Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12140 | A08 | 10634622 | C | T | missense_variant | MODERATE | c.1717G>A|p.Asp573Asn |
S274 |
2 | BAA08g12140 | A08 | 10634678 | G | A | missense_variant | MODERATE | c.1661C>T|p.Ala554Val |
S5 |
3 | BAA08g12140 | A08 | 10635150 | C | T | missense_variant | MODERATE | c.1189G>A|p.Glu397Lys |
S9 |
4 | BAA08g12140 | A08 | 10635510 | C | T | missense_variant | MODERATE | c.829G>A|p.Glu277Lys |
S177 |
5 | BAA08g12140 | A08 | 10635573 | C | T | missense_variant | MODERATE | c.766G>A|p.Val256Met |
S155 |
6 | BAA08g12140 | A08 | 10636202 | C | T | synonymous_variant | LOW | c.207G>A|p.Glu69Glu |
S259 |
7 | BAA08g12140 | A08 | 10636661 | C | T | upstream_gene_variant | MODIFIER | c.-253G>A| |
S119 |
8 | BAA08g12140 | A08 | 10636777 | G | A | upstream_gene_variant | MODIFIER | c.-369C>T| |
S177 |
9 | BAA08g12140 | A08 | 10636913 | G | A | upstream_gene_variant | MODIFIER | c.-505C>T| |
S19 |
10 | BAA08g12140 | A08 | 10639077 | C | T | upstream_gene_variant | MODIFIER | c.-2669G>A| |
S256 |
11 | BAA08g12140 | A08 | 10639196 | C | T | upstream_gene_variant | MODIFIER | c.-2788G>A| |
S284 |
12 | BAA08g12140 | A08 | 10639509 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S157 |