Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33490 | A09 | 42064974 | G | A | upstream_gene_variant | MODIFIER | c.-4607G>A| |
S160 |
2 | BAA09g33490 | A09 | 42065636 | G | A | upstream_gene_variant | MODIFIER | c.-3945G>A| |
S16 |
3 | BAA09g33490 | A09 | 42067043 | C | T | upstream_gene_variant | MODIFIER | c.-2538C>T| |
S296 |
4 | BAA09g33490 | A09 | 42067611 | C | T | upstream_gene_variant | MODIFIER | c.-1970C>T| |
S246 |
5 | BAA09g33490 | A09 | 42068013 | C | T | upstream_gene_variant | MODIFIER | c.-1568C>T| |
S182 |
6 | BAA09g33490 | A09 | 42068029 | G | A | upstream_gene_variant | MODIFIER | c.-1552G>A| |
S35 |
7 | BAA09g33490 | A09 | 42068198 | C | T | upstream_gene_variant | MODIFIER | c.-1383C>T| |
S232 |
8 | BAA09g33490 | A09 | 42068461 | C | T | upstream_gene_variant | MODIFIER | c.-1120C>T| |
S219 |
9 | BAA09g33490 | A09 | 42069614 | C | T | missense_variant | MODERATE | c.34C>T|p.Pro12Ser |
S240 |
10 | BAA09g33490 | A09 | 42069816 | G | A | synonymous_variant | LOW | c.135G>A|p.Gly45Gly |
S84 S93 |