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 |
rs105158422 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427907 | CACTCACCTATGTTT[C/T]CATACTGTTGACTTT | 60668 |
rs105159904 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474001 | ATGAAATAATTAACA[C/T]AAATAACATTAGAAC | 60668 |
rs105163875 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499001 | TGTCTTGCTCCTTCC[C/T]GTAGTGATTCTTCTC | 60668 |
rs105166094 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48365090 | GAGTTGAGATGACCT[A/T]CCCAGTGGGAGTGAC | 60668 |
rs105167942 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555867 | GTACTGGACAGGGGT[C/G]AGATGCCATGACGGG | 60668 |
rs105173345 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48314653 | CGGGGAGTCTTCCAG[G/T]AGTTAAGACTCACTT | 60668 |
rs105179269 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48491070 | GGGGAGAAAACGAAA[A/G]AAAATAAAGGAAGGG | 60668 |
rs105182404 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444359 | GAATCATCCAAACCA[C/T]ACCATATATGAAAAC | 60668 |
rs105184074 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458600 | CCCATCTGTGCAGGC[A/T]ATAGGCTGGCCTCAA | 60668 |
rs105187577 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494630 | TCACATACCCAGATA[C/T]AAATACATATACATC | 60668 |
rs105190892 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48490989 | CTTAAGACACTTAAC[A/G]CACATACTGTACAAC | 60668 |
rs105196817 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500098 | CAGAGCACCCTTCTG[C/T]CCTAGAATGCTTAGA | 60668 |
rs105199785 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489689 | CAGAGAACTCAAACA[C/T]TCTGAAGGAAAAATC | 60668 |
rs105200236 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488514 | CTAACCAGATGCTTG[C/T]CCATCATACCTGTCT | 60668 |
rs105202270 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550695 | CTTACCTTTATGGAC[G/T]GTTTGTAGCACAATC | 60668 |
rs105203440 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467293 | GACAATTTAGTTCTG[A/C]ACAGAGAGGTCTGTT | 60668 |
rs105203673 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497377 | ACCAGGAAATGGTGT[C/T]TGCTGTAGCTTAGTG | 60668 |
rs105203853 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48431078 | TGGATATTTTTTATT[C/T]ACATTTCAAATGGAT | 60668 |
rs105209222 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455898 | GCTACTGGATGACTT[C/T]ACACTATTTTAAAAT | 60668 |
rs105212369 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326567 | ACCTATCCATCTCAA[C/G]AGAAAGACCAAAGGA | 60668 |
rs105221836 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474329 | AGAGAAGAGGAAATA[C/T]GATATAAATATTCAG | 60668 |
rs105222152 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48367231 | GGTATATAAATACAT[C/G]ATTATGTATTTTATT | 60668 |
rs105223020 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48493948 | CCTAAAGACTATACA[G/T]GGACTGACCCTGGAC | 60668 |
rs105223263 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327931 | AAATAGAAATCAAGA[C/T]GAGGTTAGTTGGTGT | 60668 |
rs105224830 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494348 | GGAGGAGAATATACT[A/G]TAAGTACAAACATTC | 60668 |
rs105228375 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48486798 | ATGGATAAACTCAAC[C/T]AAAACCTCTAACCCA | 60668 |
rs105230966 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305550 | GACTGATAATAGTCT[A/G]GCTGATGAGGAAAGG | 60668 |
rs105232056 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474819 | AATATGTGGTGTTTT[C/T]AGTAATAGGACTTTA | 60668 |
rs105233833 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48420062 | GATGGGAGCAATGTA[C/G]ACTCCAGGGTCATGT | 60668 |
rs105237286 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504061 | TAAAGCCTAGTCATC[C/G]AGACCTAAAGGTACA | 60668 |
rs105240324 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360510 | CTGATAATGAAACTG[A/T]TATTTGCAAATGCTT | 60668 |
rs105242181 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362201 | AGTAGTAACACAGTA[C/T]CGCTACAACATCCGT | 60668 |
rs105247541 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556076 | CCTGCAGGTATGCAT[G/T]TAGGCAATAATAAAT | 60668 |
rs105247612 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48358260 | GTCAGATGAGCACAG[A/C]TATGCAAACAGACAT | 60668 |
rs105250186 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357927 | TTCAAATCCTATACA[C/T]CTTACATTTAATAAT | 60668 |
rs105251300 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502660 | TTTACCCATCACAAA[C/T]CCAAAGTTAGCCTAA | 60668 |
rs105254626 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48316257 | ATTCATGCATGAGAG[C/T]AGAAGGCCAGGGAAG | 60668 |
rs105257347 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48492101 | ATGGCACAGTACACT[C/G]AGTGGTAGGAATACA | 60668 |
rs105258432 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48313768 | TGTGCAGTGTGCTGG[G/T]ATGGCTGCTGCATAA | 60668 |
rs105265171 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48494365 | AAGTACAAACATTCA[G/T]AAAGGCCATAGGGTA | 60668 |
rs105266185 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423891 | ATTATCATAGCATGG[A/G]GCCCTAACCAACAGA | 60668 |
rs105266531 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499312 | TTTACCTAGAATTTT[A/G]TCTAAGGGGAAATTT | 60668 |
rs105266812 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344322 | ATTTCTAGCTGGAGG[A/G]GAATCCTCACCCTGA | 60668 |
rs105266835 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48485161 | GAAGCTAAGGGAAAT[A/G]GTGAGATACGACGAT | 60668 |
rs105269868 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327260 | TTATGCTGGAGTCAT[A/G]TATGGCAAAGTTCCT | 60668 |
rs105271442 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48313468 | CCCCAGTGAACTAGA[C/T]TGTTGGGGGGAGGGC | 60668 |
rs105275247 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552849 | TGAGAGTGAGCGTGA[A/G]TTCTTGCTCTTTTGC | 60668 |
rs105275631 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48475403 | CCTCTCCTCTTTCAC[C/T]CCATTTAACTTTTCA | 60668 |
rs105278016 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48504566 | TGACAGGGGATTTGG[A/G]GAGATTTTGACAGTT | 60668 |
rs105279499 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477861 | ACTAAGGTTGTATGC[A/T]ATAAGAAGAGTATGT | 60668 |
rs105283858 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424886 | TATTAAAAGTAAAAA[G/T]AAATATGTAATATAT | 60668 |
rs105286393 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48313907 | AACATAATAGAATTA[G/T]AAATTCAGAAACAGA | 60668 |
rs105286907 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419969 | AACCCAGAGCTGTCA[A/G]TTCTGGTAACAATAA | 60668 |
rs105288210 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48321132 | AACTGTTCATACATA[C/T]GATATGAATGAAGTG | 60668 |
rs105292521 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551434 | CCTAAAACTCTTTGG[G/T]TAGAAAGTGGTTCCC | 60668 |
rs105293166 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467774 | CAACAGCTGCTCTTG[C/T]TTCCCCTTCCTTTAT | 60668 |
rs105299237 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48487350 | TCGGTAATAATTTGA[G/T]GCTTTGGTGCCCTCC | 60668 |
rs105299364 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555974 | GTTAAGAGTGCCAAC[A/T]GCTCTTCCAGAGGTC | 60668 |
rs105302104 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551439 | AACTCTTTGGGTAGA[A/G]AGTGGTTCCCAGTGG | 60668 |
rs105302406 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48358017 | TATCTACAGCTGACC[A/T]GAGAGTCCTGTCCAC | 60668 |
rs105302767 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504960 | CCTAAGCAACAGAAA[C/G]CAAGGCCACTGGGCA | 60668 |
rs105306787 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424477 | CTAACCAACATGACT[C/G]TCTAAATGTGAGCTG | 60668 |
rs105308883 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48503534 | TTAAGAGCAGAATAT[A/G]AAATGGCAGTGATTT | 60668 |
rs105312005 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498830 | TGTTTGTTTTTGTTT[A/T]ATTTTGTCATATGTA | 60668 |
rs105313812 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48358268 | AGCACAGCTATGCAA[A/G]CAGACATCTAACTGA | 60668 |
rs105317573 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48439636 | ATCCCACAATACCTA[A/G]GCATGAGGTACTACT | 60668 |
rs105318437 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484550 | GGAGATTCTGAGCAG[C/T]ACTGTGAGGAGGTTG | 60668 |
rs105320327 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489279 | GTAGTCCTTCTCTGC[C/T]TCATCTTGGTTCCTC | 60668 |
rs105323293 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465988 | GGCAAGCAGCTGAGA[A/G]GGATTTGTACAGGGA | 60668 |
rs105326867 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551730 | TCCCAAAACCTGCCC[A/T]GGGGTAAAACACCCA | 60668 |
rs105328900 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504989 | CATCATCAGAATCCA[A/G]TTTCCCCACCACAGC | 60668 |
rs105331285 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554845 | CTACTAATTCAAAGG[A/G]TGAGTCATCTCTGAC | 60668 |
rs105333658 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327474 | GTGCTGTCACAGAAG[A/T]TTTGCATTTATTGCA | 60668 |
rs105335025 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48454017 | GCACCTTGGATATTG[G/T]CTACTTAAATGAACA | 60668 |
rs105339507 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342710 | TTGATCTCTCTTTTG[G/T]GTCACTGATACGAAT | 60668 |
rs105340028 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306791 | AGAACTTATGAAAAG[A/T]CTGCAGACAAATATT | 60668 |
rs105342419 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494558 | TGTGTATATATATGT[A/G]TATATATATATGTAT | 60668 |
rs105348168 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48499127 | GGCATGTTCTCTCAG[A/G]GATATACAGATAACA | 60668 |
rs105352094 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48440146 | GAGAATTATTGATTT[C/T]TCTTCTTATCCTTTT | 60668 |
rs105354838 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48454221 | TAGAGGAAAGGGAAT[C/G]ACTCTGTTACTTACA | 60668 |
rs105358126 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556228 | TCAGAATAGGATAGA[A/C]ATGACTGAAATGTTG | 60668 |
rs105366196 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48553971 | GCTTGAGTCTTATTT[A/C]ATAGATTCTAATTTG | 60668 |
rs105367228 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494222 | AAAAAAAAAAAGAAA[A/T]ATGGGGAGTGACATT | 60668 |
rs105368188 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48335166 | CCAGGTGGAAAGCCG[C/T]GATAACATTCGCCAT | 60668 |
rs105375266 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48431558 | CATCAATATTGTCTG[C/G]GTTTGGTGGCTGTAT | 60668 |
rs105381353 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48441825 | GAAGGAAGCAGGAAG[G/T]ACTCCTACTGTGGCC | 60668 |
rs105382581 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494200 | ATAAGAAATACTCAA[C/G]TTAATAAAAAAAAAA | 60668 |
rs105387341 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503543 | GAATATGAAATGGCA[A/G]TGATTTCTTTTCAGA | 60668 |
rs105387951 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48491047 | AGCAAGGGATGAGAG[A/G]AGGAAGGGGGGAGAA | 60668 |
rs105388523 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306420 | CAAGAGAGTTCCAGC[A/C]CTGCCAGTAAAGGGG | 60668 |
rs105395729 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484731 | GTTTCTTGGAAATAA[G/T]CTACTGCAACAAATG | 60668 |
rs105404039 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48440176 | TTATGTTCTTAGTCT[C/T]CCTTGCTTAAGGCTT | 60668 |
rs105408630 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549751 | TAAGTGGGAAGAGGA[A/T]CAATTGAGAAAACAC | 60668 |
rs105410435 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555061 | ATATTCTATATTACA[A/G]TTCTTATTTATGCTC | 60668 |
rs105412661 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424438 | CTTGCCTTCTTATAA[C/T]GTCAGAAGCTACGTC | 60668 |
rs105414883 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48465250 | GTATTAAATAAATTT[A/T]AAAAAATCAAAAAAA | 60668 |
rs105419005 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497567 | CTCCTTGCACCCTGA[G/T]CCACCCAAAATGTTC | 60668 |
rs105421681 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468886 | TAACTCTGTGAAGTG[C/T]TTCATTTGGAGCATG | 60668 |
rs105424646 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48509487 | TGTTGGTGTGATTAC[A/G]AGCTGGTACAACTAC | 60668 |
rs105425511 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498246 | CTAGTTTTCCTCGAG[A/G]CCCACACCTTCAGTC | 60668 |
rs105428505 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450039 | CTGATAAGGGCAAAT[A/G]GTGCAGACCGCAAAA | 60668 |
rs105440393 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48488819 | TACTAGCTGCACGCT[A/G]TGGCAACCCTCTCCC | 60668 |
rs105441804 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48316970 | GGCTTTTCTGGGCAA[C/T]TATTGTTGTTGTTGG | 60668 |
rs105445713 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48499263 | GACTACCCAGTGCAG[A/C]ATGATTAGATCTGCA | 60668 |
rs105447436 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468345 | TGCCCTGCTAACAAA[C/T]GGGGGTCTCCAGTTT | 60668 |
rs105450780 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48494474 | CACTGCTTTTGCAAG[A/G]ACTGAGTTTGGTTTA | 60668 |
rs105451536 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48469744 | TGAGAATCTGATACC[C/T]CTGGAGGCAGCAGTC | 60668 |
rs105454045 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48470734 | AACTGCTTGATGAGT[C/G]CGGTTGTGCTAATTG | 60668 |
rs105459038 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357788 | GTAGAAAAATTGAAA[A/G]AAAATAGGCCAGAGT | 60668 |
rs105462654 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491540 | GCAGGCACTCAAAAC[G/T]ATATGGGGATCAACA | 60668 |
rs105464524 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488617 | AGGAGGTTGGTCTGC[C/T]AATCCCAGAAATGAT | 60668 |
rs105466871 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48446975 | CCCAAAAAGATAGCA[G/T]TACCTCAGGGCTTTG | 60668 |
