Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35290 | A09 | 43715090 | C | T | upstream_gene_variant | MODIFIER | c.-4300C>T| |
S86 |
2 | BAA09g35290 | A09 | 43715128 | C | T | upstream_gene_variant | MODIFIER | c.-4262C>T| |
S237 |
3 | BAA09g35290 | A09 | 43717100 | C | G | upstream_gene_variant | MODIFIER | c.-2290C>G| |
S290 |
4 | BAA09g35290 | A09 | 43717290 | C | T | upstream_gene_variant | MODIFIER | c.-2100C>T| |
S256 |
5 | BAA09g35290 | A09 | 43717369 | C | T | upstream_gene_variant | MODIFIER | c.-2021C>T| |
S114 |
6 | BAA09g35290 | A09 | 43718787 | C | T | upstream_gene_variant | MODIFIER | c.-603C>T| |
S246 |
7 | BAA09g35290 | A09 | 43719166 | G | A | upstream_gene_variant | MODIFIER | c.-224G>A| |
S148 S210 |
8 | BAA09g35290 | A09 | 43719798 | C | T | intron_variant | MODIFIER | c.237+25C>T| |
S117 |
9 | BAA09g35290 | A09 | 43720102 | C | T | synonymous_variant | LOW | c.405C>T|p.Phe135Phe |
S213 |
10 | BAA09g35290 | A09 | 43720140 | C | T | missense_variant | MODERATE | c.443C>T|p.Ala148Val |
S58 |
11 | BAA09g35290 | A09 | 43721997 | C | T | downstream_gene_variant | MODIFIER | c.*1322C>T| |
S90 |
12 | BAA09g35290 | A09 | 43724571 | C | T | downstream_gene_variant | MODIFIER | c.*3896C>T| |
S271 |