Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66280 | A09 | 60663616 | C | T | upstream_gene_variant | MODIFIER | c.-2786C>T| |
S94 |
2 | BAA09g66280 | A09 | 60663854 | G | A | upstream_gene_variant | MODIFIER | c.-2548G>A| |
S96 |
3 | BAA09g66280 | A09 | 60664233 | C | T | upstream_gene_variant | MODIFIER | c.-2169C>T| |
S133 |
4 | BAA09g66280 | A09 | 60664568 | C | T | upstream_gene_variant | MODIFIER | c.-1834C>T| |
S157 |
5 | BAA09g66280 | A09 | 60664968 | C | T | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S26 |
6 | BAA09g66280 | A09 | 60665400 | C | T | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S232 |
7 | BAA09g66280 | A09 | 60665847 | C | T | upstream_gene_variant | MODIFIER | c.-555C>T| |
S162 S280 |
8 | BAA09g66280 | A09 | 60666036 | C | T | upstream_gene_variant | MODIFIER | c.-366C>T| |
S251 |
9 | BAA09g66280 | A09 | 60666038 | T | G | upstream_gene_variant | MODIFIER | c.-364T>G| |
S149 S156 S19 S192 S194 S211 S215 S223 S242 S258 S273 S284 S304 S4 |
10 | BAA09g66280 | A09 | 60666467 | G | T | missense_variant | MODERATE | c.66G>T|p.Lys22Asn |
S156 S18 S190 S198 S204 S228 S231 S255 S267 |
11 | BAA09g66280 | A09 | 60666472 | C | T | missense_variant | MODERATE | c.71C>T|p.Thr24Met |
S296 |
12 | BAA09g66280 | A09 | 60666502 | C | T | missense_variant | MODERATE | c.101C>T|p.Ser34Phe |
S183 S198 |
13 | BAA09g66280 | A09 | 60666657 | G | A | missense_variant | MODERATE | c.256G>A|p.Glu86Lys |
S57 |
14 | BAA09g66280 | A09 | 60666659 | G | A | synonymous_variant | LOW | c.258G>A|p.Glu86Glu |
S74 |
15 | BAA09g66280 | A09 | 60666758 | G | A | synonymous_variant | LOW | c.357G>A|p.Val119Val |
S58 |
16 | BAA09g66280 | A09 | 60667789 | G | A | synonymous_variant | LOW | c.915G>A|p.Leu305Leu |
S268 |
17 | BAA09g66280 | A09 | 60667882 | G | A | synonymous_variant | LOW | c.1008G>A|p.Lys336Lys |
S40 S49 |
18 | BAA09g66280 | A09 | 60668238 | C | T | synonymous_variant | LOW | c.1203C>T|p.Phe401Phe |
S169 |