rs105477930 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556135 | TTTAAGATAGAAAAA[A/G]CATAAGTGTTTACTA | 60668 |
rs105478955 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551379 | AGTTGCCCTGGTCAT[A/G]GTGTCTCTTCACAGC | 60668 |
rs105481957 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444326 | AGTGGGGATTAATTT[A/C]CAACAGAGGAGCTTT | 60668 |
rs105484769 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497055 | TGCCATGGATTTCCA[C/T]GTCTGAAACAGCTCT | 60668 |
rs105486048 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504766 | TACCAATTTCCCCTG[C/T]ACCTAGAGCTGACCC | 60668 |
rs105488397 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48503669 | TGCTAATCACGAGTG[A/C]GTCAGCCCTAAGCAG | 60668 |
rs105488666 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48486721 | GTCAAAAGTATCCTA[A/T]AAAAGCATCCACCAT | 60668 |
rs105491882 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48494389 | TAGGGTAGTAGGGTG[G/T]TTACATGAGAAACTA | 60668 |
rs105492810 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48363000 | GAGAGTTGCTTTTAT[A/T]TGTTTCTTCATTTGA | 60668 |
rs105512132 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48488416 | TGTATGGAAATGTTG[A/T]CGTTTAACATGATTA | 60668 |
rs105524544 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340160 | TATAGTTTTCAGTTC[A/C]AGTGCATGGTGATTG | 60668 |
rs105526392 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551622 | CAGTCCATCATAAGA[A/G]GGACCTGACACAGAA | 60668 |
rs105529658 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498380 | AGAAAACAATACAGA[A/C]TTCAAATACTGCGAC | 60668 |
rs105530194 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501590 | AGTTTCTTAGTGATT[C/G]ACTTCTACTTAGCAT | 60668 |
rs105536116 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468500 | TAAATAGTTATTAAA[A/G]CTATTTCTAGAAACC | 60668 |
rs105537127 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468385 | TACTTACTGGAGTTT[A/C]CAATATGCTCTCTTT | 60668 |
rs105541402 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466532 | TGCCCACACACACAT[A/G]GCTGCTCAACTCACC | 60668 |
rs105547138 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359178 | AATAAAAAAACTGAG[A/C]ATAAGAGGAAACACA | 60668 |
rs105548567 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48335679 | TCGCTGTCAACTCTC[A/G]CTTTTAAATTTTGGT | 60668 |
rs105551083 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425067 | TTGGAATGTTTCATG[C/T]GTGAGGCATATGCTG | 60668 |
rs105551774 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48530401 | CAAGTAGATAGTGTC[A/G]ACAATCATATTATGA | 60668 |
rs105553130 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488078 | GATTGACAGCAATGG[A/G]TAACCCCACTAGAAT | 60668 |
rs105557123 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357684 | TTGTGACATAAAAAT[G/T]ACCAATGAACTGAAG | 60668 |
rs105560614 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473971 | ACATGCAGGTTACTG[A/T]GTGATTTGGGGGATA | 60668 |
rs105567470 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48485405 | GGAAGACAACTGACA[A/G]CAGTCTGGGATTTGA | 60668 |
rs105569691 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48316019 | TTTTCCTTTGCATTA[A/T]TTTTTTTTCAGATTT | 60668 |
rs105570167 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552477 | ATTAGACATATATGT[A/G]CCTCAAAAACACAAA | 60668 |
rs105570595 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468663 | AGGATAATAATAATA[C/T]TATATAATAATAATA | 60668 |
rs105570808 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48477685 | GAAATAGTCTAAGCA[C/G]AGTTAGTACTGTCCT | 60668 |
rs105571083 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344369 | AGTCAGCAGAAGAAA[A/G]CATTCCAGTGGATAA | 60668 |
rs105572411 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48447548 | AGAAAGAAAAACAGC[A/C]CAAGAAAAAAGAGCA | 60668 |
rs105573155 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48556959 | CTTTAAAAAACAAAA[A/G]ACAAAACAACAAAAA | 60668 |
rs105579710 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48346382 | GGTCTTCAATCCCCA[C/T]GGGAATACACAAAGA | 60668 |
rs105582713 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484561 | GCAGCACTGTGAGGA[C/G]GTTGATCAGGCAAGA | 60668 |
rs105590039 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476529 | GTTGCTGCTGCTACA[C/G]CTCAGCTAAGTTCTG | 60668 |
rs105590577 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48457764 | ACCATGATTACTGAT[A/G]GCCTCCNATGTTCNA | 60668 |
rs105598464 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48335717 | TGTTGTATTTTTGAG[A/G]AATTTCTGCATTATG | 60668 |
rs105598654 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488583 | AGGACACTCACATTG[C/G]ATGAAAGCCAAACAG | 60668 |
rs105601980 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48419597 | GAGCACTATATAGCA[C/T]AGAAGCCATCATTAA | 60668 |
rs105603482 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305709 | ATTTGGAGTGAGTCA[A/C]AATCTAATGAGACCA | 60668 |
rs105603987 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425600 | CCCAAACAATTTCTT[G/T]AGGAATTTATAATGT | 60668 |
rs105606412 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48497353 | TCCTCCTCCCTTAAA[A/C]AAAAGCAAACCAGGA | 60668 |
rs105609198 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498607 | ATGTTGGAAGTGCAG[C/T]TCACAATGGGCATCA | 60668 |
rs105610893 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48316077 | CATACAATACCACAT[C/G]CCTCAGCTTGAGGGA | 60668 |
rs105613408 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48470325 | AAGCCAGGAAAAGGC[G/T]CCACACAAGACATAG | 60668 |
rs105614352 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360579 | GCCTTAGTTTCATAA[C/T]ATCCAAAAGGTAATT | 60668 |
rs105616195 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48351645 | GCTCTTATCCATTGT[A/T]CTGGTGGGTTCTTAG | 60668 |
rs105619044 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419181 | ATCATCTCATGCAGT[A/G]TGAGTCTACAGGAAT | 60668 |
rs105629719 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455387 | CTAGAAAGTCCCTCA[C/T]AGACATGTCCAGAGA | 60668 |
rs105631676 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458964 | TATAAGGCCTCTGGG[C/T]TCCCGTAGGGGAGGG | 60668 |
rs105634401 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421420 | AACAATGGGACCTCA[C/T]AAAATTGCAAAACTT | 60668 |
rs105635563 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487769 | TGACATCCCCATCAC[A/G]TACTGCAGATACAGT | 60668 |
rs105637464 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48545586 | CTCCCAAACAGTTCC[A/G]CAATCTGAGAACCAA | 60668 |
rs105644250 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499093 | ATGAACTTTAGACAA[C/T]ACAGCAGTCCCAAGA | 60668 |
rs105648341 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466094 | TGAGAAGCACCTTCT[C/T]TCCACCTCCCTGTGC | 60668 |
rs105652650 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48365168 | CAGAGTACTTGCATG[C/T]ACATAGCTGTTGCTG | 60668 |
rs105653279 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499349 | GAATGATTCTGTATA[C/T]TCGGCAACAACCAAC | 60668 |
rs105654451 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48551712 | TCTTGCTTTTTCGTA[C/G]AGTCCCAAAACCTGC | 60668 |
rs105658037 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444225 | TCTTCTTCTAAAGCT[G/T]CCCAAATGGCTTTTA | 60668 |
rs105660175 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421975 | CTATGTCCATAGTGG[A/C]CTTATTTATAATAGG | 60668 |
rs105660191 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425097 | GTATGTCACTATCAC[C/T]ACCCTGTTCTATGCT | 60668 |
rs105661403 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551340 | ACTGAACCTCTGAAC[C/T]TCAATGAAATGTTTT | 60668 |
rs105663022 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48313775 | TGTGCTGGTATGGCT[C/G]CTGCATAAACTTAAA | 60668 |
rs105669636 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48351777 | CCAATGAAGAACCAC[C/T]GTAGCAAGAGTTATC | 60668 |
rs105669797 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501556 | TAGATTGGAATCATT[C/T]TATATGTAGTAGTCA | 60668 |
rs105673175 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484564 | GCACTGTGAGGAGGT[A/T]GATCAGGCAAGAACG | 60668 |
rs105681914 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551130 | ATACTTGGCCTACAG[C/G]GAGTGGCAGTGTTAG | 60668 |
rs105684849 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306623 | ATCCCCACACAGCCA[C/T]ATATGCATACATGAA | 60668 |
rs105685010 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557340 | AGAAGAAAGATGCAT[A/G]TACACATGACTTTGT | 60668 |
rs105686054 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327668 | TCTTTAGAACTTGAG[C/T]ACAGCCTACACGAAT | 60668 |
rs105686116 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499082 | TTTAGTCAACTATGA[A/G]CTTTAGACAACACAG | 60668 |
rs105687519 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504488 | CTGAATTGTCAGTGG[C/T]GTTTAAGTCTGAGTA | 60668 |
rs105688107 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48318280 | CTCTAATAATGATCA[A/C]CATGAAATAGTGACA | 60668 |
rs105689606 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359672 | GAAACTGTCACTATT[A/G]ATTGCTCCCTGTGAA | 60668 |
rs105691711 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48485170 | GGAAATAGTGAGATA[C/T]GACGATAATTCACAA | 60668 |
rs105693216 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48554179 | CCAGTGGACACAAGC[A/G]TATTTGTGAAGGATA | 60668 |
rs105693692 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48441520 | ACTAGGAGCTTACAG[A/G]GAGGCCCTGGGTTTG | 60668 |
rs105694180 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498788 | CAAATAACCTCTTTC[C/T]TCTCCGTGTTTTTTT | 60668 |
rs105710384 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48520657 | CATAATACGGAAATA[A/G]GTCAGCTACGCTGGC | 60668 |
rs105714575 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491937 | TCTGAAAGGGCTTTG[A/G]GCTAAACGATGAGTT | 60668 |
rs105715581 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552533 | CTCACACTTAGGTCC[A/G]AACTTAATCCATAGG | 60668 |
rs105719298 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503206 | GTTGTTAGCATCCCC[C/T]AATTGTGTAAATGTC | 60668 |
rs105723785 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485735 | CTGTTCTACTATGAA[G/T]CTGTACATTCCCAGC | 60668 |
rs105725817 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327105 | GTTTTAGTGGTTTTT[G/T]GTTTCTCAATCCATC | 60668 |
rs105728400 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48500207 | GAAACAACCCAGGAG[A/C]GTAGCCCTTAAAGAA | 60668 |
rs105734349 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48488655 | TGTGTTGTGATAAAT[A/G]TTTAAAACAGCCTCT | 60668 |
rs105734352 | snp | C/T | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48342394 | GGTAAAATCATTAAA[C/T]GAACCTCCAGAAGCC | 60668 |
rs105741881 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554881 | GTCTTGACTGTGCGC[C/T]AAAGGGGCAAGTATG | 60668 |
rs105743341 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502122 | CCAAGAAAAATAGCA[A/G]TTTCGAACTTGAAGA | 60668 |
rs105743795 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48547078 | ACATTTCCAATATTC[C/T]CTAAAGCTAAGTGCT | 60668 |
rs105746639 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455923 | TAAAATATAAACATG[A/G]TCTGAAGTTTCAAAA | 60668 |
rs105747797 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556195 | TCCACTCATAAATTA[G/T]GCTTTCAACTAACTC | 60668 |
rs105749178 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48472642 | ACCAAGCCGGCAGCC[C/T]GTTTTAGATGCCAGA | 60668 |
rs105750485 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497850 | CTTCTTCCAGCTGCA[C/T]GGGCTGGGCTGCCTG | 60668 |
rs105754160 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48470189 | CTAATCCTCAGGCCT[C/G]TGGCGTTCAAGGTGT | 60668 |
rs105754593 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549593 | AAACCTTTCAGCACT[A/T]GGAATTTTTTTCAAT | 60668 |
rs105755557 | snp | A/G | 0.5 | 0 | missense | Amph | Rn_Celera | 17:48359401 | GCAGGAGATGCAGGT[A/G]CTAATGTGTGGTTGG | 60668 |
rs105756504 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501908 | GCAGAAACCTGAGCA[A/G]ATGGAGCTGTACTCT | 60668 |
rs105758683 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489771 | TGAGCTCTGTATCTC[A/T]TGTCTCTAATTTCTT | 60668 |
rs105760336 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488224 | ATTAAAATAGTTAAC[A/T]GGCTGGAACAGTAAA | 60668 |
rs105775312 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477335 | AAGATATATAATTTT[A/G]TATTTTCTTGTAAGT | 60668 |
rs105779870 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468459 | CCTAGCTCGTGGATG[A/T]GGAAGAAAAAGCTTA | 60668 |
rs105782798 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502114 | CACAGCAACCAAGAA[A/G]AATAGCAGTTTCGAA | 60668 |
rs105782924 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427921 | TCCATACTGTTGACT[G/T]TTCTGAGAAGGCAAT | 60668 |
rs105787169 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468613 | GACAGCTATAGCACA[C/T]GGTCCTACCTAAGCT | 60668 |
rs105790739 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342274 | CCAATTTTGTGCTGA[C/T]GCTCTTAATCATTTT | 60668 |
rs105795594 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478469 | ATGGCGAGAGGCAAG[C/G]GCAGGAGCCCAAGCA | 60668 |
rs105799637 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362215 | ATCGCTACAACATCC[A/G]TGTAAGGGTAAGGCT | 60668 |
rs105802246 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48445275 | TCCAGGCCTCAAGGG[A/G]GTCTAAGCAAATTCA | 60668 |
rs105804694 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468419 | TTAAGCCACACAGAC[A/G]ACTAAGAAACTAGGT | 60668 |
rs105807328 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48490969 | TTTTCTCCTGAGATC[G/T]AGGACTTAAGACACT | 60668 |
rs105808831 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555042 | AATATTTACAGCTGA[C/T]TCTATATTCTATATT | 60668 |
rs105812085 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475565 | TCAGGGTCCACCCTG[A/G]TGACCACGTTTGTTT | 60668 |
