Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19000 | A03 | 8408380 | G | A | splice_region_variant&intron_variant | LOW | c.1680+8C>T| |
S16 |
2 | BAA03g19000 | A03 | 8408817 | C | T | missense_variant | MODERATE | c.1408G>A|p.Asp470Asn |
S216 |
3 | BAA03g19000 | A03 | 8408883 | C | T | missense_variant | MODERATE | c.1342G>A|p.Glu448Lys |
S282 |
4 | BAA03g19000 | A03 | 8408984 | G | A | missense_variant | MODERATE | c.1241C>T|p.Thr414Ile |
S255 |
5 | BAA03g19000 | A03 | 8409197 | G | A | synonymous_variant | LOW | c.1119C>T|p.Val373Val |
S289 S290 |
6 | BAA03g19000 | A03 | 8409808 | C | T | missense_variant | MODERATE | c.820G>A|p.Glu274Lys |
S32 |
7 | BAA03g19000 | A03 | 8410771 | C | T | missense_variant | MODERATE | c.314G>A|p.Arg105Lys |
S163 |
8 | BAA03g19000 | A03 | 8411709 | C | T | missense_variant | MODERATE | c.46G>A|p.Gly16Arg |
S8 |
9 | BAA03g19000 | A03 | 8411945 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S68 |
10 | BAA03g19000 | A03 | 8412037 | T | C | upstream_gene_variant | MODIFIER | c.-283A>G| |
S20 |