Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00040 | A02 | 29891 | G | A | upstream_gene_variant | MODIFIER | c.-3133G>A| |
|
2 | BAA02g00040 | A02 | 31455 | C | T | upstream_gene_variant | MODIFIER | c.-1569C>T| |
S200 |
3 | BAA02g00040 | A02 | 31703 | C | T | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S174 |
4 | BAA02g00040 | A02 | 31947 | C | T | upstream_gene_variant | MODIFIER | c.-1077C>T| |
S196 |
5 | BAA02g00040 | A02 | 32144 | G | A | upstream_gene_variant | MODIFIER | c.-880G>A| |
S17 |
6 | BAA02g00040 | A02 | 32233 | C | T | upstream_gene_variant | MODIFIER | c.-791C>T| |
S115 |
7 | BAA02g00040 | A02 | 33664 | G | A | missense_variant | MODERATE | c.641G>A|p.Gly214Glu |
S33 |
8 | BAA02g00040 | A02 | 33716 | G | A | synonymous_variant | LOW | c.693G>A|p.Gly231Gly |
S118 |
9 | BAA02g00040 | A02 | 34814 | G | A | missense_variant | MODERATE | c.1711G>A|p.Ala571Thr |
S259 |
10 | BAA02g00040 | A02 | 34994 | G | A | missense_variant | MODERATE | c.1891G>A|p.Gly631Arg |
S189 |
11 | BAA02g00040 | A02 | 35186 | G | A | missense_variant | MODERATE | c.2083G>A|p.Gly695Ser |
S48 |
12 | BAA02g00040 | A02 | 36520 | C | T | downstream_gene_variant | MODIFIER | c.*636C>T| |
S167 |
13 | BAA02g00040 | A02 | 37384 | C | T | downstream_gene_variant | MODIFIER | c.*1500C>T| |
S108 |
14 | BAA02g00040 | A02 | 37741 | G | A | downstream_gene_variant | MODIFIER | c.*1857G>A| |
S237 |
15 | BAA02g00040 | A02 | 38638 | C | T | downstream_gene_variant | MODIFIER | c.*2754C>T| |
S40 S49 |