Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g55840 | A03 | 27560523 | G | A | missense_variant | MODERATE | c.3110C>T|p.Ser1037Phe |
S77 S82 |
2 | BAA03g55840 | A03 | 27560820 | G | A | missense_variant | MODERATE | c.2897C>T|p.Ser966Phe |
S297 |
3 | BAA03g55840 | A03 | 27561258 | C | A | missense_variant | MODERATE | c.2666G>T|p.Cys889Phe |
S187 |
4 | BAA03g55840 | A03 | 27562143 | C | T | missense_variant&splice_region_variant | MODERATE | c.2158G>A|p.Asp720Asn |
S136 |
5 | BAA03g55840 | A03 | 27563736 | C | T | splice_region_variant&intron_variant | LOW | c.1446+5G>A| |
S263 |
6 | BAA03g55840 | A03 | 27563812 | G | A | missense_variant | MODERATE | c.1375C>T|p.Leu459Phe |
S283 |
7 | BAA03g55840 | A03 | 27564106 | G | A | synonymous_variant | LOW | c.1152C>T|p.Val384Val |
S261 |
8 | BAA03g55840 | A03 | 27565504 | C | T | intron_variant | MODIFIER | c.408+39G>A| |
S107 |
9 | BAA03g55840 | A03 | 27565548 | G | A | missense_variant | MODERATE | c.403C>T|p.Arg135Cys |
S223 |
10 | BAA03g55840 | A03 | 27566195 | G | A | upstream_gene_variant | MODIFIER | c.-128C>T| |
S259 |
11 | BAA03g55840 | A03 | 27567578 | G | A | upstream_gene_variant | MODIFIER | c.-1511C>T| |
S132 S137 S215 S89 |
12 | BAA03g55840 | A03 | 27567717 | C | T | upstream_gene_variant | MODIFIER | c.-1650G>A| |
S6 |