Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g17200 | A08 | 14073173 | C | T | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S88 |
2 | BAA08g17200 | A08 | 14073383 | C | T | upstream_gene_variant | MODIFIER | c.-3605C>T| |
S176 |
3 | BAA08g17200 | A08 | 14073836 | C | T | upstream_gene_variant | MODIFIER | c.-3152C>T| |
S89 |
4 | BAA08g17200 | A08 | 14075189 | G | A | upstream_gene_variant | MODIFIER | c.-1799G>A| |
S115 |
5 | BAA08g17200 | A08 | 14076560 | C | T | upstream_gene_variant | MODIFIER | c.-428C>T| |
S303 |
6 | BAA08g17200 | A08 | 14077003 | G | A | missense_variant | MODERATE | c.16G>A|p.Asp6Asn |
S75 S81 |
7 | BAA08g17200 | A08 | 14077020 | C | T | synonymous_variant | LOW | c.33C>T|p.Tyr11Tyr |
S296 |
8 | BAA08g17200 | A08 | 14077053 | C | T | synonymous_variant | LOW | c.66C>T|p.Val22Val |
S6 |
9 | BAA08g17200 | A08 | 14078556 | G | A | downstream_gene_variant | MODIFIER | c.*787G>A| |
S280 |