Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69120 | A09 | 61825625 | C | T | upstream_gene_variant | MODIFIER | c.-3161C>T| |
S168 |
2 | BAA09g69120 | A09 | 61825799 | C | T | upstream_gene_variant | MODIFIER | c.-2987C>T| |
S149 |
3 | BAA09g69120 | A09 | 61826870 | G | A | upstream_gene_variant | MODIFIER | c.-1916G>A| |
S295 |
4 | BAA09g69120 | A09 | 61826973 | C | T | upstream_gene_variant | MODIFIER | c.-1813C>T| |
S41 |
5 | BAA09g69120 | A09 | 61826975 | G | A | upstream_gene_variant | MODIFIER | c.-1811G>A| |
S74 |
6 | BAA09g69120 | A09 | 61827195 | C | T | upstream_gene_variant | MODIFIER | c.-1591C>T| |
S104 |
7 | BAA09g69120 | A09 | 61828195 | C | T | upstream_gene_variant | MODIFIER | c.-591C>T| |
S199 S59 |
8 | BAA09g69120 | A09 | 61828421 | C | T | upstream_gene_variant | MODIFIER | c.-365C>T| |
S56 |
9 | BAA09g69120 | A09 | 61828553 | C | T | upstream_gene_variant | MODIFIER | c.-233C>T| |
S75 S81 |
10 | BAA09g69120 | A09 | 61828972 | G | A | missense_variant | MODERATE | c.187G>A|p.Gly63Ser |
S238 |
11 | BAA09g69120 | A09 | 61829152 | G | A | missense_variant | MODERATE | c.367G>A|p.Asp123Asn |
S84 S93 |
12 | BAA09g69120 | A09 | 61830299 | C | T | synonymous_variant | LOW | c.1303C>T|p.Leu435Leu |
S18 |
13 | BAA09g69120 | A09 | 61830931 | G | A | synonymous_variant | LOW | c.1935G>A|p.Arg645Arg |
S288 |
14 | BAA09g69120 | A09 | 61831108 | G | A | downstream_gene_variant | MODIFIER | c.*57G>A| |
S25 |
15 | BAA09g69120 | A09 | 61832726 | C | T | downstream_gene_variant | MODIFIER | c.*1675C>T| |
S104 |
16 | BAA09g69120 | A09 | 61834277 | G | A | downstream_gene_variant | MODIFIER | c.*3226G>A| |
S244 |