Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g32630 | A08 | 21440952 | G | A | missense_variant | MODERATE | c.646G>A|p.Asp216Asn |
S203 |
2 | BAA08g32630 | A08 | 21441381 | G | A | missense_variant | MODERATE | c.824G>A|p.Ser275Asn |
S33 |
3 | BAA08g32630 | A08 | 21442228 | C | T | missense_variant | MODERATE | c.1315C>T|p.Pro439Ser |
S20 |
4 | BAA08g32630 | A08 | 21442625 | G | A | splice_region_variant&intron_variant | LOW | c.1554+3G>A| |
S160 |
5 | BAA08g32630 | A08 | 21443666 | C | T | synonymous_variant | LOW | c.2115C>T|p.Phe705Phe |
S20 |
6 | BAA08g32630 | A08 | 21444378 | C | T | synonymous_variant | LOW | c.2487C>T|p.Tyr829Tyr |
S97 |
7 | BAA08g32630 | A08 | 21445160 | C | T | synonymous_variant | LOW | c.2907C>T|p.Leu969Leu |
S283 |
8 | BAA08g32630 | A08 | 21445348 | G | A | missense_variant | MODERATE | c.2977G>A|p.Ala993Thr |
S33 |