Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04470 | A09 | 2641332 | C | T | missense_variant | MODERATE | c.1954G>A|p.Glu652Lys |
S94 |
2 | BAA09g04470 | A09 | 2641661 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1715-1G>A| |
S94 |
3 | BAA09g04470 | A09 | 2642144 | C | T | missense_variant&splice_region_variant | MODERATE | c.1459G>A|p.Ala487Thr |
S303 |
4 | BAA09g04470 | A09 | 2642690 | G | A | missense_variant | MODERATE | c.1070C>T|p.Pro357Leu |
S267 |
5 | BAA09g04470 | A09 | 2643204 | C | T | missense_variant | MODERATE | c.775G>A|p.Asp259Asn |
S151 |
6 | BAA09g04470 | A09 | 2643249 | C | T | missense_variant | MODERATE | c.730G>A|p.Asp244Asn |
S67 |
7 | BAA09g04470 | A09 | 2644565 | G | A | synonymous_variant | LOW | c.202C>T|p.Leu68Leu |
S274 |
8 | BAA09g04470 | A09 | 2646148 | C | T | upstream_gene_variant | MODIFIER | c.-1269G>A| |
S302 |
9 | BAA09g04470 | A09 | 2646579 | C | G | upstream_gene_variant | MODIFIER | c.-1700G>C| |
S187 |
10 | BAA09g04470 | A09 | 2646636 | G | A | upstream_gene_variant | MODIFIER | c.-1757C>T| |
S60 |
11 | BAA09g04470 | A09 | 2648617 | G | A | upstream_gene_variant | MODIFIER | c.-3738C>T| |
S100 |
12 | BAA09g04470 | A09 | 2648957 | G | A | upstream_gene_variant | MODIFIER | c.-4078C>T| |
S167 |
13 | BAA09g04470 | A09 | 2649206 | G | A | upstream_gene_variant | MODIFIER | c.-4327C>T| |
S167 |
14 | BAA09g04470 | A09 | 2649701 | C | T | upstream_gene_variant | MODIFIER | c.-4822G>A| |
S136 S275 |