Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g29770 | A07 | 30312119 | G | A | missense_variant | MODERATE | c.184G>A|p.Asp62Asn |
S131 |
2 | BAA07g29770 | A07 | 30312551 | C | T | synonymous_variant | LOW | c.528C>T|p.Asn176Asn |
S233 |
3 | BAA07g29770 | A07 | 30312967 | G | A | missense_variant | MODERATE | c.775G>A|p.Val259Ile |
S10 S132 S89 |
4 | BAA07g29770 | A07 | 30314930 | C | T | downstream_gene_variant | MODIFIER | c.*1544C>T| |
S207 |
5 | BAA07g29770 | A07 | 30316295 | C | T | downstream_gene_variant | MODIFIER | c.*2909C>T| |
S32 |
6 | BAA07g29770 | A07 | 30316585 | C | T | downstream_gene_variant | MODIFIER | c.*3199C>T| |
S204 |
7 | BAA07g29770 | A07 | 30317534 | C | T | downstream_gene_variant | MODIFIER | c.*4148C>T| |
S15 S3 |
8 | BAA07g29770 | A07 | 30317807 | G | A | downstream_gene_variant | MODIFIER | c.*4421G>A| |
S80 S86 S90 S98 |
9 | BAA07g29770 | A07 | 30317929 | G | A | downstream_gene_variant | MODIFIER | c.*4543G>A| |
S42 |