rs105812171 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423748 | AAGGTAAGGAAATGT[A/G]TTAATGAGGAGGAGG | 60668 |
rs105812257 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467560 | GGCTGAGACATAAAA[C/T]AATCAGTTATATAAC | 60668 |
rs105814021 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557471 | CCTTAGTAGAAGATG[G/T]CCCGGCTTGTGATTC | 60668 |
rs105814398 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474387 | TCTGTATCTTGATCA[A/G]TTGGGCATCTCTTCA | 60668 |
rs105814635 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494887 | AATATGCATACCTTG[A/T]GTTGGAAACGCTGAT | 60668 |
rs105816975 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48473216 | TCAATCAGAATAGAT[C/T]GAGGCCCTCACTAGT | 60668 |
rs105818637 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48473196 | GTCTTCTTCTTGTAA[C/T]GGCATCAATCAGAAT | 60668 |
rs105829622 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486272 | TTTGAACAGAGGCTA[A/C]TAACAACAATGAAAT | 60668 |
rs105832110 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421761 | AACCTCAGGTGACCA[C/G]AGATGCTGGCAAGGA | 60668 |
rs105832551 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471154 | CACAAGAATAAATCA[G/T]CCAATGGAGCACGTC | 60668 |
rs105837681 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48491110 | GAAGGGATATGCATA[G/T]ATGGGTGAATGAATG | 60668 |
rs105845275 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48440730 | GTACTAACCAGAGAA[A/G]GCAGCAGAAAACACT | 60668 |
rs105849460 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498210 | CTGCCTTCCTCTAGG[A/T]TCTAAGTAAACACCA | 60668 |
rs105852489 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48456016 | GTACATAAAGATTTC[C/T]TGTATTGCAGACCCA | 60668 |
rs105853949 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477898 | AACCACTGGGCCATC[G/T]CTCCAGCCTACTTAG | 60668 |
rs105858509 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362091 | TATACTAATTTAGAA[C/G]ATCATTTAAAATTCC | 60668 |
rs105858609 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48451226 | ATCCAAAGATCTGCT[A/G]CTGAAACACATGGAA | 60668 |
rs105865498 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489496 | GCTTTGGTTACTTTG[C/T]CCAATTGACCCTCTT | 60668 |
rs105866245 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48353433 | TGTATCTATGTGATT[A/G]CTTTATTTTTGATAT | 60668 |
rs105866693 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486032 | GGATTGCACAGTCAC[A/G]TTGGCTTCCATATTT | 60668 |
rs105870507 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487381 | TGTGAGGTGGATTCC[A/C]AGTTGGACCAGCCAC | 60668 |
rs105874077 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48502511 | GAGGATTCAGGTACC[A/G]TGATAACAAATACCA | 60668 |
rs105879553 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48555101 | AGACAAAGAGCAAGA[C/T]GCATGGAGTATTTCC | 60668 |
rs105880631 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48448078 | TTCAAGTGGGATTGT[C/G]ACCACTTAACTTCTT | 60668 |
rs105892723 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48346202 | AGTGTTTAAACTCAA[C/G]TCCACAGCTACCTAG | 60668 |
rs105894902 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486409 | TTTATTTTGTAATAT[A/G]AATGTTGGTACTTTG | 60668 |
rs105899308 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48477109 | TCGGTTCTCTCTCTG[C/T]TCCTTCTCTCTTTCA | 60668 |
rs105903818 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504387 | AGGTAAGACAGGAGG[G/T]TGAGCCATTGGGACT | 60668 |
rs105905220 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305387 | AAATTAAAGAAAAGG[C/T]TGGATGTATCCCCTT | 60668 |
rs105911344 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504058 | GGGTAAAGCCTAGTC[A/G]TCCAGACCTAAAGGT | 60668 |
rs105914996 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48556751 | ATGTCATTTGAATGA[C/T]TACATAGAAAATTCT | 60668 |
rs105916453 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48444585 | GACTACCGTCTTTCT[C/T]GAGGGTTCTGAGCAG | 60668 |
rs105923047 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48556977 | AAAACAACAAAAAAA[C/T]TTAAAAAAATATGTT | 60668 |
rs105924238 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48472829 | AATTTAAAAAGGTAA[A/G]TCTTAGCTATAAAGT | 60668 |
rs105927585 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327269 | AGTCATATATGGCAA[A/T]GTTCCTGATGTTTGC | 60668 |
rs105932339 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48515280 | TATCAGCAGCACCAG[G/T]TGTCATGGAAGCTGA | 60668 |
rs105936357 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552180 | ATCTGACTTTTGAAG[A/C]AATTGTCAACTTGTT | 60668 |
rs105943244 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360097 | CATGACAGGTGAGAT[A/T]CTACAACTTCCTAAG | 60668 |
rs105945278 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360574 | AACATGCCTTAGTTT[C/T]ATAACATCCAAAAGG | 60668 |
rs105946533 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48318086 | ACAAGGGAGGACTTC[C/T]TGTTGCTGTCACACT | 60668 |
rs105948779 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430069 | AGGAAGAGGTGTTTT[A/T]AAAAGTGGGACTTCC | 60668 |
rs105953163 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489565 | TAGGCTAGACTGATA[A/G]TGAGGTTTCTTAACC | 60668 |
rs105953356 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474514 | TACCATATCCATTTA[A/G]CAGAATAAGAATATA | 60668 |
rs105958108 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48555018 | GGTGGAAGCTGTCAT[A/T]ACAAGGCCAATATTT | 60668 |
rs105958113 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497686 | AATCACAATCCTGTG[C/T]AAAATGCTTGCAATG | 60668 |
rs105959656 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469099 | AGTCAGTGTGGCCAT[C/T]CTACAGCAGTCATCC | 60668 |
rs105959668 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468342 | CTATGCCCTGCTAAC[A/G]AATGGGGGTCTCCAG | 60668 |
rs105964338 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48502523 | ACCATGATAACAAAT[A/G]CCAAGGTTACCTCTG | 60668 |
rs105965672 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48503597 | AATCGTGAGCATCTG[C/T]TCCCATTTCAAAACT | 60668 |
rs105966395 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498694 | GAAGAACAAGCAGCA[C/T]TCTTCCGTGGTCTCT | 60668 |
rs105966894 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48494570 | TGTATATATATATAT[A/G]TATATATATATATTA | 60668 |
rs105970034 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500108 | TTCTGCCCTAGAATG[A/C]TTAGAGCCCTAAACT | 60668 |
rs105970435 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362218 | GCTACAACATCCGTG[G/T]AAGGGTAAGGCTAGT | 60668 |
rs105982899 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48554123 | GGGCTCTGAGATGGA[G/T]GCCATATGTTTTCAC | 60668 |
rs105984440 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48443218 | ACATCCATGAAGCTT[C/G]TTTCCTGCATAATCT | 60668 |
rs105986893 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340608 | AAAATAAGACTGAGA[G/T]TCTGTTCTACATTGG | 60668 |
rs106000861 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362286 | TAAGAGCAACAGTCA[C/G]CATTACTCACCACTG | 60668 |
rs106003013 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476530 | TTGCTGCTGCTACAG[C/T]TCAGCTAAGTTCTGA | 60668 |
rs106004967 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549249 | TAATATATATATATG[C/T]ATATATATATATATA | 60668 |
rs106005172 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484802 | GCACAGATTAACAAC[A/T]TCTGCTCAATATGAG | 60668 |
rs106009185 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468913 | CATGTAAGGAATGAC[A/G]CAAAAGTAAGATTTG | 60668 |
rs106013102 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48493612 | TTGCATTTATTAAGC[A/G]ATTTGATTACTATTC | 60668 |
rs106015748 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48473314 | ATCAAATCCACTTCT[C/T]TCCTCACCCTACAAT | 60668 |
rs106019427 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476961 | CTTGTGTTCTCATCA[C/T]CCCCTAGCCTTGATG | 60668 |
rs106020385 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48430006 | TAATGAAGTGAACAG[A/T]GGAGCACACTCTGAA | 60668 |
rs106022444 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307489 | ACATCTCTGACGCCA[C/G]AGGAAAACACCAAAC | 60668 |
rs106025584 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553227 | TCTCAAGCATTCACT[G/T]CCTAGATCAAAGTCA | 60668 |
rs106026756 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48458634 | AAGCAGTTCATTTTA[C/T]GCAACACTGAGTGAT | 60668 |
rs106032901 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489024 | CTCCCTAATGGTTAT[A/G]GCATCAGCTCCCAGC | 60668 |
rs106033489 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48555383 | TAATTTAGTTGACAG[C/T]TTTCTTTCATGCATA | 60668 |
rs106035579 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474284 | ACTTACACTCTTCTG[C/T]CCCCTCCCCCACAGT | 60668 |
rs106036722 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48316232 | ATAACTGACTGTTAT[C/T]CAAAAATTAATTCAT | 60668 |
rs106036963 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48336760 | AAATATGTACCATTG[A/G]TTCAATATTGGGCCA | 60668 |
rs106040431 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499180 | GGCTCCCTGCAGTGA[C/T]CTTGTGAGTTTGAAA | 60668 |
rs106041855 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48349814 | CTCCGTGAGTGCACT[A/G]AATAGGAAATGTGAT | 60668 |
rs106041973 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502737 | CAGTGGACTCTTCTT[C/G]CCTAATGGGCTATTT | 60668 |
rs106043177 | snp | A/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486053 | TTCCATATTTCATGC[A/T]CAAGCACAGCTGGAC | 60668 |
rs106044843 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551396 | TGTCTCTTCACAGCA[A/G]TGACATTCTATCTAA | 60668 |
rs106046770 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551997 | AAATAATTAGAAATA[A/T]ATTTAATAAGTACAA | 60668 |
rs106047138 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48490244 | TCTAGATAACTGTTG[A/T]ATGCTTTGGGGCTCA | 60668 |
rs106048819 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48454400 | CTGCTCCTTCATGCG[A/G]AAATAACTGAAAGCA | 60668 |
rs106050032 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48553785 | TAAAGCATCCTATAG[C/G]GGGGGGGCACTGTTT | 60668 |
rs106051090 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424964 | CTCTAATTTTATTTT[A/C]CAAAATGAAGGTGAC | 60668 |
rs106058120 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498082 | GTGGGGCAGAGCAAG[G/T]CATGGGGTAGCACTG | 60668 |
rs106058248 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552124 | AATAATCTTTCTTCA[C/T]TTCTTATATTCATTC | 60668 |
rs106058647 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48476044 | TCACAACTCAGTAAC[A/C]TGTTAAAATCAAAAA | 60668 |
rs106067356 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48488611 | CAGAGGAGGAGGTTG[A/G]TCTGCCAATCCCAGA | 60668 |
rs106068092 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504310 | CATGCCAGTCTGTTT[A/G]TACAACTCTACGCCC | 60668 |
rs106068416 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555937 | AAAACACTTTAAGAG[A/G]GTCTGGAGAGATGGC | 60668 |
rs106069009 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455979 | GTTTATTTTAGAGCA[C/T]TTTAAATAGATCACT | 60668 |
rs106075129 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553286 | AATGTCTGCTGTGAA[G/T]AGTGGACACAAGCCT | 60668 |
rs106075329 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489452 | GCGTATAGGCATCAA[C/T]CTTTGGTCCTTTCCC | 60668 |
rs106080996 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489096 | ATCAGACTTATCTTC[A/G]TATTTATCTCAGTAA | 60668 |
rs106086304 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455101 | AATGCTAAACTTTTT[C/T]ATTGCAGAGAGGAAA | 60668 |
rs106089854 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48545588 | CCCAAACAGTTCCAC[A/C]ATCTGAGAACCAAGT | 60668 |
rs106094710 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455333 | CAATATGGTTGTCTG[C/T]ATTAAGACTGTGTCC | 60668 |
rs106095005 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476268 | TGTGGCCAGTTGAGG[C/G]CACACAGATGTGAGT | 60668 |
rs106095476 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476291 | ATGTGAGTCCTCCTG[C/T]TCCGCCCCCATCTTA | 60668 |
rs106100511 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554970 | TTTGGAACGTGTTAA[G/T]TGGGTCTCTTTTGCA | 60668 |
rs106100864 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551210 | GTCTCCTATGCTCAA[A/G]CTCTACCCAGTGTGG | 60668 |
rs106103498 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469146 | AGACCCCAAGAATTC[C/G]TCACCTGACCTGTGG | 60668 |
rs106103608 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48499823 | TGTTAATTCTAATGT[C/G]TGTGAGACTGAAACA | 60668 |
rs106103806 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485712 | GGGGGGTTGCATGTA[A/G]TAGAAAACTGTTCTA | 60668 |
rs106105053 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48457660 | ATCCTTTTAACTCAC[A/C]CCTATAGGTTGACAT | 60668 |
rs106114112 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48556398 | TAAATTTAGATTCTG[A/G]ATCAATAAGAATGCA | 60668 |
rs106117670 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503106 | CTATAATAATGACAT[A/G]ATGTGTTCAATAACA | 60668 |
rs106117764 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455911 | TTCACACTATTTTAA[A/T]ATATAAACATGATCT | 60668 |
rs106129904 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498277 | ACACCATGAAGGACC[C/G]CTCAGAGTCTCTCAG | 60668 |
rs106130992 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552339 | GGAAAAGGATGGACA[C/G]CAGGACTTGACCAAT | 60668 |
rs106133802 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48349802 | CCTCCCGATGGTCTC[C/T]GTGAGTGCACTGAAT | 60668 |
rs106137299 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552993 | ATTTAAAGTAACTAG[C/G]CAAAATTCACAGAGG | 60668 |
rs106140767 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488225 | TTAAAATAGTTAACT[A/G]GCTGGAACAGTAAAA | 60668 |
rs106141450 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48420224 | TAGATGCTCAGAAAA[C/T]ATTTCACAAAATTCA | 60668 |
