Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g67090 | A03 | 41582968 | G | A | missense_variant | MODERATE | c.1849C>T|p.Pro617Ser |
S6 |
2 | BAA03g67090 | A03 | 41583061 | C | T | missense_variant | MODERATE | c.1756G>A|p.Asp586Asn |
S139 |
3 | BAA03g67090 | A03 | 41583087 | C | T | missense_variant | MODERATE | c.1730G>A|p.Gly577Glu |
S142 |
4 | BAA03g67090 | A03 | 41583714 | G | A | missense_variant | MODERATE | c.1103C>T|p.Ala368Val |
S60 |
5 | BAA03g67090 | A03 | 41584101 | G | A | missense_variant | MODERATE | c.784C>T|p.Pro262Ser |
S182 |
6 | BAA03g67090 | A03 | 41584295 | C | T | missense_variant | MODERATE | c.590G>A|p.Arg197Lys |
S203 |
7 | BAA03g67090 | A03 | 41584318 | C | T | stop_gained | HIGH | c.567G>A|p.Trp189* |
S79 S84 |
8 | BAA03g67090 | A03 | 41584701 | A | G | synonymous_variant | LOW | c.237T>C|p.Asn79Asn |
S176 |
9 | BAA03g67090 | A03 | 41585197 | G | A | upstream_gene_variant | MODIFIER | c.-5C>T| |
S143 |
10 | BAA03g67090 | A03 | 41585898 | G | A | upstream_gene_variant | MODIFIER | c.-706C>T| |
S150 |
11 | BAA03g67090 | A03 | 41586333 | G | A | upstream_gene_variant | MODIFIER | c.-1141C>T| |
S111 |
12 | BAA03g67090 | A03 | 41586746 | C | T | upstream_gene_variant | MODIFIER | c.-1554G>A| |
S30 S31 |
13 | BAA03g67090 | A03 | 41590075 | C | T | upstream_gene_variant | MODIFIER | c.-4883G>A| |
S232 |
14 | BAA03g67090 | A03 | 41590086 | C | T | upstream_gene_variant | MODIFIER | c.-4894G>A| |
S67 |
15 | BAA03g67090 | A03 | 41590190 | C | T | upstream_gene_variant | MODIFIER | c.-4998G>A| |
S59 |