Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19040 | A08 | 15085372 | C | T | upstream_gene_variant | MODIFIER | c.-3148C>T| |
S132 S137 S89 |
2 | BAA08g19040 | A08 | 15085788 | C | T | upstream_gene_variant | MODIFIER | c.-2732C>T| |
S230 |
3 | BAA08g19040 | A08 | 15085930 | C | T | upstream_gene_variant | MODIFIER | c.-2590C>T| |
S6 |
4 | BAA08g19040 | A08 | 15088750 | C | T | missense_variant | MODERATE | c.131C>T|p.Ala44Val |
S135 |
5 | BAA08g19040 | A08 | 15088925 | G | A | missense_variant | MODERATE | c.179G>A|p.Gly60Glu |
S174 S39 |
6 | BAA08g19040 | A08 | 15090064 | G | A | missense_variant | MODERATE | c.844G>A|p.Ala282Thr |
S130 |
7 | BAA08g19040 | A08 | 15090898 | C | T | synonymous_variant | LOW | c.1311C>T|p.Asn437Asn |
S207 |
8 | BAA08g19040 | A08 | 15091428 | C | T | missense_variant | MODERATE | c.1687C>T|p.Pro563Ser |
S138 |
9 | BAA08g19040 | A08 | 15091587 | G | A | missense_variant | MODERATE | c.1780G>A|p.Asp594Asn |
S111 |
10 | BAA08g19040 | A08 | 15092765 | G | A | downstream_gene_variant | MODIFIER | c.*248G>A| |
S140 |