Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66520 | A03 | 40897948 | G | A | synonymous_variant | LOW | c.78G>A|p.Arg26Arg |
S112 |
2 | BAA03g66520 | A03 | 40898033 | C | T | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S237 |
3 | BAA03g66520 | A03 | 40898231 | G | A | missense_variant | MODERATE | c.361G>A|p.Gly121Ser |
S81 S85 |
4 | BAA03g66520 | A03 | 40898235 | G | A | missense_variant | MODERATE | c.365G>A|p.Arg122Gln |
S261 |
5 | BAA03g66520 | A03 | 40898447 | G | A | downstream_gene_variant | MODIFIER | c.*184G>A| |
S60 |
6 | BAA03g66520 | A03 | 40898674 | C | T | downstream_gene_variant | MODIFIER | c.*411C>T| |
S306 S308 |
7 | BAA03g66520 | A03 | 40898817 | C | T | downstream_gene_variant | MODIFIER | c.*554C>T| |
S10 |
8 | BAA03g66520 | A03 | 40899265 | G | A | downstream_gene_variant | MODIFIER | c.*1002G>A| |
S48 |
9 | BAA03g66520 | A03 | 40899294 | G | A | downstream_gene_variant | MODIFIER | c.*1031G>A| |
S177 |
10 | BAA03g66520 | A03 | 40899553 | C | T | downstream_gene_variant | MODIFIER | c.*1290C>T| |
S237 |
11 | BAA03g66520 | A03 | 40901264 | C | T | downstream_gene_variant | MODIFIER | c.*3001C>T| |
S42 |
12 | BAA03g66520 | A03 | 40902490 | C | T | downstream_gene_variant | MODIFIER | c.*4227C>T| |
S118 |