Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13330 | A08 | 11560514 | G | A | upstream_gene_variant | MODIFIER | c.-4553G>A| |
S164 |
2 | BAA08g13330 | A08 | 11560685 | C | T | upstream_gene_variant | MODIFIER | c.-4382C>T| |
S230 |
3 | BAA08g13330 | A08 | 11561588 | C | T | upstream_gene_variant | MODIFIER | c.-3479C>T| |
S276 |
4 | BAA08g13330 | A08 | 11561635 | G | A | upstream_gene_variant | MODIFIER | c.-3432G>A| |
S221 |
5 | BAA08g13330 | A08 | 11562940 | G | A | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S232 |
6 | BAA08g13330 | A08 | 11563446 | C | T | upstream_gene_variant | MODIFIER | c.-1621C>T| |
S269 |
7 | BAA08g13330 | A08 | 11565153 | C | T | synonymous_variant | LOW | c.87C>T|p.His29His |
S53 |
8 | BAA08g13330 | A08 | 11565660 | C | T | missense_variant | MODERATE | c.416C>T|p.Pro139Leu |
S294 |
9 | BAA08g13330 | A08 | 11566267 | C | T | synonymous_variant | LOW | c.774C>T|p.Tyr258Tyr |
S18 |
10 | BAA08g13330 | A08 | 11566274 | G | A | missense_variant | MODERATE | c.781G>A|p.Asp261Asn |
S281 |
11 | BAA08g13330 | A08 | 11566610 | C | T | missense_variant | MODERATE | c.844C>T|p.Leu282Phe |
S17 |
12 | BAA08g13330 | A08 | 11567112 | G | A | intron_variant | MODIFIER | c.1047+99G>A| |
S269 |
13 | BAA08g13330 | A08 | 11568196 | G | A | downstream_gene_variant | MODIFIER | c.*390G>A| |
S130 |
14 | BAA08g13330 | A08 | 11569245 | G | A | downstream_gene_variant | MODIFIER | c.*1439G>A| |
S245 |
15 | BAA08g13330 | A08 | 11570606 | G | A | downstream_gene_variant | MODIFIER | c.*2800G>A| |
S48 |
16 | BAA08g13330 | A08 | 11572067 | G | A | downstream_gene_variant | MODIFIER | c.*4261G>A| |
S127 |