Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g14530 | A07 | 22112070 | C | T | missense_variant | MODERATE | c.3484G>A|p.Asp1162Asn |
S259 |
2 | BAA07g14530 | A07 | 22112156 | C | T | missense_variant | MODERATE | c.3398G>A|p.Arg1133Lys |
S156 |
3 | BAA07g14530 | A07 | 22112515 | G | A | synonymous_variant | LOW | c.3039C>T|p.Asp1013Asp |
S60 |
4 | BAA07g14530 | A07 | 22112679 | G | A | missense_variant | MODERATE | c.2875C>T|p.Pro959Ser |
S67 |
5 | BAA07g14530 | A07 | 22113328 | G | A | missense_variant | MODERATE | c.2426C>T|p.Ser809Phe |
S152 S273 |
6 | BAA07g14530 | A07 | 22114930 | T | C | intron_variant | MODIFIER | c.1828-48A>G| |
S277 |
7 | BAA07g14530 | A07 | 22116422 | C | T | synonymous_variant | LOW | c.822G>A|p.Glu274Glu |
S8 |
8 | BAA07g14530 | A07 | 22119485 | C | T | upstream_gene_variant | MODIFIER | c.-2042G>A| |
S242 |
9 | BAA07g14530 | A07 | 22120603 | C | T | upstream_gene_variant | MODIFIER | c.-3160G>A| |
S230 |
10 | BAA07g14530 | A07 | 22122072 | G | A | upstream_gene_variant | MODIFIER | c.-4629C>T| |
S188 |