Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g41010 | A07 | 36145321 | G | A | missense_variant | MODERATE | c.1793C>T|p.Ser598Phe |
S117 |
2 | BAA07g41010 | A07 | 36145632 | G | A | synonymous_variant | LOW | c.1482C>T|p.Leu494Leu |
S225 S73 |
3 | BAA07g41010 | A07 | 36145889 | G | A | missense_variant | MODERATE | c.1225C>T|p.Arg409Cys |
S135 |
4 | BAA07g41010 | A07 | 36145975 | C | T | missense_variant | MODERATE | c.1139G>A|p.Arg380Lys |
S190 |
5 | BAA07g41010 | A07 | 36146621 | C | T | missense_variant | MODERATE | c.493G>A|p.Glu165Lys |
S94 |
6 | BAA07g41010 | A07 | 36146675 | C | T | missense_variant | MODERATE | c.439G>A|p.Glu147Lys |
S13 |
7 | BAA07g41010 | A07 | 36146927 | C | T | missense_variant | MODERATE | c.187G>A|p.Asp63Asn |
S286 |
8 | BAA07g41010 | A07 | 36146973 | C | T | synonymous_variant | LOW | c.141G>A|p.Val47Val |
S68 |
9 | BAA07g41010 | A07 | 36147026 | G | A | missense_variant | MODERATE | c.88C>T|p.Arg30Cys |
S302 |
10 | BAA07g41010 | A07 | 36151334 | G | A | upstream_gene_variant | MODIFIER | c.-4221C>T| |
S11 |