Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g27690 | A06 | 19002521 | G | A | missense_variant | MODERATE | c.248C>T|p.Thr83Ile |
S173 |
2 | BAA06g27690 | A06 | 19004567 | G | A | upstream_gene_variant | MODIFIER | c.-1399C>T| |
S69 |
3 | BAA06g27690 | A06 | 19006241 | C | T | upstream_gene_variant | MODIFIER | c.-3073G>A| |
S167 |
4 | BAA06g27690 | A06 | 19006530 | C | T | upstream_gene_variant | MODIFIER | c.-3362G>A| |
S87 |
5 | BAA06g27690 | A06 | 19006593 | G | A | upstream_gene_variant | MODIFIER | c.-3425C>T| |
S256 |
6 | BAA06g27690 | A06 | 19006623 | C | T | upstream_gene_variant | MODIFIER | c.-3455G>A| |
S178 |
7 | BAA06g27690 | A06 | 19007485 | C | T | upstream_gene_variant | MODIFIER | c.-4317G>A| |
S70 |
8 | BAA06g27690 | A06 | 19007763 | G | A | upstream_gene_variant | MODIFIER | c.-4595C>T| |
S123 |
9 | BAA06g27690 | A06 | 19007897 | C | T | upstream_gene_variant | MODIFIER | c.-4729G>A| |
S242 |
10 | BAA06g27690 | A06 | 19008151 | C | T | upstream_gene_variant | MODIFIER | c.-4983G>A| |
S242 |