Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40050 | A06 | 26065510 | G | A | missense_variant | MODERATE | c.1282C>T|p.Pro428Ser |
S207 |
2 | BAA06g40050 | A06 | 26065767 | C | T | synonymous_variant | LOW | c.1113G>A|p.Glu371Glu |
S168 |
3 | BAA06g40050 | A06 | 26066282 | G | A | synonymous_variant | LOW | c.747C>T|p.Asn249Asn |
S210 |
4 | BAA06g40050 | A06 | 26066582 | G | A | synonymous_variant | LOW | c.513C>T|p.Val171Val |
S56 |
5 | BAA06g40050 | A06 | 26067815 | C | T | upstream_gene_variant | MODIFIER | c.-97G>A| |
S301 |
6 | BAA06g40050 | A06 | 26068501 | T | C | upstream_gene_variant | MODIFIER | c.-783A>G| |
S116 S119 S131 S135 S246 S250 S280 S34 S60 S68 S80 |
7 | BAA06g40050 | A06 | 26069832 | G | A | upstream_gene_variant | MODIFIER | c.-2114C>T| |
S233 |
8 | BAA06g40050 | A06 | 26070708 | G | A | upstream_gene_variant | MODIFIER | c.-2990C>T| |
S13 |
9 | BAA06g40050 | A06 | 26071705 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S80 |
10 | BAA06g40050 | A06 | 26072241 | G | A | upstream_gene_variant | MODIFIER | c.-4523C>T| |
S138 |
11 | BAA06g40050 | A06 | 26072288 | C | T | upstream_gene_variant | MODIFIER | c.-4570G>A| |
S163 |