SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8156609 | snp | A/G | 0 | 0 | utr-variant-3-prime | Bfar | Rn_Celera | 10:1497312 | GTAGCACTTGGCATA[A/G]TTATACATGCTTTTA | 304709 |
rs13453608 | snp | A/G | 0.336298 | 0.234633 | missense | Bfar | Rn_Celera | 10:1496378 | CTGGTGGTCAAGGAA[A/G]TCCGACGGCTGGAAA | 304709 |
rs106038820 | snp | C/T | 0.214158 | 0.247417 | intron-variant, utr-variant-5-prime | Bfar, RGD1305537 | Rn_Celera | 10:1469637 | AGAGGTCTGGTTGCA[C/T]GCGCTGGTGGGTAAA | 304709 |
rs197224422 | snp | G/T | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485510 | TACAACCATTTCCAG[G/T]CATTTCCTGACTCCC | 304709 |
rs197302150 | snp | G/T | 0 | 0 | missense | Bfar | Rn_Celera | 10:1485083 | CTGTCTCCTTTCAGG[G/T]CATCCTGCTTGTGTA | 304709 |
rs197403385 | snp | A/C/G/T | 0 | 0 | intron-variant | Bfar, RGD1305537 | Rn_Celera | 10:1465985 | AACCCAAAGTTAAGT[A/C/G/T]TTCAGAGTGAGGCTA | 304709 |
rs197674910 | snp | A/C | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485263 | GAAGGTGAGGAATTA[A/C]AATCTGTCACACCAA | 304709 |
rs197755687 | snp | G/T | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485363 | GCCTGGCAACTATCA[G/T]GCCACAAGGTGACAT | 304709 |
rs198025834 | snp | C/G | 0 | 0 | intron-variant | Bfar, RGD1305537 | Rn_Celera | 10:1468943 | TACCAGATGGTCTTA[C/G]GCAACTCCTGCAAGA | 304709 |
rs198091826 | snp | A/G | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485929 | TTGGAGCTCTTTGAA[A/G]AGTGCTGCTAAAGTC | 304709 |
rs198223259 | snp | G/T | 0 | 0 | missense | Bfar | Rn_Celera | 10:1485151 | GTGCACAAGGCTGTA[G/T]ACAAATGGACGACAG | 304709 |
rs198547581 | snp | C/G | 0 | 0 | intron-variant | Bfar, RGD1305537 | Rn_Celera | 10:1468872 | AGGACTATTGCACTA[C/G]GAGAAAGTAAATCTA | 304709 |
rs198939916 | snp | A/T | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485338 | CAGAGCTCTTGTGAG[A/T]TTGAGGCCAGCCTGG | 304709 |
rs198982654 | snp | C/G | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485460 | AATCCTTTTCTTACA[C/G]AAGTGAATGTGTTTG | 304709 |
rs199042996 | snp | G/T | 0 | 0 | intron-variant | Bfar | Rn_Celera | 10:1485301 | GTGGTGGTGCAAGCA[G/T]GCCTTTAATCTCAGA | 304709 |