Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26900 | A08 | 19080101 | C | T | upstream_gene_variant | MODIFIER | c.-3589C>T| |
S201 |
2 | BAA08g26900 | A08 | 19080537 | G | A | upstream_gene_variant | MODIFIER | c.-3153G>A| |
S48 |
3 | BAA08g26900 | A08 | 19084003 | C | T | missense_variant | MODERATE | c.85C>T|p.Leu29Phe |
S7 |
4 | BAA08g26900 | A08 | 19084013 | G | A | missense_variant | MODERATE | c.95G>A|p.Arg32Lys |
S287 |
5 | BAA08g26900 | A08 | 19084237 | G | A | missense_variant | MODERATE | c.235G>A|p.Asp79Asn |
S150 |
6 | BAA08g26900 | A08 | 19084576 | C | T | synonymous_variant | LOW | c.498C>T|p.Phe166Phe |
S162 |
7 | BAA08g26900 | A08 | 19084823 | G | A | missense_variant | MODERATE | c.655G>A|p.Ala219Thr |
S15 S3 |
8 | BAA08g26900 | A08 | 19084940 | G | A | missense_variant | MODERATE | c.772G>A|p.Val258Ile |
S75 S81 |
9 | BAA08g26900 | A08 | 19085184 | G | A | synonymous_variant | LOW | c.927G>A|p.Lys309Lys |
S100 |
10 | BAA08g26900 | A08 | 19085617 | C | T | missense_variant | MODERATE | c.1208C>T|p.Thr403Ile |
S104 S252 S52 |
11 | BAA08g26900 | A08 | 19086075 | G | A | missense_variant | MODERATE | c.1508G>A|p.Gly503Glu |
S207 |