Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12650 | A10 | 14051848 | G | A | upstream_gene_variant | MODIFIER | c.-4795G>A| |
S197 |
2 | BAA10g12650 | A10 | 14051985 | G | A | upstream_gene_variant | MODIFIER | c.-4658G>A| |
S55 |
3 | BAA10g12650 | A10 | 14053451 | G | A | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S74 |
4 | BAA10g12650 | A10 | 14053755 | C | T | upstream_gene_variant | MODIFIER | c.-2888C>T| |
S25 |
5 | BAA10g12650 | A10 | 14055141 | T | A | upstream_gene_variant | MODIFIER | c.-1502T>A| |
S125 |
6 | BAA10g12650 | A10 | 14055463 | G | A | upstream_gene_variant | MODIFIER | c.-1180G>A| |
S267 |
7 | BAA10g12650 | A10 | 14056309 | G | A | upstream_gene_variant | MODIFIER | c.-334G>A| |
S55 |
8 | BAA10g12650 | A10 | 14056473 | G | A | upstream_gene_variant | MODIFIER | c.-170G>A| |
S57 |
9 | BAA10g12650 | A10 | 14056765 | G | A | synonymous_variant | LOW | c.123G>A|p.Thr41Thr |
S75 S81 |
10 | BAA10g12650 | A10 | 14056817 | C | T | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S167 |
11 | BAA10g12650 | A10 | 14056966 | C | T | synonymous_variant | LOW | c.324C>T|p.Asn108Asn |
S243 S299 |
12 | BAA10g12650 | A10 | 14058631 | G | A | downstream_gene_variant | MODIFIER | c.*9G>A| |
S90 |