rs106142956 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499211 | GATTGTGTTCTGAAA[C/T]AATCTTATTTATACA | 60668 |
rs106144012 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476441 | ATGAACAGAGACCCA[C/T]CTCGCTTAGCAGAAA | 60668 |
rs106146825 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48485015 | ATGGCACCCCGCAAG[A/C]GGCACCTTCCCTTCC | 60668 |
rs106151167 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478414 | GACAGTTTAGCCACG[G/T]TCAGAAATAGCAGAA | 60668 |
rs106153731 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446179 | AAGAATACTACAAAT[A/G]TATTATACACCCACT | 60668 |
rs106154160 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48444763 | CTTACATATGCATTC[C/G]CTTAGGAGGCTGTAC | 60668 |
rs106159717 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306458 | GAGTTTATATCTGAG[C/T]GGGGCTGGAGAAGCG | 60668 |
rs106161439 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502685 | GCCTAAGCTTTTAAT[A/G]CATGGGTCTATTAGA | 60668 |
rs106163954 | snp | A/G | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48362339 | CTCAAGGCTAGAGAC[A/G]TTTTTGAAAGTATTG | 60668 |
rs106164254 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494093 | GGGCAGCAAGGGGGG[G/T]AGGATGGGGAGCAGA | 60668 |
rs106172355 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48553220 | CCTATTCTCTCAAGC[A/C]TTCACTGCCTAGATC | 60668 |
rs106175291 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48423613 | CACCCCAGTAGTAGT[G/T]CACCTTACTTCCTGC | 60668 |
rs106175374 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494075 | ACTAGATTGTTGGGG[A/G]GAGGGCAGCAAGGGG | 60668 |
rs106178142 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491139 | TGAATCATAATGCCA[A/G]GCACCTCTTCAGAGC | 60668 |
rs106178777 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48492034 | CCTAGCAATGTAAAA[A/G]ATATCAGTTTCCACC | 60668 |
rs106184416 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48423109 | GAAAACAACAAAGAA[A/G]ATTTCTTTTGTAACT | 60668 |
rs106188431 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474505 | GCAATTCAATACCAT[A/G]TCCATTTAACAGAAT | 60668 |
rs106189393 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314118 | ATTACATTGAAGGAC[C/T]CTAGTACTTACTGAA | 60668 |
rs106196456 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469672 | TAAGATTCCTTCAAC[A/G]GGGGTCCCGTTCTCA | 60668 |
rs106197610 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48446903 | AAACAAAAAATGGAT[C/G]TTTGTGCAAAATCAC | 60668 |
rs106209434 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468276 | TGACAATAGGCTTCC[A/G]TACACAGTTAAGTCC | 60668 |
rs106209652 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48556980 | ACAACAAAAAAATTT[A/T]AAAAAATATGTTCTC | 60668 |
rs106209866 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328653 | ATAGAAGCAGTGGGA[G/T]TCCCAACTATAGACT | 60668 |
rs106210080 | snp | C/T | 0.480312 | 0.0972437 | intron-variant | Amph | Rn_Celera | 17:48490358 | TGAGATACTTTGACA[C/T]ATCTAAGGCCTTAGT | 60668 |
rs106211830 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484551 | GAGATTCTGAGCAGC[A/G]CTGTGAGGAGGTTGA | 60668 |
rs106215292 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553731 | AACTGAATGGTGTCT[C/T]TGACATTTAGGTAGA | 60668 |
rs106215449 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48501983 | GCTTGACTCCAATGA[C/G]CAAGGGCACCTGTAC | 60668 |
rs106216546 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497511 | ACAACCCTCTTCCTG[C/T]GGTCCTTTTTTGCAA | 60668 |
rs106217335 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48430136 | ACAAGGGGTCAGGTG[A/C]ACTGGAGGATGTAGA | 60668 |
rs106220089 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476700 | AAGTAGCTGCCCAGT[A/T]AAGAAGGGGCACAAG | 60668 |
rs106220824 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494738 | TCACTTGAATGCTCT[A/G]GTTTAGGGAACATAT | 60668 |
rs106221873 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423916 | AACAGAAGTGCAGTT[C/T]CTCACAAGTCTCTAG | 60668 |
rs106224134 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550926 | ATAGCAGGAAGACTT[A/G]GTTCAAAATATCTAA | 60668 |
rs106228201 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48305488 | TTTTGGAGAGACAGA[A/T]AAAAAACCTCACAAA | 60668 |
rs106228472 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419956 | ACATAGATGGTTCAA[C/T]CCAGAGCTGTCAATT | 60668 |
rs106232480 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48467203 | CTGCCCTTGCATAGT[C/T]CAGACATAATAAGTG | 60668 |
rs106234595 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48511932 | AAAGTACCGTAATTT[A/G]GGCTATTATTCAAAT | 60668 |
rs106247402 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487547 | AGGTGCACTCTTCAA[A/G]CTCCCGCTCCCCAGT | 60668 |
rs106249803 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48305661 | AGCCTCTAGTGTGCA[C/G]AGGAAAGGTCAGTTC | 60668 |
rs106251712 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48485117 | TTGAATGTTTAGAGC[A/G]TAGGTAGCTATAAGT | 60668 |
rs106260130 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489060 | ATTAAAATCAAAACT[C/T]CAGATGCTTGTAGTT | 60668 |
rs106261561 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48492141 | GCACCTAGACACAGC[C/T]TAAGGATGCATCACA | 60668 |
rs106262091 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48499865 | GCAAGTTCAAGGTCA[A/G]TCTGGACTAGGGCTA | 60668 |
rs106264146 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48473247 | AGCCTCTTTTAAAAA[C/T]TATTTTTCCTTTTTT | 60668 |
rs106265898 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476462 | TTAGCAGAAAACATG[A/C]TATTAAAGCTTCTTC | 60668 |
rs106266337 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48330076 | TAGAAGGGATTCAGC[A/T]GAATGAACATACTTC | 60668 |
rs106267240 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487957 | CTACGCCATTCCTCT[A/C]TCATTAAGATTTCTC | 60668 |
rs106267889 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48342753 | CATCAACCAAGAGTC[A/G]AGAGCTTTAGTGAGA | 60668 |
rs106268273 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458392 | GTATCCTCCTCTCCA[C/T]ACCCCAACCTAAGGC | 60668 |
rs106270871 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420792 | AAGATGGCAAGATCT[A/C]TCATGCTCATGGATT | 60668 |
rs106272545 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551346 | CCTCTGAACCTCAAT[A/G]AAATGTTTTCTTGTA | 60668 |
rs106274781 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48313471 | CAGTGAACTAGATTG[G/T]TGGGGGGAGGGCGGC | 60668 |
rs106281539 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48441494 | CAAAGCAGAATCTGG[A/G]GCTCAGGAAAACTAG | 60668 |
rs106283242 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556476 | TAGTTGCAATGATTA[A/G]CACTTTAATTCTGCA | 60668 |
rs106283371 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455504 | GCATACTTAAGTAGT[C/T]GTGTGTGCATATTTG | 60668 |
rs106285362 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473152 | TTTACATGGACTTTG[C/T]TTATGTGTGTTTCTT | 60668 |
rs106290787 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473739 | GGGGTCACTCTACCC[C/T]TGCTTAAGTGGCTAT | 60668 |
rs106291200 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458173 | CAAAAACCACCTCCA[C/T]CCAAAAATTTTAGGA | 60668 |
rs106293535 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469766 | GCAGCAGTCTGAAAT[C/T]GTGGCTATTCCTGTG | 60668 |
rs106294650 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48511186 | GCTTTGGATTTATTG[A/T]ACAGTGCAGAAGACA | 60668 |
rs106300356 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424260 | ATAATTATAAAGTCC[A/G]ATGTTATTAAATTGT | 60668 |
rs106308977 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425896 | TTAGTTTTCTCATGT[A/T]TACAGCAAAATGACA | 60668 |
rs106310570 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48494137 | AGGGGAGGGGGGAAG[A/G]GGATGTTTGCCCGGA | 60668 |
rs106314017 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48493886 | GCTCGAGACCCCATA[G/T]GTACAACAATGCCAA | 60668 |
rs106319515 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48520627 | TCATTGACTTTTTAG[G/T]TAAGGAGATTTTGAC | 60668 |
rs106319655 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556255 | GTTGGGTTTCTGATT[C/T]TTGTACATCTGTCCT | 60668 |
rs106321563 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469614 | TGCTTGGCATTGTTG[A/T]TCATATGAGGTCTCA | 60668 |
rs106323570 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48497228 | ACAAAGTAACAGTCT[C/T]GTCACTACAGGGTCA | 60668 |
rs106325215 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491469 | GCTGATAAAACAAAA[C/T]GAAACAAACAAACAA | 60668 |
rs106325613 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498420 | GACAGGCAGCCCCTC[C/T]CAGCTCACACTATCA | 60668 |
rs106328403 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488393 | AATATATAGCCAATT[C/T]GTATCTGTGTATGGA | 60668 |
rs106328420 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500223 | GTAGCCCTTAAAGAA[A/T]TTCATCCCACCATCC | 60668 |
rs106331894 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502931 | TAATCCTTAGCCAAG[A/G]GGACAGTGAGGTGCA | 60668 |
rs106331944 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48492355 | TTTCCATTTGAGTGA[C/T]GGCTACAATGATTGG | 60668 |
rs106332734 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556391 | GAATACTTAAATTTA[A/G]ATTCTGGATCAATAA | 60668 |
rs106334316 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488493 | TTGAAGGACAGTCTT[C/T]AAAAGCTAACCAGAT | 60668 |
rs106334671 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48551697 | TTCGTGGTTTGCTCA[C/T]CTTGCTTTTTCGTAC | 60668 |
rs106340113 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419386 | ATATTATATTATTGG[A/G]TAATTGAGACTTCAT | 60668 |
rs106342426 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48547264 | ACGTATTTGGAGCTT[A/G]AATACAGGACAGAGA | 60668 |
rs106343791 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342730 | CTGATACGAATCACT[A/G]TGATAAACATCAACC | 60668 |
rs106349037 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48305892 | CTAAGGAAAATTAAA[G/T]TTGAACTGCTTAAAA | 60668 |
rs106350428 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48454034 | TACTTAAATGAACAT[A/C]TAATCTCTGGGTGGT | 60668 |
rs106353018 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552144 | TATATTCATTCAAAG[G/T]AGTCTTTATTCAAAA | 60668 |
rs106353027 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328293 | TTTGGTCACAACAAT[A/G]GAATGAAACTAGAAC | 60668 |
rs106358900 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494156 | TGTTTGCCCGGAAAC[C/T]GGGAAAGGGAATAAC | 60668 |
rs106360381 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551238 | TGGAATCCAGTTTCT[C/T]CTTGCTGCTTGTAGA | 60668 |
rs106360469 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48346191 | TTATAAGTATTAGTG[C/T]TTAAACTCAAGTCCA | 60668 |
rs106361582 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307441 | CAGAGAGGCAGGCAC[G/T]CCTGGGAAACCAGAA | 60668 |
rs106361704 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48476072 | AAACTCAATAATTTA[C/G]TAATCTTTTTATATT | 60668 |
rs106363387 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48486609 | AAATACTTCAGGGTA[C/T]AACTAACAGCGAACA | 60668 |
rs106366308 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484836 | AAATTCAAGCAGCCT[G/T]GAAATTACCACCGTG | 60668 |
rs106367586 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469431 | TCCCCCCATTACTGC[C/T]CTCTCCCCAACAATC | 60668 |
rs106368357 | snp | A/C | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419265 | ATGGTCAAAGTCATA[A/C]ATCGAATTTAGAACG | 60668 |
rs106369212 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360500 | CTTGCTTTAACTGAT[A/T]ATGAAACTGTTATTT | 60668 |
rs106373523 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48494135 | GAAGGGGAGGGGGGA[A/G]GGGGATGTTTGCCCG | 60668 |
rs106375007 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489045 | AGCTCCCAGCAACCC[A/G]TTAAAATCAAAACTC | 60668 |
rs106375907 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503280 | CACACATGCTCACTC[C/T]CAACTTCAGGATTCC | 60668 |
rs106376209 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48440244 | TAGCAATCTGTGATT[A/G]TGTCATTCACAAGAA | 60668 |
rs106377970 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48547457 | TCTCAGAAGGTTCTG[G/T]GACTTCTTCCACCTA | 60668 |
rs106379186 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485679 | CATTTGTAGGGGGAT[A/G]TTGCTAGGATTGAAC | 60668 |
rs106379540 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48318522 | TGTGTCACTGTGGGG[A/T]GTGTGTCACTCAGAG | 60668 |
rs106379970 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466505 | AAGGGAGAAAGATGG[C/G]CTGAAGCAGGATGCC | 60668 |
rs106382682 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48429800 | GGTGAATGCGCAAAA[C/T]AAGAAACATAGGCTC | 60668 |
rs106387084 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48547436 | CCAGGAGAGAGAATC[A/T]ATGATTCTCAGAAGG | 60668 |
rs106387930 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498145 | GCACCAGGCACCCCA[A/C]AGTCCCTTAGAGGGA | 60668 |
rs106391239 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48426312 | CTATGATTGTGTGGG[A/C]ACTTGGTATGTGGGC | 60668 |
rs106392596 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419274 | GTCATACATCGAATT[G/T]AGAACGGGCTATGAT | 60668 |
rs106398000 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475592 | GTTTTCCACAGGCTC[A/G]CATGAACACATCAGT | 60668 |
rs106399672 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455414 | GAGATTTGTTCCCAG[A/G]GTGATCCTAAACCAT | 60668 |
rs106405635 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473866 | CATCAATTCCCACCT[C/T]GGTCTCCTTGTCCTG | 60668 |
rs106406065 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500093 | GCAAACAGAGCACCC[C/T]TCTGCCCTAGAATGC | 60668 |
rs106406597 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48329137 | CTACTCTAGTCTTCC[C/G]TGCAGTCCCATCAGA | 60668 |
rs106407754 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48315854 | AAGTTGAACTAAACA[A/T]GCTAGGCTAAAAAGC | 60668 |
