Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13640 | A08 | 11822618 | C | T | upstream_gene_variant | MODIFIER | c.-408C>T| |
S175 |
2 | BAA08g13640 | A08 | 11823172 | G | A | synonymous_variant | LOW | c.147G>A|p.Thr49Thr |
S62 |
3 | BAA08g13640 | A08 | 11823467 | G | A | missense_variant | MODERATE | c.346G>A|p.Glu116Lys |
S297 |
4 | BAA08g13640 | A08 | 11823548 | C | T | missense_variant | MODERATE | c.427C>T|p.Leu143Phe |
S44 |
5 | BAA08g13640 | A08 | 11823880 | C | T | missense_variant | MODERATE | c.658C>T|p.Pro220Ser |
S26 |
6 | BAA08g13640 | A08 | 11823975 | G | A | synonymous_variant | LOW | c.753G>A|p.Leu251Leu |
S103 |
7 | BAA08g13640 | A08 | 11824063 | G | A | missense_variant | MODERATE | c.841G>A|p.Glu281Lys |
S146 |
8 | BAA08g13640 | A08 | 11827549 | G | A | downstream_gene_variant | MODIFIER | c.*2949G>A| |
S116 |
9 | BAA08g13640 | A08 | 11828241 | C | T | downstream_gene_variant | MODIFIER | c.*3641C>T| |
S134 |
10 | BAA08g13640 | A08 | 11828348 | C | T | downstream_gene_variant | MODIFIER | c.*3748C>T| |
S175 |
11 | BAA08g13640 | A08 | 11829152 | C | T | downstream_gene_variant | MODIFIER | c.*4552C>T| |
S74 |
12 | BAA08g13640 | A08 | 11829365 | G | A | downstream_gene_variant | MODIFIER | c.*4765G>A| |
S183 |