Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47380 | A09 | 51707895 | C | T | upstream_gene_variant | MODIFIER | c.-621C>T| |
S240 |
2 | BAA09g47380 | A09 | 51708969 | C | T | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S151 S166 S167 S262 S263 |
3 | BAA09g47380 | A09 | 51709504 | G | A | missense_variant | MODERATE | c.989G>A|p.Arg330Lys |
S54 |
4 | BAA09g47380 | A09 | 51709671 | G | A | missense_variant | MODERATE | c.1156G>A|p.Glu386Lys |
S247 |
5 | BAA09g47380 | A09 | 51711209 | G | A | downstream_gene_variant | MODIFIER | c.*1245G>A| |
S70 |
6 | BAA09g47380 | A09 | 51712363 | C | T | downstream_gene_variant | MODIFIER | c.*2399C>T| |
S297 |
7 | BAA09g47380 | A09 | 51712366 | C | T | downstream_gene_variant | MODIFIER | c.*2402C>T| |
S211 S262 |
8 | BAA09g47380 | A09 | 51713210 | C | T | downstream_gene_variant | MODIFIER | c.*3246C>T| |
S295 |
9 | BAA09g47380 | A09 | 51713629 | C | T | downstream_gene_variant | MODIFIER | c.*3665C>T| |
S160 |
10 | BAA09g47380 | A09 | 51713745 | G | A | downstream_gene_variant | MODIFIER | c.*3781G>A| |
S42 |