Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g37230 | A07 | 34400494 | G | A | synonymous_variant | LOW | c.174G>A|p.Gln58Gln |
S297 |
2 | BAA07g37230 | A07 | 34402685 | G | A | missense_variant | MODERATE | c.1315G>A|p.Gly439Arg |
S74 |
3 | BAA07g37230 | A07 | 34402922 | C | T | missense_variant | MODERATE | c.1552C>T|p.Pro518Ser |
S111 |
4 | BAA07g37230 | A07 | 34402955 | G | A | missense_variant | MODERATE | c.1585G>A|p.Glu529Lys |
S291 |
5 | BAA07g37230 | A07 | 34403024 | C | T | missense_variant | MODERATE | c.1654C>T|p.Pro552Ser |
S277 |
6 | BAA07g37230 | A07 | 34403382 | G | A | splice_region_variant&intron_variant | LOW | c.2006+6G>A| |
S152 |
7 | BAA07g37230 | A07 | 34403805 | G | A | missense_variant | MODERATE | c.2186G>A|p.Arg729Lys |
S79 S84 |
8 | BAA07g37230 | A07 | 34405126 | G | A | missense_variant | MODERATE | c.3226G>A|p.Ala1076Thr |
S205 |
9 | BAA07g37230 | A07 | 34405214 | C | T | missense_variant | MODERATE | c.3314C>T|p.Pro1105Leu |
S27 |
10 | BAA07g37230 | A07 | 34406377 | C | T | downstream_gene_variant | MODIFIER | c.*502C>T| |
S129 |
11 | BAA07g37230 | A07 | 34406793 | C | T | downstream_gene_variant | MODIFIER | c.*918C>T| |
S23 |
12 | BAA07g37230 | A07 | 34407771 | C | T | downstream_gene_variant | MODIFIER | c.*1896C>T| |
S32 |