Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10930 | A04 | 16975301 | C | T | missense_variant | MODERATE | c.134C>T|p.Thr45Ile |
S132 S137 S215 |
2 | BAA04g10930 | A04 | 16975932 | G | A | missense_variant | MODERATE | c.559G>A|p.Ala187Thr |
S162 S69 |
3 | BAA04g10930 | A04 | 16979313 | C | T | missense_variant | MODERATE | c.1421C>T|p.Thr474Ile |
S199 |
4 | BAA04g10930 | A04 | 16979332 | C | T | synonymous_variant | LOW | c.1440C>T|p.Ser480Ser |
S90 |
5 | BAA04g10930 | A04 | 16979920 | G | A | missense_variant | MODERATE | c.1727G>A|p.Ser576Asn |
S197 |
6 | BAA04g10930 | A04 | 16980279 | C | T | missense_variant | MODERATE | c.1925C>T|p.Ala642Val |
S296 |
7 | BAA04g10930 | A04 | 16981386 | G | A | downstream_gene_variant | MODIFIER | c.*824G>A| |
S244 |
8 | BAA04g10930 | A04 | 16981408 | C | T | downstream_gene_variant | MODIFIER | c.*846C>T| |
S15 S3 |
9 | BAA04g10930 | A04 | 16982396 | C | T | downstream_gene_variant | MODIFIER | c.*1834C>T| |
S172 S217 |
10 | BAA04g10930 | A04 | 16983128 | G | A | downstream_gene_variant | MODIFIER | c.*2566G>A| |
S158 |
11 | BAA04g10930 | A04 | 16983579 | A | T | downstream_gene_variant | MODIFIER | c.*3017A>T| |
S163 |