Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29910 | A08 | 20402559 | G | A | upstream_gene_variant | MODIFIER | c.-3437G>A| |
S302 |
2 | BAA08g29910 | A08 | 20402593 | G | A | upstream_gene_variant | MODIFIER | c.-3403G>A| |
S219 S72 |
3 | BAA08g29910 | A08 | 20403549 | G | A | upstream_gene_variant | MODIFIER | c.-2447G>A| |
S78 S83 |
4 | BAA08g29910 | A08 | 20403829 | C | T | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S262 |
5 | BAA08g29910 | A08 | 20403838 | C | T | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S127 |
6 | BAA08g29910 | A08 | 20406051 | G | A | missense_variant | MODERATE | c.56G>A|p.Ser19Asn |
S291 |
7 | BAA08g29910 | A08 | 20406128 | C | T | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S90 |
8 | BAA08g29910 | A08 | 20406411 | G | A | missense_variant | MODERATE | c.214G>A|p.Gly72Ser |
S139 |
9 | BAA08g29910 | A08 | 20406496 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S282 |
10 | BAA08g29910 | A08 | 20407437 | C | T | missense_variant | MODERATE | c.688C>T|p.Leu230Phe |
S261 |
11 | BAA08g29910 | A08 | 20407814 | C | T | missense_variant | MODERATE | c.980C>T|p.Ser327Phe |
S44 |
12 | BAA08g29910 | A08 | 20407840 | G | A | missense_variant | MODERATE | c.1006G>A|p.Glu336Lys |
S48 |
13 | BAA08g29910 | A08 | 20408507 | G | A | missense_variant | MODERATE | c.1673G>A|p.Ser558Asn |
S78 S83 |
14 | BAA08g29910 | A08 | 20408518 | G | A | missense_variant | MODERATE | c.1684G>A|p.Asp562Asn |
S129 |
15 | BAA08g29910 | A08 | 20408958 | C | T | synonymous_variant | LOW | c.2124C>T|p.His708His |
S2 |