Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10190 | A08 | 9261850 | G | A | upstream_gene_variant | MODIFIER | c.-4026G>A| |
S283 |
2 | BAA08g10190 | A08 | 9262318 | G | A | upstream_gene_variant | MODIFIER | c.-3558G>A| |
S56 |
3 | BAA08g10190 | A08 | 9263155 | C | T | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S112 |
4 | BAA08g10190 | A08 | 9263315 | G | A | upstream_gene_variant | MODIFIER | c.-2561G>A| |
S241 |
5 | BAA08g10190 | A08 | 9266367 | C | T | missense_variant | MODERATE | c.22C>T|p.Pro8Ser |
S119 |
6 | BAA08g10190 | A08 | 9266371 | G | A | missense_variant | MODERATE | c.26G>A|p.Arg9Gln |
S148 S32 |
7 | BAA08g10190 | A08 | 9267687 | C | T | missense_variant | MODERATE | c.268C>T|p.Pro90Ser |
S291 |
8 | BAA08g10190 | A08 | 9268374 | C | T | missense_variant | MODERATE | c.955C>T|p.Pro319Ser |
S305 |
9 | BAA08g10190 | A08 | 9269111 | C | T | synonymous_variant | LOW | c.1692C>T|p.Ile564Ile |
S51 |
10 | BAA08g10190 | A08 | 9269595 | G | A | intron_variant | MODIFIER | c.1800+376G>A| |
S13 S92 |
11 | BAA08g10190 | A08 | 9269795 | C | T | intron_variant | MODIFIER | c.1800+576C>T| |
S256 |
12 | BAA08g10190 | A08 | 9269806 | G | A | intron_variant | MODIFIER | c.1800+587G>A| |
S125 |
13 | BAA08g10190 | A08 | 9272456 | T | C | downstream_gene_variant | MODIFIER | c.*779T>C| |
S1 S161 S228 S244 S90 |
14 | BAA08g10190 | A08 | 9274703 | A | C | downstream_gene_variant | MODIFIER | c.*3026A>C| |
S292 |