Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20690 | A01 | 10219508 | C | T | synonymous_variant | LOW | c.1608G>A|p.Glu536Glu |
S135 S185 S203 |
2 | BAA01g20690 | A01 | 10219882 | G | A | synonymous_variant | LOW | c.1440C>T|p.Leu480Leu |
S202 |
3 | BAA01g20690 | A01 | 10220583 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1033-1G>A| |
S42 |
4 | BAA01g20690 | A01 | 10220838 | C | T | missense_variant&splice_region_variant | MODERATE | c.961G>A|p.Asp321Asn |
S200 |
5 | BAA01g20690 | A01 | 10221995 | C | T | missense_variant | MODERATE | c.313G>A|p.Gly105Arg |
S143 |
6 | BAA01g20690 | A01 | 10222556 | T | A | upstream_gene_variant | MODIFIER | c.-249A>T| |
S1 S90 |
7 | BAA01g20690 | A01 | 10222615 | C | T | upstream_gene_variant | MODIFIER | c.-308G>A| |
S130 |
8 | BAA01g20690 | A01 | 10223130 | C | T | upstream_gene_variant | MODIFIER | c.-823G>A| |
S270 |
9 | BAA01g20690 | A01 | 10223333 | G | A | upstream_gene_variant | MODIFIER | c.-1026C>T| |
S211 S227 |
10 | BAA01g20690 | A01 | 10225886 | G | A | upstream_gene_variant | MODIFIER | c.-3579C>T| |
S246 |
11 | BAA01g20690 | A01 | 10226164 | C | T | upstream_gene_variant | MODIFIER | c.-3857G>A| |
S104 S184 |
12 | BAA01g20690 | A01 | 10226758 | G | A | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S209 |
13 | BAA01g20690 | A01 | 10226884 | C | T | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S158 |