Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19850 | A09 | 12223614 | C | T | downstream_gene_variant | MODIFIER | c.*1263G>A| |
S296 |
2 | BAA09g19850 | A09 | 12223831 | G | A | downstream_gene_variant | MODIFIER | c.*1046C>T| |
S244 |
3 | BAA09g19850 | A09 | 12224440 | G | A | downstream_gene_variant | MODIFIER | c.*437C>T| |
S151 |
4 | BAA09g19850 | A09 | 12224596 | G | A | downstream_gene_variant | MODIFIER | c.*281C>T| |
S170 |
5 | BAA09g19850 | A09 | 12225169 | C | T | splice_region_variant&intron_variant | LOW | c.1064-3G>A| |
S256 |
6 | BAA09g19850 | A09 | 12225204 | C | T | intron_variant | MODIFIER | c.1064-38G>A| |
S158 |
7 | BAA09g19850 | A09 | 12225458 | C | T | intron_variant | MODIFIER | c.1063+176G>A| |
S242 |
8 | BAA09g19850 | A09 | 12225840 | C | T | splice_donor_variant&intron_variant | HIGH | c.944+1G>A| |
S171 |
9 | BAA09g19850 | A09 | 12226422 | G | A | missense_variant | MODERATE | c.512C>T|p.Ala171Val |
S34 |
10 | BAA09g19850 | A09 | 12226468 | C | T | missense_variant | MODERATE | c.466G>A|p.Asp156Asn |
S242 |
11 | BAA09g19850 | A09 | 12228031 | G | A | upstream_gene_variant | MODIFIER | c.-721C>T| |
S245 |
12 | BAA09g19850 | A09 | 12228304 | C | T | upstream_gene_variant | MODIFIER | c.-994G>A| |
S293 |
13 | BAA09g19850 | A09 | 12230823 | C | T | upstream_gene_variant | MODIFIER | c.-3513G>A| |
S292 |