Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29390 | A01 | 18542214 | C | T | synonymous_variant | LOW | c.42C>T|p.Ile14Ile |
S255 |
2 | BAA01g29390 | A01 | 18542495 | G | A | missense_variant | MODERATE | c.239G>A|p.Gly80Asp |
S157 |
3 | BAA01g29390 | A01 | 18543150 | G | A | intron_variant | MODIFIER | c.404+140G>A| |
S187 |
4 | BAA01g29390 | A01 | 18544077 | G | A | intron_variant | MODIFIER | c.600+168G>A| |
S218 |
5 | BAA01g29390 | A01 | 18544088 | C | T | intron_variant | MODIFIER | c.600+179C>T| |
S295 |
6 | BAA01g29390 | A01 | 18544251 | C | T | intron_variant | MODIFIER | c.601-82C>T| |
S204 |
7 | BAA01g29390 | A01 | 18545890 | G | A | missense_variant | MODERATE | c.1162G>A|p.Val388Ile |
S168 |
8 | BAA01g29390 | A01 | 18546453 | G | A | downstream_gene_variant | MODIFIER | c.*549G>A| |
S197 |
9 | BAA01g29390 | A01 | 18547066 | C | T | downstream_gene_variant | MODIFIER | c.*1162C>T| |
S155 |
10 | BAA01g29390 | A01 | 18547411 | C | T | downstream_gene_variant | MODIFIER | c.*1507C>T| |
S210 S225 |
11 | BAA01g29390 | A01 | 18547624 | C | T | downstream_gene_variant | MODIFIER | c.*1720C>T| |
S162 |
12 | BAA01g29390 | A01 | 18548811 | G | A | downstream_gene_variant | MODIFIER | c.*2907G>A| |
S263 |