Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44290 | A01 | 29441371 | C | T | upstream_gene_variant | MODIFIER | c.-2307C>T| |
S19 |
2 | BAA01g44290 | A01 | 29442775 | G | A | upstream_gene_variant | MODIFIER | c.-903G>A| |
S202 |
3 | BAA01g44290 | A01 | 29442926 | C | T | upstream_gene_variant | MODIFIER | c.-752C>T| |
S177 |
4 | BAA01g44290 | A01 | 29443294 | C | T | upstream_gene_variant | MODIFIER | c.-384C>T| |
S153 S213 |
5 | BAA01g44290 | A01 | 29443639 | C | T | upstream_gene_variant | MODIFIER | c.-39C>T| |
S168 |
6 | BAA01g44290 | A01 | 29443852 | C | T | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S45 |
7 | BAA01g44290 | A01 | 29444415 | C | T | synonymous_variant | LOW | c.492C>T|p.Asp164Asp |
S63 |
8 | BAA01g44290 | A01 | 29444714 | C | T | missense_variant | MODERATE | c.791C>T|p.Ser264Leu |
S182 S218 |
9 | BAA01g44290 | A01 | 29446584 | G | A | missense_variant&splice_region_variant | MODERATE | c.1828G>A|p.Ala610Thr |
S296 |
10 | BAA01g44290 | A01 | 29447649 | G | A | missense_variant | MODERATE | c.2135G>A|p.Gly712Glu |
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