SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs104899705 | snp | A/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | Btbd19, Tctex1d4 | Rn_Celera | 5:135994803 | GGCCCGGGTCCCTAA[A/T]GTAGTCCTGAGGTTC | 100361234 |
rs105185842 | snp | A/T | 0 | 0 | utr-variant-3-prime | Btbd19 | Rn_Celera | 5:135989388 | GGGCCCACTGTCCAA[A/T]CCCTACTCTCCCACG | 100361234 |
rs105494044 | snp | C/T | 0 | 0 | intron-variant | Btbd19 | Rn_Celera | 5:135992406 | GGACAATTTAATAAC[C/T]CAGGACCTCTGGAAG | 100361234 |
rs105707629 | snp | G/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | Btbd19 | Rn_Celera | 5:135988790 | GAGCGAGCACTATGA[G/T]CTCAAAGCTAACCGG | 100361234 |
rs105740504 | snp | A/T | 0 | 0 | utr-variant-3-prime | Btbd19 | Rn_Celera | 5:135989522 | AACTGTAGTTTGGGG[A/T]GTGGTTAACGTCCTA | 100361234 |
rs105817018 | snp | G/T | 0 | 0 | intron-variant | Btbd19 | Rn_Celera | 5:135992632 | ACACTCTGTAGTTCA[G/T]GTTAGCCTGGGAACT | 100361234 |
rs105928530 | snp | A/C | 0 | 0 | intron-variant, missense | Btbd19 | Rn_Celera | 5:135990000 | CGCCGCTTCAGCGTC[A/C]TCGTCCAACCCCCAG | 100361234 |
rs106006739 | snp | C/T | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Btbd19, Tctex1d4 | Rn_Celera | 5:135996222 | TAGGAGGAAAAAAGT[C/T]CCACCAGACTTAGAG | 100361234 |
rs107076108 | snp | A/C | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | Btbd19, Tctex1d4 | Rn_Celera | 5:135994697 | AACAGCCCAGAAGAC[A/C]CAGCCAGGCCAACAA | 100361234 |
rs198480389 | snp | A/C | 0 | 0 | intron-variant | Btbd19 | Rn_Celera | 5:135990642 | TTTTCAAGATGGGCC[A/C]TATGTAGCCCTGGTT | 100361234 |