Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21390 | A10 | 18845040 | G | A | upstream_gene_variant | MODIFIER | c.-3121G>A| |
S265 |
2 | BAA10g21390 | A10 | 18845492 | C | T | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S98 |
3 | BAA10g21390 | A10 | 18845901 | G | A | upstream_gene_variant | MODIFIER | c.-2260G>A| |
S35 |
4 | BAA10g21390 | A10 | 18846007 | C | T | upstream_gene_variant | MODIFIER | c.-2154C>T| |
S249 |
5 | BAA10g21390 | A10 | 18846161 | C | T | upstream_gene_variant | MODIFIER | c.-2000C>T| |
S87 |
6 | BAA10g21390 | A10 | 18846718 | G | A | upstream_gene_variant | MODIFIER | c.-1443G>A| |
S139 |
7 | BAA10g21390 | A10 | 18847497 | C | T | upstream_gene_variant | MODIFIER | c.-664C>T| |
S186 |
8 | BAA10g21390 | A10 | 18847851 | C | T | upstream_gene_variant | MODIFIER | c.-310C>T| |
S67 |
9 | BAA10g21390 | A10 | 18848627 | G | A | missense_variant | MODERATE | c.467G>A|p.Cys156Tyr |
S3 |