Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g08780 | A07 | 17704241 | G | A | synonymous_variant | LOW | c.369C>T|p.Asp123Asp |
S182 |
2 | BAA07g08780 | A07 | 17705693 | G | A | intron_variant | MODIFIER | c.358+32C>T| |
S190 |
3 | BAA07g08780 | A07 | 17706609 | C | T | intron_variant | MODIFIER | c.230-324G>A| |
S232 |
4 | BAA07g08780 | A07 | 17706656 | C | T | intron_variant | MODIFIER | c.230-371G>A| |
S94 |
5 | BAA07g08780 | A07 | 17707647 | G | A | intron_variant | MODIFIER | c.230-1362C>T| |
S267 |
6 | BAA07g08780 | A07 | 17710490 | C | T | intron_variant | MODIFIER | c.229+199G>A| |
S23 |
7 | BAA07g08780 | A07 | 17710711 | G | A | synonymous_variant | LOW | c.207C>T|p.His69His |
S175 S177 |
8 | BAA07g08780 | A07 | 17710788 | C | T | missense_variant | MODERATE | c.130G>A|p.Asp44Asn |
S81 |
9 | BAA07g08780 | A07 | 17711671 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S139 |
10 | BAA07g08780 | A07 | 17713663 | G | A | upstream_gene_variant | MODIFIER | c.-2678C>T| |
S176 |
11 | BAA07g08780 | A07 | 17715387 | G | A | upstream_gene_variant | MODIFIER | c.-4402C>T| |
S61 |
12 | BAA07g08780 | A07 | 17715453 | G | A | upstream_gene_variant | MODIFIER | c.-4468C>T| |
S65 |