Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02310 | A02 | 1036985 | G | A | missense_variant | MODERATE | c.2396C>T|p.Ser799Phe |
S163 |
2 | BAA02g02310 | A02 | 1037117 | G | A | missense_variant | MODERATE | c.2264C>T|p.Thr755Met |
S78 |
3 | BAA02g02310 | A02 | 1037346 | C | T | missense_variant | MODERATE | c.2035G>A|p.Glu679Lys |
S58 |
4 | BAA02g02310 | A02 | 1037800 | G | A | synonymous_variant | LOW | c.1581C>T|p.Ile527Ile |
S202 |
5 | BAA02g02310 | A02 | 1038312 | G | A | missense_variant | MODERATE | c.1069C>T|p.Arg357Cys |
S143 |
6 | BAA02g02310 | A02 | 1038313 | C | T | synonymous_variant | LOW | c.1068G>A|p.Ser356Ser |
S61 |
7 | BAA02g02310 | A02 | 1038875 | C | T | missense_variant | MODERATE | c.506G>A|p.Arg169Gln |
S100 |
8 | BAA02g02310 | A02 | 1039171 | C | T | synonymous_variant | LOW | c.210G>A|p.Arg70Arg |
S13 |
9 | BAA02g02310 | A02 | 1041511 | C | T | upstream_gene_variant | MODIFIER | c.-2131G>A| |
S280 |