Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14190 | A10 | 14988793 | T | C | upstream_gene_variant | MODIFIER | c.-3934T>C| |
S224 |
2 | BAA10g14190 | A10 | 14988860 | G | A | upstream_gene_variant | MODIFIER | c.-3867G>A| |
S69 |
3 | BAA10g14190 | A10 | 14990952 | G | A | upstream_gene_variant | MODIFIER | c.-1775G>A| |
S265 |
4 | BAA10g14190 | A10 | 14991081 | G | A | upstream_gene_variant | MODIFIER | c.-1646G>A| |
S197 |
5 | BAA10g14190 | A10 | 14991560 | G | A | upstream_gene_variant | MODIFIER | c.-1167G>A| |
S41 |
6 | BAA10g14190 | A10 | 14992519 | C | T | upstream_gene_variant | MODIFIER | c.-208C>T| |
S117 |
7 | BAA10g14190 | A10 | 14993482 | G | A | missense_variant | MODERATE | c.142G>A|p.Glu48Lys |
S65 |
8 | BAA10g14190 | A10 | 14996048 | C | T | downstream_gene_variant | MODIFIER | c.*1168C>T| |
S255 |
9 | BAA10g14190 | A10 | 14996304 | C | T | downstream_gene_variant | MODIFIER | c.*1424C>T| |
S28 |