Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g29630 | A09 | 19847841 | C | T | synonymous_variant | LOW | c.51C>T|p.Asn17Asn |
S256 |
2 | BAA09g29630 | A09 | 19848232 | G | A | synonymous_variant | LOW | c.234G>A|p.Arg78Arg |
S46 |
3 | BAA09g29630 | A09 | 19848311 | G | A | missense_variant | MODERATE | c.313G>A|p.Asp105Asn |
S74 |
4 | BAA09g29630 | A09 | 19848548 | G | A | missense_variant | MODERATE | c.475G>A|p.Val159Ile |
S217 S248 |
5 | BAA09g29630 | A09 | 19848781 | G | A | missense_variant | MODERATE | c.640G>A|p.Ala214Thr |
S166 |
6 | BAA09g29630 | A09 | 19848805 | C | T | synonymous_variant | LOW | c.664C>T|p.Leu222Leu |
S272 |
7 | BAA09g29630 | A09 | 19849093 | C | T | synonymous_variant | LOW | c.867C>T|p.Asp289Asp |
S255 |
8 | BAA09g29630 | A09 | 19849589 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1285-1G>A| |
S129 |
9 | BAA09g29630 | A09 | 19849682 | C | T | intron_variant | MODIFIER | c.1368+9C>T| |
S247 |
10 | BAA09g29630 | A09 | 19850549 | C | T | downstream_gene_variant | MODIFIER | c.*77C>T| |
S276 |
11 | BAA09g29630 | A09 | 19850568 | G | A | downstream_gene_variant | MODIFIER | c.*96G>A| |
S121 |
12 | BAA09g29630 | A09 | 19850677 | C | T | downstream_gene_variant | MODIFIER | c.*205C>T| |
S212 |
13 | BAA09g29630 | A09 | 19852526 | C | T | downstream_gene_variant | MODIFIER | c.*2054C>T| |
S234 |
14 | BAA09g29630 | A09 | 19852567 | G | A | downstream_gene_variant | MODIFIER | c.*2095G>A| |
S13 |
15 | BAA09g29630 | A09 | 19853046 | C | T | downstream_gene_variant | MODIFIER | c.*2574C>T| |
S245 |