Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16950 | A10 | 16530245 | C | T | upstream_gene_variant | MODIFIER | c.-315C>T| |
S119 |
2 | BAA10g16950 | A10 | 16531746 | G | A | missense_variant | MODERATE | c.734G>A|p.Gly245Glu |
S271 |
3 | BAA10g16950 | A10 | 16531938 | G | A | missense_variant | MODERATE | c.926G>A|p.Ser309Asn |
S144 |
4 | BAA10g16950 | A10 | 16532873 | C | G | missense_variant | MODERATE | c.1527C>G|p.Asp509Glu |
S121 |
5 | BAA10g16950 | A10 | 16533167 | C | T | missense_variant | MODERATE | c.1735C>T|p.Pro579Ser |
S45 |
6 | BAA10g16950 | A10 | 16533683 | C | T | downstream_gene_variant | MODIFIER | c.*40C>T| |
S175 S189 S211 S226 S250 |
7 | BAA10g16950 | A10 | 16534044 | C | T | downstream_gene_variant | MODIFIER | c.*401C>T| |
S284 |
8 | BAA10g16950 | A10 | 16534126 | G | A | downstream_gene_variant | MODIFIER | c.*483G>A| |
S273 |
9 | BAA10g16950 | A10 | 16534512 | C | T | downstream_gene_variant | MODIFIER | c.*869C>T| |
S152 |
10 | BAA10g16950 | A10 | 16534771 | G | A | downstream_gene_variant | MODIFIER | c.*1128G>A| |
S179 |
11 | BAA10g16950 | A10 | 16535298 | G | A | downstream_gene_variant | MODIFIER | c.*1655G>A| |
S138 |
12 | BAA10g16950 | A10 | 16536707 | C | T | downstream_gene_variant | MODIFIER | c.*3064C>T| |
S46 |
13 | BAA10g16950 | A10 | 16536715 | C | T | downstream_gene_variant | MODIFIER | c.*3072C>T| |
S199 |