Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g25970 | A01 | 14313302 | G | A | synonymous_variant | LOW | c.2916C>T|p.Val972Val |
S299 |
2 | BAA01g25970 | A01 | 14313678 | G | A | missense_variant | MODERATE | c.2540C>T|p.Thr847Ile |
S234 |
3 | BAA01g25970 | A01 | 14313731 | G | A | synonymous_variant | LOW | c.2487C>T|p.Phe829Phe |
S181 |
4 | BAA01g25970 | A01 | 14313895 | G | A | splice_region_variant&intron_variant | LOW | c.2326-3C>T| |
S262 |
5 | BAA01g25970 | A01 | 14314257 | G | A | missense_variant | MODERATE | c.2144C>T|p.Thr715Ile |
S1 S90 |
6 | BAA01g25970 | A01 | 14314351 | G | A | stop_gained | HIGH | c.2050C>T|p.Gln684* |
S161 S228 S244 S289 S290 |
7 | BAA01g25970 | A01 | 14315257 | G | A | missense_variant | MODERATE | c.1556C>T|p.Ser519Phe |
S142 |
8 | BAA01g25970 | A01 | 14315360 | C | T | missense_variant | MODERATE | c.1453G>A|p.Ala485Thr |
S160 |
9 | BAA01g25970 | A01 | 14316061 | C | T | missense_variant | MODERATE | c.829G>A|p.Asp277Asn |
S150 |
10 | BAA01g25970 | A01 | 14316760 | C | T | missense_variant | MODERATE | c.130G>A|p.Ala44Thr |
S273 |
11 | BAA01g25970 | A01 | 14317600 | G | A | upstream_gene_variant | MODIFIER | c.-711C>T| |
S159 S243 |
12 | BAA01g25970 | A01 | 14317952 | G | A | upstream_gene_variant | MODIFIER | c.-1063C>T| |
S209 |
13 | BAA01g25970 | A01 | 14319056 | G | A | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S195 |