Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11470 | A01 | 5309628 | G | A | downstream_gene_variant | MODIFIER | c.*2433C>T| |
S274 |
2 | BAA01g11470 | A01 | 5309755 | C | T | downstream_gene_variant | MODIFIER | c.*2306G>A| |
S171 |
3 | BAA01g11470 | A01 | 5310548 | G | A | downstream_gene_variant | MODIFIER | c.*1513C>T| |
S157 S163 |
4 | BAA01g11470 | A01 | 5312256 | C | T | splice_donor_variant&intron_variant | HIGH | c.2055+1G>A| |
S155 S211 |
5 | BAA01g11470 | A01 | 5312763 | C | T | missense_variant | MODERATE | c.1724G>A|p.Gly575Glu |
S18 |
6 | BAA01g11470 | A01 | 5313649 | G | A | missense_variant | MODERATE | c.1316C>T|p.Ser439Phe |
S275 |
7 | BAA01g11470 | A01 | 5314028 | G | A | missense_variant | MODERATE | c.1028C>T|p.Pro343Leu |
S181 |
8 | BAA01g11470 | A01 | 5314978 | G | A | missense_variant | MODERATE | c.713C>T|p.Thr238Ile |
S165 |
9 | BAA01g11470 | A01 | 5316181 | G | A | synonymous_variant | LOW | c.345C>T|p.Ser115Ser |
S271 |
10 | BAA01g11470 | A01 | 5317387 | G | A | missense_variant | MODERATE | c.124C>T|p.Pro42Ser |
S28 |
11 | BAA01g11470 | A01 | 5317830 | C | T | upstream_gene_variant | MODIFIER | c.-320G>A| |
S299 |
12 | BAA01g11470 | A01 | 5318425 | G | A | upstream_gene_variant | MODIFIER | c.-915C>T| |
S169 S225 S73 |
13 | BAA01g11470 | A01 | 5318939 | T | C | upstream_gene_variant | MODIFIER | c.-1429A>G| |
S171 |