Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26120 | A06 | 17933252 | C | T | synonymous_variant | LOW | c.1107G>A|p.Glu369Glu |
S181 |
2 | BAA06g26120 | A06 | 17933655 | G | A | stop_gained | HIGH | c.883C>T|p.Gln295* |
S44 |
3 | BAA06g26120 | A06 | 17934362 | C | T | missense_variant | MODERATE | c.340G>A|p.Gly114Arg |
S68 |
4 | BAA06g26120 | A06 | 17934486 | G | A | synonymous_variant | LOW | c.216C>T|p.Leu72Leu |
S12 |
5 | BAA06g26120 | A06 | 17934662 | C | T | missense_variant | MODERATE | c.121G>A|p.Asp41Asn |
S151 S263 |
6 | BAA06g26120 | A06 | 17934774 | C | T | synonymous_variant | LOW | c.9G>A|p.Gln3Gln |
S228 |
7 | BAA06g26120 | A06 | 17937326 | G | A | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S122 |
8 | BAA06g26120 | A06 | 17938467 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S250 |
9 | BAA06g26120 | A06 | 17939489 | G | A | upstream_gene_variant | MODIFIER | c.-4707C>T| |
S38 |