Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g04910 | A03 | 2071235 | C | T | missense_variant | MODERATE | c.130C>T|p.Leu44Phe |
S221 |
2 | BAA03g04910 | A03 | 2071580 | G | A | missense_variant | MODERATE | c.475G>A|p.Asp159Asn |
S213 |
3 | BAA03g04910 | A03 | 2071586 | G | A | missense_variant | MODERATE | c.481G>A|p.Asp161Asn |
S139 |
4 | BAA03g04910 | A03 | 2072312 | G | A | missense_variant | MODERATE | c.1207G>A|p.Asp403Asn |
S77 S82 |
5 | BAA03g04910 | A03 | 2072504 | G | A | missense_variant | MODERATE | c.1399G>A|p.Glu467Lys |
S103 |
6 | BAA03g04910 | A03 | 2072590 | G | A | synonymous_variant | LOW | c.1485G>A|p.Ser495Ser |
S294 |
7 | BAA03g04910 | A03 | 2072619 | G | A | missense_variant | MODERATE | c.1514G>A|p.Arg505Lys |
S181 |
8 | BAA03g04910 | A03 | 2072632 | G | A | synonymous_variant | LOW | c.1527G>A|p.Lys509Lys |
S185 |
9 | BAA03g04910 | A03 | 2073275 | C | T | missense_variant | MODERATE | c.2084C>T|p.Ser695Phe |
S18 |
10 | BAA03g04910 | A03 | 2073713 | G | A | missense_variant | MODERATE | c.2522G>A|p.Arg841Lys |
S98 |
11 | BAA03g04910 | A03 | 2074544 | C | T | missense_variant | MODERATE | c.3353C>T|p.Ser1118Leu |
S245 |
12 | BAA03g04910 | A03 | 2074859 | C | T | missense_variant | MODERATE | c.3668C>T|p.Ser1223Leu |
S223 |
13 | BAA03g04910 | A03 | 2074976 | C | T | missense_variant | MODERATE | c.3785C>T|p.Thr1262Met |
S100 |
14 | BAA03g04910 | A03 | 2074981 | G | A | missense_variant | MODERATE | c.3790G>A|p.Glu1264Lys |
S270 |
15 | BAA03g04910 | A03 | 2075163 | G | A | synonymous_variant | LOW | c.3972G>A|p.Leu1324Leu |
S260 |
16 | BAA03g04910 | A03 | 2077197 | G | A | downstream_gene_variant | MODIFIER | c.*282G>A| |
S161 |
17 | BAA03g04910 | A03 | 2077763 | C | T | downstream_gene_variant | MODIFIER | c.*848C>T| |
S8 |