Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g07480 | A01 | 3298269 | C | T | missense_variant | MODERATE | c.2521G>A|p.Val841Met |
S99 |
2 | BAA01g07480 | A01 | 3298477 | G | A | synonymous_variant | LOW | c.2313C>T|p.Asn771Asn |
S287 |
3 | BAA01g07480 | A01 | 3299180 | G | A | missense_variant | MODERATE | c.1610C>T|p.Ser537Phe |
S187 |
4 | BAA01g07480 | A01 | 3299882 | C | T | missense_variant | MODERATE | c.908G>A|p.Ser303Asn |
S112 |
5 | BAA01g07480 | A01 | 3300052 | G | A | synonymous_variant | LOW | c.738C>T|p.Phe246Phe |
S105 S106 |
6 | BAA01g07480 | A01 | 3300332 | C | T | missense_variant | MODERATE | c.458G>A|p.Gly153Glu |
S270 |
7 | BAA01g07480 | A01 | 3303049 | G | A | upstream_gene_variant | MODIFIER | c.-2260C>T| |
S257 |
8 | BAA01g07480 | A01 | 3304782 | G | A | upstream_gene_variant | MODIFIER | c.-3993C>T| |
S9 |
9 | BAA01g07480 | A01 | 3304935 | C | T | upstream_gene_variant | MODIFIER | c.-4146G>A| |
S198 |
10 | BAA01g07480 | A01 | 3305275 | G | A | upstream_gene_variant | MODIFIER | c.-4486C>T| |
S60 |