Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g24900 | A08 | 18101664 | G | A | missense_variant | MODERATE | c.1265C>T|p.Ala422Val |
S197 |
2 | BAA08g24900 | A08 | 18102173 | G | A | missense_variant | MODERATE | c.1193C>T|p.Ser398Phe |
S265 |
3 | BAA08g24900 | A08 | 18103517 | C | T | missense_variant | MODERATE | c.902G>A|p.Gly301Asp |
S278 |
4 | BAA08g24900 | A08 | 18104165 | G | A | intron_variant | MODIFIER | c.778+147C>T| |
S40 S49 |
5 | BAA08g24900 | A08 | 18104467 | C | T | splice_region_variant&intron_variant | LOW | c.705+7G>A| |
S135 |
6 | BAA08g24900 | A08 | 18105486 | G | A | missense_variant | MODERATE | c.346C>T|p.Arg116Trp |
S35 |
7 | BAA08g24900 | A08 | 18106002 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.122-1G>A| |
S274 |
8 | BAA08g24900 | A08 | 18106817 | G | A | upstream_gene_variant | MODIFIER | c.-277C>T| |
S204 |
9 | BAA08g24900 | A08 | 18106942 | G | A | upstream_gene_variant | MODIFIER | c.-402C>T| |
S68 |
10 | BAA08g24900 | A08 | 18107734 | G | A | upstream_gene_variant | MODIFIER | c.-1194C>T| |
S183 |
11 | BAA08g24900 | A08 | 18108869 | C | T | upstream_gene_variant | MODIFIER | c.-2329G>A| |
S247 |