Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65610 | A09 | 60366723 | C | T | missense_variant | MODERATE | c.2029G>A|p.Asp677Asn |
S215 |
2 | BAA09g65610 | A09 | 60367784 | C | T | splice_region_variant&intron_variant | LOW | c.1433+5G>A| |
S103 |
3 | BAA09g65610 | A09 | 60369750 | C | T | missense_variant | MODERATE | c.176G>A|p.Gly59Asp |
S169 |
4 | BAA09g65610 | A09 | 60371458 | T | A | upstream_gene_variant | MODIFIER | c.-1533A>T| |
S151 |