Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g20180 | A07 | 25545474 | G | A | upstream_gene_variant | MODIFIER | c.-4154G>A| |
S1 S90 |
2 | BAA07g20180 | A07 | 25545565 | G | A | upstream_gene_variant | MODIFIER | c.-4063G>A| |
S60 |
3 | BAA07g20180 | A07 | 25545770 | C | T | upstream_gene_variant | MODIFIER | c.-3858C>T| |
S17 |
4 | BAA07g20180 | A07 | 25546423 | G | A | upstream_gene_variant | MODIFIER | c.-3205G>A| |
S31 |
5 | BAA07g20180 | A07 | 25548330 | G | A | upstream_gene_variant | MODIFIER | c.-1298G>A| |
S146 |
6 | BAA07g20180 | A07 | 25548454 | G | A | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S51 |
7 | BAA07g20180 | A07 | 25548456 | G | A | upstream_gene_variant | MODIFIER | c.-1172G>A| |
S112 |
8 | BAA07g20180 | A07 | 25548725 | C | T | upstream_gene_variant | MODIFIER | c.-903C>T| |
S94 |
9 | BAA07g20180 | A07 | 25549637 | C | T | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S133 |
10 | BAA07g20180 | A07 | 25550954 | G | A | splice_region_variant&intron_variant | LOW | c.601+8G>A| |
S295 |