Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39420 | A09 | 47049342 | C | T | upstream_gene_variant | MODIFIER | c.-1700C>T| |
S261 |
2 | BAA09g39420 | A09 | 47049659 | C | T | upstream_gene_variant | MODIFIER | c.-1383C>T| |
S77 S82 |
3 | BAA09g39420 | A09 | 47050202 | G | A | upstream_gene_variant | MODIFIER | c.-840G>A| |
S160 |
4 | BAA09g39420 | A09 | 47052541 | C | T | synonymous_variant | LOW | c.411C>T|p.Asn137Asn |
S292 |
5 | BAA09g39420 | A09 | 47052584 | C | T | stop_gained | HIGH | c.454C>T|p.Gln152* |
S95 |
6 | BAA09g39420 | A09 | 47052902 | G | A | missense_variant | MODERATE | c.772G>A|p.Glu258Lys |
S2 |
7 | BAA09g39420 | A09 | 47052972 | C | T | missense_variant | MODERATE | c.842C>T|p.Ser281Phe |
S238 |
8 | BAA09g39420 | A09 | 47053522 | G | A | missense_variant | MODERATE | c.1125G>A|p.Met375Ile |
S11 |
9 | BAA09g39420 | A09 | 47054148 | C | T | missense_variant | MODERATE | c.1621C>T|p.His541Tyr |
S278 |
10 | BAA09g39420 | A09 | 47055859 | C | T | synonymous_variant | LOW | c.3054C>T|p.Leu1018Leu |
S95 |
11 | BAA09g39420 | A09 | 47058433 | G | A | downstream_gene_variant | MODIFIER | c.*1317G>A| |
S157 |