| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g65940 | A09 | 60494435 | C | T | synonymous_variant | LOW | c.195C>T|p.Val65Val |
S117 |
| 2 | BAA09g65940 | A09 | 60494536 | G | A | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S246 |
| 3 | BAA09g65940 | A09 | 60496901 | C | T | synonymous_variant | LOW | c.1113C>T|p.Ile371Ile |
S35 |
| 4 | BAA09g65940 | A09 | 60497686 | C | T | synonymous_variant | LOW | c.1452C>T|p.His484His |
S208 |
| 5 | BAA09g65940 | A09 | 60498127 | C | T | intron_variant | MODIFIER | c.1504-56C>T| |
S82 S92 |
| 6 | BAA09g65940 | A09 | 60499666 | C | T | synonymous_variant | LOW | c.2187C>T|p.Ser729Ser |
S270 |
| 7 | BAA09g65940 | A09 | 60500048 | C | T | splice_region_variant&intron_variant | LOW | c.2398-3C>T| |
S159 S299 |
| 8 | BAA09g65940 | A09 | 60500050 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2398-1G>A| |
S295 |
| 9 | BAA09g65940 | A09 | 60501688 | C | T | missense_variant | MODERATE | c.3229C>T|p.Pro1077Ser |
S34 |
| 10 | BAA09g65940 | A09 | 60502000 | G | A | missense_variant | MODERATE | c.3383G>A|p.Gly1128Glu |
S54 |
| 11 | BAA09g65940 | A09 | 60502707 | C | T | synonymous_variant | LOW | c.3783C>T|p.Asn1261Asn |
S87 |