Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46630 | A09 | 51304097 | G | A | downstream_gene_variant | MODIFIER | c.*2800C>T| |
S216 |
2 | BAA09g46630 | A09 | 51304527 | G | A | downstream_gene_variant | MODIFIER | c.*2370C>T| |
S127 |
3 | BAA09g46630 | A09 | 51304557 | G | A | downstream_gene_variant | MODIFIER | c.*2340C>T| |
S264 |
4 | BAA09g46630 | A09 | 51305347 | C | T | downstream_gene_variant | MODIFIER | c.*1550G>A| |
S213 |
5 | BAA09g46630 | A09 | 51305910 | G | A | downstream_gene_variant | MODIFIER | c.*987C>T| |
S295 S30 S31 S54 |
6 | BAA09g46630 | A09 | 51306188 | G | A | downstream_gene_variant | MODIFIER | c.*709C>T| |
S221 |
7 | BAA09g46630 | A09 | 51306527 | C | T | downstream_gene_variant | MODIFIER | c.*370G>A| |
S278 |
8 | BAA09g46630 | A09 | 51307439 | C | T | splice_region_variant&intron_variant | LOW | c.489-8G>A| |
S9 |
9 | BAA09g46630 | A09 | 51307849 | C | T | missense_variant | MODERATE | c.374G>A|p.Ser125Asn |
S261 |
10 | BAA09g46630 | A09 | 51308548 | C | T | upstream_gene_variant | MODIFIER | c.-176G>A| |
S192 |
11 | BAA09g46630 | A09 | 51308811 | C | T | upstream_gene_variant | MODIFIER | c.-439G>A| |
S168 |
12 | BAA09g46630 | A09 | 51309019 | G | A | upstream_gene_variant | MODIFIER | c.-647C>T| |
S52 |
13 | BAA09g46630 | A09 | 51312279 | G | A | upstream_gene_variant | MODIFIER | c.-3907C>T| |
S132 S137 S215 |
14 | BAA09g46630 | A09 | 51312524 | G | A | upstream_gene_variant | MODIFIER | c.-4152C>T| |
S218 |
15 | BAA09g46630 | A09 | 51312793 | G | A | upstream_gene_variant | MODIFIER | c.-4421C>T| |
S165 |