Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19500 | A01 | 9600757 | C | T | stop_gained | HIGH | c.3288G>A|p.Trp1096* |
S132 S137 S89 |
2 | BAA01g19500 | A01 | 9608621 | C | T | missense_variant | MODERATE | c.1933G>A|p.Asp645Asn |
S62 |
3 | BAA01g19500 | A01 | 9608763 | C | T | missense_variant | MODERATE | c.1791G>A|p.Met597Ile |
S166 |
4 | BAA01g19500 | A01 | 9608828 | C | T | missense_variant | MODERATE | c.1726G>A|p.Asp576Asn |
S38 |
5 | BAA01g19500 | A01 | 9609222 | C | T | synonymous_variant | LOW | c.1332G>A|p.Gln444Gln |
S264 |
6 | BAA01g19500 | A01 | 9609392 | C | T | missense_variant | MODERATE | c.1162G>A|p.Glu388Lys |
S20 S36 |
7 | BAA01g19500 | A01 | 9609900 | C | T | synonymous_variant | LOW | c.654G>A|p.Ala218Ala |
S36 |
8 | BAA01g19500 | A01 | 9611090 | C | T | upstream_gene_variant | MODIFIER | c.-119G>A| |
S76 |
9 | BAA01g19500 | A01 | 9612372 | G | T | upstream_gene_variant | MODIFIER | c.-1401C>A| |
S81 S85 |
10 | BAA01g19500 | A01 | 9612497 | G | A | upstream_gene_variant | MODIFIER | c.-1526C>T| |
S139 |
11 | BAA01g19500 | A01 | 9614560 | C | T | upstream_gene_variant | MODIFIER | c.-3589G>A| |
S36 |