Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21660 | A01 | 10749107 | G | A | missense_variant | MODERATE | c.712G>A|p.Glu238Lys |
S281 |
2 | BAA01g21660 | A01 | 10749191 | C | T | missense_variant | MODERATE | c.796C>T|p.Leu266Phe |
S44 |
3 | BAA01g21660 | A01 | 10749291 | G | A | missense_variant | MODERATE | c.896G>A|p.Gly299Glu |
S162 |
4 | BAA01g21660 | A01 | 10749326 | C | T | synonymous_variant | LOW | c.931C>T|p.Leu311Leu |
S65 |
5 | BAA01g21660 | A01 | 10749527 | G | A | missense_variant | MODERATE | c.1132G>A|p.Glu378Lys |
S94 |
6 | BAA01g21660 | A01 | 10749744 | C | T | splice_region_variant&intron_variant | LOW | c.1341+8C>T| |
S166 |
7 | BAA01g21660 | A01 | 10750870 | G | A | downstream_gene_variant | MODIFIER | c.*911G>A| |
S7 S9 |
8 | BAA01g21660 | A01 | 10751482 | C | T | downstream_gene_variant | MODIFIER | c.*1523C>T| |
S136 |
9 | BAA01g21660 | A01 | 10751632 | G | A | downstream_gene_variant | MODIFIER | c.*1673G>A| |
S84 S93 |
10 | BAA01g21660 | A01 | 10754809 | C | T | downstream_gene_variant | MODIFIER | c.*4850C>T| |
S10 |