Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g28890 | A06 | 19750109 | G | A | upstream_gene_variant | MODIFIER | c.-4715G>A| |
S168 |
2 | BAA06g28890 | A06 | 19755180 | G | A | missense_variant | MODERATE | c.229G>A|p.Ala77Thr |
S95 |
3 | BAA06g28890 | A06 | 19755855 | C | T | stop_gained | HIGH | c.736C>T|p.Arg246* |
S173 |
4 | BAA06g28890 | A06 | 19755948 | G | A | missense_variant | MODERATE | c.829G>A|p.Glu277Lys |
S132 S137 S215 S89 |
5 | BAA06g28890 | A06 | 19756851 | G | A | missense_variant | MODERATE | c.1030G>A|p.Asp344Asn |
S17 |
6 | BAA06g28890 | A06 | 19756962 | G | A | missense_variant&splice_region_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S219 |
7 | BAA06g28890 | A06 | 19757086 | G | A | synonymous_variant | LOW | c.1185G>A|p.Glu395Glu |
S249 |
8 | BAA06g28890 | A06 | 19757498 | C | T | synonymous_variant | LOW | c.1527C>T|p.His509His |
S16 |