Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01390 | A07 | 968969 | C | T | upstream_gene_variant | MODIFIER | c.-2712C>T| |
S144 |
2 | BAA07g01390 | A07 | 969188 | C | T | upstream_gene_variant | MODIFIER | c.-2493C>T| |
S94 |
3 | BAA07g01390 | A07 | 971766 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S23 |
4 | BAA07g01390 | A07 | 972608 | G | A | missense_variant | MODERATE | c.259G>A|p.Val87Ile |
S158 |
5 | BAA07g01390 | A07 | 975965 | G | A | downstream_gene_variant | MODIFIER | c.*1234G>A| |
S190 |
6 | BAA07g01390 | A07 | 976119 | G | A | downstream_gene_variant | MODIFIER | c.*1388G>A| |
S123 |
7 | BAA07g01390 | A07 | 976728 | C | T | downstream_gene_variant | MODIFIER | c.*1997C>T| |
S148 |
8 | BAA07g01390 | A07 | 977830 | C | T | downstream_gene_variant | MODIFIER | c.*3099C>T| |
S18 |
9 | BAA07g01390 | A07 | 977947 | C | T | downstream_gene_variant | MODIFIER | c.*3216C>T| |
S19 |