SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs197286982 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48343938 | ACCGTCCCAACTTTC[C/T]ACTTCACTACTTTCA | 60668 |
rs197295434 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352686 | GTTGTCAAGTGCTTT[C/T]CCCACAACATTTATT | 60668 |
rs197303375 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48525415 | CCAGCATCTCTAGAA[A/C]ATTCTTGTCTGTATC | 60668 |
rs197311719 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419069 | ATCTGCAAACTCATA[A/G]TTAGAAAAGGGCCTT | 60668 |
rs197314240 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474172 | CCTGTGATGCTACAA[C/T]TTTGGCCAGCTTGAA | 60668 |
rs197327324 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554369 | CCAAGCCTTACTATC[A/C]AGAATGAGGTGAGTC | 60668 |
rs197339532 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48453074 | CACTCACTCCACACC[G/T]CATGGGAGGAAATGG | 60668 |
rs197346228 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48315397 | AGGGCTGTAGTGGTG[A/G]GTCACTGGGGTAATG | 60668 |
rs197371854 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48554227 | CTCTTCCCTCATTGA[C/T]CAGAGAGACTGGGAA | 60668 |
rs197391235 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420944 | AGAGTAACAAAAAAC[C/T]CAAGATAGCAAAAAC | 60668 |
rs197425930 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489302 | GGTTCCTCAACTCTT[C/T]TCTCTCTCTCTCTCT | 60668 |
rs197426191 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499502 | CTATTTTTTACTCAC[A/C]ATATTTTGTGAGACC | 60668 |
rs197429609 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340028 | GGTCATGAGACATGG[A/G]CCAGGAGATATGAGC | 60668 |
rs197430165 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48426945 | CTACTGACAGAAATT[A/T]CAGTTCATTTTAAAG | 60668 |
rs197436247 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446752 | CTCCACAGAGGGCAT[A/C]GAGGAAGGGAGGAGG | 60668 |
rs197444212 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48558170 | TTATAAAGTTTCTAT[C/G]ATGGACAGGACACAT | 60668 |
rs197452104 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48548909 | ATCCATGCTTGGCTC[A/G]ATTCTTTTCAGTTTA | 60668 |
rs197452149 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48440458 | AAACCATAGGACCTA[A/G]AAAACCATTCATTAA | 60668 |
rs197460333 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48443922 | AAGGTCCAGGGTGCT[G/T]AATATCCTGAAACTA | 60668 |
rs197462315 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489377 | TTACAAAAAGAGTCC[C/T]GCCTTACTTTTACTG | 60668 |
rs197473704 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48466648 | TATCTATGAACATTT[C/G]AGAGGTGTTTTCCTT | 60668 |
rs197474195 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477756 | ATGTGCTTCCATGAG[A/T]TTATGTGAAGCACTT | 60668 |
rs197481749 | snp | A/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48448517 | TAATTCACGATTTTC[A/T]TTTTTTTTTTTTTTT | 60668 |
rs197492769 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48452360 | ACACAGGAACCCAGG[A/T]GCAATCTGGGACAGG | 60668 |
rs197511087 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48443463 | CCTCTAAAACACATA[A/G]AAGAACAAGGCACCC | 60668 |
rs197514565 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498875 | GGAATTTATTTAAGA[A/C]AAACTTATAGAGAGA | 60668 |
rs197517487 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498242 | ACAGCTAGTTTTCCT[C/T]GAGACCCACACCTTC | 60668 |
rs197528866 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48439697 | AATAAAGTTGCACAA[A/G]GAAATATTTACATAA | 60668 |
rs197563426 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441136 | AATGAAATATGAATG[A/T]ACCAACATATTCACA | 60668 |
rs197578436 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48497901 | GCAGCACCATTCCAA[A/G]CAGTGGGTAAAGCTG | 60668 |
rs197588353 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48327619 | CAAATTCTGTGCTTT[G/T]GTCAAACTAATATGC | 60668 |
rs197595757 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48472547 | CACAGAGTATGTAGA[A/C]CTGGACTGTAGGGTC | 60668 |
rs197617374 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48307154 | TCCCGGCCCGCAGCA[G/T]CTCTCTGCTCCCAAA | 60668 |
rs197647306 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427713 | TATGATGAAGCAACA[C/T]ATTTTGCTTTGAGAA | 60668 |
