Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39640 | A09 | 47137654 | G | A | upstream_gene_variant | MODIFIER | c.-4763G>A| |
S176 |
2 | BAA09g39640 | A09 | 47138476 | C | T | upstream_gene_variant | MODIFIER | c.-3941C>T| |
S279 |
3 | BAA09g39640 | A09 | 47138731 | T | C | upstream_gene_variant | MODIFIER | c.-3686T>C| |
S15 S3 |
4 | BAA09g39640 | A09 | 47138885 | C | T | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S237 |
5 | BAA09g39640 | A09 | 47139009 | C | T | upstream_gene_variant | MODIFIER | c.-3408C>T| |
S68 |
6 | BAA09g39640 | A09 | 47141465 | G | A | upstream_gene_variant | MODIFIER | c.-952G>A| |
S75 S81 |
7 | BAA09g39640 | A09 | 47141873 | G | A | upstream_gene_variant | MODIFIER | c.-544G>A| |
S116 |
8 | BAA09g39640 | A09 | 47142186 | C | T | upstream_gene_variant | MODIFIER | c.-231C>T| |
S144 |
9 | BAA09g39640 | A09 | 47142502 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S61 |
10 | BAA09g39640 | A09 | 47142856 | C | T | missense_variant | MODERATE | c.440C>T|p.Ala147Val |
S32 |
11 | BAA09g39640 | A09 | 47143033 | G | A | downstream_gene_variant | MODIFIER | c.*134G>A| |
S151 S263 |
12 | BAA09g39640 | A09 | 47143057 | G | A | downstream_gene_variant | MODIFIER | c.*158G>A| |
S86 |
13 | BAA09g39640 | A09 | 47144835 | G | A | downstream_gene_variant | MODIFIER | c.*1936G>A| |
S48 |