Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30400 | A08 | 20565377 | G | A | downstream_gene_variant | MODIFIER | c.*144C>T| |
S221 |
2 | BAA08g30400 | A08 | 20566234 | G | A | missense_variant | MODERATE | c.3868C>T|p.Pro1290Ser |
S151 S263 |
3 | BAA08g30400 | A08 | 20566670 | G | A | synonymous_variant | LOW | c.3432C>T|p.Val1144Val |
S98 |
4 | BAA08g30400 | A08 | 20567286 | C | T | intron_variant | MODIFIER | c.3167-351G>A| |
S167 |
5 | BAA08g30400 | A08 | 20568651 | G | A | missense_variant | MODERATE | c.2225C>T|p.Ser742Leu |
S84 S93 |
6 | BAA08g30400 | A08 | 20568855 | G | A | missense_variant | MODERATE | c.2021C>T|p.Pro674Leu |
S203 |
7 | BAA08g30400 | A08 | 20569211 | G | A | missense_variant | MODERATE | c.1745C>T|p.Ser582Leu |
S187 |
8 | BAA08g30400 | A08 | 20569795 | G | A | synonymous_variant | LOW | c.1161C>T|p.Ser387Ser |
S27 |
9 | BAA08g30400 | A08 | 20569923 | C | T | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S13 |
10 | BAA08g30400 | A08 | 20569974 | C | T | missense_variant | MODERATE | c.982G>A|p.Glu328Lys |
S223 |
11 | BAA08g30400 | A08 | 20570724 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S38 |
12 | BAA08g30400 | A08 | 20571464 | G | A | upstream_gene_variant | MODIFIER | c.-509C>T| |
S125 |
13 | BAA08g30400 | A08 | 20571695 | C | T | upstream_gene_variant | MODIFIER | c.-740G>A| |
S274 |
14 | BAA08g30400 | A08 | 20572438 | G | A | upstream_gene_variant | MODIFIER | c.-1483C>T| |
S55 |
15 | BAA08g30400 | A08 | 20572673 | C | T | upstream_gene_variant | MODIFIER | c.-1718G>A| |
S270 |
16 | BAA08g30400 | A08 | 20572928 | G | A | upstream_gene_variant | MODIFIER | c.-1973C>T| |
S67 |
17 | BAA08g30400 | A08 | 20574813 | C | T | upstream_gene_variant | MODIFIER | c.-3858G>A| |
S103 |