SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs105764795 | snp | A/G | 0 | 0 | intron-variant | Ncf1 | Rn_Celera | 12:25501734 | TCAGGGCAGGAAGCT[A/G]GAGGTAGAAACTCAA | 114553 |
rs106071178 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB | Ncf1, LOC103691302 | Rn_Celera | 12:25500464 | TCTGCGCAGACATCA[C/T]GGGTCCCATCATCCT | 114553 |
rs106803122 | snp | C/T | 0 | 0 | intron-variant | Ncf1, LOC103691302 | Rn_Celera | 12:25498239 | AACCCCTCAGCCTTT[C/T]GTCCAAGGCTAAAAG | 114553 |
rs197082672 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | Ncf1, LOC103691302 | Rn_Celera | 12:25499128 | TCTGGTGCCCCCACG[C/T]AGCTCCCAGGTGGTA | 114553 |
rs197233523 | snp | C/T | 0 | 0 | intron-variant | Ncf1, LOC103691302 | Rn_Celera | 12:25499042 | AGGGTCCCCAGCCCC[C/T]GGGGGGGCCCCTCCT | 114553 |
rs197275371 | snp | A/C | 0 | 0 | synonymous-codon | Ncf1 | Rn_Celera | 12:25504703 | ACAGAGAGCACCAAG[A/C]GGAAACTGACGTCCG | 114553 |
rs197832993 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | Ncf1, LOC103691302 | Rn_Celera | 12:25497101 | ATAGGGAGAAGTGGC[C/T]CTGCCACTGCCCAGC | 114553 |
rs198022540 | snp | C/T | 0 | 0 | missense | Ncf1 | Rn_Celera | 12:25504722 | AACTGACGTCCGCCG[C/T]GTGAGGGGCGGCTGC | 114553 |
rs198510850 | snp | A/G | 0 | 0 | missense, upstream-variant-2KB | Ncf1, LOC103691302 | Rn_Celera | 12:25499217 | CTCATGGGACTGCCC[A/G]TGAAGATCTCCCGCT | 114553 |
rs198581637 | snp | C/T | 0 | 0 | utr-variant-3-prime | Ncf1 | Rn_Celera | 12:25504894 | TAGGATGAGAGGAGG[C/T]AGTCAGCGTTGCTGG | 114553 |
rs198644486 | snp | C/T | 0 | 0 | intron-variant | Ncf1 | Rn_Celera | 12:25503413 | GAACCCAGGGCCTTG[C/T]GCTTCCTAGGTAAGC | 114553 |
rs199101168 | snp | C/G | 0 | 0 | intron-variant | Ncf1, LOC103691302 | Rn_Celera | 12:25499050 | CAGCCCCTGGGGGGG[C/G]CCCTCCTCTGCTCTC | 114553 |