Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01660 | A10 | 805502 | A | G | synonymous_variant | LOW | c.561T>C|p.Asp187Asp |
S147 S91 |
2 | BAA10g01660 | A10 | 805523 | A | T | synonymous_variant | LOW | c.540T>A|p.Thr180Thr |
S147 S91 |
3 | BAA10g01660 | A10 | 805554 | T | G | missense_variant | MODERATE | c.509A>C|p.His170Pro |
S147 S91 |
4 | BAA10g01660 | A10 | 805555 | G | T | missense_variant | MODERATE | c.508C>A|p.His170Asn |
S147 S91 |
5 | BAA10g01660 | A10 | 805577 | G | T | missense_variant | MODERATE | c.486C>A|p.His162Gln |
S147 S91 |
6 | BAA10g01660 | A10 | 805579 | G | T | missense_variant | MODERATE | c.484C>A|p.His162Asn |
S147 S91 |
7 | BAA10g01660 | A10 | 805584 | C | G | missense_variant | MODERATE | c.479G>C|p.Cys160Ser |
S147 S91 |
8 | BAA10g01660 | A10 | 805598 | A | G | synonymous_variant | LOW | c.465T>C|p.Ser155Ser |
S147 S91 |
9 | BAA10g01660 | A10 | 806093 | C | T | missense_variant&splice_region_variant | MODERATE | c.199G>A|p.Glu67Lys |
S70 |
10 | BAA10g01660 | A10 | 810107 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S173 |
11 | BAA10g01660 | A10 | 810833 | C | T | upstream_gene_variant | MODIFIER | c.-4443G>A| |
S155 |