Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23050 | A01 | 11770619 | C | T | upstream_gene_variant | MODIFIER | c.-4795C>T| |
S200 |
2 | BAA01g23050 | A01 | 11773317 | C | T | upstream_gene_variant | MODIFIER | c.-2097C>T| |
S42 |
3 | BAA01g23050 | A01 | 11775178 | C | T | upstream_gene_variant | MODIFIER | c.-236C>T| |
S36 |
4 | BAA01g23050 | A01 | 11775279 | G | A | upstream_gene_variant | MODIFIER | c.-135G>A| |
S187 |
5 | BAA01g23050 | A01 | 11776236 | C | T | missense_variant | MODERATE | c.289C>T|p.Pro97Ser |
S55 |
6 | BAA01g23050 | A01 | 11776474 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.435-1G>A| |
S43 |
7 | BAA01g23050 | A01 | 11778442 | C | T | downstream_gene_variant | MODIFIER | c.*139C>T| |
S54 |
8 | BAA01g23050 | A01 | 11779805 | G | A | downstream_gene_variant | MODIFIER | c.*1502G>A| |
S199 |
9 | BAA01g23050 | A01 | 11780260 | C | T | downstream_gene_variant | MODIFIER | c.*1957C>T| |
S148 S210 S30 S31 |
10 | BAA01g23050 | A01 | 11780303 | C | T | downstream_gene_variant | MODIFIER | c.*2000C>T| |
S107 |
11 | BAA01g23050 | A01 | 11780642 | G | A | downstream_gene_variant | MODIFIER | c.*2339G>A| |
S246 |