Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21190 | A01 | 10475083 | G | A | upstream_gene_variant | MODIFIER | c.-4867G>A| |
S186 |
2 | BAA01g21190 | A01 | 10475728 | C | T | upstream_gene_variant | MODIFIER | c.-4222C>T| |
S44 |
3 | BAA01g21190 | A01 | 10475764 | C | T | upstream_gene_variant | MODIFIER | c.-4186C>T| |
S305 |
4 | BAA01g21190 | A01 | 10476948 | G | A | upstream_gene_variant | MODIFIER | c.-3002G>A| |
S45 |
5 | BAA01g21190 | A01 | 10476955 | C | T | upstream_gene_variant | MODIFIER | c.-2995C>T| |
S256 |
6 | BAA01g21190 | A01 | 10477443 | C | T | upstream_gene_variant | MODIFIER | c.-2507C>T| |
S81 S85 |
7 | BAA01g21190 | A01 | 10477559 | C | T | upstream_gene_variant | MODIFIER | c.-2391C>T| |
S167 |
8 | BAA01g21190 | A01 | 10479596 | A | G | upstream_gene_variant | MODIFIER | c.-354A>G| |
S122 |
9 | BAA01g21190 | A01 | 10479840 | C | T | upstream_gene_variant | MODIFIER | c.-110C>T| |
S203 |
10 | BAA01g21190 | A01 | 10480374 | T | A | missense_variant | MODERATE | c.425T>A|p.Leu142Gln |
S134 |
11 | BAA01g21190 | A01 | 10483607 | C | T | missense_variant | MODERATE | c.2567C>T|p.Ala856Val |
S182 |
12 | BAA01g21190 | A01 | 10483868 | C | T | missense_variant | MODERATE | c.2828C>T|p.Ala943Val |
S30 S31 |