Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44190 | A06 | 28342207 | G | A | upstream_gene_variant | MODIFIER | c.-2056G>A| |
S161 |
2 | BAA06g44190 | A06 | 28343261 | C | T | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S16 S259 |
3 | BAA06g44190 | A06 | 28344507 | C | T | missense_variant | MODERATE | c.245C>T|p.Pro82Leu |
S257 |
4 | BAA06g44190 | A06 | 28346409 | C | T | synonymous_variant | LOW | c.603C>T|p.Leu201Leu |
S192 |
5 | BAA06g44190 | A06 | 28346544 | C | T | synonymous_variant | LOW | c.738C>T|p.Leu246Leu |
S290 |
6 | BAA06g44190 | A06 | 28346810 | C | T | missense_variant | MODERATE | c.1004C>T|p.Thr335Ile |
S172 S217 |
7 | BAA06g44190 | A06 | 28346839 | C | T | missense_variant | MODERATE | c.1033C>T|p.Leu345Phe |
S135 |
8 | BAA06g44190 | A06 | 28347257 | G | A | missense_variant | MODERATE | c.1451G>A|p.Arg484Lys |
S117 |
9 | BAA06g44190 | A06 | 28347426 | G | A | synonymous_variant | LOW | c.1620G>A|p.Leu540Leu |
S168 |
10 | BAA06g44190 | A06 | 28347607 | C | T | missense_variant | MODERATE | c.1801C>T|p.Leu601Phe |
S37 |
11 | BAA06g44190 | A06 | 28347906 | G | A | synonymous_variant | LOW | c.2100G>A|p.Glu700Glu |
S17 |