Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11660 | A10 | 13251166 | G | A | missense_variant | MODERATE | c.266C>T|p.Ser89Phe |
S45 |
2 | BAA10g11660 | A10 | 13252928 | G | A | upstream_gene_variant | MODIFIER | c.-1427C>T| |
S198 |
3 | BAA10g11660 | A10 | 13254509 | G | A | upstream_gene_variant | MODIFIER | c.-3008C>T| |
S287 |
4 | BAA10g11660 | A10 | 13255648 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S289 |
5 | BAA10g11660 | A10 | 13255665 | G | A | upstream_gene_variant | MODIFIER | c.-4164C>T| |
S271 |
6 | BAA10g11660 | A10 | 13255674 | C | T | upstream_gene_variant | MODIFIER | c.-4173G>A| |
S54 |
7 | BAA10g11660 | A10 | 13255770 | C | T | upstream_gene_variant | MODIFIER | c.-4269G>A| |
S185 |
8 | BAA10g11660 | A10 | 13255779 | C | T | upstream_gene_variant | MODIFIER | c.-4278G>A| |
S176 |