Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39860 | A01 | 26473335 | G | A | downstream_gene_variant | MODIFIER | c.*2656C>T| |
S15 S3 |
2 | BAA01g39860 | A01 | 26474191 | G | A | downstream_gene_variant | MODIFIER | c.*1800C>T| |
S76 |
3 | BAA01g39860 | A01 | 26474773 | C | T | downstream_gene_variant | MODIFIER | c.*1218G>A| |
S204 |
4 | BAA01g39860 | A01 | 26474789 | G | A | downstream_gene_variant | MODIFIER | c.*1202C>T| |
S245 |
5 | BAA01g39860 | A01 | 26475036 | G | A | downstream_gene_variant | MODIFIER | c.*955C>T| |
S199 |
6 | BAA01g39860 | A01 | 26475186 | C | T | downstream_gene_variant | MODIFIER | c.*805G>A| |
S158 |
7 | BAA01g39860 | A01 | 26475572 | G | A | downstream_gene_variant | MODIFIER | c.*419C>T| |
S38 |
8 | BAA01g39860 | A01 | 26476611 | G | A | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S298 |
9 | BAA01g39860 | A01 | 26477209 | C | T | upstream_gene_variant | MODIFIER | c.-436G>A| |
S81 |
10 | BAA01g39860 | A01 | 26478058 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S157 |
11 | BAA01g39860 | A01 | 26478295 | G | A | upstream_gene_variant | MODIFIER | c.-1522C>T| |
S138 |
12 | BAA01g39860 | A01 | 26479693 | C | T | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S32 |
13 | BAA01g39860 | A01 | 26480063 | G | A | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S287 |
14 | BAA01g39860 | A01 | 26480362 | G | A | upstream_gene_variant | MODIFIER | c.-3589C>T| |
S86 |
15 | BAA01g39860 | A01 | 26480784 | C | T | upstream_gene_variant | MODIFIER | c.-4011G>A| |
S131 |
16 | BAA01g39860 | A01 | 26481046 | G | A | upstream_gene_variant | MODIFIER | c.-4273C>T| |
S5 |
17 | BAA01g39860 | A01 | 26481414 | C | T | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S41 |
18 | BAA01g39860 | A01 | 26481537 | T | A | upstream_gene_variant | MODIFIER | c.-4764A>T| |
S12 |