Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02600 | A09 | 1638277 | G | A | upstream_gene_variant | MODIFIER | c.-4026G>A| |
S293 |
2 | BAA09g02600 | A09 | 1639207 | C | T | upstream_gene_variant | MODIFIER | c.-3096C>T| |
S5 |
3 | BAA09g02600 | A09 | 1639433 | G | A | upstream_gene_variant | MODIFIER | c.-2870G>A| |
S172 S217 |
4 | BAA09g02600 | A09 | 1639550 | G | A | upstream_gene_variant | MODIFIER | c.-2753G>A| |
S291 |
5 | BAA09g02600 | A09 | 1640348 | C | T | upstream_gene_variant | MODIFIER | c.-1955C>T| |
S104 S52 |
6 | BAA09g02600 | A09 | 1641312 | C | T | upstream_gene_variant | MODIFIER | c.-991C>T| |
S257 |
7 | BAA09g02600 | A09 | 1642553 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.170-1G>A| |
S306 S308 |
8 | BAA09g02600 | A09 | 1643047 | G | A | synonymous_variant | LOW | c.501G>A|p.Lys167Lys |
S19 |
9 | BAA09g02600 | A09 | 1643076 | C | T | missense_variant | MODERATE | c.530C>T|p.Ala177Val |
S94 |
10 | BAA09g02600 | A09 | 1643875 | C | T | downstream_gene_variant | MODIFIER | c.*456C>T| |
S203 |
11 | BAA09g02600 | A09 | 1645666 | G | A | downstream_gene_variant | MODIFIER | c.*2247G>A| |
S291 |
12 | BAA09g02600 | A09 | 1646117 | C | T | downstream_gene_variant | MODIFIER | c.*2698C>T| |
S256 |
13 | BAA09g02600 | A09 | 1647681 | G | A | downstream_gene_variant | MODIFIER | c.*4262G>A| |
S97 |
14 | BAA09g02600 | A09 | 1647769 | G | A | downstream_gene_variant | MODIFIER | c.*4350G>A| |
S46 |