SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8155443 | snp | A/C | 0 | 0 | missense | Amph | Rn_Celera | 17:48319067 | GGAACTGAGGGGTCC[A/C]CAGGGGAGGAAGCAG | 60668 |
rs8156244 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48360099 | TGACAGGTGAGATTC[C/T]ACAACTTCCTAAGAA | 60668 |
rs13452713 | snp | C/T | | | synonymous-codon | Amph | Rnor_6.0 | 17:48304346 | GGGATTCAAAGGCCT[C/T]TTTCCAGAGAACTTC | 60668 |
rs64220668 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48366796 | GAGCCACCAGCCAAG[A/T]AGCATACACTAACTG | 60668 |
rs65129576 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48318573 | GGTGCACTGTCTCTT[C/T]CTGCTGCTTGTGGAC | 60668 |
rs65980534 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48366656 | TTACACCCAACCAAT[A/G]GACAGAAGCTCGGGA | 60668 |
rs66248789 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48342837 | CTCTGTTGCTCATAG[A/T]TTAGCACATTTTGGT | 60668 |
rs104895913 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48545189 | GCTTGGCTTCAGCTA[C/T]GTCTCCTCACTGAGT | 60668 |
rs104898589 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503075 | AAATTATAGACTACA[C/G]AAAATATTATGCCAC | 60668 |
rs104900980 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48456007 | ACTAGAAATGTACAT[A/G]AAGATTTCCTGTATT | 60668 |
rs104901436 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502573 | GCTTCTAGCTTCAAG[A/T]TATCGTCGTATACAT | 60668 |
rs104902332 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48369661 | TCTGGATCCTCTGGT[C/T]TCTGGTACTTTTTGG | 60668 |
rs104911942 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503920 | TCATAGATTCTGTAC[G/T]AAGCATTTCACACAT | 60668 |
rs104912723 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48308044 | CAAGAAAGACGTAAA[A/G]AACTCCCTTAGAGAA | 60668 |
rs104916359 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362463 | TATGTTCCTAATATA[A/T]AACTTTGAAAAATAT | 60668 |
rs104923766 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359570 | CAATATTCTTTACCC[A/C]AGAGAAATCCTGAAG | 60668 |
rs104924366 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474339 | AAATACGATATAAAT[A/G]TTCAGTTTAGAGATG | 60668 |
rs104925481 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474043 | ACATGGATATAGAAA[C/T]ATGGGTAGCCTTTCA | 60668 |
rs104928037 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48478189 | GGCAGCACCCCGCGA[A/G]CAAACTTGAGCCTCA | 60668 |
rs104932607 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477803 | GAGATGACATCAAAT[C/T]CTCTATGACAGATGT | 60668 |
rs104937896 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467354 | ACTGGAACTTTTCCA[C/T]ACCAAATGAGTTCTC | 60668 |
rs104940335 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446332 | TCTTGGAAACTTCTA[C/G]GAAGTTTCTAAAGTC | 60668 |
rs104940898 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48451018 | TTTATTTTATGTTTT[C/T]AAGAAGCAGCCAATG | 60668 |
rs104941032 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48477688 | ATAGTCTAAGCAGAG[C/T]TAGTACTGTCCTTTC | 60668 |
rs104944274 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48470020 | GGAGACTGAGATCTT[C/T]TTGAACTAATCATGC | 60668 |
rs104947857 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484670 | GCAATTGTCATGAAC[A/G]AGAAAATGAAAATGT | 60668 |
rs104959432 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504857 | ACACACAGGCTTACA[C/T]GAGGGTCAAGCCACT | 60668 |
rs104969266 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424139 | ATCCCAAAATACAGG[C/T]GCATCCCTAGGTCCT | 60668 |
rs104969935 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504674 | GAGGTCCTCTGAACT[A/T]AATGCTTAAAAGAAA | 60668 |
rs104970734 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557541 | TGGCCAGAGTCTTCA[C/T]TTCTTCCCCTATTAT | 60668 |
rs104972689 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48474203 | CTTAGTCAGATCTTA[A/C]GCAGGTAGTCATAAG | 60668 |
rs104975711 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501927 | GAGCTGTACTCTCAC[G/T]ACTCCTACCTAAATA | 60668 |
rs104978848 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498353 | TCAGATGTTAGCTGA[A/G]GCAACTGGTATAGAA | 60668 |
