Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21140 | A10 | 18698414 | G | A | upstream_gene_variant | MODIFIER | c.-2142G>A| |
S262 |
2 | BAA10g21140 | A10 | 18700096 | G | A | upstream_gene_variant | MODIFIER | c.-460G>A| |
S131 |
3 | BAA10g21140 | A10 | 18700422 | G | A | upstream_gene_variant | MODIFIER | c.-134G>A| |
S122 |
4 | BAA10g21140 | A10 | 18701035 | G | A | synonymous_variant | LOW | c.384G>A|p.Glu128Glu |
S261 |
5 | BAA10g21140 | A10 | 18701344 | G | A | missense_variant | MODERATE | c.590G>A|p.Arg197His |
S57 |
6 | BAA10g21140 | A10 | 18701939 | G | A | intron_variant | MODIFIER | c.887+31G>A| |
S213 |
7 | BAA10g21140 | A10 | 18701999 | C | T | intron_variant | MODIFIER | c.888-9C>T| |
S98 |
8 | BAA10g21140 | A10 | 18702239 | C | T | intron_variant | MODIFIER | c.964-28C>T| |
S11 |
9 | BAA10g21140 | A10 | 18703642 | C | T | intron_variant | MODIFIER | c.1594-21C>T| |
S150 |