Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21600 | A09 | 13476024 | C | T | downstream_gene_variant | MODIFIER | c.*1905G>A| |
S36 |
2 | BAA09g21600 | A09 | 13477955 | C | T | missense_variant | MODERATE | c.1732G>A|p.Asp578Asn |
S174 S27 |
3 | BAA09g21600 | A09 | 13478025 | G | A | synonymous_variant | LOW | c.1662C>T|p.Leu554Leu |
S246 |
4 | BAA09g21600 | A09 | 13478325 | G | A | synonymous_variant | LOW | c.1362C>T|p.Thr454Thr |
S11 |
5 | BAA09g21600 | A09 | 13478793 | C | T | synonymous_variant | LOW | c.894G>A|p.Lys298Lys |
S11 |
6 | BAA09g21600 | A09 | 13479057 | C | T | synonymous_variant | LOW | c.630G>A|p.Gln210Gln |
S10 |
7 | BAA09g21600 | A09 | 13479240 | C | T | synonymous_variant | LOW | c.447G>A|p.Lys149Lys |
S286 |
8 | BAA09g21600 | A09 | 13479434 | C | T | missense_variant | MODERATE | c.253G>A|p.Asp85Asn |
S230 S54 |
9 | BAA09g21600 | A09 | 13479544 | G | A | missense_variant | MODERATE | c.143C>T|p.Ser48Phe |
S40 S49 |
10 | BAA09g21600 | A09 | 13481669 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S19 |
11 | BAA09g21600 | A09 | 13483038 | C | T | upstream_gene_variant | MODIFIER | c.-3352G>A| |
S160 |
12 | BAA09g21600 | A09 | 13483501 | G | A | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S42 |