Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05630 | A09 | 3198976 | C | T | missense_variant | MODERATE | c.22C>T|p.Arg8Trp |
S37 |
2 | BAA09g05630 | A09 | 3199505 | C | T | missense_variant | MODERATE | c.551C>T|p.Ser184Phe |
S156 |
3 | BAA09g05630 | A09 | 3199541 | C | T | missense_variant | MODERATE | c.587C>T|p.Ser196Phe |
S260 |
4 | BAA09g05630 | A09 | 3199776 | G | A | synonymous_variant | LOW | c.822G>A|p.Arg274Arg |
S192 |
5 | BAA09g05630 | A09 | 3199913 | G | A | missense_variant | MODERATE | c.959G>A|p.Gly320Glu |
S167 |
6 | BAA09g05630 | A09 | 3200008 | G | A | missense_variant | MODERATE | c.1054G>A|p.Ala352Thr |
S23 |
7 | BAA09g05630 | A09 | 3201152 | C | T | downstream_gene_variant | MODIFIER | c.*968C>T| |
S281 |
8 | BAA09g05630 | A09 | 3202637 | C | T | downstream_gene_variant | MODIFIER | c.*2453C>T| |
S39 |
9 | BAA09g05630 | A09 | 3203061 | G | A | downstream_gene_variant | MODIFIER | c.*2877G>A| |
S262 |
10 | BAA09g05630 | A09 | 3203311 | G | A | downstream_gene_variant | MODIFIER | c.*3127G>A| |
S162 |