rs104979159 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48555422 | CTATAGAAAGTCCAT[A/G]TCCAGATCAACCCCA | 60668 |
rs104980282 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471792 | CTCTTGGGTATGGTT[A/G]CCAATACTTTACAAT | 60668 |
rs104985688 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48556940 | ATATATATAATAAGT[A/G]AGTCTTTAAAAAACA | 60668 |
rs104985989 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48554065 | TTTCAGGTTCTTCCT[C/T]TATGTTTAAGGAGTA | 60668 |
rs104992398 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424084 | GTTTAGGACTCACCC[A/T]CATGACCTCATGTAA | 60668 |
rs104999973 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484796 | ATGACAGCACAGATT[A/T]ACAACTTCTGCTCAA | 60668 |
rs105003826 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487879 | TTAGCCTTTCCTATG[A/G]CCCACTAAAGCACAG | 60668 |
rs105008137 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498771 | GATTACAACCTGTAA[A/G]CCAAATAACCTCTTT | 60668 |
rs105009784 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488151 | AGTGAATGTCTTTTC[C/T]CTATTTCTTCTATGC | 60668 |
rs105012122 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48477068 | GCCGTCCCATTCCAC[C/T]GCACGCCCCTCTGCA | 60668 |
rs105014217 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468583 | ACCTAGATGAAGGAG[A/G]GACATGACTGCTGGG | 60668 |
rs105014379 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360254 | AATAAGAGTACAGAC[A/G]CAGCAGCATGATCTA | 60668 |
rs105016779 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551646 | CACAGAAACAGAAGC[A/G]GAGTCTATGGAAGAG | 60668 |
rs105019953 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48459017 | CGCCTGAGATACCGC[A/C]GGAACCTGAAGGAAA | 60668 |
rs105024106 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444219 | TATCCTTCTTCTTCT[A/G]AAGCTTCCCAAATGG | 60668 |
rs105024299 | snp | A/C | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48428777 | TCACCACCACCACCA[A/C]CACCACCAACAAACA | 60668 |
rs105025069 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48559701 | GAAAAGCCTTGAAAC[A/C]GACTTGATAGATTTA | 60668 |
rs105027213 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48426560 | ACAACATCTCAGATG[A/G]TCATTACCTTGGTAT | 60668 |
rs105028971 | snp | A/G | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48359433 | ACTAGCCGTTGGGCT[A/G]GGGAGGGGTGAAGCC | 60668 |
rs105036768 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473504 | GCTTCTCGTTACTGC[C/T]CCAATGTTGTACATT | 60668 |
rs105036949 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48441582 | GAAATTCTTCTTCTT[A/G]GTGTCCACAGGTTGA | 60668 |
rs105037757 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549275 | ATATATATATATATA[C/T]ACACACACACACACA | 60668 |
rs105040722 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467679 | TCAGTGATGGAGAGA[A/G]GTCAGCCCCGGGCAA | 60668 |
rs105042554 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498811 | GTTTTTTTGTCTGTT[C/T]GTTTGTTTGTTTTTG | 60668 |
rs105052899 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498549 | CAGTCACCTTCCTGT[C/T]CATTCAAATATGTTT | 60668 |
rs105060996 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473967 | GCAGACATGCAGGTT[A/C]CTGAGTGATTTGGGG | 60668 |
rs105061488 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446356 | TAAAGTCCAGTGTCT[A/C]TATCACCACCAGTGT | 60668 |
rs105061867 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557291 | TTTAAACATGATTTC[C/T]TGTGGTCTTAATTCT | 60668 |
rs105066806 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444334 | TTAATTTCCAACAGA[G/T]GAGCTTTGGGAATCA | 60668 |
rs105069688 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491318 | GGAACTGTAGAAGCC[C/T]GGTAACCTCCAGGTG | 60668 |
rs105070982 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48445198 | TTCAGAGAAGAACCT[A/G]TAGAGGTGGTTTTTC | 60668 |
rs105071212 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499699 | TCCATAAATGGTAAA[C/T]TTTAGCTTTTTTATA | 60668 |
rs105073464 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489772 | GAGCTCTGTATCTCA[C/T]GTCTCTAATTTCTTT | 60668 |
