Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00500 | A01 | 219016 | C | T | upstream_gene_variant | MODIFIER | c.-1798C>T| |
S158 |
2 | BAA01g00500 | A01 | 219257 | C | T | upstream_gene_variant | MODIFIER | c.-1557C>T| |
S203 |
3 | BAA01g00500 | A01 | 221464 | C | T | synonymous_variant | LOW | c.651C>T|p.Val217Val |
S135 |
4 | BAA01g00500 | A01 | 221705 | G | A | missense_variant | MODERATE | c.892G>A|p.Ala298Thr |
S185 |
5 | BAA01g00500 | A01 | 222201 | C | T | missense_variant | MODERATE | c.1388C>T|p.Ser463Phe |
S284 |
6 | BAA01g00500 | A01 | 222378 | G | A | missense_variant | MODERATE | c.1565G>A|p.Arg522Gln |
S104 S52 |
7 | BAA01g00500 | A01 | 222813 | A | C | missense_variant | MODERATE | c.2000A>C|p.Tyr667Ser |
S11 S110 S133 S168 S175 S194 S195 S197 S277 S284 S303 S45 S54 |
8 | BAA01g00500 | A01 | 222815 | A | C | missense_variant | MODERATE | c.2002A>C|p.Ile668Leu |
S110 S133 S168 S175 S195 S303 S45 S54 |
9 | BAA01g00500 | A01 | 223540 | G | A | synonymous_variant | LOW | c.2727G>A|p.Lys909Lys |
S209 |
10 | BAA01g00500 | A01 | 226183 | C | T | downstream_gene_variant | MODIFIER | c.*1785C>T| |
S192 |
11 | BAA01g00500 | A01 | 226263 | C | T | downstream_gene_variant | MODIFIER | c.*1865C>T| |
S135 |
12 | BAA01g00500 | A01 | 226319 | G | A | downstream_gene_variant | MODIFIER | c.*1921G>A| |
S278 |
13 | BAA01g00500 | A01 | 228421 | C | T | downstream_gene_variant | MODIFIER | c.*4023C>T| |
S107 |