Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02730 | A03 | 1186048 | C | T | synonymous_variant | LOW | c.3096G>A|p.Lys1032Lys |
S263 |
2 | BAA03g02730 | A03 | 1186224 | C | T | missense_variant | MODERATE | c.3017G>A|p.Gly1006Glu |
S40 S49 |
3 | BAA03g02730 | A03 | 1187257 | C | T | missense_variant&splice_region_variant | MODERATE | c.2737G>A|p.Glu913Lys |
S81 |
4 | BAA03g02730 | A03 | 1189631 | G | A | intron_variant | MODIFIER | c.1830+17C>T| |
S39 |
5 | BAA03g02730 | A03 | 1190196 | C | T | intron_variant | MODIFIER | c.1482+33G>A| |
S184 |
6 | BAA03g02730 | A03 | 1191581 | C | T | missense_variant | MODERATE | c.1147G>A|p.Asp383Asn |
S215 |
7 | BAA03g02730 | A03 | 1192179 | C | T | missense_variant | MODERATE | c.907G>A|p.Glu303Lys |
S122 |
8 | BAA03g02730 | A03 | 1192400 | C | T | missense_variant | MODERATE | c.769G>A|p.Asp257Asn |
S177 |
9 | BAA03g02730 | A03 | 1192699 | C | T | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S210 |
10 | BAA03g02730 | A03 | 1197065 | C | T | upstream_gene_variant | MODIFIER | c.-3111G>A| |
S236 |