Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12660 | A07 | 20879393 | C | T | downstream_gene_variant | MODIFIER | c.*2217G>A| |
S94 |
2 | BAA07g12660 | A07 | 20881682 | C | T | synonymous_variant | LOW | c.1959G>A|p.Lys653Lys |
S81 S85 |
3 | BAA07g12660 | A07 | 20881943 | C | T | missense_variant&splice_region_variant | MODERATE | c.1771G>A|p.Glu591Lys |
S259 |
4 | BAA07g12660 | A07 | 20882413 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1386-1G>A| |
S107 |
5 | BAA07g12660 | A07 | 20883916 | G | A | missense_variant | MODERATE | c.469C>T|p.Pro157Ser |
S105 S106 |
6 | BAA07g12660 | A07 | 20884280 | G | A | missense_variant | MODERATE | c.271C>T|p.Pro91Ser |
S80 |
7 | BAA07g12660 | A07 | 20884499 | G | A | missense_variant | MODERATE | c.52C>T|p.Leu18Phe |
S151 |
8 | BAA07g12660 | A07 | 20887908 | G | A | upstream_gene_variant | MODIFIER | c.-3358C>T| |
S54 |
9 | BAA07g12660 | A07 | 20887989 | C | T | upstream_gene_variant | MODIFIER | c.-3439G>A| |
S197 |
10 | BAA07g12660 | A07 | 20888748 | G | A | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S161 |