Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02610 | A02 | 1178723 | C | T | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S267 |
2 | BAA02g02610 | A02 | 1178885 | C | T | upstream_gene_variant | MODIFIER | c.-2869C>T| |
S178 |
3 | BAA02g02610 | A02 | 1180505 | G | A | upstream_gene_variant | MODIFIER | c.-1249G>A| |
S161 |
4 | BAA02g02610 | A02 | 1181772 | G | A | missense_variant | MODERATE | c.19G>A|p.Gly7Ser |
S176 |
5 | BAA02g02610 | A02 | 1183253 | G | A | missense_variant | MODERATE | c.637G>A|p.Val213Ile |
S197 |
6 | BAA02g02610 | A02 | 1183764 | G | A | missense_variant | MODERATE | c.994G>A|p.Asp332Asn |
S57 |
7 | BAA02g02610 | A02 | 1183847 | G | A | synonymous_variant | LOW | c.1077G>A|p.Glu359Glu |
S184 |
8 | BAA02g02610 | A02 | 1184498 | G | A | missense_variant | MODERATE | c.1401G>A|p.Met467Ile |
S68 |
9 | BAA02g02610 | A02 | 1184649 | C | T | splice_region_variant&intron_variant | LOW | c.1432-6C>T| |
S66 |
10 | BAA02g02610 | A02 | 1184810 | C | T | synonymous_variant | LOW | c.1587C>T|p.Asp529Asp |
S16 |
11 | BAA02g02610 | A02 | 1185664 | C | T | synonymous_variant | LOW | c.2077C>T|p.Leu693Leu |
S167 |
12 | BAA02g02610 | A02 | 1186094 | G | A | missense_variant | MODERATE | c.2347G>A|p.Glu783Lys |
S64 |
13 | BAA02g02610 | A02 | 1186281 | G | A | splice_region_variant&intron_variant | LOW | c.2448+8G>A| |
S265 |
14 | BAA02g02610 | A02 | 1187092 | G | A | synonymous_variant | LOW | c.2853G>A|p.Lys951Lys |
S168 |