Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g35170 | A03 | 16285336 | G | A | synonymous_variant | LOW | c.4842C>T|p.Leu1614Leu |
S274 |
2 | BAA03g35170 | A03 | 16285976 | G | A | missense_variant | MODERATE | c.4403C>T|p.Ala1468Val |
S123 |
3 | BAA03g35170 | A03 | 16286169 | G | A | missense_variant | MODERATE | c.4288C>T|p.Pro1430Ser |
S197 |
4 | BAA03g35170 | A03 | 16287240 | C | T | missense_variant | MODERATE | c.3352G>A|p.Glu1118Lys |
S232 |
5 | BAA03g35170 | A03 | 16287804 | G | A | missense_variant | MODERATE | c.2873C>T|p.Ala958Val |
S12 |
6 | BAA03g35170 | A03 | 16288045 | G | A | missense_variant | MODERATE | c.2632C>T|p.His878Tyr |
S20 |
7 | BAA03g35170 | A03 | 16289346 | G | A | missense_variant | MODERATE | c.1814C>T|p.Thr605Ile |
|
8 | BAA03g35170 | A03 | 16289395 | C | T | intron_variant | MODIFIER | c.1792-27G>A| |
S120 S122 S55 S65 |
9 | BAA03g35170 | A03 | 16289961 | G | A | missense_variant | MODERATE | c.1606C>T|p.Arg536Cys |
S161 |
10 | BAA03g35170 | A03 | 16290121 | G | A | synonymous_variant | LOW | c.1542C>T|p.Ile514Ile |
S272 |
11 | BAA03g35170 | A03 | 16290579 | G | A | intron_variant | MODIFIER | c.1245+10C>T| |
S12 |
12 | BAA03g35170 | A03 | 16292529 | C | T | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S165 |
13 | BAA03g35170 | A03 | 16292554 | C | T | synonymous_variant | LOW | c.180G>A|p.Gln60Gln |
S92 |
14 | BAA03g35170 | A03 | 16294600 | G | A | upstream_gene_variant | MODIFIER | c.-1629C>T| |
S177 S212 |
15 | BAA03g35170 | A03 | 16294662 | G | A | upstream_gene_variant | MODIFIER | c.-1691C>T| |
S135 |
16 | BAA03g35170 | A03 | 16295990 | C | T | upstream_gene_variant | MODIFIER | c.-3019G>A| |
S67 |
17 | BAA03g35170 | A03 | 16297621 | C | T | upstream_gene_variant | MODIFIER | c.-4650G>A| |
S279 |