Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38050 | A09 | 46087656 | C | T | missense_variant | MODERATE | c.1583G>A|p.Ser528Asn |
S183 S198 |
2 | BAA09g38050 | A09 | 46087936 | C | T | missense_variant&splice_region_variant | MODERATE | c.1387G>A|p.Glu463Lys |
S296 |
3 | BAA09g38050 | A09 | 46088356 | G | A | intron_variant | MODIFIER | c.1225-10C>T| |
S151 S263 |
4 | BAA09g38050 | A09 | 46090456 | C | T | synonymous_variant | LOW | c.15G>A|p.Gln5Gln |
S272 |
5 | BAA09g38050 | A09 | 46091116 | C | T | upstream_gene_variant | MODIFIER | c.-646G>A| |
S152 |
6 | BAA09g38050 | A09 | 46092591 | G | A | upstream_gene_variant | MODIFIER | c.-2121C>T| |
S123 |
7 | BAA09g38050 | A09 | 46093709 | G | A | upstream_gene_variant | MODIFIER | c.-3239C>T| |
S173 |
8 | BAA09g38050 | A09 | 46094303 | C | T | upstream_gene_variant | MODIFIER | c.-3833G>A| |
S287 |
9 | BAA09g38050 | A09 | 46094502 | C | T | upstream_gene_variant | MODIFIER | c.-4032G>A| |
S256 |
10 | BAA09g38050 | A09 | 46094541 | C | T | upstream_gene_variant | MODIFIER | c.-4071G>A| |
S191 |
11 | BAA09g38050 | A09 | 46094896 | C | T | upstream_gene_variant | MODIFIER | c.-4426G>A| |
S251 |