Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g15020 | A08 | 12688256 | G | A | missense_variant&splice_region_variant | MODERATE | c.1217C>T|p.Ser406Phe |
S130 |
2 | BAA08g15020 | A08 | 12688481 | C | T | missense_variant | MODERATE | c.992G>A|p.Gly331Glu |
S36 |
3 | BAA08g15020 | A08 | 12688776 | C | T | missense_variant | MODERATE | c.860G>A|p.Arg287His |
S122 |
4 | BAA08g15020 | A08 | 12689212 | G | A | synonymous_variant | LOW | c.582C>T|p.Phe194Phe |
S20 |
5 | BAA08g15020 | A08 | 12689233 | G | A | synonymous_variant | LOW | c.561C>T|p.Leu187Leu |
S16 S94 |
6 | BAA08g15020 | A08 | 12690729 | C | T | intron_variant | MODIFIER | c.414+147G>A| |
S173 S273 |
7 | BAA08g15020 | A08 | 12690939 | C | T | synonymous_variant | LOW | c.351G>A|p.Ser117Ser |
S166 |
8 | BAA08g15020 | A08 | 12690991 | G | A | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S264 |
9 | BAA08g15020 | A08 | 12692154 | C | T | upstream_gene_variant | MODIFIER | c.-865G>A| |
S173 |
10 | BAA08g15020 | A08 | 12692306 | G | A | upstream_gene_variant | MODIFIER | c.-1017C>T| |
S20 |
11 | BAA08g15020 | A08 | 12695524 | G | A | upstream_gene_variant | MODIFIER | c.-4235C>T| |
S188 |
12 | BAA08g15020 | A08 | 12695888 | C | T | upstream_gene_variant | MODIFIER | c.-4599G>A| |
S53 |