Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15760 | A04 | 20431595 | C | T | upstream_gene_variant | MODIFIER | c.-4166C>T| |
S1 |
2 | BAA04g15760 | A04 | 20431964 | G | A | upstream_gene_variant | MODIFIER | c.-3797G>A| |
S94 |
3 | BAA04g15760 | A04 | 20432641 | C | T | upstream_gene_variant | MODIFIER | c.-3120C>T| |
S200 |
4 | BAA04g15760 | A04 | 20433360 | G | A | upstream_gene_variant | MODIFIER | c.-2401G>A| |
S50 |
5 | BAA04g15760 | A04 | 20434272 | G | A | upstream_gene_variant | MODIFIER | c.-1489G>A| |
S174 S27 |
6 | BAA04g15760 | A04 | 20435190 | G | A | upstream_gene_variant | MODIFIER | c.-571G>A| |
S43 |
7 | BAA04g15760 | A04 | 20435504 | G | A | upstream_gene_variant | MODIFIER | c.-257G>A| |
S60 |
8 | BAA04g15760 | A04 | 20436986 | G | A | synonymous_variant | LOW | c.645G>A|p.Arg215Arg |
S36 |
9 | BAA04g15760 | A04 | 20437659 | G | A | missense_variant | MODERATE | c.1030G>A|p.Gly344Ser |
S233 |
10 | BAA04g15760 | A04 | 20437874 | C | T | missense_variant | MODERATE | c.1153C>T|p.Pro385Ser |
S202 |
11 | BAA04g15760 | A04 | 20439717 | C | T | missense_variant | MODERATE | c.2032C>T|p.Leu678Phe |
S210 |
12 | BAA04g15760 | A04 | 20439864 | C | T | missense_variant | MODERATE | c.2179C>T|p.Leu727Phe |
S167 |
13 | BAA04g15760 | A04 | 20440164 | G | A | missense_variant | MODERATE | c.2287G>A|p.Gly763Arg |
S169 |
14 | BAA04g15760 | A04 | 20440802 | G | A | downstream_gene_variant | MODIFIER | c.*462G>A| |
S261 |
15 | BAA04g15760 | A04 | 20441609 | G | A | downstream_gene_variant | MODIFIER | c.*1269G>A| |
S156 |
16 | BAA04g15760 | A04 | 20442357 | C | T | downstream_gene_variant | MODIFIER | c.*2017C>T| |
S296 |