Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16980 | A05 | 9494009 | T | A | upstream_gene_variant | MODIFIER | c.-4539T>A| |
S199 |
2 | BAA05g16980 | A05 | 9494076 | C | T | upstream_gene_variant | MODIFIER | c.-4472C>T| |
S84 S93 |
3 | BAA05g16980 | A05 | 9494247 | G | A | upstream_gene_variant | MODIFIER | c.-4301G>A| |
S272 |
4 | BAA05g16980 | A05 | 9495459 | C | T | upstream_gene_variant | MODIFIER | c.-3089C>T| |
S130 |
5 | BAA05g16980 | A05 | 9495744 | C | T | upstream_gene_variant | MODIFIER | c.-2804C>T| |
S182 |
6 | BAA05g16980 | A05 | 9496223 | C | T | upstream_gene_variant | MODIFIER | c.-2325C>T| |
S162 |
7 | BAA05g16980 | A05 | 9496683 | C | T | upstream_gene_variant | MODIFIER | c.-1865C>T| |
S18 |
8 | BAA05g16980 | A05 | 9498534 | G | A | upstream_gene_variant | MODIFIER | c.-14G>A| |
S158 |
9 | BAA05g16980 | A05 | 9499350 | G | A | missense_variant | MODERATE | c.637G>A|p.Asp213Asn |
S216 |
10 | BAA05g16980 | A05 | 9499626 | G | A | missense_variant | MODERATE | c.913G>A|p.Val305Ile |
S221 |
11 | BAA05g16980 | A05 | 9500037 | C | T | downstream_gene_variant | MODIFIER | c.*16C>T| |
S185 |