Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08060 | A05 | 4006027 | C | T | missense_variant | MODERATE | c.749G>A|p.Ser250Asn |
S191 |
2 | BAA05g08060 | A05 | 4006304 | G | A | missense_variant | MODERATE | c.553C>T|p.Pro185Ser |
S278 |
3 | BAA05g08060 | A05 | 4009180 | G | A | upstream_gene_variant | MODIFIER | c.-1476C>T| |
S298 |
4 | BAA05g08060 | A05 | 4011053 | G | A | upstream_gene_variant | MODIFIER | c.-3349C>T| |
S79 S91 |
5 | BAA05g08060 | A05 | 4011495 | C | T | upstream_gene_variant | MODIFIER | c.-3791G>A| |
S205 |
6 | BAA05g08060 | A05 | 4011608 | G | A | upstream_gene_variant | MODIFIER | c.-3904C>T| |
S283 |
7 | BAA05g08060 | A05 | 4012001 | C | T | upstream_gene_variant | MODIFIER | c.-4297G>A| |
S98 |
8 | BAA05g08060 | A05 | 4012114 | A | T | upstream_gene_variant | MODIFIER | c.-4410T>A| |
S105 |
9 | BAA05g08060 | A05 | 4012636 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S241 |