Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12080 | A07 | 20533347 | C | T | upstream_gene_variant | MODIFIER | c.-2979C>T| |
S204 |
2 | BAA07g12080 | A07 | 20533894 | G | A | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S125 |
3 | BAA07g12080 | A07 | 20534420 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S211 S227 |
4 | BAA07g12080 | A07 | 20534675 | G | A | upstream_gene_variant | MODIFIER | c.-1651G>A| |
S240 |
5 | BAA07g12080 | A07 | 20534889 | C | T | upstream_gene_variant | MODIFIER | c.-1437C>T| |
S132 S215 S89 |
6 | BAA07g12080 | A07 | 20535025 | C | T | upstream_gene_variant | MODIFIER | c.-1301C>T| |
S232 |
7 | BAA07g12080 | A07 | 20535876 | G | A | upstream_gene_variant | MODIFIER | c.-450G>A| |
S98 |
8 | BAA07g12080 | A07 | 20536985 | G | A | intron_variant | MODIFIER | c.304+16G>A| |
S187 |
9 | BAA07g12080 | A07 | 20537210 | C | T | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S217 S248 |
10 | BAA07g12080 | A07 | 20537438 | G | A | missense_variant | MODERATE | c.691G>A|p.Asp231Asn |
S225 S73 |