Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08630 | A08 | 7886034 | C | T | synonymous_variant | LOW | c.324C>T|p.Leu108Leu |
S44 |
2 | BAA08g08630 | A08 | 7886101 | C | T | stop_gained | HIGH | c.391C>T|p.Gln131* |
S50 |
3 | BAA08g08630 | A08 | 7886427 | G | A | synonymous_variant | LOW | c.717G>A|p.Pro239Pro |
S148 |
4 | BAA08g08630 | A08 | 7886734 | G | A | splice_region_variant&intron_variant | LOW | c.1019+5G>A| |
S188 |
5 | BAA08g08630 | A08 | 7886850 | G | A | missense_variant | MODERATE | c.1063G>A|p.Gly355Arg |
S28 |
6 | BAA08g08630 | A08 | 7887024 | C | T | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S12 |
7 | BAA08g08630 | A08 | 7890502 | G | A | downstream_gene_variant | MODIFIER | c.*3416G>A| |
S275 |
8 | BAA08g08630 | A08 | 7890710 | G | A | downstream_gene_variant | MODIFIER | c.*3624G>A| |
S116 |
9 | BAA08g08630 | A08 | 7890878 | G | A | downstream_gene_variant | MODIFIER | c.*3792G>A| |
S204 |
10 | BAA08g08630 | A08 | 7891085 | G | A | downstream_gene_variant | MODIFIER | c.*3999G>A| |
S200 |