Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20390 | A01 | 10032761 | C | T | downstream_gene_variant | MODIFIER | c.*4050G>A| |
S41 |
2 | BAA01g20390 | A01 | 10033676 | G | A | downstream_gene_variant | MODIFIER | c.*3135C>T| |
S14 S251 |
3 | BAA01g20390 | A01 | 10034618 | G | A | downstream_gene_variant | MODIFIER | c.*2193C>T| |
S186 |
4 | BAA01g20390 | A01 | 10035010 | C | T | downstream_gene_variant | MODIFIER | c.*1801G>A| |
S302 |
5 | BAA01g20390 | A01 | 10035102 | C | T | downstream_gene_variant | MODIFIER | c.*1709G>A| |
S107 |
6 | BAA01g20390 | A01 | 10036601 | C | T | downstream_gene_variant | MODIFIER | c.*210G>A| |
S10 |
7 | BAA01g20390 | A01 | 10036753 | C | T | downstream_gene_variant | MODIFIER | c.*58G>A| |
S231 |
8 | BAA01g20390 | A01 | 10037374 | G | A | missense_variant | MODERATE | c.286C>T|p.Pro96Ser |
S279 |
9 | BAA01g20390 | A01 | 10037608 | C | T | missense_variant | MODERATE | c.52G>A|p.Asp18Asn |
S230 |
10 | BAA01g20390 | A01 | 10037717 | G | A | upstream_gene_variant | MODIFIER | c.-58C>T| |
S306 S308 |
11 | BAA01g20390 | A01 | 10037999 | G | A | upstream_gene_variant | MODIFIER | c.-340C>T| |
S245 |
12 | BAA01g20390 | A01 | 10039743 | C | T | upstream_gene_variant | MODIFIER | c.-2084G>A| |
S38 |
13 | BAA01g20390 | A01 | 10041193 | C | T | upstream_gene_variant | MODIFIER | c.-3534G>A| |
S230 |
14 | BAA01g20390 | A01 | 10041523 | C | T | upstream_gene_variant | MODIFIER | c.-3864G>A| |
S159 S243 |
15 | BAA01g20390 | A01 | 10042289 | C | T | upstream_gene_variant | MODIFIER | c.-4630G>A| |
S18 |