SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3021536 | in-del | -/C | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499567 | TTTTTCAAAGATAAT[-/C]TTAGACAGAGTGAAA | 11622 |
rs3021537 | in-del | -/C | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499587 | CAGAGTGAAATGAGT[-/C]GCTCTGCTTAACATA | 11622 |
rs3021538 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35501303 | AGCACGGGCTGAAGG[C/T]TTTTTTTAAAAACAA | 11622 |
rs3021539 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Ahr | Mm_Celera | 12:35497840 | GCTCAAACAGAGAAT[C/T]TAAGTAACCCTTTCA | 11622 |
rs3021543 | snp | C/T | 0.437045 | 0.165874 | missense | Ahr | Mm_Celera | 12:35503847 | GAGGACTGACCATGG[C/T]GGACTGTGAGTTTAT | 11622 |
rs3021544 | snp | A/G | 0.499405 | 0.0172311 | missense | Ahr | Mm_Celera | 12:35506263 | AGTGGTCTCTGAGTG[A/G]CGATGATGTAATCTG | 11622 |
rs3021545 | snp | A/G | 0.470868 | 0.117121 | missense | Ahr | Mm_Celera | 12:35506345 | GACTGTGTTTTGCAA[A/G]AAGCCGGAAAACTGT | 11622 |
rs3021546 | snp | C/T | 0.49948 | 0.0161206 | intron-variant | Ahr | Mm_Celera | 12:35510130 | CAGTCTACCTTACAT[C/T]TGCTGTGAAATCAAG | 11622 |
rs3021547 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35512161 | GTCCCTAAATGTGAC[C/T]GTGGTTTCACAGTTC | 11622 |
rs3021548 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35512199 | GCTCTGTCTTAGTGA[C/T]ACTTCCATGGCTGAC | 11622 |
rs3021549 | snp | A/G | 0.466392 | 0.125197 | intron-variant | Ahr | Mm_Celera | 12:35512828 | TTTCTAAAAACCTTC[A/G]TTTGAGATGATGGAA | 11622 |
rs3021550 | in-del | -/GGTA | | | intron-variant | Ahr | GRCm38.p3 | 12:35513011 | CCTGACAGTTAGGTA[-/GGTA]ACAGGCTGTTTCTCT | 11622 |
rs3021551 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522249 | TAATTTCTAGGACAG[C/T]GAGACTACCAAGAGA | 11622 |
rs3021553 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35522326 | TGATCTTTTTATCCC[A/T]TGTGAGGCAGTAGCT | 11622 |
rs3021554 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522354 | GCTCCTGCTTGATCA[C/T]TGTTCAACAGACATG | 11622 |
rs3021555 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522358 | CTGCTTGATCATTGT[C/T]CAACAGACATGATAC | 11622 |
rs3021556 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522388 | CAGGAGAAATGGCCT[C/T]TCTGTTAACATAAGC | 11622 |
rs3021557 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35522390 | GGAGAAATGGCCTCT[C/G]TGTTAACATAAGCCA | 11622 |
rs3021558 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35522457 | ATTCATAAATAAAGT[C/T]CTACTGATCATAGTC | 11622 |
rs3021559 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahr | GRCm38.p3 | 12:35522544 | GAGACGGCTTCAAAC[C/T]TCACACTACCTAAAA | 11622 |
rs3021560 | in-del | -/ACTAC | | | intron-variant | Ahr | Mm_Celera | 12:35522553 | CAAACTTCACACTAC[-/ACTAC]CTAAAACACGACTAA | 11622 |
rs3021561 | snp | A/G | 0.4352 | 0.167931 | utr-variant-5-prime, synonymous-codon | Ahr | Mm_Celera | 12:35526790 | CAGGCTGGCCAGGCG[A/G]TCTAACTCTGTGTTC | 11622 |
rs3021562 | snp | G/T | 0.452663 | 0.146382 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535497 | AGACAATAAAACATC[G/T]TTTCCTCCATCAGAC | 11622 |
rs3021563 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536090 | GCAAGGAAAAGGATA[G/T]CGAGAAAACTAAGAA | 11622 |
