Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10690 | A09 | 5869727 | C | T | upstream_gene_variant | MODIFIER | c.-3441C>T| |
S83 S88 |
2 | BAA09g10690 | A09 | 5871307 | G | A | upstream_gene_variant | MODIFIER | c.-1861G>A| |
S124 |
3 | BAA09g10690 | A09 | 5871733 | C | T | upstream_gene_variant | MODIFIER | c.-1435C>T| |
S153 |
4 | BAA09g10690 | A09 | 5871867 | G | A | upstream_gene_variant | MODIFIER | c.-1301G>A| |
S15 S3 |
5 | BAA09g10690 | A09 | 5872066 | C | T | upstream_gene_variant | MODIFIER | c.-1102C>T| |
S107 |
6 | BAA09g10690 | A09 | 5872925 | C | T | upstream_gene_variant | MODIFIER | c.-243C>T| |
S95 |
7 | BAA09g10690 | A09 | 5873271 | G | A | synonymous_variant | LOW | c.36G>A|p.Glu12Glu |
S144 S44 |
8 | BAA09g10690 | A09 | 5873784 | C | T | intron_variant | MODIFIER | c.381+63C>T| |
S256 |
9 | BAA09g10690 | A09 | 5874745 | G | A | missense_variant | MODERATE | c.541G>A|p.Asp181Asn |
S11 |
10 | BAA09g10690 | A09 | 5878556 | C | T | downstream_gene_variant | MODIFIER | c.*3611C>T| |
S19 |
11 | BAA09g10690 | A09 | 5878815 | C | T | downstream_gene_variant | MODIFIER | c.*3870C>T| |
S33 |
12 | BAA09g10690 | A09 | 5879663 | C | T | downstream_gene_variant | MODIFIER | c.*4718C>T| |
S2 |
13 | BAA09g10690 | A09 | 5879728 | C | T | downstream_gene_variant | MODIFIER | c.*4783C>T| |
S208 |