Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04220 | A09 | 2540985 | G | A | upstream_gene_variant | MODIFIER | c.-3137G>A| |
S152 |
2 | BAA09g04220 | A09 | 2544075 | C | T | upstream_gene_variant | MODIFIER | c.-47C>T| |
S280 |
3 | BAA09g04220 | A09 | 2544814 | G | A | missense_variant | MODERATE | c.272G>A|p.Gly91Asp |
S45 |
4 | BAA09g04220 | A09 | 2545614 | G | A | missense_variant | MODERATE | c.796G>A|p.Ala266Thr |
S262 |
5 | BAA09g04220 | A09 | 2545782 | C | T | missense_variant | MODERATE | c.874C>T|p.Leu292Phe |
S249 |
6 | BAA09g04220 | A09 | 2546110 | C | T | missense_variant | MODERATE | c.1051C>T|p.Leu351Phe |
S297 |
7 | BAA09g04220 | A09 | 2546476 | C | T | missense_variant | MODERATE | c.1250C>T|p.Thr417Ile |
S138 |
8 | BAA09g04220 | A09 | 2547001 | G | A | splice_region_variant&intron_variant | LOW | c.1546-8G>A| |
S229 |
9 | BAA09g04220 | A09 | 2548444 | G | A | synonymous_variant | LOW | c.2256G>A|p.Glu752Glu |
S13 |
10 | BAA09g04220 | A09 | 2549633 | G | A | synonymous_variant | LOW | c.3030G>A|p.Arg1010Arg |
S1 S90 |
11 | BAA09g04220 | A09 | 2551670 | C | T | downstream_gene_variant | MODIFIER | c.*1959C>T| |
S246 |
12 | BAA09g04220 | A09 | 2551720 | C | T | downstream_gene_variant | MODIFIER | c.*2009C>T| |
S176 |
13 | BAA09g04220 | A09 | 2552125 | G | A | downstream_gene_variant | MODIFIER | c.*2414G>A| |
S89 |