Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17160 | A05 | 9607735 | G | A | downstream_gene_variant | MODIFIER | c.*2577C>T| |
S303 |
2 | BAA05g17160 | A05 | 9610475 | G | A | missense_variant | MODERATE | c.1076C>T|p.Pro359Leu |
S122 |
3 | BAA05g17160 | A05 | 9610545 | C | T | missense_variant | MODERATE | c.1006G>A|p.Asp336Asn |
S276 |
4 | BAA05g17160 | A05 | 9610738 | G | A | synonymous_variant | LOW | c.813C>T|p.Asp271Asp |
S11 |
5 | BAA05g17160 | A05 | 9611026 | C | T | synonymous_variant | LOW | c.525G>A|p.Gln175Gln |
S2 |
6 | BAA05g17160 | A05 | 9611279 | G | A | missense_variant | MODERATE | c.272C>T|p.Ala91Val |
S245 |
7 | BAA05g17160 | A05 | 9611683 | C | T | synonymous_variant | LOW | c.54G>A|p.Gln18Gln |
S221 |
8 | BAA05g17160 | A05 | 9612049 | G | A | upstream_gene_variant | MODIFIER | c.-313C>T| |
S178 |
9 | BAA05g17160 | A05 | 9612618 | G | A | upstream_gene_variant | MODIFIER | c.-882C>T| |
S173 |
10 | BAA05g17160 | A05 | 9612980 | G | A | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S224 |
11 | BAA05g17160 | A05 | 9614156 | G | A | upstream_gene_variant | MODIFIER | c.-2420C>T| |
S294 |
12 | BAA05g17160 | A05 | 9615162 | G | A | upstream_gene_variant | MODIFIER | c.-3426C>T| |
S105 S106 |
13 | BAA05g17160 | A05 | 9615321 | C | T | upstream_gene_variant | MODIFIER | c.-3585G>A| |
S259 |
14 | BAA05g17160 | A05 | 9615803 | G | A | upstream_gene_variant | MODIFIER | c.-4067C>T| |
S272 |
15 | BAA05g17160 | A05 | 9616668 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S288 |