Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17070 | A01 | 8282553 | G | A | downstream_gene_variant | MODIFIER | c.*4918C>T| |
S175 |
2 | BAA01g17070 | A01 | 8282883 | C | T | downstream_gene_variant | MODIFIER | c.*4588G>A| |
S38 |
3 | BAA01g17070 | A01 | 8287854 | G | A | synonymous_variant | LOW | c.916C>T|p.Leu306Leu |
S70 |
4 | BAA01g17070 | A01 | 8287865 | G | A | missense_variant | MODERATE | c.905C>T|p.Ser302Phe |
S139 |
5 | BAA01g17070 | A01 | 8287929 | G | A | missense_variant | MODERATE | c.841C>T|p.Pro281Ser |
S174 S216 S241 S27 S39 |
6 | BAA01g17070 | A01 | 8287959 | G | A | missense_variant | MODERATE | c.811C>T|p.Leu271Phe |
S188 |
7 | BAA01g17070 | A01 | 8287998 | G | A | missense_variant | MODERATE | c.772C>T|p.Leu258Phe |
S124 |
8 | BAA01g17070 | A01 | 8288015 | G | A | missense_variant | MODERATE | c.755C>T|p.Ser252Phe |
S110 |
9 | BAA01g17070 | A01 | 8288564 | C | T | missense_variant | MODERATE | c.288G>A|p.Met96Ile |
S164 |
10 | BAA01g17070 | A01 | 8290553 | C | T | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S213 |