Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g34090 | A09 | 42603463 | C | T | missense_variant | MODERATE | c.2114G>A|p.Gly705Glu |
S180 |
2 | BAA09g34090 | A09 | 42603873 | C | T | missense_variant | MODERATE | c.1783G>A|p.Asp595Asn |
S247 |
3 | BAA09g34090 | A09 | 42604757 | C | T | intron_variant | MODIFIER | c.1007-31G>A| |
S152 |
4 | BAA09g34090 | A09 | 42605085 | C | T | stop_gained | HIGH | c.873G>A|p.Trp291* |
S302 |
5 | BAA09g34090 | A09 | 42605588 | G | A | missense_variant | MODERATE | c.448C>T|p.Leu150Phe |
S100 |
6 | BAA09g34090 | A09 | 42605632 | C | T | intron_variant | MODIFIER | c.441-37G>A| |
S192 |
7 | BAA09g34090 | A09 | 42605830 | C | T | missense_variant | MODERATE | c.287G>A|p.Arg96Lys |
S58 |
8 | BAA09g34090 | A09 | 42606269 | G | A | missense_variant | MODERATE | c.37C>T|p.Leu13Phe |
S252 |
9 | BAA09g34090 | A09 | 42607060 | C | T | upstream_gene_variant | MODIFIER | c.-755G>A| |
S5 |
10 | BAA09g34090 | A09 | 42607279 | C | T | upstream_gene_variant | MODIFIER | c.-974G>A| |
S240 |
11 | BAA09g34090 | A09 | 42608400 | G | A | upstream_gene_variant | MODIFIER | c.-2095C>T| |
S71 |
12 | BAA09g34090 | A09 | 42608835 | G | A | upstream_gene_variant | MODIFIER | c.-2530C>T| |
S72 |
13 | BAA09g34090 | A09 | 42610528 | G | A | upstream_gene_variant | MODIFIER | c.-4223C>T| |
S15 S3 |