rs197650655 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48484910 | GCTCAGCTTCAATCC[G/T]GAAGCAATCTTTTGA | 60668 |
rs197651631 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550610 | GAATGCCATGTTCAA[A/G]TGAAGAAAAAGCCAC | 60668 |
rs197653841 | snp | A/G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465539 | ATTATGAACAGCAGG[A/G/T]ATTGAATTACACAAT | 60668 |
rs197657117 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48355989 | CATTATAAAAATAGC[C/T]ACTGTGGCCATAAAT | 60668 |
rs197689753 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342144 | GAACTAGTGGAACAA[A/C]TGGCATAGCACTATG | 60668 |
rs197691393 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48356952 | CAGATTAAATGACAA[A/G]GAACATCTCTGGTGG | 60668 |
rs197695211 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425073 | TGTTTCATGCGTGAG[A/G]CATATGCTGTATGTC | 60668 |
rs197696064 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48336394 | AACTTGTAACCATGA[A/G]TATGTAATGAAAAAA | 60668 |
rs197697567 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48492498 | CCTGGTTAAGAGCTC[C/T]GCTTTCTAATTATGA | 60668 |
rs197698145 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48457200 | CTCAATAAAAAAAAA[A/G]AAAGAAAGAAAAATA | 60668 |
rs197705265 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340860 | AAATAAAGATCGAGA[C/T]TTTCCCCAGATTTCT | 60668 |
rs197713638 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550427 | TTGAAGGCCAAGCTG[G/T]GAAACCTGACATATT | 60668 |
rs197714731 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48336662 | GGATCTCTAACCCAG[C/G]ACAAAAGGTATCCTT | 60668 |
rs197715365 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475348 | GTTTTCAAAGGTCTT[A/G]AGTATGTCTTCCCTT | 60668 |
rs197716635 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425187 | TTCAGTGTGTTAAAA[A/G]TAGTAATCTGGCAAG | 60668 |
rs197717175 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421239 | GCAAATTGAACCAGT[C/T]ATTGTCTTATACAAA | 60668 |
rs197718582 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48556094 | GGCAATAATAAATAA[A/T]AAATAAATCTTTAAA | 60668 |
rs197719125 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48305307 | TTACAAAGAGGGATG[A/G]TCAGATTTAATCTGA | 60668 |
rs197726345 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447216 | CATGGCCTCTGATAC[C/T]ATGGATAAAAGAAGA | 60668 |
rs197729984 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48487108 | CGTATGCTCCTATTC[A/G]GTGGCTCAGTCTCTG | 60668 |
rs197731180 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359888 | CTGCTCTACAACAGA[A/G]TCATGTCACCCCACA | 60668 |
rs197746309 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48478009 | TAAAATTATAATTTT[A/G]CTACCTAAGATAATA | 60668 |
rs197752378 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457643 | ATCACAATCCATTTT[C/G]TATCCTTTTAACTCA | 60668 |
rs197756755 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554585 | TTGACTATGTTCATC[C/T]CCCAACACGCTCCTT | 60668 |
rs197760716 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48453515 | CTCCTGATTGTGGCT[G/T]GGATGTGTGGTAAGC | 60668 |
rs197768629 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450308 | TGTTTGTGTAATGAG[A/G]CACTGTCTCATCACA | 60668 |
rs197785512 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48360614 | TATTCTTATTATTCT[A/C]TTATTCTTAGCTCAA | 60668 |
rs197793641 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48348408 | TCAGGACTAGAAATT[C/G]AAGTCAGTTCTTAAT | 60668 |
rs197793874 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457333 | CATCTGTGCTTTCAG[C/T]CTTTAATTTCTATGA | 60668 |
rs197806969 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48422179 | ATAAGCAGATATTAG[C/T]CCAAAAGCCCAGAAT | 60668 |
rs197814023 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441984 | CAGCCAAGCCACCCG[A/G]CCTTTCATTATAGCC | 60668 |
rs197823233 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48522726 | ACTGTCCATTCCTGG[A/G]CTCCATGTTGGAAAA | 60668 |
rs197829194 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557745 | CGAACAGTACATCCC[A/G]GAAGGAGATAAAAGT | 60668 |
rs197830738 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48353590 | TAGCTTATGGAAAGA[C/T]AAATTGGGGCTTTTT | 60668 |
rs197831655 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48442178 | TCTGCCACTTATTAG[A/G]AACTCTAATAAAAGA | 60668 |
