Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66270 | A03 | 40593521 | C | T | upstream_gene_variant | MODIFIER | c.-4698C>T| |
S57 |
2 | BAA03g66270 | A03 | 40594736 | C | T | upstream_gene_variant | MODIFIER | c.-3483C>T| |
S201 |
3 | BAA03g66270 | A03 | 40595242 | C | T | upstream_gene_variant | MODIFIER | c.-2977C>T| |
S140 |
4 | BAA03g66270 | A03 | 40595491 | G | A | upstream_gene_variant | MODIFIER | c.-2728G>A| |
S233 |
5 | BAA03g66270 | A03 | 40596219 | C | T | upstream_gene_variant | MODIFIER | c.-2000C>T| |
S91 |
6 | BAA03g66270 | A03 | 40596541 | G | A | upstream_gene_variant | MODIFIER | c.-1678G>A| |
S140 S168 S278 S279 |
7 | BAA03g66270 | A03 | 40596668 | T | A | upstream_gene_variant | MODIFIER | c.-1551T>A| |
S175 |
8 | BAA03g66270 | A03 | 40598344 | C | T | synonymous_variant | LOW | c.126C>T|p.Leu42Leu |
S298 |
9 | BAA03g66270 | A03 | 40599377 | C | T | missense_variant | MODERATE | c.1159C>T|p.Pro387Ser |
S200 |
10 | BAA03g66270 | A03 | 40600133 | G | A | synonymous_variant | LOW | c.1605G>A|p.Ser535Ser |
S114 |
11 | BAA03g66270 | A03 | 40600273 | G | A | missense_variant | MODERATE | c.1745G>A|p.Arg582Lys |
S267 |
12 | BAA03g66270 | A03 | 40601215 | C | T | downstream_gene_variant | MODIFIER | c.*914C>T| |
S205 |
13 | BAA03g66270 | A03 | 40601228 | C | T | downstream_gene_variant | MODIFIER | c.*927C>T| |
S195 |
14 | BAA03g66270 | A03 | 40601996 | G | A | downstream_gene_variant | MODIFIER | c.*1695G>A| |
S259 |
15 | BAA03g66270 | A03 | 40603233 | C | T | downstream_gene_variant | MODIFIER | c.*2932C>T| |
S32 |
16 | BAA03g66270 | A03 | 40603523 | C | T | downstream_gene_variant | MODIFIER | c.*3222C>T| |
S172 |
17 | BAA03g66270 | A03 | 40603974 | G | A | downstream_gene_variant | MODIFIER | c.*3673G>A| |
S136 |
18 | BAA03g66270 | A03 | 40604707 | G | A | downstream_gene_variant | MODIFIER | c.*4406G>A| |
S282 |
19 | BAA03g66270 | A03 | 40605092 | G | A | downstream_gene_variant | MODIFIER | c.*4791G>A| |
S221 |
20 | BAA03g66270 | A03 | 40605247 | C | T | downstream_gene_variant | MODIFIER | c.*4946C>T| |
S39 |