rs106409637 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485842 | CCTGTGCTGGTACTG[A/T]ATTTACAACTCTCAT | 60668 |
rs106413807 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484822 | CTCAATATGAGAGAA[A/C]ATTCAAGCAGCCTGG | 60668 |
rs106414822 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48361048 | CAAATTGACCTTAAA[G/T]GTATGTAACTGAAAC | 60668 |
rs106416829 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501783 | GGCCTGCTATAACCT[A/G]GAAGGCTGGTTCCTG | 60668 |
rs106421857 | snp | G/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48313541 | GGGAGGGGGGAGAGG[G/T]ATGTTTGCCCGGAAA | 60668 |
rs106425150 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359275 | TAGAAACTTTCTATA[A/T]TGCTTATAATGCTTA | 60668 |
rs106426575 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48329719 | TCCATGTGTGTTTGT[A/G]GAGGCCAGAGTTCAG | 60668 |
rs106431737 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477670 | CCTCAAATCCAAATC[A/G]AAATAGTCTAAGCAG | 60668 |
rs106433551 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48317837 | CCACCCACACTTTCT[C/T]TATCCTACTAACCCG | 60668 |
rs106437607 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48500114 | CCTAGAATGCTTAGA[A/G]CCCTAAACTAAGCTG | 60668 |
rs106438310 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552572 | TACCTGGTTTAGGGC[C/T]ACAACTACAAATTAA | 60668 |
rs106438443 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48500402 | TATTTTTCATATATA[A/T]GGTGACTGAGAGAAT | 60668 |
rs106438836 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424020 | TCCTTACCACATGCA[C/T]GTACTCCTGTAGTCT | 60668 |
rs106451085 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501661 | AAATGTCTCCCAAAT[C/T]GGTTACTCGGAAAAA | 60668 |
rs106451282 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48476073 | AACTCAATAATTTAC[C/T]AATCTTTTTATATTT | 60668 |
rs106453738 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498325 | ACATTCAAGGGCAAA[A/G]TAAGAAACCGAATCA | 60668 |
rs106454613 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484849 | CTGGAAATTACCACC[A/G]TGAATGCTGGGAGTC | 60668 |
rs106459419 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425997 | GAATATTTCAAAAAC[A/G]AACACCTTCATATTT | 60668 |
rs106467393 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491308 | AGTACTGCTTGGAAC[C/T]GTAGAAGCCTGGTAA | 60668 |
rs106470921 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48555515 | AAATTCATATCTATA[C/T]CAAAACTTAAAAAGT | 60668 |
rs106472216 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477055 | GATTCATCCTCTTGC[C/T]GTCCCATTCCACCGC | 60668 |
rs106479908 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326822 | AACCTAATAAGAGGA[A/T]GGCAAATAAAAGTCA | 60668 |
rs106484444 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500116 | TAGAATGCTTAGAGC[A/C]CTAAACTAAGCTGCA | 60668 |
rs106488961 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555957 | GGAGAGATGGCTCAG[A/G]GGTTAAGAGTGCCAA | 60668 |
rs106493019 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469740 | CTTATGAGAATCTGA[C/T]ACCTCTGGAGGCAGC | 60668 |
rs106495482 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477759 | TGCTTCCATGAGTTT[A/G]TGTGAAGCACTTGTG | 60668 |
rs106500606 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48476418 | AAGACAACAATCTAC[A/G]CGTCAGGATGAACAG | 60668 |
rs106502665 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48517196 | ACCTCACCAACCTGG[A/C]ATTCCCCTATACTGA | 60668 |
rs106505310 | snp | A/C | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465645 | ATTAGACAAAGCTTA[A/C]CCTTTAAAAATATAC | 60668 |
rs106509889 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48341526 | AAATAAACAAGCTCA[A/T]AGTCAGATTCTACAA | 60668 |
rs106514598 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344392 | GTGGATAATCTCATG[C/T]CTCGCTCTGCTTCAG | 60668 |
rs106515350 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488717 | ATGGCATTAGGGGTA[C/T]AATCATCTCAGAGGC | 60668 |
rs106515575 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48552307 | GTAACATCATAAGGC[A/G]GCATGATACAGTTTT | 60668 |
rs106528682 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423665 | CATGAATGGCAGCTC[C/T]ACCTATCACATCCTT | 60668 |
rs106532362 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48493874 | GAGCTTAAAGGGGCT[C/T]GAGACCCCATAGGTA | 60668 |
rs106532592 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557450 | CAAACAGAGGGGATG[A/C]GATTGCCTTAGTAGA | 60668 |
rs106533683 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477637 | AGTCTCAGGCTTACA[A/C]ACCAAAGCCATTATG | 60668 |
rs106542053 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430459 | AAATGAAGGCAAGAC[A/C]GAACAATTAAGATTT | 60668 |
rs106545348 | snp | A/C | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314740 | CCAGCTGACCCTCGA[A/C]ATGTTCAATATGGCT | 60668 |
rs106547016 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455320 | CCTCTAACTCATGCA[A/G]TATGGTTGTCTGCAT | 60668 |
rs106548545 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491221 | AACACAATTATACTA[C/T]AAGTGACAACAGACA | 60668 |
rs106549832 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48446964 | ATGGTGCCTTTCCCA[A/C]AAAGATAGCATTACC | 60668 |
rs106552062 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48318261 | CTCTAGGGAATCTGC[G/T]ATGCTCTAATAATGA | 60668 |
rs106563055 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477595 | TAAGGATGCTGTCAA[A/G]ATGTTATGCAAAACT | 60668 |
rs106564888 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494518 | ACATGACTTGCAGCC[A/G]CCTATAACTCCAGAT | 60668 |
rs106569549 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48556831 | GAGAGATGGCTCAGC[A/G]GTTAAGAGCACTGAC | 60668 |
rs106573646 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423738 | CTACTGTGTCAAGGT[A/G]AGGAAATGTGTTAAT | 60668 |
rs106574903 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48491065 | GAAGGGGGGAGAAAA[C/T]GAAAGAAAATAAAGG | 60668 |
rs106581172 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484846 | AGCCTGGAAATTACC[A/G]CCGTGAATGCTGGGA | 60668 |
rs106583955 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467216 | GTTCAGACATAATAA[A/G]TGCAAGTGGGATATA | 60668 |
rs106585237 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474620 | CTTGTGGACTTGGAT[A/G]TAACTCAAAGTAGAA | 60668 |
rs106585858 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421290 | GGATCTCCACGTAAA[A/G]CCAGATACACTGAAA | 60668 |
rs106587990 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48502538 | ACCAAGGTTACCTCT[A/G]AATAAGATCCTAATA | 60668 |
rs106592001 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553329 | TGTTTCCTGGAAAAC[A/G]GAGAATCTCCTAGTA | 60668 |
rs106594023 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502167 | TCTAAATCCTTAAGC[C/T]TCAAGGTCAATGATA | 60668 |
rs106604310 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455820 | AATATTAAGGGCCAA[A/G]CCACAGGATTACACA | 60668 |
rs106611968 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497107 | GAGTTTCCCTGTCAG[C/T]TTGCAGACATTACTG | 60668 |
rs106615824 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48368330 | ATATCCGAAGTTCTC[A/G]TGCATTTGGTCTTCC | 60668 |
rs106622493 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48321247 | ACCTATGACCAATCC[A/G]ATGATTTCAATAGTT | 60668 |
rs106625853 | snp | A/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48514707 | ATCAGGGGTATATTT[A/T]AAAAAAAAAAAAAAA | 60668 |
rs106628003 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420630 | TTCTTCTACTCAAAG[G/T]ATAAACAGGCTGAGA | 60668 |
rs106632247 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342481 | TATTCATTAGACAAG[C/T]AGGAAAGAAACTACT | 60668 |
rs106641110 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48338983 | TACAATACCCCTTAT[A/G]CACTGAATCAGGTCT | 60668 |
rs106641143 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444271 | CTGACAGGCCTTGCC[G/T]CTAAATACTGTAGTA | 60668 |
rs106646857 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504237 | CAATTATTCTGATCA[G/T]TGGGTGTGTGGTATC | 60668 |
rs106648991 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48485442 | AGAGCCTAGGGCACA[C/T]CCTACCTATTGGGCA | 60668 |
rs106649923 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307443 | GAGAGGCAGGCACTC[C/T]TGGGAAACCAGAAGA | 60668 |
rs106656383 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503065 | TCTCTAATATAAATT[A/G]TAGACTACACAAAAT | 60668 |
rs106659894 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48331516 | TTGATAGAGTTAGAC[C/T]GCCTGAAAAATTTAT | 60668 |
rs106659913 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476361 | CCCTACCTTACTTTT[C/T]CACTGCCCTCACCTT | 60668 |
rs106660714 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503114 | ATGACATGATGTGTT[A/C]AATAACATGCAAACG | 60668 |
rs106664594 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48522855 | ATAAGGATCATGAAC[C/T]GGCTTCTCAGGAGAT | 60668 |
rs106664964 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48443725 | GACTCACACCCACTT[A/G]CTTCTGAGGTAAGCA | 60668 |
rs106666076 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551154 | GTGTTAGGAGGTGTG[C/G]CCTTGTTGGAGGAAG | 60668 |
rs106666638 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424096 | CCCTCATGACCTCAT[G/T]TAACCTAATCAACAA | 60668 |
rs106666922 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552670 | TTACAAATAAAATTA[C/T]AAAGTCACCGTATTA | 60668 |
rs106668064 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48314009 | AATGTTGTGAGTCAA[A/T]GAAGCAAAATGAATC | 60668 |
rs106668394 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497755 | GACTGTTTTAGATCC[C/T]GCATCCTTTTCTTCT | 60668 |
rs106670846 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455902 | CTGGATGACTTCACA[C/T]TATTTTAAAATATAA | 60668 |
rs106670998 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362454 | AATTAAGACTATGTT[C/T]CTAATATAAAACTTT | 60668 |
rs106675917 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504106 | GAAGCTTTAGTCCCA[A/C]GTAATGCAGACTAAA | 60668 |
rs106683661 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503336 | CATACTCTCATCAAC[A/G]TTATTATTATTTTCT | 60668 |
rs106686762 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458342 | TATCAGTGACAGCCT[C/T]ACTAACCCAGACTGG | 60668 |
rs106689549 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307228 | CTGAGGCTGCAGAGC[A/G]GAGGAGACCACCAAC | 60668 |
rs106691374 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491944 | GGGCTTTGGGCTAAA[C/T]GATGAGTTCCTGGAC | 60668 |
rs106695962 | snp | A/C | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48428783 | CCACCACCACCACCA[A/C]CAACAAACACACACA | 60668 |
rs106698182 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48518052 | CATCCACATATTGGA[C/T]GTCCTTCTTGAGATT | 60668 |
rs106698645 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327438 | GGAACCAGCTTTGAT[G/T]GTGAATGTAGCATTC | 60668 |
rs106701512 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488694 | TATTGCCAGCATTGT[C/T]GAGCCATATGGCATT | 60668 |
rs106701949 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498331 | AAGGGCAAAGTAAGA[A/C]ACCGAATCAGATGTT | 60668 |
rs106705530 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48451620 | CTTTCTGGGTTCAGT[A/G]AAAAGAAGGTAAGTA | 60668 |
rs106709430 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477580 | CTAGACAATAGATGC[C/T]AAGGATGCTGTCAAA | 60668 |
rs106712616 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504091 | AAATTCTCCTCTTGA[C/G]AAGCTTTAGTCCCAA | 60668 |
rs106715367 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475941 | ATGGGTGGCCACCTC[A/G]CCGGTTCCATACAGA | 60668 |
rs106716747 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48329175 | AGCAGCTGGGTTCTA[G/T]TCCAACTCAACCAAC | 60668 |
rs106717931 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449508 | AAAATCAAATTAAGA[A/G]TCAAAGGGAGAGGCA | 60668 |
rs106721242 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494497 | TTGGTTTAGAACACC[C/T]ATGTTACATGACTTG | 60668 |
rs106722791 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446342 | TTCTACGAAGTTTCT[A/G]AAGTCCAGTGTCTAT | 60668 |
rs106724225 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467182 | TGTGAGGCTGCCACA[C/T]GACAGCTGCCCTTGC | 60668 |
rs106726286 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48329393 | CTGTCCCATTCTCTG[A/G]ATGTCCTACCCCTGT | 60668 |
rs106728095 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504838 | CTGGTCTCCAGGAGT[G/T]CTGACACACAGGCTT | 60668 |
rs106728589 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48500344 | CATCTACCTTAACCC[G/T]TGAAAAACACTTGAC | 60668 |
rs106734970 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327437 | AGGAACCAGCTTTGA[C/T]GGTGAATGTAGCATT | 60668 |
rs106735121 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497078 | ACAGCTCTGAGCACC[A/G]GCTCACAGCTCTTGA | 60668 |
rs106739987 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504241 | TATTCTGATCATTGG[A/G]TGTGTGGTATCTGGT | 60668 |
rs106746768 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340229 | ATGCTGGGCAGGACA[A/G]GTTGTGATCCTCAGC | 60668 |
rs106752406 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503894 | TATAGCTATTTTCTG[A/C]TGACCCACTGTCATA | 60668 |
rs106753063 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471954 | CAGGAGCATTAAGCA[G/T]AGTTCAAAGGTTTTC | 60668 |
rs106754142 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48429303 | GGTGCTGAGGCACAG[A/G]ACAAGGAGGTAGAAA | 60668 |
rs106755282 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503131 | ATAACATGCAAACGA[A/T]GGCTTTAAGAAGTTA | 60668 |
rs106755514 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328661 | AGTGGGAGTCCCAAC[C/T]ATAGACTGCTGCTGC | 60668 |
rs106761734 | snp | A/C | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48361695 | ACCAAGTTTCGTCAT[A/C]ACTTCATAAAGCTTG | 60668 |
