Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07380 | A09 | 4111981 | G | A | synonymous_variant | LOW | c.375G>A|p.Arg125Arg |
S167 |
2 | BAA09g07380 | A09 | 4112201 | C | T | synonymous_variant | LOW | c.595C>T|p.Leu199Leu |
S120 |
3 | BAA09g07380 | A09 | 4112237 | G | A | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S162 |
4 | BAA09g07380 | A09 | 4112580 | C | T | missense_variant | MODERATE | c.872C>T|p.Ala291Val |
S95 |
5 | BAA09g07380 | A09 | 4113343 | C | T | missense_variant | MODERATE | c.1321C>T|p.His441Tyr |
S117 |
6 | BAA09g07380 | A09 | 4113470 | G | A | missense_variant | MODERATE | c.1448G>A|p.Gly483Asp |
S172 S217 |
7 | BAA09g07380 | A09 | 4113634 | G | A | synonymous_variant | LOW | c.1521G>A|p.Gln507Gln |
S276 |
8 | BAA09g07380 | A09 | 4113809 | G | A | missense_variant | MODERATE | c.1696G>A|p.Val566Ile |
S17 |
9 | BAA09g07380 | A09 | 4116972 | C | T | downstream_gene_variant | MODIFIER | c.*2556C>T| |
S87 |
10 | BAA09g07380 | A09 | 4119209 | G | A | downstream_gene_variant | MODIFIER | c.*4793G>A| |
S166 |