rs197839442 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427331 | ATATATCTCTTTTAT[C/T]TCCTTCAGACCAGGG | 60668 |
rs197840411 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48551576 | ATGAAAAGCAACTTG[A/G]AGAAGAAAGTTTATT | 60668 |
rs197844367 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48467921 | CATGTGTTTGCCTTC[A/T]TGGATCTCTGCAGGC | 60668 |
rs197844527 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48546703 | CACATTTCAGGGTTA[C/T]AATTGCGGGTTGCAT | 60668 |
rs197850628 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48468122 | AAGGACAAAGATGGA[A/T]ATCTAACTTTTAGGT | 60668 |
rs197856056 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450623 | AAGAGTTTATTTTGG[A/C]TTACAGTTCCAGAAT | 60668 |
rs197863974 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352240 | GAGACAGATCAGTGA[A/G]GGGATTGGTATTACT | 60668 |
rs197867385 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48484185 | TTTAAAAAGTAGCAG[A/T]GTTAGCTAGCATTTG | 60668 |
rs197877559 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550611 | AATGCCATGTTCAAG[G/T]GAAGAAAAAGCCACC | 60668 |
rs197878917 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499605 | ACAGCAATTAAGTAT[C/T]TCATGAGTTTGTGAG | 60668 |
rs197879101 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48414974 | AATGCAGGGAAAAGG[A/G]ATGGAGCAGACACTG | 60668 |
rs197879975 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48454922 | TAGAGAATAAAGGGG[A/G]AAAACATCGCCAGGA | 60668 |
rs197884653 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48465824 | ACAAGGAAGAAGCAC[A/G]ATTACAGATAAATAC | 60668 |
rs197890346 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447524 | CACATCAGACTAGGA[C/T]ATTACAGAAGAAAGA | 60668 |
rs197906848 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469173 | GTGGAATTGAGAAGT[G/T]AAAAATGTTTGCTGT | 60668 |
rs197907958 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48432231 | GGGACTTTAGGGTCA[C/T]TATATTGTAGACATA | 60668 |
rs197909980 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550533 | TCTCAGTGACCCAGT[A/G]TGAGGCTATAATGTC | 60668 |
rs197927524 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48451285 | CTCAGAAATACTAGT[C/T]GCTAGAATTGTTGAC | 60668 |
rs197948217 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314907 | ATATTTAAAAGGAAT[C/T]AGTTACTTTTAGAAA | 60668 |
rs197960617 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48501345 | TTGTGTCATTTTTTA[A/G]ATGACCCTAGGTGGT | 60668 |
rs197963321 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489905 | GTCATTTCCCTATGA[G/T]GTTTTGCTGTTCTGT | 60668 |
rs197969902 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48472235 | GCAATAAAGTTTACT[C/T]ATATTTCATATATGA | 60668 |
rs197970250 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48448246 | CAACCTTATGGCATA[C/T]ACTACCAAGTTTGTA | 60668 |
rs197976955 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48558053 | TAGGAGACAACATTT[C/T]TTTTTCATTTCATTC | 60668 |
rs197991733 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48351351 | AAAGTGGTAGGAGGC[A/G]TCAGGGAAGAGTTGA | 60668 |
rs198002378 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48343977 | CTCCCCTTGCTCTGC[G/T]AGGTTTTTGAGATCA | 60668 |
rs198004810 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48452267 | TCTCAGAAGTGCTGA[G/T]AATTCTGAGAGCACA | 60668 |
rs198014446 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48423534 | CTCCTTAAATATCTA[A/G]AGCACAATATTGAAT | 60668 |
rs198017050 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48357280 | GTAACTGAGCCAGAA[A/T]ACTTGAAATAAAAAC | 60668 |
rs198021717 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446201 | ACACCCACTACAAGC[A/G]TAATATCACAGACGA | 60668 |
rs198024615 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314983 | TCTGGCAGGACACTA[C/G]TCATGACTTCAAGCC | 60668 |
rs198038954 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48452735 | ATGGTTGGCCTTAAG[C/T]ATTGGCCTCTGTATT | 60668 |
rs198042325 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420929 | TTTCCAAATTCATTT[A/G]GAGTAACAAAAAACC | 60668 |
rs198043843 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48547983 | AACTTCTTCCAAATA[G/T]TCAGTGTCCTCTCAT | 60668 |
rs198050076 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48440085 | TCGTGTTTCCAAGAC[C/G]CGGCTTTGTTTTGTT | 60668 |
