Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29170 | A01 | 18396044 | G | A | missense_variant | MODERATE | c.3575C>T|p.Ala1192Val |
S7 |
2 | BAA01g29170 | A01 | 18396302 | C | T | missense_variant | MODERATE | c.3317G>A|p.Gly1106Glu |
S255 |
3 | BAA01g29170 | A01 | 18396807 | C | T | synonymous_variant | LOW | c.2901G>A|p.Leu967Leu |
S115 |
4 | BAA01g29170 | A01 | 18396861 | C | T | synonymous_variant | LOW | c.2847G>A|p.Arg949Arg |
S77 S82 |
5 | BAA01g29170 | A01 | 18397097 | C | T | missense_variant | MODERATE | c.2611G>A|p.Glu871Lys |
S177 |
6 | BAA01g29170 | A01 | 18399094 | G | A | missense_variant | MODERATE | c.2114C>T|p.Ser705Phe |
S60 |
7 | BAA01g29170 | A01 | 18400009 | C | T | intron_variant | MODIFIER | c.1343+29G>A| |
S41 |
8 | BAA01g29170 | A01 | 18400164 | C | T | missense_variant | MODERATE | c.1217G>A|p.Gly406Glu |
S182 |
9 | BAA01g29170 | A01 | 18400367 | C | T | missense_variant | MODERATE | c.1090G>A|p.Gly364Arg |
S94 |
10 | BAA01g29170 | A01 | 18401787 | C | T | upstream_gene_variant | MODIFIER | c.-283G>A| |
S272 |
11 | BAA01g29170 | A01 | 18404552 | C | T | upstream_gene_variant | MODIFIER | c.-3048G>A| |
S205 |
12 | BAA01g29170 | A01 | 18405336 | G | A | upstream_gene_variant | MODIFIER | c.-3832C>T| |
S74 |