 | Mm_Celera | 4:72177133 | ACAGGATACCAGGCG[C/T]AGATGTTCGCTGAGA | 21885 |
rs27839977 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72176842 | CAGAGGGTATGATTC[A/G]TGTAGGGAACACACT | 21885 |
rs27839978 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Tle1 | Mm_Celera | 4:72176481 | AGGGTTAATGACTAG[A/G]TATGACCATATATAA | 21885 |
rs27839979 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Tle1 | Mm_Celera | 4:72176443 | ATGTAGCTCAATTGA[C/G]GGAATGGATACAAGA | 21885 |
rs27839980 | snp | A/G | 0.5 | 0 | intron-variant | Tle1 | Mm_Celera | 4:72170980 | TTAAAAGATAATGAT[A/G]GAGTTAGAGAAATGG | 21885 |
rs27839981 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle1 | Mm_Celera | 4:72170907 | AATTACCTGGAAATA[C/T]ACTGTAGATACCAGA | 21885 |
rs27839982 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72170533 | GTTGAGATACTGTCA[C/T]CCCTCCAGCAGCCTG | 21885 |
rs27839983 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72170259 | ACAGGCCTAGCCAGC[A/G]GTGGTGGCATCGAGA | 21885 |
rs27839984 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72170222 | GGGTACCCGAACCAT[A/G]TCAAGCACATATTAC | 21885 |
rs27839985 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72170187 | AGTGACTTTTCAAGT[C/T]AGCTCAAGAAAACAG | 21885 |
rs27839986 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Tle1 | Mm_Celera | 4:72169547 | TGTATTTTCTCTGAT[G/T]TAAAAAAAAAAAAAA | 21885 |
rs27839987 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle1 | Mm_Celera | 4:72169446 | AACAGGACATGGATG[A/G]CTGTTCTAGGTTATG | 21885 |
rs27839988 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72169399 | ATATCAGAATGGACA[G/T]CAATGGTGACCTGTC | 21885 |
rs27839989 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle1 | Mm_Celera | 4:72169353 | TTTCTGAAGGGTTCC[A/G]GGCATCACTATACTC | 21885 |
rs27839990 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72169330 | ACAATGAGCGGTGCT[G/T]CCCTTTATTTCTGAA | 21885 |
rs27839991 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72169273 | AACAAAGACCAAAAC[C/T]GGGTCATCATGCAAG | 21885 |
rs27839992 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72169237 | TTAGCATCAGCTAAG[A/C]ATGTCCCTGTTCACT | 21885 |
rs27839993 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant | Tle1 | Mm_Celera | 4:72169194 | GGCCACCTGTTGTTG[A/G]TGCTTTGAAAACAAG | 21885 |
rs27839994 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72168908 | AGGAGAGTTACTTCC[A/G]TCCTCTTCTAGTGTT | 21885 |
rs27839995 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72168877 | TCTCTGGATAAACGT[C/T]TCTACTTCTCCATTT | 21885 |
rs27839996 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Tle1 | GRCm38.p3 | 4:72168673 | GGAACAAGAAAGAAA[C/G/T]GAATCAAACAACCAC | 21885 |
rs27839997 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle1 | Mm_Celera | 4:72168003 | CTGCCAACAGCTTAC[C/T]ACAGGCACCCCAACT | 21885 |
rs27839998 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Tle1 | Mm_Celera | 4:72167995 | CTAATTGACTGCCAA[C/T]AGCTTACCACAGGCA | 21885 |
rs27839999 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle1 | Mm_Celera | 4:72167468 | TCAGAAAACAAACAT[A/G]TCCCACAAAGTTGAA | 21885 |
rs27840000 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle1 | Mm_Celera | 4:72167262 | AAGTAGGTACAAAGA[C/T]TTTCCAGGTCTGAGC | 21885 |
rs27840001 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle1 | Mm_Celera | 4:72167082 | GTTATTACTATCAAG[C/T]TAATCTTACTTTATA | 21885 |
rs27840002 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle1 | Mm_Celera | 4:72166694 | TAGAACAATCTGACA[A/G]CTGCTATCAAACAGG | 21885 |
rs27840003 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Tle1 | Mm_Celera | 4:72166570 | GTACTCTTTCATGAT[A/C]TTTCACACTTAAAAT | 21885 |