Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g31120 | A05 | 33949089 | C | T | missense_variant | MODERATE | c.2755G>A|p.Val919Ile |
S152 |
2 | BAA05g31120 | A05 | 33950640 | C | T | missense_variant | MODERATE | c.1615G>A|p.Glu539Lys |
S103 |
3 | BAA05g31120 | A05 | 33950817 | G | A | missense_variant | MODERATE | c.1438C>T|p.Pro480Ser |
S131 |
4 | BAA05g31120 | A05 | 33951375 | G | A | missense_variant | MODERATE | c.1316C>T|p.Pro439Leu |
S50 |
5 | BAA05g31120 | A05 | 33952547 | G | A | splice_region_variant&synonymous_variant | LOW | c.471C>T|p.Gly157Gly |
S225 S73 |
6 | BAA05g31120 | A05 | 33952842 | C | T | missense_variant | MODERATE | c.341G>A|p.Arg114His |
S202 |
7 | BAA05g31120 | A05 | 33953062 | G | A | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S47 |
8 | BAA05g31120 | A05 | 33953582 | G | A | upstream_gene_variant | MODIFIER | c.-400C>T| |
S270 |
9 | BAA05g31120 | A05 | 33954557 | C | T | upstream_gene_variant | MODIFIER | c.-1375G>A| |
S169 |
10 | BAA05g31120 | A05 | 33956789 | C | T | upstream_gene_variant | MODIFIER | c.-3607G>A| |
S137 S215 |