Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41430 | A01 | 27539160 | C | T | missense_variant&splice_region_variant | MODERATE | c.680C>T|p.Ala227Val |
S128 |
2 | BAA01g41430 | A01 | 27539780 | G | A | splice_region_variant&intron_variant | LOW | c.1122+5G>A| |
S95 |
3 | BAA01g41430 | A01 | 27541522 | C | T | intron_variant | MODIFIER | c.1713+53C>T| |
S264 |
4 | BAA01g41430 | A01 | 27542627 | C | T | missense_variant | MODERATE | c.2104C>T|p.Pro702Ser |
S236 |
5 | BAA01g41430 | A01 | 27544399 | G | A | synonymous_variant | LOW | c.2871G>A|p.Lys957Lys |
S138 |
6 | BAA01g41430 | A01 | 27545143 | C | T | splice_region_variant&intron_variant | LOW | c.3030+5C>T| |
S7 |
7 | BAA01g41430 | A01 | 27545329 | C | T | missense_variant | MODERATE | c.3118C>T|p.Leu1040Phe |
S228 |
8 | BAA01g41430 | A01 | 27545509 | C | T | missense_variant | MODERATE | c.3178C>T|p.Pro1060Ser |
S8 |