rs106777754 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501896 | ATCACCACTTCAGCA[A/G]AAACCTGAGCAGATG | 60668 |
rs106781019 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494073 | GAACTAGATTGTTGG[A/G]GAGAGGGCAGCAAGG | 60668 |
rs106782522 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478512 | ACTACATGGCATCAA[C/T]GGAGCCCAATTCTCC | 60668 |
rs106785190 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423999 | GAAAAAGTTGGCCTT[A/C]GAGAATCCTTACCAC | 60668 |
rs106785300 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494029 | GTGGAAGGGGAAGCC[A/C]TGGGTCCTGCTAAGA | 60668 |
rs106790424 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497541 | AACATCCCACTGAAG[A/G]GATAAATGTTCTCCT | 60668 |
rs106791081 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468452 | CATCCTACCTAGCTC[A/G]TGGATGTGGAAGAAA | 60668 |
rs106799947 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485685 | TAGGGGGATATTGCT[A/G]GGATTGAACCTGGGG | 60668 |
rs106803038 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362164 | TAATAAAATCTTCAA[A/T]ACCAGTGCAAATAGT | 60668 |
rs106803541 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48488418 | TATGGAAATGTTGAC[A/G]TTTAACATGATTAGC | 60668 |
rs106806945 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424270 | AGTCCGATGTTATTA[A/G]ATTGTTCCTTTATTA | 60668 |
rs106807167 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430290 | TCTCTATCATGATCC[C/G]TAAAGAGAAAAGGCT | 60668 |
rs106811971 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48340276 | TGCTCAGGAGAATAT[A/G]TGTAGAGAGGACTAG | 60668 |
rs106813221 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48427260 | TAGGTTACAAAACAA[A/C]CTGCTGTGGCCTACC | 60668 |
rs106814684 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430507 | CAGACACACATTTAG[A/G]AGGAAGTCAAGGGAC | 60668 |
rs106820430 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458943 | CCCTGGCCTAAGAGG[A/C]AACTGTATAAGGCCT | 60668 |
rs106830081 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557438 | CAATTTTGAATTCAA[A/C]CAGAGGGGATGCGAT | 60668 |
rs106835198 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473027 | TGTTAGGATGGTCAC[A/G]TTAAAGTACTTCAGC | 60668 |
rs106835490 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557341 | GAAGAAAGATGCATA[A/T]ACACATGACTTTGTG | 60668 |
rs106837974 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48475608 | CATGAACACATCAGT[A/G]TTGCAGTAATTTTAA | 60668 |
rs106838717 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468729 | AATGCTGTTAGCCAG[A/G]GTGTTGAAATTACAG | 60668 |
rs106840831 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473953 | TCAGTATCTTACAGG[C/T]AGACATGCAGGTTAC | 60668 |
rs106842519 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455281 | GCTGCCTGGCTCCTT[C/T]TCTCCTCTTTATTTA | 60668 |
rs106847969 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48497229 | CAAAGTAACAGTCTT[A/G]TCACTACAGGGTCAC | 60668 |
rs106850022 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424009 | GCCTTCGAGAATCCT[C/T]ACCACATGCACGTAC | 60668 |
rs106852035 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48488904 | GGACTCTAGAGATCC[C/T]AGCAGTGACTAGTCT | 60668 |
rs106854899 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551926 | AAAAATTAGAGTTCT[C/T]ATAGAAATCTAGTTA | 60668 |
rs106856524 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48555241 | TCTGCTTCTAGGTTA[A/G]TTCCCTGCATAGCAA | 60668 |
rs106857537 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48497238 | AGTCTTGTCACTACA[A/G]GGTCACAGCACAGAG | 60668 |
rs106858265 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552568 | TCTATACCTGGTTTA[A/G]GGCTACAACTACAAA | 60668 |
rs106858298 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340637 | GGGTGTACAAAAACA[C/T]GATAACACATTGACA | 60668 |
rs106858792 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48555400 | TTCTTTCATGCATAA[A/G]CATAACCTATAGAAA | 60668 |
rs106858811 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357944 | TTACATTTAATAATC[A/C]TTTGATTACAAAGCA | 60668 |
rs106858912 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48555297 | GTTTTCATGGCTTCT[C/T]ATACAGTTTCTTATA | 60668 |
rs106860845 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48414641 | GAGGTTGAGAATTGG[A/G]AGGAATAAAGGTGGG | 60668 |
rs106863743 | snp | G/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48504815 | ACCCATCTCCCACTG[G/T]GAAAAAGCTGGTCTC | 60668 |
rs106866692 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468484 | AGCTTATGGGTGTTG[A/G]TAAATAGTTATTAAA | 60668 |
rs106866693 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555901 | CATTTATTCAAGTGC[C/T]ATGAGCATTTCATTA | 60668 |
rs106868661 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48304796 | GCTGGCAGGGAGGGT[C/T]AAACACCTTAAGTTG | 60668 |
rs106869930 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342926 | AGGGAGAGAGAAAGA[C/G]AGACTCAGGAAGCGG | 60668 |
rs106874958 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503175 | ATATGCTTAATATTT[A/G]TAAATATTTTAAAAG | 60668 |
rs106878052 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48493604 | TAATTCACTTGCATT[C/T]ATTAAGCAATTTGAT | 60668 |
rs106879350 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48525599 | CAGTTAGTGCACACA[A/G]TGATATCCCAACTGC | 60668 |
rs106880665 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48361023 | TTGGACTTGAATAAG[A/G]AAAACAAAGCAAATT | 60668 |
rs106882571 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468988 | ACACCCACCCCAATC[C/G]CAATCTGGACAAACT | 60668 |
rs106884889 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48490713 | CTCTCTCTCAGCATG[C/T]CTTCCCTCTTCTGCC | 60668 |
rs106886517 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498460 | CTGATCCCTTGTCCT[C/G]GACCTGCCGTCTTAA | 60668 |
rs106886913 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471859 | TTTTCTCGTTGGTTT[A/T]ATGCACTATTCCCAG | 60668 |
rs106887759 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357977 | GAAACAAGCACAAGT[A/G]ATAAAATTTTATTAA | 60668 |
rs106889240 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553050 | CAATAGACTTTATCC[A/G]TACAAAAAATTTTAA | 60668 |
rs106890895 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489547 | GCACACTCTATAACT[A/G]TCTAGGCTAGACTGA | 60668 |
rs106893040 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48361087 | TCTGACTGCTCAAGG[C/T]TTGTTAGGTAAGATA | 60668 |
rs106893202 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362132 | CTAACAGAGGAGGAA[A/G]TAAAATAGTGGGGCT | 60668 |
rs106894656 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48549702 | CTGCTGCTGCTGCTG[C/T]TGTTTCATTTTTTAC | 60668 |
rs106895631 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475519 | CTTGACTTCTGTGGG[C/T]GCTCTAAAGGCATGT | 60668 |
rs106895774 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498845 | AATTTTGTCATATGT[A/T]CTATCACAGCAACAG | 60668 |
rs106897398 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457570 | TGGTCTGTTTCTGTA[A/C]TGTTCTGGAGGCATT | 60668 |
rs106898113 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48493865 | GAACTGGAAGAGCTT[A/G]AAGGGGCTCGAGACC | 60668 |
rs106901643 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326999 | TAAATTTTGAAAATA[C/T]AGCACTTGGGAAACT | 60668 |
rs106902831 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344057 | CAGGACCTTCTATTG[C/T]CTTGATATCAATACC | 60668 |
rs106903348 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502127 | AAAAATAGCAGTTTC[A/G]AACTTGAAGAGATAG | 60668 |
rs106905871 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48363719 | GTCATGCAGTTCACA[G/T]GTAGAGAAAATCAAT | 60668 |
rs106905929 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556511 | ACCATATATATGTAT[A/G]TGTTTATATGTATAG | 60668 |
rs106907066 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48492405 | CGTAATAATCTGTAG[C/G]TATGACTGAATTTTT | 60668 |
rs106911227 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48307231 | AGGCTGCAGAGCGGA[A/G]GAGACCACCAACACT | 60668 |
rs106915135 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48423081 | ATGGGGATGTAAGGA[A/T]GATCATGAAACAGAA | 60668 |
rs106916832 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48502794 | CATCTTTCAGCACTG[A/C]AGTGTGGTATATTGT | 60668 |
rs106918567 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48335551 | AGCTTGCTTACTGTT[C/G]GTATTTATTGCTTTT | 60668 |
rs106921831 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423863 | AGCTATTTTCTAAGT[A/G]TTTCTATTAAAAATT | 60668 |
rs106926819 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48452901 | AGTTGCTCTTCTTCT[A/G]TGTTCATGGGGAAAT | 60668 |
rs106932683 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499919 | GACAATAGCAAAGAA[A/G]TCACTCACAATACGC | 60668 |
rs106936453 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48551685 | ATGGGATTTCTCTTC[A/G]TGGTTTGCTCATCTT | 60668 |
rs106940408 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503896 | TAGCTATTTTCTGCT[C/G]ACCCACTGTCATAGA | 60668 |
rs106941205 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500211 | CAACCCAGGAGCGTA[A/G]CCCTTAAAGAAATTC | 60668 |
rs106943189 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476065 | AAATCAAAAACTCAA[C/T]AATTTACTAATCTTT | 60668 |
rs106943743 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48487719 | TTTTTCCTGGCGTCT[A/C]ATAGGTGCCAGATGA | 60668 |
rs106945183 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48335468 | AAGATGTTGGGCGCA[C/T]GACACACTGACATTC | 60668 |
rs106945445 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352165 | ACATGTACTTCAAAA[C/T]TAGACCTCATAACTT | 60668 |
rs106947136 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48477029 | CCATAAGCAAATAGA[C/T]CTCTGTCTCTGATTC | 60668 |
rs106947570 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502944 | AGAGGACAGTGAGGT[C/G]CAGCACTACCGAGAT | 60668 |
rs106949524 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555939 | AACACTTTAAGAGAG[G/T]CTGGAGAGATGGCTC | 60668 |
rs106950549 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449719 | GGTTTCCACACTTTC[C/T]TCATGATATAAAGGC | 60668 |
rs106953629 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314088 | ACACACACCATATCA[C/T]TGTTAAACTCATCTA | 60668 |
rs106956902 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557593 | GTGGGGAGGACACCA[A/C]AGGCAGCTGCAAGTC | 60668 |
rs106960507 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478454 | ACTAGAGATAATCTG[A/G]TGGCGAGAGGCAAGC | 60668 |
rs106965078 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476527 | GTGTTGCTGCTGCTA[C/G]AGCTCAGCTAAGTTC | 60668 |
rs106965670 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549248 | ATAATATATATATAT[A/G]CATATATATATATAT | 60668 |
rs106968383 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48473592 | TTAATATGTTTTAAA[C/T]AGCACAATAGCCTGG | 60668 |
rs106973972 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48445254 | CGGAAATGTAGCAGC[A/T]TTCGTTCCAGGCCTC | 60668 |
rs106976722 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327576 | AAGGAATTTGCTCGA[A/G]TAGTGAAAAGGTTTG | 60668 |
rs106977053 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498306 | AGTTACCTTTCATAC[A/G]TCCACATTCAAGGGC | 60668 |
rs106977335 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48305616 | GGACAGTTATATCTA[C/T]ATGAAGGACAGATAA | 60668 |
rs106979970 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48447893 | AGGGTAAGGAATGGG[A/G]ACATGTGCAACCTAT | 60668 |
rs106985617 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48497272 | GGAGGATGCTGGAGA[A/G]TCAAAAAATAAAACA | 60668 |
rs106987823 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48331219 | AATGCCGCCCAACAA[A/T]AATAGCAGGACAGGG | 60668 |
rs106988807 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503883 | CTGTGTTTAATTATA[A/G]CTATTTTCTGCTGAC | 60668 |
rs106988951 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476320 | TAGTTCTCTCTCTCC[C/T]CTCCCCTGCCTTACA | 60668 |
rs106990887 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488950 | CCTGCTCTGGTACCA[G/T]TGGTAGCTGTCCTAT | 60668 |
rs106994193 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478511 | GACTACATGGCATCA[A/T]TGGAGCCCAATTCTC | 60668 |
rs106997053 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48492072 | CAGCCTCACTCACCA[C/T]GGTGAAATTTCACAT | 60668 |
rs106998033 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476419 | AGACAACAATCTACA[C/T]GTCAGGATGAACAGA | 60668 |
rs107000730 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48556892 | CAGCAACCACATGGT[A/G]GCTCACAACCATCTG | 60668 |
rs107002465 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48420022 | TTGGAAAGGAGGTAT[A/T]GGTCATGGAAAGAAT | 60668 |
rs107003583 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553108 | AACAACCTGAACCTA[C/G]ATTGCCTCACTGGTG | 60668 |
rs107006124 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469502 | CCCCTTCCACTGGTG[A/C]TCTTACTAGGCTATT | 60668 |
rs107021728 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48429120 | CTGATACTAAAATCT[A/G]GTTCCCTAATTGGCT | 60668 |
rs107024663 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48501926 | GGAGCTGTACTCTCA[C/T]TACTCCTACCTAAAT | 60668 |
rs107025478 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469508 | CCACTGGTGCTCTTA[C/G]TAGGCTATTCATTGC | 60668 |
rs107032110 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504767 | ACCAATTTCCCCTGC[A/G]CCTAGAGCTGACCCT | 60668 |
rs107043440 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469567 | ACCATGTATAGTCTT[C/T]GGGTAGTGGCTTAGT | 60668 |
rs107044640 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48491222 | ACACAATTATACTAC[A/G]AGTGACAACAGACAC | 60668 |
rs107050876 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494149 | AAGGGGATGTTTGCC[C/T]GGAAACTGGGAAAGG | 60668 |
rs107052408 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327595 | TGAAAAGGTTTGGAA[C/T]AGACTGTCCAAATTC | 60668 |
