SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346432073 | snp | A/G | | | intron-variant | RCE1 | TAIR10 | 4:17341963 | ATCTGCACAGTTCAA[A/G]ATCGGAAAAAACACC | 829833 |
rs346565920 | snp | C/T | | | intron-variant, utr-variant-5-prime | RCE1 | TAIR10 | 4:17342670 | GATTAATCTCTCTCT[C/T]TCGCCTACCGGATTG | 829833 |
rs346618059 | snp | G/T | | | intron-variant | RCE1 | TAIR10 | 4:17342511 | TCAAAACAACGACTA[G/T]GTCGAAACATCGAAA | 829833 |
rs346750155 | snp | G/T | | | intron-variant, utr-variant-5-prime | RCE1 | TAIR10 | 4:17342673 | TAATCTCTCTCTCTC[G/T]CCTACCGGATTGTCG | 829833 |
rs346888573 | snp | A/T | | | utr-variant-3-prime | RCE1 | TAIR10 | 4:17341073 | TTCTCACGAACTTAA[A/T]GTTGACAAGATTTCG | 829833 |
rs346902009 | snp | G/T | | | intron-variant, utr-variant-5-prime | RCE1 | TAIR10 | 4:17342648 | CGAATTAAAAAGGTC[G/T]CCGATTGATTAATCT | 829833 |
rs346907732 | snp | C/G | | | missense | RCE1 | TAIR10 | 4:17341240 | ACCAGAGCTTTGTTA[C/G]ATACAACGCGGGAAA | 829833 |
rs346996502 | snp | A/G | | | intron-variant | RCE1 | TAIR10 | 4:17342461 | CAGGTTCAAAGATCG[A/G]AGACTTTCCTTCCAC | 829833 |
rs347034156 | snp | A/C | | | intron-variant | RCE1 | TAIR10 | 4:17342277 | CGATATATCAAATCA[A/C]AACTGCAACTAAACT | 829833 |
rs347037594 | snp | A/G | | | utr-variant-3-prime | RCE1 | TAIR10 | 4:17341002 | ATTTATAAGGAACCC[A/G]AGAAATGACAAAGAT | 829833 |
rs347110278 | snp | A/G | | | intron-variant | RCE1 | TAIR10 | 4:17342515 | AACAACGACTAGGTC[A/G]AAACATCGAAAGTTA | 829833 |
rs347187311 | snp | C/T | | | intron-variant | RCE1 | TAIR10 | 4:17341595 | AAAACCAACAAAGAG[C/T]TTCTACAACACAAAC | 829833 |
rs347224793 | snp | C/T | | | intron-variant | RCE1 | TAIR10 | 4:17342280 | TATATCAAATCACAA[C/T]TGCAACTAAACTCAT | 829833 |
rs347249920 | snp | G/T | | | utr-variant-5-prime | RCE1 | TAIR10 | 4:17342681 | CTCTCTCGCCTACCG[G/T]ATTGTCGTCCTCTGA | 829833 |
rs347366184 | snp | A/T | | | synonymous-codon | RCE1 | TAIR10 | 4:17341927 | TATTGAACAAGAGCT[A/T]GGAAGGTTCAACTCT | 829833 |