Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09960 | A08 | 9064445 | T | C | upstream_gene_variant | MODIFIER | c.-4413T>C| |
S115 S117 S120 S122 |
2 | BAA08g09960 | A08 | 9065472 | C | T | upstream_gene_variant | MODIFIER | c.-3386C>T| |
S236 |
3 | BAA08g09960 | A08 | 9065666 | C | T | upstream_gene_variant | MODIFIER | c.-3192C>T| |
S15 S3 |
4 | BAA08g09960 | A08 | 9066231 | G | A | upstream_gene_variant | MODIFIER | c.-2627G>A| |
S261 S274 |
5 | BAA08g09960 | A08 | 9066942 | G | A | upstream_gene_variant | MODIFIER | c.-1916G>A| |
S269 |
6 | BAA08g09960 | A08 | 9067198 | G | A | upstream_gene_variant | MODIFIER | c.-1660G>A| |
S86 |
7 | BAA08g09960 | A08 | 9068455 | G | A | upstream_gene_variant | MODIFIER | c.-403G>A| |
S280 |
8 | BAA08g09960 | A08 | 9068645 | G | A | upstream_gene_variant | MODIFIER | c.-213G>A| |
S155 |
9 | BAA08g09960 | A08 | 9069097 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.148-1G>A| |
S116 |
10 | BAA08g09960 | A08 | 9070908 | C | T | synonymous_variant | LOW | c.1722C>T|p.Ile574Ile |
S157 S163 |
11 | BAA08g09960 | A08 | 9070946 | C | T | missense_variant | MODERATE | c.1760C>T|p.Ser587Phe |
S88 |
12 | BAA08g09960 | A08 | 9071507 | G | A | missense_variant | MODERATE | c.2321G>A|p.Ser774Asn |
S234 |