Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38660 | A09 | 46416913 | G | A | upstream_gene_variant | MODIFIER | c.-1103G>A| |
S71 |
2 | BAA09g38660 | A09 | 46418574 | G | A | missense_variant | MODERATE | c.559G>A|p.Glu187Lys |
S274 |
3 | BAA09g38660 | A09 | 46418634 | G | A | missense_variant | MODERATE | c.619G>A|p.Asp207Asn |
S202 |
4 | BAA09g38660 | A09 | 46418860 | G | A | missense_variant | MODERATE | c.845G>A|p.Gly282Glu |
S236 |
5 | BAA09g38660 | A09 | 46419527 | G | A | missense_variant&splice_region_variant | MODERATE | c.1439G>A|p.Arg480Lys |
S281 |
6 | BAA09g38660 | A09 | 46419604 | G | A | intron_variant | MODIFIER | c.1439+77G>A| |
S221 |
7 | BAA09g38660 | A09 | 46420057 | G | A | splice_region_variant&intron_variant | LOW | c.1551+5G>A| |
S128 |
8 | BAA09g38660 | A09 | 46421577 | G | A | downstream_gene_variant | MODIFIER | c.*587G>A| |
S15 S3 |
9 | BAA09g38660 | A09 | 46421841 | G | A | downstream_gene_variant | MODIFIER | c.*851G>A| |
S188 |
10 | BAA09g38660 | A09 | 46422133 | G | A | downstream_gene_variant | MODIFIER | c.*1143G>A| |
S271 |