rs3021564 | snp | C/G | 0.486111 | 0.0821678 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536092 | AAGGAAAAGGATAGC[C/G]AGAAAACTAAGAACA | 11622 |
rs3021565 | snp | A/G | 0.486111 | 0.0821678 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536104 | AGCGAGAAAACTAAG[A/G]ACAACAAATGGTGCC | 11622 |
rs3021566 | snp | C/T | 0.477041 | 0.104654 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536143 | GGAGGAAGAAGAACC[C/T]GCATCACTGTGGGTG | 11622 |
rs3021567 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536172 | TGGTTGTAAACTGGT[C/T]CAGCCACTGTGGAAC | 11622 |
rs3021568 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536249 | CCTGCTATTCTCCTG[C/T]GCACATACCTGATAG | 11622 |
rs3021569 | snp | A/G | 0.497041 | 0.0383476 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536324 | CATCAACCTATGGAT[A/G]GATAAATAAAATGTA | 11622 |
rs3021570 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536370 | GGCATTTTATGGGAC[C/T]CTGAATAAAACTGAA | 11622 |
rs3021571 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536376 | TTATGGGACTCTGAA[G/T]AAAACTGAAATCATG | 11622 |
rs3021572 | snp | C/G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536407 | GCATTTGCAGGTAAA[C/G/T]AAGTGGAACTGGAGG | 11622 |
rs3021573 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536408 | CATTTGCAGGTAAAC[A/G]AGTGGAACTGGAGGC | 11622 |
rs3021574 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536463 | AGAAGGCAAATACCA[C/T]GTTTTCTCTAGATGT | 11622 |
rs3021586 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499737 | AGCAGCGTTATCTCA[C/T]GTCTCAGAAAACACG | 11622 |
rs3021588 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ahr | Mm_Celera | 12:35510194 | TTGAATTAAAAATAC[A/C]ATTTCGAAAATAATT | 11622 |
rs3021589 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35511335 | TTCACATCAGCCATC[A/G]CCTCCTGACACGACG | 11622 |
rs3021590 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35511350 | GCCTCCTGACACGAC[A/G]GCTCTGGCTCACAAG | 11622 |
rs3021592 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35512692 | AAGAACAATAACCGC[A/G]AAGCAATATAGCAAA | 11622 |
rs3021593 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35526940 | TAAAACGTCCCCTCA[A/G]GGACTGCTCTACCGA | 11622 |
rs3021596 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522254 | TCTAGGACAGTGAGA[C/T]TACCAAGAGAAACCA | 11622 |
rs3021599 | snp | A/G | | | downstream-variant-500B | Ahr | Mm_Celera | 12:35497616 | CACAGAGATCAGAAT[A/G]AATACATGATTGTAG | 11622 |
rs3021600 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499027 | ATTTGAATACATCTC[A/G]GTTTGGGATCTCATC | 11622 |
rs3021601 | snp | C/T | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499599 | GAGTGCTCTGCTTAA[C/T]ATAGCTAACAGGCTT | 11622 |
rs3021602 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499675 | CTTTAGCACTTTCTA[C/T]GGTGGCCTTCTGATC | 11622 |
rs3021603 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499813 | AATTTGGGCAACATG[C/T]TATTTTTCAAATTTT | 11622 |
rs3021604 | in-del | -/CA | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499949 | AGTAGTGCACACACA[-/CA]GCGGGGTCATAGAAA | 11622 |
rs3021605 | in-del | -/A/C/T | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500431 | GTATAGGGAGCATCT[-/A/C/T]TCCCTACATCTCAGG | 11622 |