rs198062326 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48320989 | TGGAACTCAGTGGTA[C/G]AGTGCTCCCAGCTGA | 60668 |
rs198070401 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486345 | AGCTAGTTTAATGTC[C/T]AATAAGTCTACACAT | 60668 |
rs198071384 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48496898 | AAGACAATACCTCTG[C/T]CAGACTGCCTATGGG | 60668 |
rs198085217 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48501545 | AAGCTCTCTAATAGA[C/T]TGGAATCATTTTATA | 60668 |
rs198088806 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48456794 | TCACAACTGTCCCTC[C/T]TTTGTTCTAGTAAAA | 60668 |
rs198089847 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498769 | TGGATTACAACCTGT[A/G]AACCAAATAACCTCT | 60668 |
rs198089964 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48492010 | AAAAAATGAAATGAC[A/C]TTTGGAAACCTAGCA | 60668 |
rs198093357 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48440483 | CATTAAATTAATTGT[C/T]ACTAAAATGAAAGCA | 60668 |
rs198094391 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306891 | GGAACAAAGCTAAAT[A/G]ACCTTTAGATATAGA | 60668 |
rs198100184 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48443474 | CATAAAAGAACAAGG[C/T]ACCCACTGTCTCCAT | 60668 |
rs198102378 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474326 | CTTAGAGAAGAGGAA[A/T]TACGATATAAATATT | 60668 |
rs198120395 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466986 | AAAAGAAGGAAACCC[G/T]CAGGAGACCATGGGG | 60668 |
rs198123262 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449095 | GCTGGGTCTTGTCAA[C/T]GACTTGACACAAACC | 60668 |
rs198126590 | snp | C/T | 0.5 | 0 | synonymous-codon | Amph | Rn_Celera | 17:48337874 | GGATAGTGCTCTCAC[C/T]GCTGCCTCCTCCTTT | 60668 |
rs198128329 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48446842 | GGCGCATTCTCTTTC[A/G]ATTGACCCTTAAAAC | 60668 |
rs198135249 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48491694 | GAATGTATTTAAATA[C/T]TTACTAAATCATTTA | 60668 |
rs198142699 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474194 | CAGCTTGAACTTAGT[C/G]AGATCTTACGCAGGT | 60668 |
rs198145750 | snp | A/C/G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48457771 | TTACTGATGGCCTCC[A/C/G/T]ATGTTCNAGGAATAG | 60668 |
rs198148876 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342846 | TCATAGTTTAGCACA[C/T]TTTGGTGTCTGAAAC | 60668 |
rs198157844 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340750 | GAAACACCAATCCAA[C/T]GCCTGTTTCATGCCA | 60668 |
rs198162650 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430625 | AAAGTAAATGGAACA[C/T]ATTCCTCCACATGTC | 60668 |
rs198177608 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427527 | TTCAGTAATATCTCT[G/T]GCTTTCTCACTGAGC | 60668 |
rs198192129 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48466332 | TTTCCAGAGTATAGA[C/T]CATGACAGGTCACCA | 60668 |
rs198226757 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554377 | TACTATCAAGAATGA[A/G]GTGAGTCTGCAAGGC | 60668 |
rs198234298 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352688 | TGTCAAGTGCTTTCC[C/T]CACAACATTTATTAT | 60668 |
rs198235115 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499049 | AATCCTAAGTCACTC[C/G]CATTCATGTCTTATA | 60668 |
rs198266205 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554315 | GTGTCAAATTCTGAG[A/G]AACTTTCGATCAAAG | 60668 |
rs198269257 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48315826 | AGCTATTTATTGCTA[C/T]TGATGACTGTTTAAG | 60668 |
rs198272476 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48524384 | TGCTACAGTTGCAGA[A/G]GTCCCAGATTTAGTT | 60668 |
rs198280990 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48339465 | AGCAAGTATGAAACA[C/T]TGTATAACGCCCACT | 60668 |
rs198283797 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48336524 | TGCTCTAAGACCCCC[C/G]TGACCACTAAACCTG | 60668 |
rs198291847 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48449312 | TTAATTTCATCCATA[C/T]TGATACTTTCCTATT | 60668 |
rs198298594 | snp | A/C/G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48520773 | TGTCTTTATGTTTAT[A/C/G/T]GAAGTCATTATAGTA | 60668 |
rs198301167 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557858 | ACAACCAGATAAGCT[A/G]TTCTTCTGCAGAAAA | 60668 |
