Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15780 | A10 | 15996044 | G | A | missense_variant | MODERATE | c.64G>A|p.Glu22Lys |
S234 |
2 | BAA10g15780 | A10 | 15997210 | C | T | missense_variant | MODERATE | c.487C>T|p.Pro163Ser |
S174 S27 S39 |
3 | BAA10g15780 | A10 | 15997628 | G | A | missense_variant | MODERATE | c.766G>A|p.Asp256Asn |
S303 |
4 | BAA10g15780 | A10 | 15997652 | G | A | missense_variant | MODERATE | c.790G>A|p.Ala264Thr |
S80 |
5 | BAA10g15780 | A10 | 15997950 | G | A | missense_variant | MODERATE | c.992G>A|p.Ser331Asn |
S1 S90 |
6 | BAA10g15780 | A10 | 15999734 | C | T | downstream_gene_variant | MODIFIER | c.*1329C>T| |
S260 |
7 | BAA10g15780 | A10 | 16000067 | C | T | downstream_gene_variant | MODIFIER | c.*1662C>T| |
S186 |
8 | BAA10g15780 | A10 | 16001613 | C | T | downstream_gene_variant | MODIFIER | c.*3208C>T| |
S133 |
9 | BAA10g15780 | A10 | 16002375 | C | T | downstream_gene_variant | MODIFIER | c.*3970C>T| |
S301 S304 |
10 | BAA10g15780 | A10 | 16002782 | C | T | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S282 |
11 | BAA10g15780 | A10 | 16002934 | C | T | downstream_gene_variant | MODIFIER | c.*4529C>T| |
S176 |
12 | BAA10g15780 | A10 | 16002988 | C | T | downstream_gene_variant | MODIFIER | c.*4583C>T| |
S121 |