Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18920 | A06 | 9708828 | C | T | upstream_gene_variant | MODIFIER | c.-722C>T| |
S160 |
2 | BAA06g18920 | A06 | 9710370 | G | A | missense_variant | MODERATE | c.611G>A|p.Gly204Glu |
S33 |
3 | BAA06g18920 | A06 | 9710561 | G | A | missense_variant | MODERATE | c.703G>A|p.Ala235Thr |
S139 |
4 | BAA06g18920 | A06 | 9712312 | G | A | missense_variant | MODERATE | c.1876G>A|p.Val626Ile |
S261 |
5 | BAA06g18920 | A06 | 9712818 | C | T | synonymous_variant | LOW | c.2140C>T|p.Leu714Leu |
S100 |
6 | BAA06g18920 | A06 | 9713444 | G | A | missense_variant | MODERATE | c.2459G>A|p.Arg820Gln |
S48 |
7 | BAA06g18920 | A06 | 9714311 | C | T | missense_variant | MODERATE | c.2812C>T|p.Pro938Ser |
S266 |
8 | BAA06g18920 | A06 | 9714836 | G | A | missense_variant | MODERATE | c.3145G>A|p.Asp1049Asn |
S284 |
9 | BAA06g18920 | A06 | 9714875 | G | A | missense_variant | MODERATE | c.3184G>A|p.Asp1062Asn |
S302 |