rs198329047 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48336692 | TAAGGTCCCTTATAG[A/T]TGCAAAGCCTGTATA | 60668 |
rs198349026 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557976 | AATAATAAACCCAAA[C/T]GTCACCATCAACAAA | 60668 |
rs198356132 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48553427 | CAGACCATAACAAAA[C/T]GGACATGATAAGAGT | 60668 |
rs198365319 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441930 | ATATGCTCACATCCC[C/T]ATCACCAAGATGTGA | 60668 |
rs198374046 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48358351 | CCCCTTGGGTGCCTC[A/T]CCAAACACTGACAGG | 60668 |
rs198384729 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48356376 | AATGGGCCATCATTA[C/T]ACAGCCTTGGACTGG | 60668 |
rs198391475 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425498 | TTGTCACCATGGACC[G/T]CCCCTCCATAATTAA | 60668 |
rs198405900 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48422844 | AGAAGCAGGGATGGG[A/G]GTAGCATAGCAGGTT | 60668 |
rs198408587 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48439211 | TGATGTTCACCTAAT[C/T]GGATTCCACAAGTGT | 60668 |
rs198409251 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48442090 | CCCTCCTTCCAGAAC[A/C]TTTTCTGCACTTATT | 60668 |
rs198413612 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550559 | ATGTCATGACATTGG[A/G]CTTTGGCTAAGTCCA | 60668 |
rs198427657 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48356971 | CATCTCTGGTGGGTA[C/G]TAATTTCAAATTCAG | 60668 |
rs198442447 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48501505 | TTCATGCAGAAAGAA[C/G]AGCTGTACAGTTATC | 60668 |
rs198444417 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48422909 | AAAATGTAAATAAAT[A/G]AAAGCCATTAAAGAA | 60668 |
rs198448143 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48477132 | CTCTTTCATTTGAAG[A/T]CTTTATGGGACTTCT | 60668 |
rs198476980 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48492626 | GCTAAGCTCCTCACT[C/T]ACCAAATCTCTTTTG | 60668 |
rs198497696 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457253 | CCCTAGAAGGACATC[C/T]GACAGCAGCTCAGAA | 60668 |
rs198503030 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48341365 | CAATATGTTAGTCAA[A/T]ACAAATTCTTGAGAC | 60668 |
rs198505458 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48328396 | GAATATGAAAGTGCA[A/G]AAGGTCTTGGGATCT | 60668 |
rs198541021 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48345784 | AGTTTTGCTTTTGAT[A/C]TGTTTCAAGGATCCT | 60668 |
rs198541301 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475010 | GTATAGGGTAATTTC[A/G]TTTAAACTCCATTTA | 60668 |
rs198546839 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48489320 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 60668 |
rs198550386 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450324 | CACTGTCTCATCACA[C/T]TTTCTACCTTGACCA | 60668 |
rs198551791 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48548161 | ATAGAAATAGGACCC[A/G]GAGGTCAAATGTCAA | 60668 |
rs198553822 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420992 | GAACTTATGTGGAAA[G/T]TTCCATCCCTAACCT | 60668 |
rs198554367 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48520995 | TTAAACAATTCATTA[C/T]TTCTTTCAATTAAGT | 60668 |
rs198555767 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447042 | AATATCAAGGGAAAG[C/T]TTGACTGGCTTTCAG | 60668 |
rs198560992 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421065 | TTAGTACAGAGACAG[A/G]CAGGTAGATCAATGG | 60668 |
rs198565433 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441420 | GGGAATACAGTCAAG[C/T]ATCAGCAAGTATGTG | 60668 |
rs198581596 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48315179 | AGGGAGGGAGGGAGG[A/G]AGGAAGGAAGGAAGG | 60668 |
rs198618750 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48458837 | CTGCTCCCAAACCCC[A/G]TGGGAGAGAGACCTC | 60668 |
rs198621466 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359123 | AAGATGAGTATAGTC[C/G]AGGCCAAGAAGGTGG | 60668 |
rs198637866 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499679 | TTAGAAAATATGATA[G/T]ATGATCCATAAATGG | 60668 |
rs198638979 | snp | A/G | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48338568 | AGAGAGGAGAGAGAG[A/G]AGAGAGAGAAAGAGA | 60668 |
rs198639439 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48493831 | GAAATATGGGGAGTC[A/G]TTGAAGGAATCAGAG | 60668 |
