Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18470 | A01 | 9055601 | G | A | missense_variant | MODERATE | c.2102C>T|p.Ser701Phe |
S86 |
2 | BAA01g18470 | A01 | 9055643 | G | A | missense_variant | MODERATE | c.2060C>T|p.Ser687Phe |
S169 |
3 | BAA01g18470 | A01 | 9055983 | G | A | synonymous_variant | LOW | c.1720C>T|p.Leu574Leu |
S58 |
4 | BAA01g18470 | A01 | 9056044 | G | A | synonymous_variant | LOW | c.1659C>T|p.Leu553Leu |
S287 |
5 | BAA01g18470 | A01 | 9056158 | G | A | synonymous_variant | LOW | c.1545C>T|p.Ser515Ser |
S34 |
6 | BAA01g18470 | A01 | 9056207 | G | A | missense_variant | MODERATE | c.1496C>T|p.Ser499Phe |
S138 |
7 | BAA01g18470 | A01 | 9056239 | G | A | synonymous_variant | LOW | c.1464C>T|p.Asn488Asn |
S252 |
8 | BAA01g18470 | A01 | 9056958 | G | A | synonymous_variant | LOW | c.745C>T|p.Leu249Leu |
S131 |
9 | BAA01g18470 | A01 | 9056965 | G | A | synonymous_variant | LOW | c.738C>T|p.Tyr246Tyr |
S168 |
10 | BAA01g18470 | A01 | 9056982 | G | A | stop_gained | HIGH | c.721C>T|p.Gln241* |
S86 |
11 | BAA01g18470 | A01 | 9057144 | C | T | missense_variant | MODERATE | c.559G>A|p.Glu187Lys |
S305 |
12 | BAA01g18470 | A01 | 9057722 | G | A | upstream_gene_variant | MODIFIER | c.-20C>T| |
S212 |
13 | BAA01g18470 | A01 | 9057775 | G | A | upstream_gene_variant | MODIFIER | c.-73C>T| |
S84 S93 |
14 | BAA01g18470 | A01 | 9060621 | C | T | upstream_gene_variant | MODIFIER | c.-2919G>A| |
S295 |