Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14000 | A01 | 6660922 | C | T | upstream_gene_variant | MODIFIER | c.-1729C>T| |
S148 S30 S31 |
2 | BAA01g14000 | A01 | 6661255 | C | T | upstream_gene_variant | MODIFIER | c.-1396C>T| |
S50 |
3 | BAA01g14000 | A01 | 6661656 | C | T | upstream_gene_variant | MODIFIER | c.-995C>T| |
S242 |
4 | BAA01g14000 | A01 | 6661691 | C | T | upstream_gene_variant | MODIFIER | c.-960C>T| |
S169 |
5 | BAA01g14000 | A01 | 6662033 | C | T | upstream_gene_variant | MODIFIER | c.-618C>T| |
S48 |
6 | BAA01g14000 | A01 | 6662530 | C | T | upstream_gene_variant | MODIFIER | c.-121C>T| |
S184 |
7 | BAA01g14000 | A01 | 6663293 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.225-1G>A| |
S161 |
8 | BAA01g14000 | A01 | 6665078 | C | T | missense_variant | MODERATE | c.1073C>T|p.Ser358Leu |
S33 |
9 | BAA01g14000 | A01 | 6666067 | C | T | missense_variant | MODERATE | c.1903C>T|p.Leu635Phe |
S219 S72 |
10 | BAA01g14000 | A01 | 6666315 | G | A | missense_variant | MODERATE | c.2072G>A|p.Gly691Glu |
S257 |
11 | BAA01g14000 | A01 | 6666622 | C | T | downstream_gene_variant | MODIFIER | c.*258C>T| |
S230 |