Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17250 | A09 | 10294627 | G | A | upstream_gene_variant | MODIFIER | c.-4325G>A| |
S265 |
2 | BAA09g17250 | A09 | 10294646 | C | T | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S64 |
3 | BAA09g17250 | A09 | 10295267 | C | T | upstream_gene_variant | MODIFIER | c.-3685C>T| |
S69 |
4 | BAA09g17250 | A09 | 10295977 | C | T | upstream_gene_variant | MODIFIER | c.-2975C>T| |
S133 |
5 | BAA09g17250 | A09 | 10297610 | C | T | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S116 |
6 | BAA09g17250 | A09 | 10298117 | G | A | upstream_gene_variant | MODIFIER | c.-835G>A| |
S69 |
7 | BAA09g17250 | A09 | 10298315 | G | A | upstream_gene_variant | MODIFIER | c.-637G>A| |
S105 S106 |
8 | BAA09g17250 | A09 | 10299933 | C | T | synonymous_variant | LOW | c.208C>T|p.Leu70Leu |
S107 |
9 | BAA09g17250 | A09 | 10300444 | C | T | intron_variant | MODIFIER | c.556-22C>T| |
S216 |
10 | BAA09g17250 | A09 | 10301039 | C | T | splice_region_variant&intron_variant | LOW | c.876-3C>T| |
S143 |
11 | BAA09g17250 | A09 | 10304396 | C | T | synonymous_variant | LOW | c.1470C>T|p.Ile490Ile |
S111 S17 |
12 | BAA09g17250 | A09 | 10304473 | C | T | missense_variant | MODERATE | c.1547C>T|p.Ser516Phe |
S107 |
13 | BAA09g17250 | A09 | 10304546 | C | T | synonymous_variant | LOW | c.1620C>T|p.Phe540Phe |
S83 S88 |