Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00260 | A04 | 151416 | C | T | upstream_gene_variant | MODIFIER | c.-4780C>T| |
S136 |
2 | BAA04g00260 | A04 | 151606 | C | T | upstream_gene_variant | MODIFIER | c.-4590C>T| |
S263 |
3 | BAA04g00260 | A04 | 156405 | G | A | synonymous_variant | LOW | c.138G>A|p.Arg46Arg |
S40 S49 |
4 | BAA04g00260 | A04 | 156714 | G | A | synonymous_variant | LOW | c.327G>A|p.Lys109Lys |
S91 |
5 | BAA04g00260 | A04 | 156916 | G | A | missense_variant | MODERATE | c.529G>A|p.Glu177Lys |
S64 |
6 | BAA04g00260 | A04 | 157871 | C | T | missense_variant&splice_region_variant | MODERATE | c.1133C>T|p.Ser378Phe |
S92 |
7 | BAA04g00260 | A04 | 158498 | C | T | synonymous_variant | LOW | c.1467C>T|p.Asn489Asn |
S129 |
8 | BAA04g00260 | A04 | 159576 | G | A | missense_variant | MODERATE | c.2416G>A|p.Asp806Asn |
S295 |
9 | BAA04g00260 | A04 | 159967 | C | T | missense_variant | MODERATE | c.2807C>T|p.Ala936Val |
S134 |
10 | BAA04g00260 | A04 | 160030 | C | T | missense_variant | MODERATE | c.2870C>T|p.Ser957Phe |
S37 |