Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19820 | A01 | 9768188 | G | A | upstream_gene_variant | MODIFIER | c.-2966G>A| |
S232 |
2 | BAA01g19820 | A01 | 9768218 | C | T | upstream_gene_variant | MODIFIER | c.-2936C>T| |
S211 |
3 | BAA01g19820 | A01 | 9768527 | C | T | upstream_gene_variant | MODIFIER | c.-2627C>T| |
S284 |
4 | BAA01g19820 | A01 | 9768645 | C | T | upstream_gene_variant | MODIFIER | c.-2509C>T| |
S19 |
5 | BAA01g19820 | A01 | 9771576 | G | A | synonymous_variant | LOW | c.342G>A|p.Gly114Gly |
S287 |
6 | BAA01g19820 | A01 | 9771587 | G | A | missense_variant | MODERATE | c.353G>A|p.Gly118Glu |
S34 |
7 | BAA01g19820 | A01 | 9772121 | G | A | synonymous_variant | LOW | c.669G>A|p.Ala223Ala |
S245 |
8 | BAA01g19820 | A01 | 9772669 | G | A | missense_variant | MODERATE | c.1136G>A|p.Gly379Asp |
S238 |
9 | BAA01g19820 | A01 | 9772690 | G | A | missense_variant | MODERATE | c.1157G>A|p.Arg386Gln |
S199 |
10 | BAA01g19820 | A01 | 9772704 | G | A | missense_variant | MODERATE | c.1171G>A|p.Asp391Asn |
S124 |