SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs106048609 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64759157 | GCATCCACATTTTGG[C/T]CATCCTTCTTCCTGT | 503446 |
rs107453467 | snp | C/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64759136 | CCCTTTTAAGAAGGA[C/G]TCAAGAATCCACACT | 503446 |
rs107518276 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64759121 | GTCCTTCTTAAACTG[A/G]GGAACAAACATATTC | 503446 |
rs197032195 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64745039 | TGGTACACAGGAGGG[A/G]GCCTCCCCCTTCTGG | 503446 |
rs197044275 | snp | A/C | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64789892 | GAGATTCCACTCACA[A/C]CAGTCAGAATGGTTA | 503446 |
rs197090484 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64734052 | ACCATAGACTTTTTT[C/T]CCTCTGTTTATTTGA | 503446 |
rs197095017 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64763224 | TGAGATGTCATCTTA[C/T]ACTTCTCAGGATGGC | 503446 |
rs197211980 | snp | A/G | 0.5 | 0 | intron-variant | Asb12 | Rn_Celera | X:64755339 | TATCAATTGCAAATT[A/G]TTTCTTGGCTGATGG | 503446 |
rs197230029 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64729628 | TCCTGAGTGCTCAGA[A/G]TAAAGACACGTGCCA | 503446 |
rs197271245 | snp | C/T | 0 | 0 | upstream-variant-2KB | Asb12 | Rn_Celera | X:64802493 | TGTTCCCTTAGATGT[C/T]CCTGATTAAATTAAA | 503446 |
rs197289171 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64768184 | AAAAATTGGCCAGGC[A/G]ACAGGGTAGTGGTGG | 503446 |
rs197360872 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64735790 | CTCCCCCACCCCCGG[A/G]AAGGGGAACTCTGAT | 503446 |
rs197368144 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64757774 | GAGAGCGCAATTAGG[C/T]GTCTCTCTGCAGCTG | 503446 |
rs197444222 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64728657 | TGGACTAGAAGAAGT[C/T]AATGGATCTCTTTGT | 503446 |
rs197461823 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64748420 | CCCAGGCTAGACCCT[G/T]CCCTGCTTATCCCCC | 503446 |
rs197528712 | snp | C/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64728968 | TATATAGAATGTTTT[C/G]ATAACAAATTGCCTA | 503446 |
rs197576429 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64776922 | AAAAGAAAAGAAAAA[A/G]AAAGAAAGAAAAGCA | 503446 |
rs197598542 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64761714 | ACAATCAAAGCCCAG[C/T]TATCCTACCATAGCA | 503446 |
rs197647018 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64772568 | AAACCCATAGTTTGA[A/G]AACTGTTGTTCTAAA | 503446 |
rs197662722 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64797195 | CAATCTACAGATTAA[A/G]TGTAATCCCCATCAA | 503446 |
rs197692247 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64762792 | AAGTACATACATACA[C/T]ACACACACACACACA | 503446 |
rs197753131 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64782599 | CAGAATATCCAAGCA[C/T]ACCAGAAAGGCAAGA | 503446 |
rs197881247 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64771966 | ACATTATTGATTGCA[A/T]CCCACAATCTGGTGG | 503446 |
rs197903240 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64789117 | CTCTCTCTCCCTCTC[C/T]CTCTCTCTCTTTCTT | 503446 |
rs197915178 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64766871 | AATATAACTTTAATG[A/G]TATTGAAGACTGGAC | 503446 |
rs197972748 | snp | A/C | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64756477 | CACACACACACACAC[A/C]CCAGAAGGAAAGGGA | 503446 |
rs197991482 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64743523 | GCCCTTCTCCAGGTA[G/T]AATCTTGCATCTACA | 503446 |
rs198008482 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64730258 | CACTGGAGAAAATTT[C/T]CTGAACAAAACATCA | 503446 |
rs198047602 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64745675 | TGGCTTTTTTCAGGG[A/T]TCTCTTTCCTTTCTT | 503446 |
rs198107220 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64728695 | GCCAATGTGACCACA[C/T]TGAATAAATACCCTT | 503446 |
rs198184723 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64753650 | CAGTGATTCTCACCT[C/T]CCTAATGTGACCCTT | 503446 |
