Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24160 | A10 | 20005115 | C | T | synonymous_variant | LOW | c.792G>A|p.Glu264Glu |
S12 |
2 | BAA10g24160 | A10 | 20006047 | C | T | missense_variant | MODERATE | c.349G>A|p.Asp117Asn |
S269 |
3 | BAA10g24160 | A10 | 20006786 | C | T | upstream_gene_variant | MODIFIER | c.-37G>A| |
S92 |
4 | BAA10g24160 | A10 | 20006820 | C | T | upstream_gene_variant | MODIFIER | c.-71G>A| |
S205 |
5 | BAA10g24160 | A10 | 20007658 | C | T | upstream_gene_variant | MODIFIER | c.-909G>A| |
S42 |
6 | BAA10g24160 | A10 | 20007819 | C | T | upstream_gene_variant | MODIFIER | c.-1070G>A| |
S162 |
7 | BAA10g24160 | A10 | 20010238 | C | T | upstream_gene_variant | MODIFIER | c.-3489G>A| |
S67 |
8 | BAA10g24160 | A10 | 20010590 | G | C | upstream_gene_variant | MODIFIER | c.-3841C>G| |
S299 |
9 | BAA10g24160 | A10 | 20010614 | C | T | upstream_gene_variant | MODIFIER | c.-3865G>A| |
S218 |