Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16890 | A09 | 10023639 | G | A | upstream_gene_variant | MODIFIER | c.-3081G>A| |
S164 |
2 | BAA09g16890 | A09 | 10023661 | G | A | upstream_gene_variant | MODIFIER | c.-3059G>A| |
S170 |
3 | BAA09g16890 | A09 | 10023849 | T | C | upstream_gene_variant | MODIFIER | c.-2871T>C| |
S178 |
4 | BAA09g16890 | A09 | 10023907 | G | A | upstream_gene_variant | MODIFIER | c.-2813G>A| |
S89 |
5 | BAA09g16890 | A09 | 10024176 | C | T | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S242 |
6 | BAA09g16890 | A09 | 10026650 | C | T | upstream_gene_variant | MODIFIER | c.-70C>T| |
S84 S93 |
7 | BAA09g16890 | A09 | 10026860 | C | T | intron_variant | MODIFIER | c.57-35C>T| |
S68 |
8 | BAA09g16890 | A09 | 10026986 | G | A | missense_variant | MODERATE | c.148G>A|p.Ala50Thr |
S95 |
9 | BAA09g16890 | A09 | 10027271 | G | A | missense_variant | MODERATE | c.433G>A|p.Asp145Asn |
S105 S106 |
10 | BAA09g16890 | A09 | 10027524 | G | A | missense_variant | MODERATE | c.686G>A|p.Arg229His |
S44 |
11 | BAA09g16890 | A09 | 10027674 | C | T | downstream_gene_variant | MODIFIER | c.*134C>T| |
S156 |
12 | BAA09g16890 | A09 | 10027761 | C | T | downstream_gene_variant | MODIFIER | c.*221C>T| |
S36 |
13 | BAA09g16890 | A09 | 10030034 | G | A | downstream_gene_variant | MODIFIER | c.*2494G>A| |
S33 |
14 | BAA09g16890 | A09 | 10030051 | G | A | downstream_gene_variant | MODIFIER | c.*2511G>A| |
S170 |