rs198328580 | snp | A/G | 0 | 0 | upstream-variant-2KB | Asb12 | Rn_Celera | X:64801282 | AATAAAGCAAAAAAA[A/G]TAGGAAGATTACTCT | 503446 |
rs198338225 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64794005 | AGGAACATAGGAACA[G/T]TCAGCTGCGGGTATC | 503446 |
rs198364730 | snp | A/T | 0.5 | 0 | intron-variant | Asb12 | Rn_Celera | X:64755284 | GGTTTACCCAGTGAC[A/T]CTTCTTTGGAGAAAA | 503446 |
rs198415471 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64776435 | CTCCACCTCAGTCTA[C/T]CTCCGGGATCCCTGT | 503446 |
rs198435955 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64759359 | TGCTGAGTAGTACTC[C/T]ATTGTGTAGATGTAC | 503446 |
rs198459964 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64729787 | TATTTATCTATTTAT[C/T]TATTATTTAATATAA | 503446 |
rs198536142 | snp | A/C | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64734345 | CATCAATATCACCTT[A/C]ACTGATGGAACCACA | 503446 |
rs198540251 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64777278 | GGCCAGACTCAGCTA[C/T]AGTGAGTTAAAGTCT | 503446 |
rs198566012 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64760031 | ACAAACTCTCTGATC[C/T]TCTGTCTCTTTGATT | 503446 |
rs198596798 | snp | A/C | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64765885 | TGACATTAAAAAAAA[A/C]AACAACAACCAAAGA | 503446 |
rs198689480 | snp | C/G | 0.5 | 0 | intron-variant | Asb12 | Rn_Celera | X:64755377 | TCGTGTCTACTTCCT[C/G]TTTTCAGTGCAGTGA | 503446 |
rs198731237 | snp | C/T | 0 | 0 | upstream-variant-2KB | Asb12 | Rn_Celera | X:64802655 | TTTATATGTTATATA[C/T]GTTTATGTTAATGTA | 503446 |
rs198766498 | snp | C/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64728319 | CTTGTTACTGGCCTG[C/G]CAAAACATCAAAATA | 503446 |
rs198807676 | snp | A/C | 0 | 0 | upstream-variant-2KB | Asb12 | Rn_Celera | X:64800738 | GTCAACCCGCCCACC[A/C]TTGTTCTGTGTGATA | 503446 |
rs198811316 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64770802 | ATTAGTATGGAGAAC[A/T]TTAGAAAGAAAAGTC | 503446 |
rs198811942 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64759883 | TGAGTTCTTTGTATA[A/T]TTTGGATATTAGCCC | 503446 |
rs198861502 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64781484 | AGACACACCTGGGAA[A/G]CCAGAAGAACTACAC | 503446 |
rs198867840 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64772177 | AACCAGCCTGCATGA[C/T]ATACCGATGCATTAG | 503446 |
rs198869945 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64789111 | CCCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 503446 |
rs198878450 | snp | C/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64752958 | ATCTCTAACCTCTTA[C/T]TAGTCCTAGACCTAG | 503446 |
rs198952452 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64753929 | AATAGTTTAACTACA[G/T]TACTTCTCAGAGAAT | 503446 |
rs199034184 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64743138 | CCAACTATTTTTAAG[A/T]CCTCTCTCAGTAAAA | 503446 |
rs199073314 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64761793 | AAGCAGCTATATGAA[G/T]ATGATAGAGGTCGAT | 503446 |
rs199107222 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64745191 | GAGAGAGAAGGAAGG[A/G]AGGAAAGAAAGAAAG | 503446 |
rs199134248 | snp | C/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64773759 | TATGTGGAAATCAAT[C/G]TGAATATACATATAT | 503446 |
rs199176829 | snp | A/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64734344 | GCATCAATATCACCT[A/T]CACTGATGGAACCAC | 503446 |
rs199219800 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Asb12 | Rn_Celera | X:64728087 | AGCTATGGTATATAT[A/G]GTAACATATGGTATA | 503446 |
rs199236933 | snp | G/T | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64790985 | GAGGGAGGGAGGGAG[G/T]GAGTGGGTGGAGGAG | 503446 |
rs199238299 | snp | C/T | 0 | 0 | upstream-variant-2KB | Asb12 | Rn_Celera | X:64802427 | TCCTAATGGTCACTA[C/T]TACTACCTACTGGTG | 503446 |
rs199293947 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64770025 | CATCCTTTCAATGTA[A/G]ACATTATATCATAGT | 503446 |
rs199330245 | snp | A/G | 0 | 0 | intron-variant | Asb12 | Rn_Celera | X:64753908 | GATAAATGTTATCCT[A/G]GGAAAAATAGTTTAA | 503446 |