Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g40330 | A07 | 35813855 | C | T | missense_variant | MODERATE | c.122C>T|p.Thr41Ile |
S125 |
2 | BAA07g40330 | A07 | 35814228 | G | A | synonymous_variant | LOW | c.495G>A|p.Leu165Leu |
S170 |
3 | BAA07g40330 | A07 | 35814459 | G | A | synonymous_variant | LOW | c.726G>A|p.Glu242Glu |
S120 |
4 | BAA07g40330 | A07 | 35814581 | G | A | splice_donor_variant&intron_variant | HIGH | c.847+1G>A| |
S52 |
5 | BAA07g40330 | A07 | 35815374 | C | T | synonymous_variant | LOW | c.1233C>T|p.Leu411Leu |
S192 |
6 | BAA07g40330 | A07 | 35815408 | G | A | missense_variant | MODERATE | c.1267G>A|p.Gly423Arg |
S96 |
7 | BAA07g40330 | A07 | 35815759 | G | A | missense_variant | MODERATE | c.1618G>A|p.Gly540Ser |
S86 |
8 | BAA07g40330 | A07 | 35816110 | G | A | missense_variant | MODERATE | c.1969G>A|p.Gly657Arg |
S115 |
9 | BAA07g40330 | A07 | 35816349 | G | A | synonymous_variant | LOW | c.2208G>A|p.Arg736Arg |
S263 |