rs198643079 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48456188 | GACATAAACATATTC[C/T]CAAGTAGTCATTGTC | 60668 |
rs198648602 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352577 | TATGTTGCAGATGGA[C/T]TGTAGTTAACCTGAA | 60668 |
rs198654967 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48467015 | GGTTCTTGAGATTAT[A/T]AACATCCTCCTTATT | 60668 |
rs198666386 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48472473 | CCAGAAAGGCCTGGA[C/G]TGTCTAAAGTCAACA | 60668 |
rs198696022 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550439 | CTGGGAAACCTGACA[C/T]ATTAGAAGATGACTC | 60668 |
rs198696492 | snp | A/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420880 | GCAATCGTCATCAAA[A/T]ATCCCCAGTCAACTC | 60668 |
rs198699307 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48452896 | ATTTCAGTTGCTCTT[A/C]TTCTGTGTTCATGGG | 60668 |
rs198700846 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48448272 | TTGTAGTGAAGAAAA[C/T]TGAACAGTGAGAAGG | 60668 |
rs198712013 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48419214 | CAATCATTAACCTTA[G/T]AATTTTTGGCCTTTT | 60668 |
rs198746810 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48359842 | GCTCCACATCCCAAC[A/G]TAAGGCATAGTAAGA | 60668 |
rs198750665 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550492 | ATGGGCTTTTGCATC[A/G]GATTCCATTTGTTCA | 60668 |
rs198752618 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48365002 | GCCTCACCACTACTT[C/T]ATAGATGTTAGAAGC | 60668 |
rs198760134 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48431951 | ATGACCTGGAATAAT[C/G]CTCACTACAGTAATA | 60668 |
rs198767559 | snp | A/C | 0 | 0 | upstream-variant-2KB | Amph | Rn_Celera | 17:48563304 | CCAAATGACTGCCCC[A/C]TAAAAATACCTTGAG | 60668 |
rs198770906 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441895 | TCTTCCAACACTGCC[A/G]TTGGACCTGGCCTGG | 60668 |
rs198784392 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494292 | CATTTGCAAAAATCA[C/T]CACTGACAATGATCT | 60668 |
rs198788719 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48550372 | GAAGTTTACCTCCCC[A/G]AAGCTGCCCATTATA | 60668 |
rs198789706 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48486138 | TCTTTTTCATGTTTG[C/T]TGGTTTGTACTTTGT | 60668 |
rs198796895 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48453845 | GGTCTATAGATAAAT[G/T]GTCTGTGCGTGGAAG | 60668 |
rs198806522 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48524494 | GCACTAAACATTCAC[A/G]TGCTACAACACATAC | 60668 |
rs198809837 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554318 | TCAAATTCTGAGGAA[C/T]TTTCGATCAAAGGCA | 60668 |
rs198810697 | snp | A/G | 0 | 0 | upstream-variant-2KB | Amph | Rn_Celera | 17:48562971 | GCAGAGGAGGCAACG[A/G]GTGAGGGAGGGGCGC | 60668 |
rs198812060 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48422137 | AACTAGAAAATATCA[A/T]TTTGAGTGAGGTAAC | 60668 |
rs198818061 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48441935 | CTCACATCCCTATCA[C/T]CAAGATGTGATCTGA | 60668 |
rs198818409 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48510068 | CCCCACCTTGGGATC[A/C]GCCAAACAGCCAAAC | 60668 |
rs198832706 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457313 | TCCAGCAGGGCTGAC[A/G]GGGTCATCTGTGCTT | 60668 |
rs198838543 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48470478 | CCTTGGGCTGAGAAG[C/G]CAGGAGAACATAGGA | 60668 |
rs198856345 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48336649 | TGAGAAGTTGGGTGG[A/G]TCTCTAACCCAGGAC | 60668 |
rs198856469 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557635 | GCATCCATCCATCCC[C/T]GAGGCTGTGTTTCTC | 60668 |
rs198873881 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48457011 | GTGCATACTTAATCG[A/G]CTGCAAGTTCTTAAG | 60668 |
rs198874147 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447187 | GAAACTTTTGTGATA[G/T]GTGGCAAAGTTGACA | 60668 |
rs198879077 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306658 | AAAAGAAAAATAAAT[A/G]TTAAAAATAATGCAA | 60668 |
rs198885712 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48306920 | GAAAACAGACTCTAG[C/T]TCCCTACAGTGTAGT | 60668 |
rs198894113 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48345949 | CTCTCTCTCTCCCAG[A/G]TCTAAATTCTGAAAA | 60668 |