rs105073935 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449404 | TACAAAGTCCAACAT[A/G]TACTGTCCCTCAGTG | 60668 |
rs105078177 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344551 | CCACTGTTAGGAGTT[C/T]CCTCCATGATGAGGT | 60668 |
rs105080544 | snp | A/T | 0.5 | 0 | missense | Amph | Rn_Celera | 17:48444443 | AAGTTCTGAACATAT[A/T]CTTCAAACTGTTCAT | 60668 |
rs105082959 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48486541 | CACTCTGAATATCAA[A/G]TACATAATTTATATT | 60668 |
rs105085256 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467114 | CAACAGATGGCCCTG[A/G]CCTGGGAAGATTTCC | 60668 |
rs105087738 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419981 | TCAATTCTGGTAACA[A/C]TAATAATTAGAGAAG | 60668 |
rs105089501 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362246 | AGTTGGCAATTCTAT[A/G]CAATGCCCTTTGCAT | 60668 |
rs105091341 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48485462 | CCTATTGGGCAGAGA[A/C]GGAAAGAGCTGGTAG | 60668 |
rs105093733 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501828 | AACACAACACTCAGC[C/T]GTTGTGGAAACTTTC | 60668 |
rs105093778 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499160 | CAAGGCTTGAGTCAA[A/G]AGCAGGCTCCCTGCA | 60668 |
rs105094260 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488072 | CAGCTGGATTGACAG[A/C]AATGGATAACCCCAC | 60668 |
rs105097269 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557474 | TAGTAGAAGATGTCC[C/T]GGCTTGTGATTCTGT | 60668 |
rs105100679 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475217 | GAAGGAACAAAGGGG[G/T]AGGAGCAAGAGAGCA | 60668 |
rs105105300 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48428823 | ACACACACACACACA[C/T]ACACACACACACATA | 60668 |
rs105107174 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458595 | ACCCTCCCATCTGTG[C/T]AGGCAATAGGCTGGC | 60668 |
rs105109518 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551258 | CTGCTTGTAGATCAA[C/T]CAAGATGTAGAACTC | 60668 |
rs105111443 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474260 | CAATCATGATTCACT[A/T]CTTCAGGCACTTACA | 60668 |
rs105115310 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554747 | GAAAATTTTATGATT[C/T]GCTTTTATTTTGAAT | 60668 |
rs105117250 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499962 | CAAAGTATTTATGGG[A/G]TACTATGTAGATAGT | 60668 |
rs105121916 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502631 | TGATCTTTCTGCCAG[A/G]CTCTGCAATTTGCTT | 60668 |
rs105122731 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48316563 | ACTTAACCTACACGC[A/G]CGCACACACACACAC | 60668 |
rs105126172 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48470710 | ATGGATTGTCAGGCC[A/G]TGCCAGTCAACTGCT | 60668 |
rs105127833 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498009 | CTGGCTGATGGGCCA[C/T]CTGCCCTTCCCACGC | 60668 |
rs105130921 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48521888 | TTCCACAGTCTCCAA[C/G]TCCTAGACAGGATAC | 60668 |
rs105133307 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306846 | CTTCCACAAATTTAG[G/T]GTAATAAGTTAGTAA | 60668 |
rs105134706 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48517227 | GGAAAAGAGCCTTCA[C/T]AGGACCAAGGGCCTC | 60668 |
rs105134965 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471683 | AAAATAATTTAATAC[C/T]TGTACCCAGCTATCC | 60668 |
rs105134991 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48477594 | CTAAGGATGCTGTCA[A/T]AATGTTATGCAAAAC | 60668 |
rs105138949 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48476377 | CACTGCCCTCACCTT[A/G]TCTTGTGCCTCTCTT | 60668 |
rs105141122 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419963 | TGGTTCAACCCAGAG[C/T]TGTCAATTCTGGTAA | 60668 |
rs105141868 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48361959 | ATGAAGCAGAAATGA[C/T]AAGGTGATTATCTTA | 60668 |
rs105144699 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362729 | TACTTAATTCTTTTC[A/C]TTTAGTTGGGTAACA | 60668 |
rs105149060 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306516 | GTGAGCACCAGAGTT[C/T]GGCTCCAAGCATTTG | 60668 |
rs105156444 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48320791 | GAACAAGAAAAATTT[A/C]AAATGTAAATTATAC | 60668 |