Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g39980 | A07 | 35677607 | C | T | synonymous_variant | LOW | c.885G>A|p.Lys295Lys |
S168 |
2 | BAA07g39980 | A07 | 35677635 | G | A | missense_variant | MODERATE | c.857C>T|p.Pro286Leu |
S216 S265 S39 |
3 | BAA07g39980 | A07 | 35677901 | G | A | synonymous_variant | LOW | c.591C>T|p.Tyr197Tyr |
S92 |
4 | BAA07g39980 | A07 | 35678104 | C | T | missense_variant | MODERATE | c.388G>A|p.Asp130Asn |
S252 |
5 | BAA07g39980 | A07 | 35678302 | C | T | missense_variant | MODERATE | c.190G>A|p.Glu64Lys |
S124 |
6 | BAA07g39980 | A07 | 35678356 | C | T | missense_variant | MODERATE | c.136G>A|p.Glu46Lys |
S61 |
7 | BAA07g39980 | A07 | 35678468 | G | A | synonymous_variant | LOW | c.24C>T|p.Cys8Cys |
S242 |
8 | BAA07g39980 | A07 | 35682563 | C | T | upstream_gene_variant | MODIFIER | c.-4072G>A| |
S132 S137 S215 S241 |
9 | BAA07g39980 | A07 | 35682683 | G | A | upstream_gene_variant | MODIFIER | c.-4192C>T| |
S287 |