Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00840 | A10 | 389379 | C | T | downstream_gene_variant | MODIFIER | c.*3474G>A| |
S265 |
2 | BAA10g00840 | A10 | 393083 | C | T | missense_variant | MODERATE | c.862G>A|p.Gly288Ser |
S162 |
3 | BAA10g00840 | A10 | 393246 | G | A | synonymous_variant | LOW | c.699C>T|p.Asn233Asn |
S148 S30 |
4 | BAA10g00840 | A10 | 393827 | G | A | missense_variant | MODERATE | c.118C>T|p.Leu40Phe |
S81 S85 |
5 | BAA10g00840 | A10 | 396884 | C | T | upstream_gene_variant | MODIFIER | c.-2940G>A| |
S181 |
6 | BAA10g00840 | A10 | 398103 | G | A | upstream_gene_variant | MODIFIER | c.-4159C>T| |
S295 |
7 | BAA10g00840 | A10 | 398296 | C | T | upstream_gene_variant | MODIFIER | c.-4352G>A| |
S142 S247 |