Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06400 | A05 | 3103019 | C | T | missense_variant | MODERATE | c.2447G>A|p.Ser816Asn |
S19 |
2 | BAA05g06400 | A05 | 3103223 | G | A | missense_variant | MODERATE | c.2243C>T|p.Thr748Ile |
S284 |
3 | BAA05g06400 | A05 | 3104617 | C | T | missense_variant | MODERATE | c.1604G>A|p.Gly535Asp |
S182 |
4 | BAA05g06400 | A05 | 3104960 | G | A | synonymous_variant | LOW | c.1542C>T|p.His514His |
S48 |
5 | BAA05g06400 | A05 | 3106237 | C | T | splice_region_variant&synonymous_variant | LOW | c.1200G>A|p.Lys400Lys |
S19 |
6 | BAA05g06400 | A05 | 3108138 | G | A | missense_variant | MODERATE | c.581C>T|p.Ser194Phe |
S167 |
7 | BAA05g06400 | A05 | 3108513 | C | T | synonymous_variant | LOW | c.276G>A|p.Glu92Glu |
S115 |
8 | BAA05g06400 | A05 | 3109340 | C | T | upstream_gene_variant | MODIFIER | c.-552G>A| |
S13 S140 S168 S279 |
9 | BAA05g06400 | A05 | 3110553 | G | A | upstream_gene_variant | MODIFIER | c.-1765C>T| |
S11 |
10 | BAA05g06400 | A05 | 3111431 | C | T | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S183 S198 |