Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01000 | A09 | 753119 | G | A | upstream_gene_variant | MODIFIER | c.-3780G>A| |
S271 |
2 | BAA09g01000 | A09 | 754068 | C | T | upstream_gene_variant | MODIFIER | c.-2831C>T| |
S270 |
3 | BAA09g01000 | A09 | 754453 | C | T | upstream_gene_variant | MODIFIER | c.-2446C>T| |
S177 |
4 | BAA09g01000 | A09 | 754840 | G | A | upstream_gene_variant | MODIFIER | c.-2059G>A| |
S146 |
5 | BAA09g01000 | A09 | 754858 | C | T | upstream_gene_variant | MODIFIER | c.-2041C>T| |
S55 |
6 | BAA09g01000 | A09 | 755030 | G | A | upstream_gene_variant | MODIFIER | c.-1869G>A| |
S46 |
7 | BAA09g01000 | A09 | 755433 | C | T | upstream_gene_variant | MODIFIER | c.-1466C>T| |
S43 |
8 | BAA09g01000 | A09 | 757639 | G | A | missense_variant | MODERATE | c.500G>A|p.Gly167Glu |
S175 |
9 | BAA09g01000 | A09 | 757656 | C | T | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S35 |
10 | BAA09g01000 | A09 | 758685 | C | T | synonymous_variant | LOW | c.1293C>T|p.Ile431Ile |
S57 |
11 | BAA09g01000 | A09 | 759723 | G | A | downstream_gene_variant | MODIFIER | c.*915G>A| |
S231 |
12 | BAA09g01000 | A09 | 759871 | C | T | downstream_gene_variant | MODIFIER | c.*1063C>T| |
S64 |