Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19950 | A09 | 12293372 | C | T | missense_variant | MODERATE | c.2320G>A|p.Gly774Ser |
S76 |
2 | BAA09g19950 | A09 | 12293474 | C | T | missense_variant | MODERATE | c.2218G>A|p.Ala740Thr |
S208 S93 |
3 | BAA09g19950 | A09 | 12293631 | C | T | synonymous_variant | LOW | c.2061G>A|p.Arg687Arg |
S6 |
4 | BAA09g19950 | A09 | 12294744 | C | T | stop_gained | HIGH | c.948G>A|p.Trp316* |
S263 |
5 | BAA09g19950 | A09 | 12295022 | C | T | missense_variant | MODERATE | c.670G>A|p.Ala224Thr |
S11 |
6 | BAA09g19950 | A09 | 12295607 | G | A | synonymous_variant | LOW | c.253C>T|p.Leu85Leu |
S188 |
7 | BAA09g19950 | A09 | 12295646 | C | T | missense_variant | MODERATE | c.214G>A|p.Asp72Asn |
S272 S287 |
8 | BAA09g19950 | A09 | 12296227 | G | A | upstream_gene_variant | MODIFIER | c.-368C>T| |
S89 |
9 | BAA09g19950 | A09 | 12296285 | C | T | upstream_gene_variant | MODIFIER | c.-426G>A| |
S303 |
10 | BAA09g19950 | A09 | 12296917 | C | T | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S143 |
11 | BAA09g19950 | A09 | 12297505 | G | A | upstream_gene_variant | MODIFIER | c.-1646C>T| |
S47 |
12 | BAA09g19950 | A09 | 12298550 | G | A | upstream_gene_variant | MODIFIER | c.-2691C>T| |
S47 |
13 | BAA09g19950 | A09 | 12298959 | G | A | upstream_gene_variant | MODIFIER | c.-3100C>T| |
S152 |
14 | BAA09g19950 | A09 | 12299356 | G | A | upstream_gene_variant | MODIFIER | c.-3497C>T| |
S189 |
15 | BAA09g19950 | A09 | 12299374 | G | A | upstream_gene_variant | MODIFIER | c.-3515C>T| |
S167 |
16 | BAA09g19950 | A09 | 12299381 | C | T | upstream_gene_variant | MODIFIER | c.-3522G>A| |
S289 S290 |
17 | BAA09g19950 | A09 | 12299770 | G | A | upstream_gene_variant | MODIFIER | c.-3911C>T| |
S207 |
18 | BAA09g19950 | A09 | 12300390 | C | T | upstream_gene_variant | MODIFIER | c.-4531G>A| |
|