SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs197167082 | snp | C/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67697330 | AGGTATGTATGCTGA[C/T]GCACATCATGACCTG | 315745 |
rs197248649 | snp | A/C | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67696942 | ATTTTTTTAACGTGA[A/C]GAATACTCTCTACTG | 315745 |
rs197341159 | snp | A/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67701309 | CATATGTGCACGTGC[A/T]GGCTGGGAGTGTGAT | 315745 |
rs197461233 | snp | C/T | 0 | 0 | utr-variant-5-prime | Fem1b | Rn_Celera | 8:67708245 | GTGGCCGAGCGCCGC[C/T]GGAGGCACAACTGTG | 315745 |
rs197533841 | snp | A/G | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67705407 | CCTAACTATAATTTT[A/G]CTGTTATGAATCATA | 315745 |
rs197937383 | snp | A/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67697063 | CAAATCTCCAGAACA[A/T]ACTTAGTGACAAGAG | 315745 |
rs198098694 | snp | A/G | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67697499 | AGTTCTCAACCTGTG[A/G]GTCACTACCCTTTTT | 315745 |
rs198130611 | snp | C/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67706184 | AGCTCAGTGGTAGAG[C/T]GCTTGCCTAGCAAGT | 315745 |
rs198361708 | snp | A/G | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67703088 | ATTTTGTGAGACAGG[A/G]TCTCACTAGCTAGCT | 315745 |
rs198611617 | snp | C/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67705287 | ATTCTAGGTGGTAGT[C/T]CCGTTGCTCTAGAGC | 315745 |
rs198873687 | snp | A/C | 0 | 0 | upstream-variant-2KB | Fem1b | Rn_Celera | 8:67710038 | CTGCATGAATGCCTG[A/C]ATGCCTTCAAAAGAA | 315745 |
rs199192094 | snp | C/T | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67699505 | TATAAAATGTAGGGG[C/T]ACAGATGCCACTGCA | 315745 |
rs199336662 | snp | C/G | 0 | 0 | intron-variant | Fem1b | Rn_Celera | 8:67707277 | GTACAACCAAAAATA[C/G]CGGCCAGCATTGTGG | 315745 |