Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14130 | A05 | 7426415 | G | A | upstream_gene_variant | MODIFIER | c.-4903G>A| |
S158 |
2 | BAA05g14130 | A05 | 7427314 | C | T | upstream_gene_variant | MODIFIER | c.-4004C>T| |
S36 |
3 | BAA05g14130 | A05 | 7427751 | G | A | upstream_gene_variant | MODIFIER | c.-3567G>A| |
S115 |
4 | BAA05g14130 | A05 | 7428154 | C | T | upstream_gene_variant | MODIFIER | c.-3164C>T| |
S139 |
5 | BAA05g14130 | A05 | 7429505 | C | T | upstream_gene_variant | MODIFIER | c.-1813C>T| |
S111 |
6 | BAA05g14130 | A05 | 7430294 | G | A | upstream_gene_variant | MODIFIER | c.-1024G>A| |
S187 |
7 | BAA05g14130 | A05 | 7430484 | C | T | upstream_gene_variant | MODIFIER | c.-834C>T| |
S100 |
8 | BAA05g14130 | A05 | 7430492 | C | T | upstream_gene_variant | MODIFIER | c.-826C>T| |
S247 |
9 | BAA05g14130 | A05 | 7432459 | G | A | missense_variant | MODERATE | c.364G>A|p.Val122Ile |
S153 |
10 | BAA05g14130 | A05 | 7432654 | G | A | missense_variant | MODERATE | c.472G>A|p.Asp158Asn |
S185 |
11 | BAA05g14130 | A05 | 7432905 | C | T | missense_variant | MODERATE | c.575C>T|p.Pro192Leu |
S295 |
12 | BAA05g14130 | A05 | 7433319 | C | T | missense_variant | MODERATE | c.989C>T|p.Pro330Leu |
S182 |