Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01850 | A01 | 867803 | G | A | missense_variant | MODERATE | c.2329C>T|p.Pro777Ser |
S32 |
2 | BAA01g01850 | A01 | 867822 | C | T | synonymous_variant | LOW | c.2310G>A|p.Arg770Arg |
S189 |
3 | BAA01g01850 | A01 | 867873 | G | A | synonymous_variant | LOW | c.2259C>T|p.Phe753Phe |
S201 |
4 | BAA01g01850 | A01 | 868405 | C | T | missense_variant | MODERATE | c.1907G>A|p.Gly636Glu |
S19 |
5 | BAA01g01850 | A01 | 869050 | C | T | missense_variant&splice_region_variant | MODERATE | c.1645G>A|p.Ala549Thr |
S18 |
6 | BAA01g01850 | A01 | 869735 | G | A | missense_variant | MODERATE | c.1187C>T|p.Ser396Phe |
S116 |
7 | BAA01g01850 | A01 | 869761 | G | A | synonymous_variant | LOW | c.1161C>T|p.Cys387Cys |
S6 |
8 | BAA01g01850 | A01 | 869906 | C | T | missense_variant | MODERATE | c.1016G>A|p.Cys339Tyr |
S19 |
9 | BAA01g01850 | A01 | 869991 | G | A | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S239 |
10 | BAA01g01850 | A01 | 870197 | C | T | missense_variant | MODERATE | c.818G>A|p.Ser273Asn |
S44 |
11 | BAA01g01850 | A01 | 871075 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S288 |
12 | BAA01g01850 | A01 | 871227 | C | T | upstream_gene_variant | MODIFIER | c.-213G>A| |
S80 |
13 | BAA01g01850 | A01 | 871331 | G | A | upstream_gene_variant | MODIFIER | c.-317C>T| |
S281 |
14 | BAA01g01850 | A01 | 874546 | C | T | upstream_gene_variant | MODIFIER | c.-3532G>A| |
S287 |
15 | BAA01g01850 | A01 | 875341 | G | A | upstream_gene_variant | MODIFIER | c.-4327C>T| |
S173 |