Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40140 | A01 | 26699893 | G | A | splice_region_variant&intron_variant | LOW | c.933+5C>T| |
S267 |
2 | BAA01g40140 | A01 | 26700148 | G | A | synonymous_variant | LOW | c.759C>T|p.Phe253Phe |
S139 |
3 | BAA01g40140 | A01 | 26700273 | C | T | missense_variant | MODERATE | c.634G>A|p.Gly212Arg |
S8 |
4 | BAA01g40140 | A01 | 26701049 | G | A | missense_variant | MODERATE | c.151C>T|p.Pro51Ser |
S86 |
5 | BAA01g40140 | A01 | 26701225 | C | T | missense_variant | MODERATE | c.40G>A|p.Val14Ile |
S161 |
6 | BAA01g40140 | A01 | 26701364 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S257 |
7 | BAA01g40140 | A01 | 26701520 | G | A | upstream_gene_variant | MODIFIER | c.-256C>T| |
S169 |
8 | BAA01g40140 | A01 | 26701545 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S263 |
9 | BAA01g40140 | A01 | 26702339 | C | T | upstream_gene_variant | MODIFIER | c.-1075G>A| |
S144 |
10 | BAA01g40140 | A01 | 26704359 | C | T | upstream_gene_variant | MODIFIER | c.-3095G>A| |
S69 |