rs3021606 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500575 | CTACAGGAATCCACC[A/G]GGTGTGATATCGGGA | 11622 |
rs3021607 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500685 | AGGTTTCATTGAAAA[C/T]ACCTCAACTCTGCAC | 11622 |
rs3021608 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35500744 | TTAGGATCTGAGGAA[C/G]ACCTTAAAAACGACT | 11622 |
rs3021609 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35500809 | ACAGTCCTGTACTGA[A/T]GATGCTCATGGCTAA | 11622 |
rs3021610 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahr | Mm_Celera | 12:35500858 | CACACAGAGGAAACG[C/T]TCACACACTGACTTC | 11622 |
rs3021611 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35501119 | TCTGGATTTTAAATG[C/T]TTCTTGCTATTCTTG | 11622 |
rs3021612 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35501206 | AAATTGTTCTGCAAG[C/T]TACCAAATAAAAAAG | 11622 |
rs3021613 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35501738 | AGTAGAAAGTACTCT[G/T]CCATGGCCTCTGCAT | 11622 |
rs3021614 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35501861 | CTCTTTCTTCTCAGA[C/G]AGCTTTTGGTCACGC | 11622 |
rs3021615 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35501923 | CTTCTTACCAGTCTC[A/G]TATCCAGAACTGCTA | 11622 |
rs3021616 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35502956 | ACTATCTGTCTGTTA[C/T]TACCCAATAGCCAGC | 11622 |
rs3021617 | in-del | -/A/AATAA/AGTA | 0.24537 | 0.265428 | intron-variant | Ahr | Mm_Celera | 12:35503537 | AAGAAAATTATTTAA[-/A/AATAA/AGTA]NNNNTTTATTATTCA | 11622 |
rs3021618 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Ahr | Mm_Celera | 12:35503935 | AGTGGGATGCAGGGA[C/T]GGTTCAAAATCCCTT | 11622 |
rs3021619 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Ahr | Mm_Celera | 12:35504439 | GTCAACCTCACCAGC[A/G]GCGGTGGAGTCAGTT | 11622 |
rs3021620 | snp | C/T | 0.265928 | 0.249492 | missense | Ahr | Mm_Celera | 12:35504521 | AGGTTCCTCATGATG[C/T]TGTACAAGTCATTAT | 11622 |
rs3021621 | snp | G/T | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35505042 | GATTTAAGTAAGATA[G/T]TTCTAAAAGGAAGAA | 11622 |
rs3021622 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35505196 | ACCAAAATAGAAATA[C/T]ACCTAAATAAAATAA | 11622 |
rs3021623 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35505278 | TAAATGAAATGTCTA[C/T]GCCTGGAAGACACTG | 11622 |
rs3021624 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35505787 | CAGTGCTCAGACTCT[-/T]GTCAAGAGTTTGTCT | 11622 |
rs3021625 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ahr | Mm_Celera | 12:35506188 | TCTTTTTCANCTTTC[A/G]TGTAAGAAGACTTAT | 11622 |
rs3021626 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35506513 | CTCGCTCACTGGCTA[A/G]AGGAACTTGATGCTC | 11622 |
rs3021627 | in-del | -/AACT | | | intron-variant | Ahr | Mm_Celera | 12:35507255 | CCACCAAGCCTGACT[-/AACT]GAGGTTGATCCTAGG | 11622 |
rs3021628 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35507355 | AATCAAAGGATTTTT[A/T]AAAAGCTTAATATGT | 11622 |
rs3021629 | snp | A/C | 0.237812 | 0.249703 | intron-variant | Ahr | Mm_Celera | 12:35507388 | TAATACATGTGCCGT[A/C]TATCAGGCGGGTCAC | 11622 |
rs3021630 | snp | A/G | 0.237812 | 0.249703 | synonymous-codon | Ahr | Mm_Celera | 12:35507460 | AAGTATGTCTGCAGC[A/G]TGGATGAACTGGTAC | 11622 |
