Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11770 | A06 | 5960153 | G | A | missense_variant | MODERATE | c.202C>T|p.Leu68Phe |
S152 |
2 | BAA06g11770 | A06 | 5960215 | C | T | missense_variant | MODERATE | c.140G>A|p.Gly47Glu |
S23 |
3 | BAA06g11770 | A06 | 5960352 | C | T | splice_donor_variant&intron_variant | HIGH | c.105+1G>A| |
S103 |
4 | BAA06g11770 | A06 | 5964593 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S139 |
5 | BAA06g11770 | A06 | 5965007 | C | T | upstream_gene_variant | MODIFIER | c.-4550G>A| |
S252 |