rs107054982 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489628 | TGACAAAATTAAGAA[C/T]GAAAACCTACCTTCA | 60668 |
rs107058692 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455469 | AACAGACAAGTGAAA[A/G]AAGAAGAAAAAAAAA | 60668 |
rs107064176 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327996 | AAGAAAGCCATAACA[A/G]AGGAATTGCCTGGAT | 60668 |
rs107064193 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48503858 | ACTAGACAGGTGACA[C/G]GTCCTCCTTCTGTGT | 60668 |
rs107071644 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468212 | AGATGCACTCTGTCC[C/T]CAGTGGAATGAGCCA | 60668 |
rs107072401 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444522 | ATGAAACAAAATGCT[C/T]CGATTTAACAATTAT | 60668 |
rs107075090 | snp | C/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48556849 | TAAGAGCACTGACTG[C/G]TCTTCCAGAGGTCCT | 60668 |
rs107077111 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359182 | AAAAAACTGAGAATA[A/G]GAGGAAACACAAAAA | 60668 |
rs107079160 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552069 | ATGAAGTAAATAAAT[A/G]AAGAAACATTCTATG | 60668 |
rs107091392 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477781 | GCACTTGTGTGAAAG[A/T]GGCCACGAGATGACA | 60668 |
rs107100448 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48487867 | GCAGCCCAAGAATTA[C/G]CCTTTCCTATGACCC | 60668 |
rs107106350 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468458 | ACCTAGCTCGTGGAT[A/G]TGGAAGAAAAAGCTT | 60668 |
rs107109701 | snp | A/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48346850 | TACTAGTCTAATACA[A/T]TCAAAACTTAAATTT | 60668 |
rs107112922 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430370 | GGAATTTAATCTCTG[A/G]GTTTGGCCAAAGACA | 60668 |
rs107115961 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487928 | TACACTCACAAGAAC[A/G]CTGCAAATTTCCACT | 60668 |
rs107116637 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48490653 | ATGCCTGCCATGACT[C/T]TTGGCCTACAGATTT | 60668 |
rs107118916 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48471724 | CAGGCTATTGCTATT[C/G]TTCTTGATTGCTCAA | 60668 |
rs107126815 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360664 | TGGAGCCTTAATTCT[C/G]TTCTTTTCTTAGATT | 60668 |
rs107127202 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468858 | TGTTTCTGCATGCCT[A/T]CGGTTTGAATTTTAA | 60668 |
rs107127234 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48315766 | CTATATTTATTAATT[A/C]AGTGCAATATACAGT | 60668 |
rs107129383 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48432040 | ACAACAGCTCAACTG[A/G]CTTGAGAGAGCCCTC | 60668 |
rs107131948 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455586 | GCCATCACCTTATTT[G/T]GCAGCCAGCATTGAG | 60668 |
rs107138590 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48502510 | AGAGGATTCAGGTAC[C/G]ATGATAACAAATACC | 60668 |
rs107139046 | snp | A/G | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48444430 | CTCTTGCCGCTTGAA[A/G]TTCTGAACATATTCT | 60668 |
rs107145157 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48443055 | CTTCAATGTTTCTAT[G/T]GTATGTTGAGGGAGA | 60668 |
rs107147594 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48446949 | CATAACCCATTCACT[A/C]TGGTGCCTTTCCCAA | 60668 |
rs107147737 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327542 | ATTTCCTGGGAGTTA[A/T]CTATGATGAAAAGAG | 60668 |
rs107150979 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48447598 | GAAACTCACTCATTT[C/G]CACACTCAGGGACCT | 60668 |
rs107178595 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476459 | CGCTTAGCAGAAAAC[A/G]TGCTATTAAAGCTTC | 60668 |
rs107179376 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501750 | CTTGAGTCAGGGAAT[A/G]TGGGAGAAAAGAAAA | 60668 |
rs107181472 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444033 | ATTGGGTTAGTCACC[G/T]TTGTATTACCAGAGA | 60668 |
rs107184377 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48426359 | CCCTACACTTAAACA[C/T]GTGCCTTGGTCTAGG | 60668 |
rs107184798 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48507964 | AATAGTAAAGGCAAT[A/T]TAGAGCAAATCAGTA | 60668 |
rs107185220 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362566 | ATCTCAAACACATTT[A/G]TAAGGGGAAGCTATG | 60668 |
rs107191271 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48492389 | GTACTGTGTTGGCTG[A/G]CGTAATAATCTGTAG | 60668 |
rs107191624 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48497318 | AACAAACAAAACCCC[A/C]AAAAAACAAAAACAA | 60668 |
rs107191824 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48453265 | CATCAGGATGAACTC[A/G]AAGAAGCAAAACACA | 60668 |
rs107193187 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48364923 | GAAGCAGAGAAACTG[G/T]CTGTAAGGTGAGGCC | 60668 |
rs107196309 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486365 | AGTCTACACATGCCA[C/G]ATAGGTTCAGCTGTT | 60668 |
rs107209451 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423747 | CAAGGTAAGGAAATG[C/T]GTTAATGAGGAGGAG | 60668 |
rs107210419 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48475747 | TATTTACCCACATTG[A/C]AAATGTTATCCCCTT | 60668 |
rs107215274 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48354745 | AAAAACCCATTCCTG[G/T]TACCATTGTTGGGCT | 60668 |
rs107215440 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419281 | ATCGAATTTAGAACG[A/G]GCTATGATTTATAAG | 60668 |
rs107217541 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444332 | GATTAATTTCCAACA[C/G]AGGAGCTTTGGGAAT | 60668 |
rs107222545 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48553767 | TGAAGAATATGGATA[C/T]TCTAAAGCATCCTAT | 60668 |
rs107226341 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551645 | ACACAGAAACAGAAG[C/T]AGAGTCTATGGAAGA | 60668 |
rs107226662 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478498 | CAACAGAAACCAAGA[A/C]TACATGGCATCAATG | 60668 |
rs107226684 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499683 | AAAATATGATAGATG[A/T]TCCATAAATGGTAAA | 60668 |
rs107230573 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477917 | CAGCCTACTTAGAGA[C/T]GCATCTTTTAACATT | 60668 |
rs107230804 | snp | A/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48420025 | GAAAGGAGGTATAGG[A/T]CATGGAAAGAATGAT | 60668 |
rs107237509 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48345506 | TCCTTCTAGAAGGTA[A/T]CTTTGCCCTTATCTC | 60668 |
rs107238377 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352018 | TTCCTAATTTTTATC[G/T]TGTACTTTGTTTAAT | 60668 |
rs107238387 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48365174 | ACTTGCATGCACATA[A/G]CTGTTGCTGACTTCT | 60668 |
rs107239736 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500089 | CTCGGCAAACAGAGC[A/G]CCCTTCTGCCCTAGA | 60668 |
rs107250439 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557758 | CCAGAAGGAGATAAA[A/T]GTTTGAAGTAGGCAA | 60668 |
rs107251102 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423838 | CGCCACTTATAAAAG[C/T]TGCATTGTGAGCTAT | 60668 |
rs107253677 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48504883 | CCACTGTCAGAAACA[A/G]CAAGATGAGCTAACA | 60668 |
rs107255976 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498147 | ACCAGGCACCCCAAA[C/G]TCCCTTAGAGGGAAC | 60668 |
rs107261188 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307505 | AGGAAAACACCAAAC[A/G]CCATCTGGAACCCTG | 60668 |
rs107261239 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484807 | GATTAACAACTTCTG[A/C]TCAATATGAGAGAAA | 60668 |
rs107263044 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48344454 | TGGCGTCATCTCCTG[C/G]CTGACACTGTCTGTC | 60668 |
rs107269281 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501823 | ATGGGAACACAACAC[G/T]CAGCCGTTGTGGAAA | 60668 |
rs107270192 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48493908 | CAATGCCAAGCAACC[A/T]GAGCTTCCAGGGACT | 60668 |
rs107270473 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499370 | AACAACCAACGTATT[G/T]AAAATTACATGTTTT | 60668 |
rs107270876 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48440123 | CCATTTCACTGCTTT[C/T]TGACTCTGAGAATTA | 60668 |
rs107271491 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48490765 | TCAGGATTTCATAGC[A/C]CTCTATCCTTCTCCT | 60668 |
rs107271761 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502925 | TTTACATAATCCTTA[A/G]CCAAGAGGACAGTGA | 60668 |
rs107273188 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552879 | CCTGCATCCCATTCT[C/G]GCATCAGTGGCAGGC | 60668 |
rs107274914 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48555314 | TACAGTTTCTTATAT[C/G]TATAAAGTTGCAGGT | 60668 |
rs107278973 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357965 | TTACAAAGCAATGAA[A/G]CAAGCACAAGTAATA | 60668 |
rs107279429 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48446283 | AACTATGTAACACCT[A/G]AAGAATTAGGATCAC | 60668 |
rs107279782 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477557 | GCTGTCATGCTGAAA[A/C]CACAGTTCTAGACAA | 60668 |
rs107283158 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458242 | GCTGGCAAGAAATCT[A/G]GGAATTACAGGCCAA | 60668 |
rs107286392 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48491995 | TCTAAATCGAGTAAG[A/G]AAAAATGAAATGACC | 60668 |
rs107288941 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465507 | TTGAAGCCCATGAAG[C/T]AAATACATTACCAGA | 60668 |
rs107290973 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48499364 | CTCGGCAACAACCAA[C/T]GTATTGAAAATTACA | 60668 |
rs107291582 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48530448 | CAAAAAAGGAAAGCA[C/G]GGGTATCAAGTAAGT | 60668 |
rs107293592 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455429 | GGTGATCCTAAACCA[C/T]GTCACTTGAATCAAC | 60668 |
rs107298265 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491319 | GAACTGTAGAAGCCT[A/G]GTAACCTCCAGGTGA | 60668 |
rs107300701 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48429257 | GGTTACAATCTACTT[G/T]GAGCAAGGGGAACCA | 60668 |
rs107302938 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340486 | ACAACTGATAATTTT[A/T]AAAAAAGAAACCTCA | 60668 |
rs107308114 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497881 | ACATGCAGAACCACA[A/C]AGCAGCAGCACCATT | 60668 |
rs107308764 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425025 | AGGCTGAGCAGTGAG[A/G]TCCATGAAAGTCTCA | 60668 |
rs107310726 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48346359 | CCTTCCACTATGACA[A/G]CTCTTTAGGTCTTCA | 60668 |
rs107311738 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473985 | GAGTGATTTGGGGGA[G/T]ATGAAATAATTAACA | 60668 |
rs107312298 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48476136 | ATCTTAAATTCTCAT[A/C]CCACAAAACATCCAC | 60668 |
rs107314173 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362109 | CATTTAAAATTCCAA[A/C]TTTTCAGCTAACAGA | 60668 |
rs107317469 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425619 | AATTTATAATGTTGT[C/T]CTTGTTCACTTGTAC | 60668 |
rs107319066 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48478561 | ATATCCAAACACACC[A/T]GAAAAGCAAGATCTA | 60668 |
rs107319428 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48467824 | ATACAGGAATTCCGA[A/G]TTCAAGAAAAGTTTA | 60668 |
rs107320171 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499300 | AATTCTTATTATTTT[A/T]CCTAGAATTTTGTCT | 60668 |
rs107325314 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484400 | GAGCACAGCTTCTTC[C/T]GCTTGCTTATAAATG | 60668 |
rs107328337 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48351816 | CACAGCCTTACAATG[A/C]AATCATCCTGTTGTT | 60668 |
rs107335991 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48469075 | TGATAACAAATCAAC[C/T]ACTGGTCAAGTCAGT | 60668 |
rs107338870 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48353445 | ATTACTTTATTTTTG[A/T]TATGAAGTATTAAGA | 60668 |
rs107341072 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48443495 | CTGTCTCCATTCAGT[G/T]GTCTAAACTGCAAAA | 60668 |
rs107348698 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444162 | CTCAGAGTCAGAAAG[A/T]GTCATCACAGGTCAG | 60668 |
rs107348941 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48554211 | AAGGTAAATCTGGAA[C/T]CTCTTCCCTCATTGA | 60668 |
rs107349860 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48490471 | TATAATTACAAAGCA[A/G]TTCTACAGAATAGGA | 60668 |
rs107350108 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360661 | TGTTGGAGCCTTAAT[C/T]CTCTTCTTTTCTTAG | 60668 |
rs107352622 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48358028 | GACCTGAGAGTCCTG[C/T]CCACCATGGCACTTT | 60668 |
rs107353310 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48442817 | ACATTAATTATTCTA[C/G]ACTCTGTAGAGGTGA | 60668 |
rs107359528 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48432116 | ATGGAACAGGATAAT[C/T]ACAGTCAACTCAAGC | 60668 |
rs107359543 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476105 | AAAAAAGCTTCTAAT[G/T]TAGCAACAGATTTAT | 60668 |
rs107361751 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551116 | ACTCATGTGTTTGAA[G/T]ACTTGGCCTACAGGG | 60668 |
rs107365910 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551003 | TGGGCAATACCTCCA[A/G]AAGCTAAACTGTGTC | 60668 |
rs107374713 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48351027 | AATTTTTTCAGTCAA[C/T]CATGCTTTGACCATG | 60668 |
rs107380063 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48455650 | GCATGGCTCTGCCTC[A/T]TTTCTGCTGCTCTCA | 60668 |
rs107380407 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48490482 | AGCAATTCTACAGAA[C/T]AGGAGGGAAGTTGTG | 60668 |
rs107380838 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48552709 | AACTTGGTCCTTCAA[A/G]TGACACTAAGTAAAT | 60668 |
rs107382225 | snp | A/G | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48498386 | CAATACAGACTTCAA[A/G]TACTGCGACAGCCGG | 60668 |
rs107385038 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48476002 | GACTCTGCTCACATT[A/G]TCAGCATCCACCCAC | 60668 |
