Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40590 | A05 | 39196696 | C | T | upstream_gene_variant | MODIFIER | c.-966C>T| |
S219 S72 |
2 | BAA05g40590 | A05 | 39196857 | G | A | upstream_gene_variant | MODIFIER | c.-805G>A| |
S206 S26 |
3 | BAA05g40590 | A05 | 39196859 | G | A | upstream_gene_variant | MODIFIER | c.-803G>A| |
S229 |
4 | BAA05g40590 | A05 | 39196895 | G | A | upstream_gene_variant | MODIFIER | c.-767G>A| |
S17 |
5 | BAA05g40590 | A05 | 39196939 | C | T | upstream_gene_variant | MODIFIER | c.-723C>T| |
S182 |
6 | BAA05g40590 | A05 | 39197047 | C | T | upstream_gene_variant | MODIFIER | c.-615C>T| |
S33 |
7 | BAA05g40590 | A05 | 39197821 | G | A | missense_variant | MODERATE | c.160G>A|p.Gly54Arg |
S110 |
8 | BAA05g40590 | A05 | 39198305 | G | A | missense_variant | MODERATE | c.443G>A|p.Gly148Asp |
S283 |
9 | BAA05g40590 | A05 | 39198452 | G | A | missense_variant | MODERATE | c.590G>A|p.Gly197Glu |
S247 |
10 | BAA05g40590 | A05 | 39199874 | G | A | missense_variant | MODERATE | c.1453G>A|p.Asp485Asn |
S242 |
11 | BAA05g40590 | A05 | 39200140 | C | T | synonymous_variant | LOW | c.1719C>T|p.Asp573Asp |
S185 S203 S273 |
12 | BAA05g40590 | A05 | 39200264 | G | A | missense_variant | MODERATE | c.1843G>A|p.Asp615Asn |
S149 |
13 | BAA05g40590 | A05 | 39200588 | C | T | missense_variant | MODERATE | c.2167C>T|p.Pro723Ser |
S66 |
14 | BAA05g40590 | A05 | 39200679 | G | A | missense_variant | MODERATE | c.2258G>A|p.Arg753Lys |
S140 |