rs198902275 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48355478 | AGAATGAGAAGTTGT[C/T]GTCAGTGTCAATGAC | 60668 |
rs198922547 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48456345 | TGAGTCTGTTATCCT[C/T]GTCTGTTTTCCAGTG | 60668 |
rs198924136 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48326978 | AACAGCCTCCTGGTC[A/G]TAGCTTAAATTTTGA | 60668 |
rs198934219 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48364134 | ACACTGTACCTTAAC[C/T]GTCCATGGGTTAAAC | 60668 |
rs198934356 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340856 | ATTTAAATAAAGATC[C/G]AGACTTTCCCCAGAT | 60668 |
rs198937621 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450908 | CAATACTAGGGTGCA[A/G]TGTACGCCAGTCTAC | 60668 |
rs198950590 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48485773 | ATTGTCCTCTTTTAT[A/T]TTTAGACAATGCCTC | 60668 |
rs198953369 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48514982 | CACACTGGTCTGGAG[C/T]CTATCAGCACAGGAT | 60668 |
rs198962929 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48492493 | AAGCTCCTGGTTAAG[A/C]GCTCCGCTTTCTAAT | 60668 |
rs198967591 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48475295 | ATATATGCATGCAAA[C/T]TTTAGAAAGCTTCTA | 60668 |
rs198971389 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48431933 | ATTATTTCTTTTCTC[A/G]ACATGACCTGGAATA | 60668 |
rs198971856 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314072 | ACACACACACACACA[C/T]ACACACACCATATCA | 60668 |
rs198985427 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554594 | TTCATCCCCCAACAC[A/G]CTCCTTTTTCTCTTC | 60668 |
rs198988995 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48346566 | TTCCTCACAGGTGAA[A/C]AAATATATTAAAGTT | 60668 |
rs199010131 | snp | G/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425226 | CACAAGTTTGACCCC[G/T]GGAATCCATACAGAC | 60668 |
rs199018863 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48444898 | CAAGGCTATAGGGCT[A/T]AAGTATGCATCTAGG | 60668 |
rs199020015 | snp | A/C | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48543279 | ACACACAAACACACA[A/C]ACACACACACACACA | 60668 |
rs199036606 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427719 | GAAGCAACATATTTT[C/G]CTTTGAGAAGATTCC | 60668 |
rs199037608 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554435 | GCACCCATTATACAG[C/T]ATGGTTGAGAAGATT | 60668 |
rs199042320 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48492698 | ATGAGATCAGTCCCT[C/T]GCTTACTAAGACACA | 60668 |
rs199048973 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48474075 | TGGCTTCATTCCCAA[C/T]GGAAAGTGTTCTCCC | 60668 |
rs199049372 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48487230 | GGGTCCCTGACTTCA[A/G]TCCAATGGTTGAGTG | 60668 |
rs199055193 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48546868 | AATAAAGAGCATTGC[A/G]TGAAAGAAATCCAGA | 60668 |
rs199061537 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48494823 | AATGATCTGACTGCT[G/T]TTTGAAGAAGACGTT | 60668 |
rs199065239 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48439842 | CAACATGGAGTTAGA[A/T]GTTTCTTTATCAAAC | 60668 |
rs199066119 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48429164 | ATAAAGAAGGTAATA[A/G]CTGGTGGTTTGGCCA | 60668 |
rs199068824 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48442247 | CAGGCAAGGAGGAAT[G/T]AACATCAGATTTTGT | 60668 |
rs199083236 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48457447 | TTCCTCCAACTCCAC[A/G]GACTGGAACAGTTCT | 60668 |
rs199087389 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48453599 | AACTGTACCCCTTAG[C/T]TTGCATGTGGCATGG | 60668 |
rs199088313 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447238 | AAAAGAAGAAAAGTT[C/T]GTTATATAGGCTGTC | 60668 |
rs199101701 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48348590 | CTTTTTGTCCTCCTC[C/T]TACATCTCCCTGAGT | 60668 |
rs199106597 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48443333 | CCAACAAATTTTAAA[A/G]GTAAAAGAGAACTCA | 60668 |
rs199112766 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48313778 | GCTGGTATGGCTGCT[A/G]CATAAACTTAAAAAA | 60668 |
rs199128451 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48447973 | CACTTCATCCCTATC[C/T]TGGCATTTCCTGACA | 60668 |
