Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01790 | A07 | 1303675 | G | A | missense_variant | MODERATE | c.521C>T|p.Ala174Val |
S134 |
2 | BAA07g01790 | A07 | 1304474 | C | T | missense_variant | MODERATE | c.7G>A|p.Gly3Ser |
S247 |
3 | BAA07g01790 | A07 | 1305199 | C | T | upstream_gene_variant | MODIFIER | c.-719G>A| |
S112 |
4 | BAA07g01790 | A07 | 1305234 | C | T | upstream_gene_variant | MODIFIER | c.-754G>A| |
S168 |
5 | BAA07g01790 | A07 | 1305669 | C | T | upstream_gene_variant | MODIFIER | c.-1189G>A| |
S165 |
6 | BAA07g01790 | A07 | 1306321 | A | G | upstream_gene_variant | MODIFIER | c.-1841T>C| |
S165 |
7 | BAA07g01790 | A07 | 1306915 | G | A | upstream_gene_variant | MODIFIER | c.-2435C>T| |
S142 |
8 | BAA07g01790 | A07 | 1306919 | C | T | upstream_gene_variant | MODIFIER | c.-2439G>A| |
S18 |
9 | BAA07g01790 | A07 | 1307026 | G | A | upstream_gene_variant | MODIFIER | c.-2546C>T| |
S216 |
10 | BAA07g01790 | A07 | 1307804 | G | A | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S124 |