Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35640 | A09 | 44028915 | G | A | downstream_gene_variant | MODIFIER | c.*2735C>T| |
S301 |
2 | BAA09g35640 | A09 | 44029080 | C | T | downstream_gene_variant | MODIFIER | c.*2570G>A| |
S267 |
3 | BAA09g35640 | A09 | 44029903 | C | T | downstream_gene_variant | MODIFIER | c.*1747G>A| |
S208 S219 |
4 | BAA09g35640 | A09 | 44031000 | G | A | downstream_gene_variant | MODIFIER | c.*650C>T| |
S150 |
5 | BAA09g35640 | A09 | 44031714 | G | A | missense_variant | MODERATE | c.2498C>T|p.Ser833Phe |
S137 |
6 | BAA09g35640 | A09 | 44032195 | C | T | missense_variant | MODERATE | c.2017G>A|p.Ala673Thr |
S134 |
7 | BAA09g35640 | A09 | 44032235 | C | T | synonymous_variant | LOW | c.1977G>A|p.Glu659Glu |
S155 S211 |
8 | BAA09g35640 | A09 | 44032323 | G | A | missense_variant | MODERATE | c.1889C>T|p.Ser630Phe |
S149 |
9 | BAA09g35640 | A09 | 44032468 | C | T | missense_variant | MODERATE | c.1744G>A|p.Val582Met |
S296 |
10 | BAA09g35640 | A09 | 44032935 | G | A | missense_variant | MODERATE | c.1277C>T|p.Ser426Leu |
S67 |
11 | BAA09g35640 | A09 | 44033240 | C | T | synonymous_variant | LOW | c.972G>A|p.Arg324Arg |
S77 S82 |
12 | BAA09g35640 | A09 | 44033882 | G | A | synonymous_variant | LOW | c.330C>T|p.Leu110Leu |
S291 |
13 | BAA09g35640 | A09 | 44034084 | G | A | missense_variant | MODERATE | c.128C>T|p.Thr43Ile |
S78 S83 |
14 | BAA09g35640 | A09 | 44034919 | C | T | upstream_gene_variant | MODIFIER | c.-708G>A| |
S247 |
15 | BAA09g35640 | A09 | 44035505 | G | A | upstream_gene_variant | MODIFIER | c.-1294C>T| |
S125 |
16 | BAA09g35640 | A09 | 44037386 | C | T | upstream_gene_variant | MODIFIER | c.-3175G>A| |
S68 |
17 | BAA09g35640 | A09 | 44037921 | C | T | upstream_gene_variant | MODIFIER | c.-3710G>A| |
S108 |