Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04980 | A05 | 2412885 | C | T | upstream_gene_variant | MODIFIER | c.-4871C>T| |
S98 |
2 | BAA05g04980 | A05 | 2413694 | C | T | upstream_gene_variant | MODIFIER | c.-4062C>T| |
S100 |
3 | BAA05g04980 | A05 | 2414420 | C | T | upstream_gene_variant | MODIFIER | c.-3336C>T| |
S59 |
4 | BAA05g04980 | A05 | 2415066 | C | T | upstream_gene_variant | MODIFIER | c.-2690C>T| |
S123 |
5 | BAA05g04980 | A05 | 2415376 | C | T | upstream_gene_variant | MODIFIER | c.-2380C>T| |
S280 |
6 | BAA05g04980 | A05 | 2415763 | C | T | upstream_gene_variant | MODIFIER | c.-1993C>T| |
S304 |
7 | BAA05g04980 | A05 | 2416744 | C | T | upstream_gene_variant | MODIFIER | c.-1012C>T| |
S2 |
8 | BAA05g04980 | A05 | 2418918 | C | T | missense_variant | MODERATE | c.1163C>T|p.Ser388Phe |
S160 |
9 | BAA05g04980 | A05 | 2419774 | C | T | synonymous_variant | LOW | c.1362C>T|p.Pro454Pro |
S298 |
10 | BAA05g04980 | A05 | 2419789 | C | T | synonymous_variant | LOW | c.1377C>T|p.Ala459Ala |
S10 |