rs199128796 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498152 | GCACCCCAAAGTCCC[A/T]TAGAGGGAACTGAAC | 60668 |
rs199131996 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48340026 | TGGGTCATGAGACAT[A/G]GACCAGGAGATATGA | 60668 |
rs199140288 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48498685 | GAATAAGAAGAAGAA[C/T]AAGCAGCACTCTTCC | 60668 |
rs199159507 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48499387 | AAATTACATGTTTTA[G/T]TACTGATGGGAATAG | 60668 |
rs199167140 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48472520 | CAGGGAACAAAGCCC[A/G]CATGAGAAGGGCACA | 60668 |
rs199184034 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48505553 | ATATCTTCAAAAAAA[A/G]TTATAGAAGCAAACT | 60668 |
rs199187408 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48331048 | GCTCTGAGAGTTATG[C/T]TTGGTCTTGATCTCT | 60668 |
rs199196012 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48414692 | GGGTTAGGTGTGCGA[A/G]GAGATGGGAAAGACG | 60668 |
rs199198573 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48420942 | TTAGAGTAACAAAAA[A/G]CCCAAGATAGCAAAA | 60668 |
rs199199861 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48452330 | CCCAAGAGGAACCTG[C/T]CTGGAGCCCTCTGGA | 60668 |
rs199204056 | snp | C/T | 0 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48314955 | CTCTGCCTGTAACCC[C/T]GGCACCCAGGAGTCT | 60668 |
rs199204150 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48445545 | ATGTTATTTTTTTTT[A/T]AAAAAGAGCTCTACT | 60668 |
rs199207235 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421022 | TCAAGCTGTATTGCA[C/G]AGTAATAGTGATAAA | 60668 |
rs199208181 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48361368 | TAACAAGGAGAAATG[A/G]TGACTATCCCAACTG | 60668 |
rs199223151 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48485507 | ACACGGCATGAACAC[A/C]ACAGCACCTGTCTTC | 60668 |
rs199236481 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48558077 | TTCATTCAATTGACA[C/G]TGGAAAAAAAACACA | 60668 |
rs199261283 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48469280 | CTATCAGTATGCTAA[A/G]CCATGTGTCCACCTT | 60668 |
rs199271252 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rnor_6.0 | 17:48450443 | AACACCAGGCAATTT[A/G]GCTTTTTATTGATGG | 60668 |
rs199272835 | snp | C/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48426167 | ACTATGATTCCATCA[C/G]AGGATGACTTGTTGG | 60668 |
rs199277390 | snp | C/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48430846 | CATTGTGGGCAGGGA[C/G]ATAATCCTGATCCAG | 60668 |
rs199280006 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48550409 | TGGTGAAGACACGAG[G/T]ACTTGAAGGCCAAGC | 60668 |
rs199298306 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48342108 | ACAGCTGAGTATCTT[A/T]TGGATCGGAGTCACT | 60668 |
rs199303574 | snp | A/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554379 | CTATCAAGAATGAGG[A/T]GAGTCTGCAAGGCTT | 60668 |
rs199316104 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48425108 | TCACTACCCTGTTCT[A/G]TGCTTTTCAAATGTT | 60668 |
rs199318030 | snp | C/T | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48489358 | TCTCTCTCTCTCTCT[C/T]TTCTTACAAAAAGAG | 60668 |
rs199326633 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48453073 | ACACTCACTCCACAC[C/T]TCATGGGAGGAAATG | 60668 |
rs199357166 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48453306 | ATCACCTAGTGGCAT[A/G]ATTTACTGTCAACCT | 60668 |
rs199370200 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48554517 | CATAGATCCAGGACC[A/G]CTGCCTACCAACAAG | 60668 |
rs199372903 | snp | A/G | 0 | 0 | intron-variant | Amph | Rn_Celera | 17:48421084 | GTAGATCAATGGAAT[A/G]GAATTGAAGTCCCAG | 60668 |
rs199375983 | snp | A/G | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48500300 | GAGACAAAAAATGCT[A/G]ATGTGTTTGGGATTT | 60668 |
rs199394911 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48317160 | GACTGCATGACTCTG[C/T]TTCCTGTCTGTTTGA | 60668 |
rs199399836 | snp | G/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48557559 | CTTCCCCTATTATCG[G/T]AGTAGCAGAAGGCTG | 60668 |
rs199403904 | snp | C/T | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48352879 | ATTTTGTTTTTGTTT[C/T]CTTGGAAGCCAGTTG | 60668 |
rs199417222 | snp | A/C | 0.5 | 0 | intron-variant | Amph | Rn_Celera | 17:48427556 | GCTTGGAGAGTCCAG[A/C]TCTGAGAGGTGTTTA | 60668 |