Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11840 | A01 | 5531180 | C | T | missense_variant | MODERATE | c.200C>T|p.Ser67Leu |
S282 |
2 | BAA01g11840 | A01 | 5532066 | G | A | missense_variant&splice_region_variant | MODERATE | c.997G>A|p.Asp333Asn |
S251 |
3 | BAA01g11840 | A01 | 5532955 | C | T | missense_variant | MODERATE | c.1886C>T|p.Ser629Phe |
S18 |
4 | BAA01g11840 | A01 | 5533804 | C | T | synonymous_variant | LOW | c.2547C>T|p.Asn849Asn |
S38 |
5 | BAA01g11840 | A01 | 5533912 | C | T | synonymous_variant | LOW | c.2655C>T|p.Asn885Asn |
S284 |
6 | BAA01g11840 | A01 | 5535391 | G | A | missense_variant | MODERATE | c.3953G>A|p.Gly1318Asp |
S5 |
7 | BAA01g11840 | A01 | 5539655 | G | A | downstream_gene_variant | MODIFIER | c.*3707G>A| |
S109 |
8 | BAA01g11840 | A01 | 5540100 | G | A | downstream_gene_variant | MODIFIER | c.*4152G>A| |
S12 |
9 | BAA01g11840 | A01 | 5540789 | C | T | downstream_gene_variant | MODIFIER | c.*4841C>T| |
S113 |