Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11630 | A08 | 10292322 | C | T | downstream_gene_variant | MODIFIER | c.*4910G>A| |
S50 |
2 | BAA08g11630 | A08 | 10293515 | C | T | downstream_gene_variant | MODIFIER | c.*3717G>A| |
S7 |
3 | BAA08g11630 | A08 | 10294174 | G | A | downstream_gene_variant | MODIFIER | c.*3058C>T| |
S12 |
4 | BAA08g11630 | A08 | 10294422 | G | A | downstream_gene_variant | MODIFIER | c.*2810C>T| |
S95 |
5 | BAA08g11630 | A08 | 10294633 | G | A | downstream_gene_variant | MODIFIER | c.*2599C>T| |
S158 |
6 | BAA08g11630 | A08 | 10297303 | C | T | missense_variant | MODERATE | c.550G>A|p.Glu184Lys |
S273 |
7 | BAA08g11630 | A08 | 10297369 | G | A | missense_variant | MODERATE | c.484C>T|p.Pro162Ser |
S263 |
8 | BAA08g11630 | A08 | 10297654 | G | A | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S33 |
9 | BAA08g11630 | A08 | 10297676 | G | A | synonymous_variant | LOW | c.177C>T|p.Ser59Ser |
S192 |
10 | BAA08g11630 | A08 | 10297776 | G | A | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S263 |
11 | BAA08g11630 | A08 | 10298060 | C | T | upstream_gene_variant | MODIFIER | c.-208G>A| |
S83 S88 |
12 | BAA08g11630 | A08 | 10300036 | G | A | upstream_gene_variant | MODIFIER | c.-2184C>T| |
S11 |
13 | BAA08g11630 | A08 | 10300108 | G | A | upstream_gene_variant | MODIFIER | c.-2256C>T| |
S282 |
14 | BAA08g11630 | A08 | 10300318 | C | T | upstream_gene_variant | MODIFIER | c.-2466G>A| |
S104 S52 |