Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59280 | A03 | 29711071 | G | A | upstream_gene_variant | MODIFIER | c.-748G>A| |
S167 |
2 | BAA03g59280 | A03 | 29711577 | C | T | upstream_gene_variant | MODIFIER | c.-242C>T| |
S125 |
3 | BAA03g59280 | A03 | 29712836 | G | A | synonymous_variant | LOW | c.678G>A|p.Gly226Gly |
S48 |
4 | BAA03g59280 | A03 | 29712925 | C | T | missense_variant | MODERATE | c.767C>T|p.Thr256Ile |
S273 |
5 | BAA03g59280 | A03 | 29713252 | C | T | synonymous_variant | LOW | c.924C>T|p.Ile308Ile |
S19 |
6 | BAA03g59280 | A03 | 29713531 | G | A | intron_variant | MODIFIER | c.1081+122G>A| |
S236 |
7 | BAA03g59280 | A03 | 29713601 | C | T | intron_variant | MODIFIER | c.1081+192C>T| |
S172 S217 |
8 | BAA03g59280 | A03 | 29713648 | G | A | intron_variant | MODIFIER | c.1081+239G>A| |
S190 |
9 | BAA03g59280 | A03 | 29713809 | G | A | intron_variant | MODIFIER | c.1082-152G>A| |
S170 |
10 | BAA03g59280 | A03 | 29714443 | C | T | missense_variant | MODERATE | c.1427C>T|p.Ala476Val |
S57 |
11 | BAA03g59280 | A03 | 29714573 | C | T | splice_region_variant&intron_variant | LOW | c.1477-8C>T| |
S273 |
12 | BAA03g59280 | A03 | 29714635 | G | A | splice_region_variant&intron_variant | LOW | c.1526+5G>A| |
S62 |
13 | BAA03g59280 | A03 | 29715213 | C | T | synonymous_variant | LOW | c.1695C>T|p.Leu565Leu |
S99 |
14 | BAA03g59280 | A03 | 29715468 | G | A | missense_variant | MODERATE | c.1886G>A|p.Ser629Asn |
S271 |