Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31440 | A01 | 20445307 | G | A | upstream_gene_variant | MODIFIER | c.-820G>A| |
S191 |
2 | BAA01g31440 | A01 | 20445311 | G | A | upstream_gene_variant | MODIFIER | c.-816G>A| |
S274 |
3 | BAA01g31440 | A01 | 20445325 | G | A | upstream_gene_variant | MODIFIER | c.-802G>A| |
S55 |
4 | BAA01g31440 | A01 | 20446215 | G | A | missense_variant | MODERATE | c.89G>A|p.Cys30Tyr |
S218 |
5 | BAA01g31440 | A01 | 20446831 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.250-1G>A| |
S95 |
6 | BAA01g31440 | A01 | 20447030 | C | T | missense_variant&splice_region_variant | MODERATE | c.359C>T|p.Ser120Leu |
S271 |
7 | BAA01g31440 | A01 | 20447149 | G | A | missense_variant | MODERATE | c.394G>A|p.Val132Ile |
S278 |
8 | BAA01g31440 | A01 | 20447506 | C | T | missense_variant | MODERATE | c.509C>T|p.Thr170Ile |
S76 |
9 | BAA01g31440 | A01 | 20447703 | C | T | missense_variant | MODERATE | c.617C>T|p.Ser206Phe |
S81 S85 |
10 | BAA01g31440 | A01 | 20452428 | G | A | downstream_gene_variant | MODIFIER | c.*4278G>A| |
S86 |
11 | BAA01g31440 | A01 | 20452526 | C | T | downstream_gene_variant | MODIFIER | c.*4376C>T| |
S20 |
12 | BAA01g31440 | A01 | 20452950 | G | A | downstream_gene_variant | MODIFIER | c.*4800G>A| |
S274 |