Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11970 | A08 | 10527738 | G | A | missense_variant | MODERATE | c.1271C>T|p.Ala424Val |
S211 |
2 | BAA08g11970 | A08 | 10528257 | G | A | missense_variant | MODERATE | c.958C>T|p.Leu320Phe |
S62 |
3 | BAA08g11970 | A08 | 10529698 | C | T | synonymous_variant | LOW | c.261G>A|p.Thr87Thr |
S157 S163 |
4 | BAA08g11970 | A08 | 10529861 | G | A | splice_region_variant&intron_variant | LOW | c.189-6C>T| |
S72 |
5 | BAA08g11970 | A08 | 10530883 | G | A | upstream_gene_variant | MODIFIER | c.-682C>T| |
S78 |
6 | BAA08g11970 | A08 | 10531744 | G | A | upstream_gene_variant | MODIFIER | c.-1543C>T| |
S217 |
7 | BAA08g11970 | A08 | 10532670 | G | A | upstream_gene_variant | MODIFIER | c.-2469C>T| |
S32 |
8 | BAA08g11970 | A08 | 10533676 | C | T | upstream_gene_variant | MODIFIER | c.-3475G>A| |
S67 |
9 | BAA08g11970 | A08 | 10534292 | G | A | upstream_gene_variant | MODIFIER | c.-4091C>T| |
S288 |