Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g31300 | A07 | 31223277 | C | T | missense_variant | MODERATE | c.14C>T|p.Ser5Leu |
S301 S304 |
2 | BAA07g31300 | A07 | 31223728 | C | T | missense_variant | MODERATE | c.284C>T|p.Ala95Val |
S200 |
3 | BAA07g31300 | A07 | 31224433 | G | A | synonymous_variant | LOW | c.615G>A|p.Thr205Thr |
S76 |
4 | BAA07g31300 | A07 | 31224710 | C | T | missense_variant | MODERATE | c.806C>T|p.Ser269Phe |
S261 S303 |
5 | BAA07g31300 | A07 | 31225155 | G | A | missense_variant | MODERATE | c.1162G>A|p.Ala388Thr |
S76 |
6 | BAA07g31300 | A07 | 31225392 | G | A | missense_variant | MODERATE | c.1399G>A|p.Glu467Lys |
S67 |
7 | BAA07g31300 | A07 | 31225704 | C | T | missense_variant | MODERATE | c.1711C>T|p.Pro571Ser |
S47 |
8 | BAA07g31300 | A07 | 31228104 | G | A | downstream_gene_variant | MODIFIER | c.*2170G>A| |
S170 |
9 | BAA07g31300 | A07 | 31228118 | C | T | downstream_gene_variant | MODIFIER | c.*2184C>T| |
S276 |
10 | BAA07g31300 | A07 | 31229735 | G | A | downstream_gene_variant | MODIFIER | c.*3801G>A| |
S185 |
11 | BAA07g31300 | A07 | 31230050 | A | G | downstream_gene_variant | MODIFIER | c.*4116A>G| |
S149 S170 |