Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08690 | A10 | 10645383 | C | T | downstream_gene_variant | MODIFIER | c.*4817G>A| |
S175 |
2 | BAA10g08690 | A10 | 10645452 | G | A | downstream_gene_variant | MODIFIER | c.*4748C>T| |
S59 |
3 | BAA10g08690 | A10 | 10645464 | C | T | downstream_gene_variant | MODIFIER | c.*4736G>A| |
S197 |
4 | BAA10g08690 | A10 | 10645670 | C | T | downstream_gene_variant | MODIFIER | c.*4530G>A| |
S116 |
5 | BAA10g08690 | A10 | 10645814 | G | A | downstream_gene_variant | MODIFIER | c.*4386C>T| |
S16 |
6 | BAA10g08690 | A10 | 10648190 | G | A | downstream_gene_variant | MODIFIER | c.*2010C>T| |
S15 |
7 | BAA10g08690 | A10 | 10650034 | G | A | downstream_gene_variant | MODIFIER | c.*166C>T| |
S296 |
8 | BAA10g08690 | A10 | 10650161 | G | A | downstream_gene_variant | MODIFIER | c.*39C>T| |
S288 |
9 | BAA10g08690 | A10 | 10650318 | G | A | missense_variant | MODERATE | c.338C>T|p.Ser113Phe |
S261 |
10 | BAA10g08690 | A10 | 10650834 | G | A | upstream_gene_variant | MODIFIER | c.-86C>T| |
S212 |
11 | BAA10g08690 | A10 | 10655010 | G | A | upstream_gene_variant | MODIFIER | c.-4262C>T| |
S36 |