Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
5051 | BAA01g04130 | A01 | 1865347 | C | T | upstream_gene_variant | MODIFIER | c.-3758G>A| |
S51 |
5052 | BAA01g04130 | A01 | 1865558 | G | A | upstream_gene_variant | MODIFIER | c.-3969C>T| |
S156 |
5053 | BAA01g04130 | A01 | 1865648 | T | A | upstream_gene_variant | MODIFIER | c.-4059A>T| |
S38 |
5054 | BAA01g04150 | A01 | 1867631 | G | A | splice_region_variant&synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S116 |
5055 | BAA01g04140 | A01 | 1867958 | G | A | upstream_gene_variant | MODIFIER | c.-4823C>T| |
S174 S241 S265 S27 |
5056 | BAA01g04140 | A01 | 1868073 | C | T | upstream_gene_variant | MODIFIER | c.-4938G>A| |
S270 |
5057 | BAA01g04160 | A01 | 1869756 | G | A | upstream_gene_variant | MODIFIER | c.-106C>T| |
S216 |
5058 | BAA01g04160 | A01 | 1869862 | G | A | upstream_gene_variant | MODIFIER | c.-212C>T| |
S34 |
5059 | BAA01g04160 | A01 | 1869982 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S276 |
5060 | BAA01g04160 | A01 | 1871421 | G | A | upstream_gene_variant | MODIFIER | c.-1771C>T| |
S34 |
5061 | BAA01g04160 | A01 | 1871650 | A | T | upstream_gene_variant | MODIFIER | c.-2000T>A| |
S26 |
5062 | BAA01g04160 | A01 | 1872389 | G | A | upstream_gene_variant | MODIFIER | c.-2739C>T| |
S272 |
5063 | BAA01g04160 | A01 | 1873739 | C | T | upstream_gene_variant | MODIFIER | c.-4089G>A| |
S256 |
5064 | BAA01g04160 | A01 | 1873889 | G | A | upstream_gene_variant | MODIFIER | c.-4239C>T| |
S229 |
5065 | BAA01g04170 | A01 | 1874745 | C | T | downstream_gene_variant | MODIFIER | c.*2687G>A| |
S45 |
5066 | BAA01g04170 | A01 | 1876504 | G | A | downstream_gene_variant | MODIFIER | c.*928C>T| |
S178 |
5067 | BAA01g04170 | A01 | 1876670 | G | A | downstream_gene_variant | MODIFIER | c.*762C>T| |
S39 |
5068 | BAA01g04170 | A01 | 1877737 | C | T | missense_variant | MODERATE | c.2146G>A|p.Asp716Asn |
S204 |
5069 | BAA01g04170 | A01 | 1878265 | C | T | synonymous_variant | LOW | c.1695G>A|p.Glu565Glu |
S7 |
5070 | BAA01g04170 | A01 | 1879422 | C | T | synonymous_variant | LOW | c.852G>A|p.Thr284Thr |
S59 |
5071 | BAA01g04170 | A01 | 1880037 | G | A | synonymous_variant | LOW | c.237C>T|p.Thr79Thr |
S251 |
5072 | BAA01g04170 | A01 | 1880947 | G | A | upstream_gene_variant | MODIFIER | c.-674C>T| |
S183 S198 |
5073 | BAA01g04170 | A01 | 1882207 | C | T | upstream_gene_variant | MODIFIER | c.-1934G>A| |
S155 |
5074 | BAA01g04170 | A01 | 1882226 | C | T | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S8 |
5075 | BAA01g04180 | A01 | 1882548 | C | T | missense_variant | MODERATE | c.1301G>A|p.Gly434Glu |
S148 |