Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50080 | A09 | 53112525 | G | A | missense_variant | MODERATE | c.2393C>T|p.Ala798Val |
S128 |
2 | BAA09g50080 | A09 | 53113623 | C | T | synonymous_variant | LOW | c.2019G>A|p.Lys673Lys |
S13 |
3 | BAA09g50080 | A09 | 53113691 | C | T | missense_variant | MODERATE | c.1951G>A|p.Glu651Lys |
S41 |
4 | BAA09g50080 | A09 | 53114436 | C | T | intron_variant | MODIFIER | c.1621-77G>A| |
S289 S290 |
5 | BAA09g50080 | A09 | 53114664 | C | T | missense_variant | MODERATE | c.1499G>A|p.Gly500Asp |
S20 |
6 | BAA09g50080 | A09 | 53114687 | G | A | splice_region_variant&intron_variant | LOW | c.1483-7C>T| |
S201 |
7 | BAA09g50080 | A09 | 53115312 | G | A | intron_variant | MODIFIER | c.1344+84C>T| |
S184 |
8 | BAA09g50080 | A09 | 53116133 | G | A | synonymous_variant | LOW | c.858C>T|p.Cys286Cys |
S289 S290 |
9 | BAA09g50080 | A09 | 53117256 | C | T | stop_gained | HIGH | c.204G>A|p.Trp68* |
S139 |
10 | BAA09g50080 | A09 | 53118808 | C | T | upstream_gene_variant | MODIFIER | c.-993G>A| |
S303 |
11 | BAA09g50080 | A09 | 53119672 | G | A | upstream_gene_variant | MODIFIER | c.-1857C>T| |
S69 |