Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g33740 | A03 | 15635675 | G | A | splice_region_variant&intron_variant | LOW | c.3356-3C>T| |
S69 |
2 | BAA03g33740 | A03 | 15635995 | C | T | missense_variant | MODERATE | c.3103G>A|p.Asp1035Asn |
S268 |
3 | BAA03g33740 | A03 | 15636220 | C | T | missense_variant | MODERATE | c.2878G>A|p.Asp960Asn |
S232 |
4 | BAA03g33740 | A03 | 15636494 | C | T | synonymous_variant | LOW | c.2604G>A|p.Lys868Lys |
S153 |
5 | BAA03g33740 | A03 | 15636595 | G | A | synonymous_variant | LOW | c.2503C>T|p.Leu835Leu |
S169 |
6 | BAA03g33740 | A03 | 15636627 | G | A | missense_variant | MODERATE | c.2471C>T|p.Thr824Ile |
S59 |
7 | BAA03g33740 | A03 | 15636991 | C | T | missense_variant | MODERATE | c.2107G>A|p.Val703Met |
S255 |
8 | BAA03g33740 | A03 | 15637162 | G | A | missense_variant | MODERATE | c.1936C>T|p.Pro646Ser |
S199 |
9 | BAA03g33740 | A03 | 15638995 | C | T | synonymous_variant | LOW | c.414G>A|p.Glu138Glu |
S172 |
10 | BAA03g33740 | A03 | 15639049 | C | T | synonymous_variant | LOW | c.360G>A|p.Gln120Gln |
S15 S3 |
11 | BAA03g33740 | A03 | 15639330 | C | T | missense_variant | MODERATE | c.79G>A|p.Asp27Asn |
S133 S172 S217 |
12 | BAA03g33740 | A03 | 15639879 | C | T | upstream_gene_variant | MODIFIER | c.-471G>A| |
S120 |