Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g07530 | A07 | 16784911 | C | T | missense_variant | MODERATE | c.2116G>A|p.Glu706Lys |
S153 |
2 | BAA07g07530 | A07 | 16785051 | C | T | missense_variant | MODERATE | c.1976G>A|p.Ser659Asn |
S166 |
3 | BAA07g07530 | A07 | 16785075 | C | T | missense_variant | MODERATE | c.1952G>A|p.Arg651Lys |
S70 |
4 | BAA07g07530 | A07 | 16785133 | G | A | missense_variant | MODERATE | c.1894C>T|p.His632Tyr |
S72 S78 |
5 | BAA07g07530 | A07 | 16786020 | C | T | missense_variant | MODERATE | c.1283G>A|p.Ser428Asn |
S91 |
6 | BAA07g07530 | A07 | 16786039 | C | T | missense_variant | MODERATE | c.1264G>A|p.Val422Met |
S53 |
7 | BAA07g07530 | A07 | 16786705 | C | T | missense_variant | MODERATE | c.598G>A|p.Glu200Lys |
S217 S248 |
8 | BAA07g07530 | A07 | 16786792 | C | T | missense_variant | MODERATE | c.511G>A|p.Ala171Thr |
S37 |
9 | BAA07g07530 | A07 | 16786800 | T | A | missense_variant | MODERATE | c.503A>T|p.Glu168Val |
S55 |
10 | BAA07g07530 | A07 | 16789059 | G | A | upstream_gene_variant | MODIFIER | c.-1757C>T| |
S201 |
11 | BAA07g07530 | A07 | 16791416 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S201 |