rs107386550 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48491423 | ACATAACCCAATCTG[C/T]CTTGAGTCATTAAAG | 60668 |
rs107387184 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555777 | GATTCTTAACAAATC[C/T]CCAAGTGAAGTAAAA | 60668 |
rs107387305 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48319708 | GAACACTAGAGGATG[A/T]GGGGAAATGGCTTCA | 60668 |
rs107389920 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421665 | CCTAAAGAAATGTTC[A/G]ACATCCTTAGTCATT | 60668 |
rs107390216 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48335995 | TCACTGGCCAGGAGA[A/C]TTGGCAACAGATTCA | 60668 |
rs107390550 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425601 | CCAAACAATTTCTTG[A/G]GGAATTTATAATGTT | 60668 |
rs107400208 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477951 | TGTCATTTAAAGATC[C/T]AAGCTTTATCTACTT | 60668 |
rs107402119 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48429212 | GGTAGAGTGAAGATA[A/G]CAGCTCCCAGACTTC | 60668 |
rs107405451 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424494 | CTAAATGTGAGCTGA[A/G]CAAGGATAACACCAA | 60668 |
rs107405521 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484610 | ATAGCTAGATATTTT[A/G]AAGTATTATTTATAT | 60668 |
rs107407012 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555967 | CTCAGAGGTTAAGAG[A/T]GCCAACTGCTCTTCC | 60668 |
rs107410558 | snp | C/G | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48556944 | ATATAATAAGTGAGT[C/G]TTTAAAAAACAAAAG | 60668 |
rs107414901 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48424451 | AATGTCAGAAGCTAC[A/G]TCCATGAACTCTAAC | 60668 |
rs107424571 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553078 | TAATAATAATTGAAG[C/T]TTCCCAGAAATAAAA | 60668 |
rs107426397 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326875 | CCAGGGAATAAACCA[C/T]CAGCTGTTGGAAGAC | 60668 |
rs107426968 | snp | A/C | 0.5 | 0 | missense | Amph | Rn_Celera | 17:48444429 | CCTCTTGCCGCTTGA[A/C]GTTCTGAACATATTC | 60668 |
rs107428243 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48555956 | TGGAGAGATGGCTCA[G/T]AGGTTAAGAGTGCCA | 60668 |
rs107430509 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48502200 | TAACCCCAAGAATAA[G/T]AGTCTACAGTAATTA | 60668 |
rs107430605 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469465 | TTCACTGGGGGTTCA[A/G]TCTTGGCAGGACCAA | 60668 |
rs107432930 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489915 | TATGATGTTTTGCTG[C/T]TCTGTCTTTGTTACT | 60668 |
rs107433573 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469770 | CAGTCTGAAATCGTG[A/G]CTATTCCTGTGTCTA | 60668 |
rs107435363 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475549 | TATCTAAAAAGAAGG[A/G]TCAGGGTCCACCCTG | 60668 |
rs107439918 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48504364 | TGAAAGCCAGTGTTT[C/T]CTAAGGCAGGTAAGA | 60668 |
rs107451047 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430071 | GAAGAGGTGTTTTTA[A/C]AAGTGGGACTTCCAT | 60668 |
rs107452739 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48473322 | CACTTCTTTCCTCAC[C/T]CTACAATGCTTCCCT | 60668 |
rs107453634 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494082 | TGTTGGGGAGAGGGC[A/G]GCAAGGGGGGGAGGA | 60668 |
rs107460012 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48555368 | TGTGTATGCAGAGGA[C/T]AATTTAGTTGACAGT | 60668 |
rs107466441 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48424905 | TATGTAATATATTAT[A/C]TCTGTCCTTCTAGCT | 60668 |
rs107469002 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458855 | GGAGAGAGACCTCAC[A/C]GCCTGGTCAGGTGGG | 60668 |
rs107471633 | snp | A/G | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48444436 | CCGCTTGAAGTTCTG[A/G]ACATATTCTTCAAAC | 60668 |
rs107473834 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48487703 | CTACTTATAAAACTC[A/G]TTTTTCCTGGCGTCT | 60668 |
rs107474961 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48430127 | TAGGCAGTCACAAGG[A/G]GTCAGGTGAACTGGA | 60668 |
rs107477904 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48307484 | TGCACACATCTCTGA[C/T]GCCAGAGGAAAACAC | 60668 |
rs107478132 | snp | A/C | 0.375 | 0.216506 | intron-variant | Amph | Rn_Celera | 17:48551723 | CGTACAGTCCCAAAA[A/C]CTGCCCAGGGGTAAA | 60668 |
rs107484410 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556222 | ACTCCATCAGAATAG[C/G]ATAGAAATGACTGAA | 60668 |
rs107485101 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474456 | TGGTTAAGAGACATG[A/C]TAATGTATGCACATA | 60668 |
rs107487067 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48314310 | CAGTTCTTGGGAGGA[A/G]CAGGGACATTCTCGA | 60668 |
rs107489023 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494440 | AGGGGGCAGAGAAGA[C/T]TCAGGGAACAAAAGC | 60668 |
rs107490428 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499176 | AGCAGGCTCCCTGCA[G/T]TGATCTTGTGAGTTT | 60668 |
rs107490664 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48488030 | AGTTGATGCTCATAT[A/G]GTCTTTGCCACTAAG | 60668 |
rs107496782 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359653 | GAAGTAGTAATGGAT[A/G]TTGGAAACTGTCACT | 60668 |
rs107505137 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553701 | AGTAACTGGAAGCCA[A/G]TTTGGCTTCCAGAAA | 60668 |
rs107505582 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497681 | ATAAAAATCACAATC[C/G]TGTGTAAAATGCTTG | 60668 |
rs107513193 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328558 | AAGGATCGAAGGAGT[A/G]CTGAAGGCAGGGCTG | 60668 |
rs107514978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Amph | Rnor_6.0 | 17:48554159 | GTTCAAGAACACTAT[C/T]TATTCCAGTGGACAC | 60668 |
rs107515566 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477527 | TCTCCATGTGTTCAA[G/T]AGACAGAGCTATTGG | 60668 |
rs107517432 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494566 | TATATGTATATATAT[A/G]TATGTATATATATAT | 60668 |
rs107517644 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484504 | CAAAACAAACTGAGT[G/T]CAAGATTGGAAAGGA | 60668 |
rs107527672 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48453121 | TTCTGTGAAAAGTTA[C/G]ATAAACTTGCTTTTG | 60668 |
rs107529597 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48473595 | ATATGTTTTAAACAG[A/C]ACAATAGCCTGGCTA | 60668 |
rs107531972 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48316770 | GACAAAAGTTTGTAG[A/C]AAAGTGGCAGGATGC | 60668 |
rs107537294 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326878 | GGGAATAAACCACCA[A/G]CTGTTGGAAGACTCC | 60668 |
rs107540114 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446281 | TTAACTATGTAACAC[C/T]TAAAGAATTAGGATC | 60668 |
rs107549003 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360984 | CTATAGATATTTAAA[C/T]GGGTTCTTTAATTCC | 60668 |
rs107549731 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48432111 | TCATGATGGAACAGG[A/G]TAATTACAGTCAACT | 60668 |
rs107551488 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328709 | TAAATGATGCTGTAG[C/T]TGAAGCTCTTGACAG | 60668 |
rs107562866 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Amph | Rn_Celera | 17:48551557 | ATTGTGACAAAACAA[A/C]ATAATGAAAAGCAAC | 60668 |
rs107563917 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48549279 | ATATATATATACACA[C/T]ACACACACACACACA | 60668 |
rs107569685 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48474878 | CAATGGCTATAGTCT[A/G]TAATATCCAGGGGTC | 60668 |
rs107573141 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489019 | AACAGCTCCCTAATG[A/G]TTATAGCATCAGCTC | 60668 |
rs107576101 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48362236 | GGGTAAGGCTAGTTG[A/G]CAATTCTATGCAATG | 60668 |
rs107576972 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550895 | CTGACAGGTTAATGA[C/G]AACTTTGGGTAAAGG | 60668 |
rs107584171 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359668 | GTTGGAAACTGTCAC[C/T]ATTGATTGCTCCCTG | 60668 |
rs107588482 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360998 | ACGGGTTCTTTAATT[A/C]CAAAGGTTATTGGAC | 60668 |
rs107590605 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48498634 | ATCATGGTCTCTGAG[A/C]AAAGCATGCTGAGCA | 60668 |
rs196968767 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48501529 | AGTTATCATTGCCTC[C/T]AAGCTCTCTAATAGA | 60668 |
rs196977323 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48492816 | CATTGCTCCAACTCT[A/G]AGCGCAAAAACACAA | 60668 |
rs196980432 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48338817 | TTTTGATTCACTCCC[C/T]TTTTTTTTACTTCCA | 60668 |
rs196985412 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357069 | CTACAGAAATGGTAC[A/G]TAACTCAGGTAGCAG | 60668 |
rs196989014 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48485206 | AAAAGCAAGCTATTC[C/T]TCTGACTGAATAGAA | 60668 |
rs196991391 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305931 | AGAGAAGAATTTCCA[C/G]TTTTGAATATGGTGG | 60668 |
rs196991656 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48452207 | CCTGGGGCTGACCCT[G/T]TGCCACAGCTCTCTG | 60668 |
rs196994237 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475554 | AAAAAGAAGGGTCAG[G/T]GTCCACCCTGATGAC | 60668 |
rs196994302 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48361490 | TAAGAGCCAAAAACC[C/T]AAGTTTGGGATCACT | 60668 |
rs197001932 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48428298 | GCTGATCCCCTTACA[A/G]GACAAAATAGGACAA | 60668 |
rs197004424 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48439955 | TGTGTTGCAGTATTC[A/G]CTTACTGTATTTTAA | 60668 |
rs197014253 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457497 | TGAGAATACTGACCA[C/T]CATAGCGAGGCTGTA | 60668 |
rs197027410 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48442417 | CTATAGTTGGAAATC[A/C]AACAGACTAATAGGG | 60668 |
rs197030321 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48492675 | AGGGTAGAGAGGACA[A/G]ATGCAATATGAGATC | 60668 |
rs197033016 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48329948 | GCCAACCACTGAGCC[A/G]TCTCCTCAGCCTCTG | 60668 |
rs197035880 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446104 | AAGAGGAGCTGCCAC[A/G]TTCTGAGCTCTACAA | 60668 |
rs197036722 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48454561 | TTACACAAAATAAGA[C/T]ATGGGCTTTCTTTCA | 60668 |
rs197043346 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48451051 | TCCCATGGGAGGGCT[A/G]TATGACATGAGGCAG | 60668 |
rs197046768 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48358288 | CATCTAACTGAAACT[A/G]ATCTATACAAAGGTG | 60668 |
rs197048954 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420914 | ACAGAGTTAGAGCAA[A/T]TTCCAAATTCATTTA | 60668 |
rs197054888 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425489 | ATACACATGTTGTCA[C/G]CATGGACCGCCCCTC | 60668 |
rs197081651 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48414753 | TGAAGCAATGGTGGA[C/T]GAAAAATGGGGTTTG | 60668 |
rs197104166 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497808 | AGTGAACACCTTTGC[C/G]ATTTTTGAAACACTT | 60668 |
rs197110661 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450977 | GGACAAGTCTTCCCT[C/G]ACCAGCAGCCTTGTT | 60668 |
rs197122154 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465715 | GTCTGACTTTCCTAA[C/T]GTAAACATTATCAGA | 60668 |
rs197129696 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48558016 | CTCAGAAAGCCTACA[A/T]GCCACATTAGATGGC | 60668 |
rs197149448 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489926 | GCTGTTCTGTCTTTG[C/T]TACTTTTTCCTGTTT | 60668 |
rs197160020 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48500490 | ATCAGAGGACTATAG[A/T]TTCTTCAAGTTAACA | 60668 |
rs197170071 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484178 | CATGCTCTTTAAAAA[C/G]TAGCAGTGTTAGCTA | 60668 |
rs197187833 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48445095 | CTGGCAGTCTAGGAG[A/C]ATTCTACAAAAACAA | 60668 |
rs197191665 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557797 | CCTTCAAGAAATCAT[A/G]AAGTGTTCCACAAAT | 60668 |
rs197194809 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551626 | CCATCATAAGAGGGA[A/C]CTGACACAGAAACAG | 60668 |
rs197203292 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305698 | CACAGGATTCTATTT[A/G]GAGTGAGTCAAAATC | 60668 |
rs197214252 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491482 | AACGAAACAAACAAA[C/G]AAAGAAAAACAAGTG | 60668 |
rs197215640 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48550561 | GTCATGACATTGGAC[C/T]TTGGCTAAGTCCAGA | 60668 |
rs197221166 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48356781 | CAGTTATTGGAGGCA[G/T]GGTACTTCTCAGGTA | 60668 |
rs197221597 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48337699 | AGTGGCTCCTTAGCA[G/T]TTTCCCTAGCATACA | 60668 |
rs197231937 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466356 | GTCACCAAACGGGAT[A/G]GGAAGGAGATACAGA | 60668 |
rs197233011 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48420090 | TGTGTGAAGTTCACA[C/T]AAAACATTGTTAAAA | 60668 |
rs197233864 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48454327 | GTGAAGTTTTCCCTA[C/G]CCATGATCCAAAGTG | 60668 |
rs197234831 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48448161 | AATAACTACTCATTT[A/G]ATTGAGCTTTACTGT | 60668 |
rs197237337 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314079 | CACACACACACACAC[A/C]CCATATCATTGTTAA | 60668 |
rs197237974 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48442147 | TGAACTGAAAATAAT[C/T]GGTGCCCATACCAAT | 60668 |
rs197244763 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48439531 | ACTGTACTATAAACA[G/T]GGAACTCTCAGCTGG | 60668 |
rs197249318 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485772 | CATTGTCCTCTTTTA[A/T]TTTTAGACAATGCCT | 60668 |
rs197270252 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449240 | CACTGTGGATAATAC[C/T]ATCGTTTGGCTGTTG | 60668 |
rs197272551 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48472497 | GTCAACATGGACTCA[A/C]AGGGATGCAGGGAAC | 60668 |