Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67780 | A09 | 61248360 | G | A | missense_variant | MODERATE | c.1589C>T|p.Ser530Phe |
S144 |
2 | BAA09g67780 | A09 | 61248393 | G | A | missense_variant | MODERATE | c.1556C>T|p.Ser519Leu |
S23 |
3 | BAA09g67780 | A09 | 61249097 | C | T | synonymous_variant | LOW | c.1023G>A|p.Lys341Lys |
S305 |
4 | BAA09g67780 | A09 | 61249105 | C | T | missense_variant | MODERATE | c.1015G>A|p.Ala339Thr |
S138 |
5 | BAA09g67780 | A09 | 61249426 | G | A | missense_variant | MODERATE | c.694C>T|p.Leu232Phe |
S57 |
6 | BAA09g67780 | A09 | 61251489 | G | A | upstream_gene_variant | MODIFIER | c.-936C>T| |
S291 |
7 | BAA09g67780 | A09 | 61252201 | C | T | upstream_gene_variant | MODIFIER | c.-1648G>A| |
S44 |
8 | BAA09g67780 | A09 | 61255284 | C | T | upstream_gene_variant | MODIFIER | c.-4731G>A| |
S298 |