Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00560 | A08 | 380256 | C | T | synonymous_variant | LOW | c.2463G>A|p.Val821Val |
S138 |
2 | BAA08g00560 | A08 | 380862 | G | A | missense_variant | MODERATE | c.1928C>T|p.Ser643Phe |
S58 |
3 | BAA08g00560 | A08 | 381691 | C | T | missense_variant | MODERATE | c.1189G>A|p.Asp397Asn |
S51 |
4 | BAA08g00560 | A08 | 383595 | G | A | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S119 |
5 | BAA08g00560 | A08 | 383879 | G | A | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S212 |
6 | BAA08g00560 | A08 | 384530 | G | A | upstream_gene_variant | MODIFIER | c.-566C>T| |
S108 |
7 | BAA08g00560 | A08 | 385590 | G | A | upstream_gene_variant | MODIFIER | c.-1626C>T| |
S115 |
8 | BAA08g00560 | A08 | 387805 | C | T | upstream_gene_variant | MODIFIER | c.-3841G>A| |
S287 |
9 | BAA08g00560 | A08 | 388034 | G | A | upstream_gene_variant | MODIFIER | c.-4070C>T| |
S297 |