Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47850 | A09 | 51927355 | C | T | missense_variant | MODERATE | c.37C>T|p.Arg13Cys |
S92 |
2 | BAA09g47850 | A09 | 51927886 | G | A | missense_variant | MODERATE | c.490G>A|p.Gly164Arg |
S287 |
3 | BAA09g47850 | A09 | 51927895 | C | T | missense_variant | MODERATE | c.499C>T|p.Pro167Ser |
S152 |
4 | BAA09g47850 | A09 | 51928044 | C | T | synonymous_variant | LOW | c.648C>T|p.Phe216Phe |
S104 |
5 | BAA09g47850 | A09 | 51929067 | G | A | missense_variant | MODERATE | c.1435G>A|p.Asp479Asn |
S246 |
6 | BAA09g47850 | A09 | 51929146 | G | A | missense_variant | MODERATE | c.1514G>A|p.Gly505Asp |
S178 |
7 | BAA09g47850 | A09 | 51929191 | C | T | missense_variant | MODERATE | c.1559C>T|p.Pro520Leu |
S18 |
8 | BAA09g47850 | A09 | 51931918 | G | A | downstream_gene_variant | MODIFIER | c.*2327G>A| |
S178 |
9 | BAA09g47850 | A09 | 51931933 | G | A | downstream_gene_variant | MODIFIER | c.*2342G>A| |
S292 |
10 | BAA09g47850 | A09 | 51932354 | C | T | downstream_gene_variant | MODIFIER | c.*2763C>T| |
S8 |
11 | BAA09g47850 | A09 | 51933789 | C | T | downstream_gene_variant | MODIFIER | c.*4198C>T| |
S139 |
12 | BAA09g47850 | A09 | 51933871 | C | T | downstream_gene_variant | MODIFIER | c.*4280C>T| |
S191 |