Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44570 | A09 | 50179761 | G | A | missense_variant | MODERATE | c.2557C>T|p.Pro853Ser |
S51 |
2 | BAA09g44570 | A09 | 50180019 | C | T | missense_variant | MODERATE | c.2299G>A|p.Gly767Arg |
S61 |
3 | BAA09g44570 | A09 | 50180333 | G | A | missense_variant | MODERATE | c.2065C>T|p.Leu689Phe |
S288 |
4 | BAA09g44570 | A09 | 50181166 | C | T | missense_variant | MODERATE | c.1312G>A|p.Gly438Arg |
S96 |
5 | BAA09g44570 | A09 | 50181793 | C | T | missense_variant | MODERATE | c.685G>A|p.Asp229Asn |
S245 |
6 | BAA09g44570 | A09 | 50181995 | C | T | synonymous_variant | LOW | c.483G>A|p.Val161Val |
S117 |
7 | BAA09g44570 | A09 | 50182160 | C | T | synonymous_variant | LOW | c.318G>A|p.Lys106Lys |
S63 |
8 | BAA09g44570 | A09 | 50184312 | G | A | upstream_gene_variant | MODIFIER | c.-1835C>T| |
S281 |
9 | BAA09g44570 | A09 | 50184807 | C | T | upstream_gene_variant | MODIFIER | c.-2330G>A| |
S237 |
10 | BAA09g44570 | A09 | 50185898 | G | A | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S62 |
11 | BAA09g44570 | A09 | 50186804 | C | T | upstream_gene_variant | MODIFIER | c.-4327G>A| |
S183 S198 |