Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g38960 | A07 | 35191362 | C | T | missense_variant | MODERATE | c.1138G>A|p.Val380Ile |
S85 |
2 | BAA07g38960 | A07 | 35191705 | C | T | missense_variant | MODERATE | c.875G>A|p.Arg292His |
S245 |
3 | BAA07g38960 | A07 | 35192358 | C | T | missense_variant | MODERATE | c.734G>A|p.Gly245Glu |
S73 S91 |
4 | BAA07g38960 | A07 | 35192435 | C | T | synonymous_variant | LOW | c.657G>A|p.Val219Val |
S181 |
5 | BAA07g38960 | A07 | 35192473 | C | T | missense_variant | MODERATE | c.619G>A|p.Gly207Arg |
S250 |
6 | BAA07g38960 | A07 | 35192835 | G | A | missense_variant | MODERATE | c.257C>T|p.Pro86Leu |
S170 |
7 | BAA07g38960 | A07 | 35194333 | G | A | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S296 |
8 | BAA07g38960 | A07 | 35197538 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S161 |