Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06280 | A07 | 15657633 | C | T | upstream_gene_variant | MODIFIER | c.-485C>T| |
S144 |
2 | BAA07g06280 | A07 | 15658163 | G | A | missense_variant | MODERATE | c.46G>A|p.Asp16Asn |
S259 |
3 | BAA07g06280 | A07 | 15659220 | T | G | missense_variant | MODERATE | c.1103T>G|p.Val368Gly |
S104 S146 S199 S222 S240 S26 S280 S302 S74 |
4 | BAA07g06280 | A07 | 15659236 | C | T | synonymous_variant | LOW | c.1119C>T|p.Pro373Pro |
S36 |
5 | BAA07g06280 | A07 | 15660567 | C | T | synonymous_variant | LOW | c.2286C>T|p.Asn762Asn |
S27 |
6 | BAA07g06280 | A07 | 15661148 | C | T | splice_region_variant&intron_variant | LOW | c.2862+5C>T| |
S266 |
7 | BAA07g06280 | A07 | 15662525 | C | T | downstream_gene_variant | MODIFIER | c.*1216C>T| |
S32 |
8 | BAA07g06280 | A07 | 15663694 | C | T | downstream_gene_variant | MODIFIER | c.*2385C>T| |
S247 |
9 | BAA07g06280 | A07 | 15664078 | C | T | downstream_gene_variant | MODIFIER | c.*2769C>T| |
S18 |