Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08660 | A10 | 10622876 | G | A | intron_variant | MODIFIER | c.152-102G>A| |
S43 |
2 | BAA10g08660 | A10 | 10622923 | G | A | intron_variant | MODIFIER | c.152-55G>A| |
S241 |
3 | BAA10g08660 | A10 | 10623170 | C | T | missense_variant | MODERATE | c.344C>T|p.Ser115Phe |
S143 |
4 | BAA10g08660 | A10 | 10623192 | C | T | synonymous_variant | LOW | c.366C>T|p.Ala122Ala |
S162 |
5 | BAA10g08660 | A10 | 10623497 | C | T | downstream_gene_variant | MODIFIER | c.*32C>T| |
S156 |
6 | BAA10g08660 | A10 | 10623767 | G | A | downstream_gene_variant | MODIFIER | c.*302G>A| |
S139 |
7 | BAA10g08660 | A10 | 10623857 | G | A | downstream_gene_variant | MODIFIER | c.*392G>A| |
S264 |
8 | BAA10g08660 | A10 | 10624065 | G | A | downstream_gene_variant | MODIFIER | c.*600G>A| |
S198 |
9 | BAA10g08660 | A10 | 10624106 | C | T | downstream_gene_variant | MODIFIER | c.*641C>T| |
S146 |