Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40710 | A05 | 39243614 | C | T | downstream_gene_variant | MODIFIER | c.*1679G>A| |
S132 S137 S215 S89 |
2 | BAA05g40710 | A05 | 39243844 | C | T | downstream_gene_variant | MODIFIER | c.*1449G>A| |
S245 |
3 | BAA05g40710 | A05 | 39243887 | C | T | downstream_gene_variant | MODIFIER | c.*1406G>A| |
S243 S299 |
4 | BAA05g40710 | A05 | 39244249 | G | A | downstream_gene_variant | MODIFIER | c.*1044C>T| |
S35 |
5 | BAA05g40710 | A05 | 39244344 | G | A | downstream_gene_variant | MODIFIER | c.*949C>T| |
S237 |
6 | BAA05g40710 | A05 | 39244800 | C | T | downstream_gene_variant | MODIFIER | c.*493G>A| |
S282 |
7 | BAA05g40710 | A05 | 39245385 | C | T | missense_variant | MODERATE | c.442G>A|p.Val148Ile |
S251 |
8 | BAA05g40710 | A05 | 39245424 | G | A | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S67 |
9 | BAA05g40710 | A05 | 39245436 | G | A | missense_variant | MODERATE | c.391C>T|p.Leu131Phe |
S230 |
10 | BAA05g40710 | A05 | 39245979 | G | A | synonymous_variant | LOW | c.168C>T|p.Asp56Asp |
S32 |
11 | BAA05g40710 | A05 | 39246772 | G | A | upstream_gene_variant | MODIFIER | c.-626C>T| |
S32 |
12 | BAA05g40710 | A05 | 39246923 | G | A | upstream_gene_variant | MODIFIER | c.-777C>T| |
S116 |
13 | BAA05g40710 | A05 | 39247090 | C | T | upstream_gene_variant | MODIFIER | c.-944G>A| |
S264 |
14 | BAA05g40710 | A05 | 39249092 | C | T | upstream_gene_variant | MODIFIER | c.-2946G>A| |
S9 |
15 | BAA05g40710 | A05 | 39249715 | C | T | upstream_gene_variant | MODIFIER | c.-3569G>A| |
S123 |
16 | BAA05g40710 | A05 | 39250310 | G | A | upstream_gene_variant | MODIFIER | c.-4164C>T| |
S157 |