Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46260 | A01 | 30870814 | G | A | missense_variant | MODERATE | c.3377C>T|p.Ala1126Val |
S291 |
2 | BAA01g46260 | A01 | 30871029 | C | T | missense_variant | MODERATE | c.3162G>A|p.Met1054Ile |
S8 |
3 | BAA01g46260 | A01 | 30871212 | C | T | stop_gained | HIGH | c.2979G>A|p.Trp993* |
S8 |
4 | BAA01g46260 | A01 | 30871484 | C | T | missense_variant | MODERATE | c.2707G>A|p.Glu903Lys |
S78 S83 |
5 | BAA01g46260 | A01 | 30871511 | C | T | missense_variant | MODERATE | c.2680G>A|p.Val894Ile |
S77 S82 |
6 | BAA01g46260 | A01 | 30871543 | G | A | missense_variant | MODERATE | c.2648C>T|p.Ala883Val |
S284 |
7 | BAA01g46260 | A01 | 30871826 | C | T | missense_variant | MODERATE | c.2365G>A|p.Val789Ile |
S75 S81 |
8 | BAA01g46260 | A01 | 30871962 | C | T | synonymous_variant | LOW | c.2229G>A|p.Lys743Lys |
S57 |
9 | BAA01g46260 | A01 | 30873625 | G | A | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S140 |
10 | BAA01g46260 | A01 | 30874583 | C | T | synonymous_variant | LOW | c.312G>A|p.Thr104Thr |
S112 |
11 | BAA01g46260 | A01 | 30874682 | C | T | synonymous_variant | LOW | c.213G>A|p.Pro71Pro |
S221 |
12 | BAA01g46260 | A01 | 30874781 | C | T | synonymous_variant | LOW | c.114G>A|p.Arg38Arg |
S60 |
13 | BAA01g46260 | A01 | 30878276 | C | T | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S32 |