Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06690 | A07 | 16038645 | G | A | missense_variant | MODERATE | c.1865C>T|p.Thr622Ile |
S262 |
2 | BAA07g06690 | A07 | 16039050 | G | A | missense_variant | MODERATE | c.1460C>T|p.Ala487Val |
S278 |
3 | BAA07g06690 | A07 | 16039374 | T | C | missense_variant | MODERATE | c.1433A>G|p.Asp478Gly |
S249 |
4 | BAA07g06690 | A07 | 16039378 | C | T | missense_variant | MODERATE | c.1429G>A|p.Asp477Asn |
S267 |
5 | BAA07g06690 | A07 | 16039527 | G | A | missense_variant | MODERATE | c.1280C>T|p.Thr427Ile |
S264 |
6 | BAA07g06690 | A07 | 16039578 | G | A | missense_variant | MODERATE | c.1229C>T|p.Pro410Leu |
S252 S292 |
7 | BAA07g06690 | A07 | 16039613 | G | A | synonymous_variant | LOW | c.1194C>T|p.Val398Val |
S12 |
8 | BAA07g06690 | A07 | 16040070 | G | A | synonymous_variant | LOW | c.837C>T|p.Asp279Asp |
S156 |
9 | BAA07g06690 | A07 | 16040183 | C | T | missense_variant | MODERATE | c.724G>A|p.Glu242Lys |
S261 |
10 | BAA07g06690 | A07 | 16040644 | C | T | missense_variant | MODERATE | c.263G>A|p.Gly88Asp |
S11 |
11 | BAA07g06690 | A07 | 16045486 | G | A | upstream_gene_variant | MODIFIER | c.-4580C>T| |
S264 |
12 | BAA07g06690 | A07 | 16045814 | G | A | upstream_gene_variant | MODIFIER | c.-4908C>T| |
S178 |