Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30660 | A01 | 19613531 | G | A | upstream_gene_variant | MODIFIER | c.-4989G>A| |
S229 |
2 | BAA01g30660 | A01 | 19613641 | C | T | upstream_gene_variant | MODIFIER | c.-4879C>T| |
S98 |
3 | BAA01g30660 | A01 | 19618920 | G | A | intron_variant | MODIFIER | c.150+251G>A| |
S67 |
4 | BAA01g30660 | A01 | 19619415 | C | T | downstream_gene_variant | MODIFIER | c.*126C>T| |
S166 |
5 | BAA01g30660 | A01 | 19620283 | C | T | downstream_gene_variant | MODIFIER | c.*994C>T| |
S48 |
6 | BAA01g30660 | A01 | 19620848 | C | T | downstream_gene_variant | MODIFIER | c.*1559C>T| |
S286 |
7 | BAA01g30660 | A01 | 19621240 | C | T | downstream_gene_variant | MODIFIER | c.*1951C>T| |
S278 |
8 | BAA01g30660 | A01 | 19621476 | C | T | downstream_gene_variant | MODIFIER | c.*2187C>T| |
S107 |
9 | BAA01g30660 | A01 | 19621868 | C | T | downstream_gene_variant | MODIFIER | c.*2579C>T| |
S35 |
10 | BAA01g30660 | A01 | 19621899 | A | G | downstream_gene_variant | MODIFIER | c.*2610A>G| |
S39 |
11 | BAA01g30660 | A01 | 19624042 | G | A | downstream_gene_variant | MODIFIER | c.*4753G>A| |
S223 |