rs3021631 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ahr | Mm_Celera | 12:35507549 | TCAAATAAAAGAATC[A/G]GATTGTAAAATAATC | 11622 |
rs3021632 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35507642 | GAAAACATCCTTTTA[A/G]TTTTTTTTTTAATTT | 11622 |
rs3021633 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35507691 | AATTTTCAATTTTAG[C/T]CTTTTTTCTTAACTT | 11622 |
rs3021635 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35508002 | AGTCAGATTATTTGT[A/C]AAATTGATTAACTGA | 11622 |
rs3021636 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35508068 | TCACACACTTACAAA[C/T]CTGCTAAAATAAAAA | 11622 |
rs3021637 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Ahr | Mm_Celera | 12:35508109 | ATTCTTGAAGAATTA[A/T]GAGTGAAAAAGTTCC | 11622 |
rs3021639 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Ahr | Mm_Celera | 12:35508267 | TTGTGGAGGAAGCAG[C/T]GCTCCGTCCTTCCCT | 11622 |
rs3021641 | snp | A/C/G/T | | | intron-variant | Ahr | Mm_Celera | 12:35508365 | ATTAAAATTAACATT[A/C/G/T]TGTAATGGTTTCATT | 11622 |
rs3021643 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35510393 | TGATTCTTGCATGTG[C/T]TAGTGTATATTCTTA | 11622 |
rs3021644 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35510498 | TACCAGTGTTGGTTT[A/T]AAAACAAAGAAAGAA | 11622 |
rs3021646 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35510577 | TAGCTCAATAGGTAA[C/T]GTGCCATGCAAGTAT | 11622 |
rs3021647 | snp | A/G | 0.237812 | 0.249703 | intron-variant | Ahr | Mm_Celera | 12:35511174 | GATGACATCAGACTA[A/G]AGGAAAGGGGCATGA | 11622 |
rs3021648 | snp | G/T | 0.2688 | 0.249292 | intron-variant | Ahr | Mm_Celera | 12:35511228 | GAGTGATAAGGTTTC[G/T]TAAAGCAGTTTCAAA | 11622 |
rs3021649 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35511440 | CACACCAGCTGATAA[C/T]ATTCTAGAACAGTGG | 11622 |
rs3021650 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35511501 | GAGGGGGTCCCATAT[C/T]AGATATTTATATAAC | 11622 |
rs3021651 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35511641 | GGAGCCACTGTTCTA[A/G]ACCCTATCTCATCCA | 11622 |
rs3021652 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35511803 | TAAATCACCTTGGTG[C/T]ATCAGTTACATAGTT | 11622 |
rs3021653 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35511860 | AGCATCTATTTTCTC[C/T]CTAATGAGAGGTACC | 11622 |
rs3021654 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35511930 | ACGTAAATGGTCTGT[A/G]GTATGCAGACCCGGA | 11622 |
rs3021655 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35511936 | ATGGTCTGTAGTATG[C/T]AGACCCGGCGGAGCC | 11622 |
rs3021656 | in-del | -/A/C | | | intron-variant | Ahr | Mm_Celera | 12:35511944 | AGTATGTAGACCCGG[-/A/C]GGAGCCTTGTGAGTT | 11622 |
rs3021657 | in-del | -/A/G | | | intron-variant | Ahr | Mm_Celera | 12:35511946 | GTATGTAGACCCGGC[-/A/G]GAGCCTTGTGAGTTT | 11622 |
rs3021659 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35512075 | TGTTAAAATGTGAGA[A/G]TCAGATACAGAAGAA | 11622 |
rs3021660 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35512398 | TACTCATAGTGTAAA[G/T]GCAGCAGAACTAAAC | 11622 |
rs3021661 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35512459 | GGCTGCACAGCCTCT[C/G]CTTAGTTTCATAACT | 11622 |
rs3021662 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35512582 | GATCTGTCAGACTAA[A/T]GACTTAACCCAGCAT | 11622 |