Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04100 | A10 | 1995229 | T | A | missense_variant | MODERATE | c.1171A>T|p.Ile391Phe |
S16 S181 S217 S248 S56 |
2 | BAA10g04100 | A10 | 1996955 | G | A | splice_region_variant&intron_variant | LOW | c.269+5C>T| |
S231 |
3 | BAA10g04100 | A10 | 1997110 | G | A | missense_variant | MODERATE | c.119C>T|p.Pro40Leu |
S306 |
4 | BAA10g04100 | A10 | 1997814 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S302 |
5 | BAA10g04100 | A10 | 2001050 | G | A | upstream_gene_variant | MODIFIER | c.-3822C>T| |
S295 |
6 | BAA10g04100 | A10 | 2001658 | G | A | upstream_gene_variant | MODIFIER | c.-4430C>T| |
S172 |