Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g34770 | A08 | 22297986 | C | T | upstream_gene_variant | MODIFIER | c.-3604C>T| |
S286 |
2 | BAA08g34770 | A08 | 22301704 | C | T | missense_variant | MODERATE | c.115C>T|p.Pro39Ser |
S209 |
3 | BAA08g34770 | A08 | 22302016 | G | A | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S247 |
4 | BAA08g34770 | A08 | 22302546 | C | T | splice_region_variant&intron_variant | LOW | c.703-4C>T| |
S134 |
5 | BAA08g34770 | A08 | 22302557 | G | A | missense_variant | MODERATE | c.710G>A|p.Arg237Lys |
S75 S81 |
6 | BAA08g34770 | A08 | 22302932 | C | T | synonymous_variant | LOW | c.912C>T|p.Ala304Ala |
S103 |
7 | BAA08g34770 | A08 | 22303391 | G | A | missense_variant | MODERATE | c.1022G>A|p.Arg341Lys |
S156 |
8 | BAA08g34770 | A08 | 22303862 | G | A | missense_variant | MODERATE | c.1180G>A|p.Glu394Lys |
S48 |
9 | BAA08g34770 | A08 | 22304324 | C | T | missense_variant | MODERATE | c.1436C>T|p.Ala479Val |
S100 |
10 | BAA08g34770 | A08 | 22306183 | C | T | missense_variant | MODERATE | c.2699C>T|p.Ala900Val |
S59 |
11 | BAA08g34770 | A08 | 22306365 | C | T | splice_region_variant&synonymous_variant | LOW | c.2796C>T|p.Val932Val |
S58 |
12 | BAA08g34770 | A08 | 22306577 | C | T | missense_variant | MODERATE | c.3008C>T|p.Ser1003Phe |
S117 |
13 | BAA08g34770 | A08 | 22308086 | C | T | downstream_gene_variant | MODIFIER | c.*1475C>T| |
S7 |