Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00670 | A01 | 294528 | C | T | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S208 |
2 | BAA01g00670 | A01 | 295232 | C | T | upstream_gene_variant | MODIFIER | c.-2461C>T| |
S282 |
3 | BAA01g00670 | A01 | 295852 | C | T | upstream_gene_variant | MODIFIER | c.-1841C>T| |
S111 |
4 | BAA01g00670 | A01 | 298443 | C | T | missense_variant | MODERATE | c.302C>T|p.Ser101Phe |
S94 |
5 | BAA01g00670 | A01 | 298927 | C | T | missense_variant | MODERATE | c.352C>T|p.Pro118Ser |
S132 S137 S215 S89 |
6 | BAA01g00670 | A01 | 298961 | G | A | missense_variant | MODERATE | c.386G>A|p.Gly129Asp |
S9 |
7 | BAA01g00670 | A01 | 299166 | G | A | synonymous_variant | LOW | c.591G>A|p.Lys197Lys |
S108 |
8 | BAA01g00670 | A01 | 299619 | G | A | missense_variant | MODERATE | c.970G>A|p.Asp324Asn |
S73 S91 |
9 | BAA01g00670 | A01 | 299661 | C | T | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S255 |
10 | BAA01g00670 | A01 | 299707 | C | T | missense_variant | MODERATE | c.1058C>T|p.Thr353Ile |
S230 |
11 | BAA01g00670 | A01 | 302613 | G | A | downstream_gene_variant | MODIFIER | c.*2002G>A| |
S257 |
12 | BAA01g00670 | A01 | 304103 | G | A | downstream_gene_variant | MODIFIER | c.*3492G>A| |
S89 |
13 | BAA01g00670 | A01 | 304421 | G | A | downstream_gene_variant | MODIFIER | c.*3810G>A| |
S23 |
14 | BAA01g00670 | A01 | 304764 | C | T | downstream_gene_variant | MODIFIER | c.*4153C>T| |
S79 S84 |
15 | BAA01g00670 | A01 | 304835 | C | T | downstream_gene_variant | MODIFIER | c.*4224C>T| |
S164 |
16 | BAA01g00670 | A01 | 304876 | G | A | downstream_gene_variant | MODIFIER | c.*4265G>A| |
S70 |