Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22140 | A01 | 11073592 | G | A | upstream_gene_variant | MODIFIER | c.-692G>A| |
S122 |
2 | BAA01g22140 | A01 | 11074235 | G | A | upstream_gene_variant | MODIFIER | c.-49G>A| |
S293 |
3 | BAA01g22140 | A01 | 11074461 | C | T | stop_gained | HIGH | c.178C>T|p.Gln60* |
S295 |
4 | BAA01g22140 | A01 | 11074616 | G | A | missense_variant | MODERATE | c.239G>A|p.Gly80Asp |
S45 |
5 | BAA01g22140 | A01 | 11074687 | G | A | missense_variant&splice_region_variant | MODERATE | c.310G>A|p.Glu104Lys |
S280 |
6 | BAA01g22140 | A01 | 11075677 | C | T | missense_variant | MODERATE | c.899C>T|p.Ser300Phe |
S130 |
7 | BAA01g22140 | A01 | 11075714 | C | T | synonymous_variant | LOW | c.936C>T|p.Ile312Ile |
S295 |
8 | BAA01g22140 | A01 | 11075742 | G | A | splice_donor_variant&intron_variant | HIGH | c.963+1G>A| |
S116 |
9 | BAA01g22140 | A01 | 11076758 | C | T | missense_variant | MODERATE | c.1274C>T|p.Pro425Leu |
S208 |
10 | BAA01g22140 | A01 | 11077023 | C | T | synonymous_variant | LOW | c.1539C>T|p.Phe513Phe |
S211 S227 |