Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38400 | A05 | 37818477 | C | T | synonymous_variant | LOW | c.505C>T|p.Leu169Leu |
S211 S227 |
2 | BAA05g38400 | A05 | 37818612 | G | A | missense_variant | MODERATE | c.640G>A|p.Asp214Asn |
S241 S39 |
3 | BAA05g38400 | A05 | 37818681 | G | A | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S128 |
4 | BAA05g38400 | A05 | 37818820 | C | T | missense_variant | MODERATE | c.848C>T|p.Thr283Ile |
S139 |
5 | BAA05g38400 | A05 | 37818950 | C | T | synonymous_variant | LOW | c.978C>T|p.Phe326Phe |
S286 |
6 | BAA05g38400 | A05 | 37819063 | C | T | missense_variant | MODERATE | c.1091C>T|p.Ser364Phe |
S67 |
7 | BAA05g38400 | A05 | 37819109 | G | A | synonymous_variant | LOW | c.1137G>A|p.Pro379Pro |
S179 |
8 | BAA05g38400 | A05 | 37819135 | C | T | missense_variant | MODERATE | c.1163C>T|p.Ser388Leu |
S37 |
9 | BAA05g38400 | A05 | 37819553 | G | A | missense_variant | MODERATE | c.1517G>A|p.Ser506Asn |
S69 |