Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g63720 | A09 | 59488848 | G | A | upstream_gene_variant | MODIFIER | c.-3776G>A| |
S225 |
2 | BAA09g63720 | A09 | 59488923 | G | A | upstream_gene_variant | MODIFIER | c.-3701G>A| |
S36 |
3 | BAA09g63720 | A09 | 59489248 | C | T | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S50 |
4 | BAA09g63720 | A09 | 59489974 | G | A | upstream_gene_variant | MODIFIER | c.-2650G>A| |
S180 |
5 | BAA09g63720 | A09 | 59490529 | G | A | upstream_gene_variant | MODIFIER | c.-2095G>A| |
S57 |
6 | BAA09g63720 | A09 | 59490636 | C | T | upstream_gene_variant | MODIFIER | c.-1988C>T| |
S219 S72 |
7 | BAA09g63720 | A09 | 59491241 | C | T | upstream_gene_variant | MODIFIER | c.-1383C>T| |
S138 |
8 | BAA09g63720 | A09 | 59492712 | C | T | missense_variant | MODERATE | c.89C>T|p.Thr30Ile |
S5 |
9 | BAA09g63720 | A09 | 59493809 | C | T | missense_variant | MODERATE | c.1186C>T|p.Pro396Ser |
S302 |
10 | BAA09g63720 | A09 | 59494003 | G | A | synonymous_variant | LOW | c.1380G>A|p.Glu460Glu |
S262 |