Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g02590 | A05 | 1400824 | C | T | synonymous_variant | LOW | c.1203G>A|p.Val401Val |
S47 |
2 | BAA05g02590 | A05 | 1401034 | C | T | splice_region_variant&synonymous_variant | LOW | c.1077G>A|p.Gln359Gln |
S13 |
3 | BAA05g02590 | A05 | 1402819 | C | T | missense_variant | MODERATE | c.439G>A|p.Asp147Asn |
S247 |
4 | BAA05g02590 | A05 | 1403292 | C | T | missense_variant | MODERATE | c.227G>A|p.Gly76Glu |
S268 |
5 | BAA05g02590 | A05 | 1405622 | C | T | upstream_gene_variant | MODIFIER | c.-2104G>A| |
S263 |
6 | BAA05g02590 | A05 | 1405966 | G | A | upstream_gene_variant | MODIFIER | c.-2448C>T| |
S242 |
7 | BAA05g02590 | A05 | 1406351 | C | T | upstream_gene_variant | MODIFIER | c.-2833G>A| |
S99 |
8 | BAA05g02590 | A05 | 1407460 | C | T | upstream_gene_variant | MODIFIER | c.-3942G>A| |
S167 |
9 | BAA05g02590 | A05 | 1407641 | C | T | upstream_gene_variant | MODIFIER | c.-4123G>A| |
S99 |
10 | BAA05g02590 | A05 | 1407857 | C | T | upstream_gene_variant | MODIFIER | c.-4339G>A| |
S25 |
11 | BAA05g02590 | A05 | 1408250 | T | A | upstream_gene_variant | MODIFIER | c.-4732A>T| |
S299 |