Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g62440 | A03 | 31733094 | C | T | upstream_gene_variant | MODIFIER | c.-4761C>T| |
S34 |
2 | BAA03g62440 | A03 | 31737987 | C | T | stop_gained | HIGH | c.133C>T|p.Gln45* |
S289 S290 |
3 | BAA03g62440 | A03 | 31738409 | G | A | missense_variant | MODERATE | c.463G>A|p.Glu155Lys |
S294 |
4 | BAA03g62440 | A03 | 31738533 | C | T | missense_variant | MODERATE | c.587C>T|p.Pro196Leu |
S33 |
5 | BAA03g62440 | A03 | 31738657 | C | T | synonymous_variant | LOW | c.711C>T|p.Leu237Leu |
S207 |
6 | BAA03g62440 | A03 | 31739329 | G | A | splice_region_variant&intron_variant | LOW | c.953+7G>A| |
S291 |
7 | BAA03g62440 | A03 | 31739842 | C | T | synonymous_variant | LOW | c.1240C>T|p.Leu414Leu |
S118 |
8 | BAA03g62440 | A03 | 31739985 | C | T | missense_variant | MODERATE | c.1285C>T|p.Leu429Phe |
S200 |
9 | BAA03g62440 | A03 | 31740516 | C | T | missense_variant | MODERATE | c.1619C>T|p.Ser540Phe |
S297 |
10 | BAA03g62440 | A03 | 31742617 | C | T | downstream_gene_variant | MODIFIER | c.*1495C>T| |
S53 |
11 | BAA03g62440 | A03 | 31742786 | C | T | downstream_gene_variant | MODIFIER | c.*1664C>T| |
S52 |
12 | BAA03g62440 | A03 | 31743619 | C | T | downstream_gene_variant | MODIFIER | c.*2497C>T| |
S174 |
13 | BAA03g62440 | A03 | 31744100 | G | A | downstream_gene_variant | MODIFIER | c.*2978G>A| |
S242 |