Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09640 | A02 | 4236760 | G | A | synonymous_variant | LOW | c.687C>T|p.Cys229Cys |
S136 |
2 | BAA02g09640 | A02 | 4237444 | G | A | splice_region_variant&intron_variant | LOW | c.273-8C>T| |
S200 S261 S303 |
3 | BAA02g09640 | A02 | 4237533 | G | A | missense_variant&splice_region_variant | MODERATE | c.272C>T|p.Ala91Val |
S171 |
4 | BAA02g09640 | A02 | 4239141 | G | A | missense_variant | MODERATE | c.98C>T|p.Pro33Leu |
S84 S93 |
5 | BAA02g09640 | A02 | 4240415 | C | T | upstream_gene_variant | MODIFIER | c.-1177G>A| |
S144 |
6 | BAA02g09640 | A02 | 4242309 | G | A | upstream_gene_variant | MODIFIER | c.-3071C>T| |
S171 |
7 | BAA02g09640 | A02 | 4242369 | C | T | upstream_gene_variant | MODIFIER | c.-3131G>A| |
S174 S216 S265 S39 |
8 | BAA02g09640 | A02 | 4243254 | C | T | upstream_gene_variant | MODIFIER | c.-4016G>A| |
S31 |
9 | BAA02g09640 | A02 | 4243609 | C | T | upstream_gene_variant | MODIFIER | c.-4371G>A| |
S123 |