Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12780 | A01 | 6046074 | C | T | missense_variant | MODERATE | c.2018G>A|p.Gly673Glu |
S90 |
2 | BAA01g12780 | A01 | 6046248 | G | A | missense_variant | MODERATE | c.1844C>T|p.Thr615Ile |
S191 |
3 | BAA01g12780 | A01 | 6046285 | T | G | missense_variant | MODERATE | c.1807A>C|p.Lys603Gln |
S263 |
4 | BAA01g12780 | A01 | 6047080 | G | A | missense_variant | MODERATE | c.1106C>T|p.Ala369Val |
S114 |
5 | BAA01g12780 | A01 | 6047248 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.939-1G>A| |
S260 |
6 | BAA01g12780 | A01 | 6047410 | G | A | synonymous_variant | LOW | c.861C>T|p.Ile287Ile |
S181 |
7 | BAA01g12780 | A01 | 6047926 | C | T | missense_variant | MODERATE | c.418G>A|p.Asp140Asn |
S128 |
8 | BAA01g12780 | A01 | 6050802 | C | T | upstream_gene_variant | MODIFIER | c.-2215G>A| |
S144 |
9 | BAA01g12780 | A01 | 6050892 | C | T | upstream_gene_variant | MODIFIER | c.-2305G>A| |
S277 |
10 | BAA01g12780 | A01 | 6051036 | C | T | upstream_gene_variant | MODIFIER | c.-2449G>A| |
S128 |