Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22250 | A07 | 26653554 | C | T | synonymous_variant | LOW | c.2121G>A|p.Ala707Ala |
S13 |
2 | BAA07g22250 | A07 | 26653886 | G | A | missense_variant | MODERATE | c.1789C>T|p.Pro597Ser |
S264 |
3 | BAA07g22250 | A07 | 26654771 | G | A | stop_gained&splice_region_variant | HIGH | c.1555C>T|p.Gln519* |
S237 |
4 | BAA07g22250 | A07 | 26655523 | C | T | missense_variant | MODERATE | c.889G>A|p.Asp297Asn |
S176 |
5 | BAA07g22250 | A07 | 26655694 | G | A | missense_variant | MODERATE | c.718C>T|p.Leu240Phe |
S67 |
6 | BAA07g22250 | A07 | 26655943 | C | T | missense_variant | MODERATE | c.469G>A|p.Asp157Asn |
S255 |
7 | BAA07g22250 | A07 | 26655959 | G | A | synonymous_variant | LOW | c.453C>T|p.His151His |
S276 |
8 | BAA07g22250 | A07 | 26659291 | G | A | upstream_gene_variant | MODIFIER | c.-2880C>T| |
S6 |
9 | BAA07g22250 | A07 | 26659845 | C | T | upstream_gene_variant | MODIFIER | c.-3434G>A| |
S27 |