Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50760 | A09 | 53478595 | G | A | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S107 |
2 | BAA09g50760 | A09 | 53482159 | C | T | splice_region_variant&intron_variant | LOW | c.28-6C>T| |
S236 |
3 | BAA09g50760 | A09 | 53482455 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S281 |
4 | BAA09g50760 | A09 | 53482496 | G | A | missense_variant&splice_region_variant | MODERATE | c.268G>A|p.Gly90Arg |
S291 |
5 | BAA09g50760 | A09 | 53482750 | C | T | synonymous_variant | LOW | c.340C>T|p.Leu114Leu |
S7 |
6 | BAA09g50760 | A09 | 53482989 | C | T | missense_variant | MODERATE | c.499C>T|p.Pro167Ser |
S204 |
7 | BAA09g50760 | A09 | 53485062 | G | A | synonymous_variant | LOW | c.1230G>A|p.Gly410Gly |
S133 |
8 | BAA09g50760 | A09 | 53485164 | C | T | synonymous_variant | LOW | c.1332C>T|p.Val444Val |
S297 |
9 | BAA09g50760 | A09 | 53485806 | G | A | synonymous_variant | LOW | c.1974G>A|p.Leu658Leu |
S82 S92 |
10 | BAA09g50760 | A09 | 53486010 | G | A | synonymous_variant | LOW | c.2178G>A|p.Lys726Lys |
S12 |
11 | BAA09g50760 | A09 | 53486811 | G | A | missense_variant | MODERATE | c.2277G>A|p.Met759Ile |
S13 |
12 | BAA09g50760 | A09 | 53487066 | G | A | synonymous_variant | LOW | c.2532G>A|p.Lys844Lys |
S135 |
13 | BAA09g50760 | A09 | 53487359 | C | T | missense_variant | MODERATE | c.2825C>T|p.Thr942Ile |
S100 |
14 | BAA09g50760 | A09 | 53487865 | C | T | downstream_gene_variant | MODIFIER | c.*406C>T| |
S67 |