Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67600 | A09 | 61178818 | G | A | missense_variant | MODERATE | c.2728C>T|p.Leu910Phe |
S14 |
2 | BAA09g67600 | A09 | 61180686 | G | A | missense_variant | MODERATE | c.1885C>T|p.Pro629Ser |
S180 |
3 | BAA09g67600 | A09 | 61180924 | C | T | missense_variant&splice_region_variant | MODERATE | c.1747G>A|p.Glu583Lys |
S229 |
4 | BAA09g67600 | A09 | 61182977 | C | T | missense_variant | MODERATE | c.602G>A|p.Gly201Glu |
S256 |
5 | BAA09g67600 | A09 | 61183578 | C | T | missense_variant | MODERATE | c.245G>A|p.Arg82Lys |
S54 |
6 | BAA09g67600 | A09 | 61183671 | G | A | missense_variant | MODERATE | c.152C>T|p.Ala51Val |
S161 |
7 | BAA09g67600 | A09 | 61185144 | C | T | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S152 |
8 | BAA09g67600 | A09 | 61186375 | G | A | upstream_gene_variant | MODIFIER | c.-2553C>T| |
S190 |
9 | BAA09g67600 | A09 | 61186427 | G | A | upstream_gene_variant | MODIFIER | c.-2605C>T| |
S244 |
10 | BAA09g67600 | A09 | 61187261 | G | A | upstream_gene_variant | MODIFIER | c.-3439C>T| |
S184 |
11 | BAA09g67600 | A09 | 61187343 | C | T | upstream_gene_variant | MODIFIER | c.-3521G>A| |
S15 S153 S2 S213 S3 S34 |
12 | BAA09g67600 | A09 | 61187647 | C | T | upstream_gene_variant | MODIFIER | c.-3825G>A| |
S303 |
13 | BAA09g67600 | A09 | 61188333 | G | A | upstream_gene_variant | MODIFIER | c.-4511C>T| |
S107 |