Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10120 | A04 | 16345835 | C | T | missense_variant&splice_region_variant | MODERATE | c.772G>A|p.Gly258Ser |
S263 |
2 | BAA04g10120 | A04 | 16346084 | G | A | missense_variant | MODERATE | c.701C>T|p.Pro234Leu |
S130 |
3 | BAA04g10120 | A04 | 16346948 | G | A | missense_variant | MODERATE | c.400C>T|p.Leu134Phe |
S125 |
4 | BAA04g10120 | A04 | 16347190 | G | A | missense_variant | MODERATE | c.301C>T|p.Leu101Phe |
S266 |
5 | BAA04g10120 | A04 | 16347694 | G | A | missense_variant | MODERATE | c.196C>T|p.Leu66Phe |
S241 |
6 | BAA04g10120 | A04 | 16348363 | C | T | upstream_gene_variant | MODIFIER | c.-474G>A| |
S180 |
7 | BAA04g10120 | A04 | 16349282 | C | T | upstream_gene_variant | MODIFIER | c.-1393G>A| |
S148 |
8 | BAA04g10120 | A04 | 16351729 | G | A | upstream_gene_variant | MODIFIER | c.-3840C>T| |
S161 |
9 | BAA04g10120 | A04 | 16352045 | C | T | upstream_gene_variant | MODIFIER | c.-4156G>A| |
S268 |
10 | BAA04g10120 | A04 | 16352215 | C | T | upstream_gene_variant | MODIFIER | c.-4326G>A| |
S192 |
11 | BAA04g10120 | A04 | 16352660 | G | A | upstream_gene_variant | MODIFIER | c.-4771C>T| |
S259 |
12 | BAA04g10120 | A04 | 16352669 | G | A | upstream_gene_variant | MODIFIER | c.-4780C>T| |
S218 |