Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29350 | A10 | 22118130 | G | A | synonymous_variant | LOW | c.3477C>T|p.Ile1159Ile |
S203 |
2 | BAA10g29350 | A10 | 22120885 | G | A | synonymous_variant | LOW | c.2887C>T|p.Leu963Leu |
S200 |
3 | BAA10g29350 | A10 | 22121007 | G | A | missense_variant | MODERATE | c.2846C>T|p.Thr949Ile |
S219 S72 |
4 | BAA10g29350 | A10 | 22123495 | G | A | missense_variant | MODERATE | c.1745C>T|p.Pro582Leu |
S136 |
5 | BAA10g29350 | A10 | 22123532 | G | A | missense_variant | MODERATE | c.1708C>T|p.Pro570Ser |
S88 |
6 | BAA10g29350 | A10 | 22125103 | G | A | synonymous_variant | LOW | c.783C>T|p.Asn261Asn |
S231 |
7 | BAA10g29350 | A10 | 22130317 | G | A | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S28 |
8 | BAA10g29350 | A10 | 22130339 | G | A | upstream_gene_variant | MODIFIER | c.-3990C>T| |
S71 |
9 | BAA10g29350 | A10 | 22130887 | G | A | upstream_gene_variant | MODIFIER | c.-4538C>T| |
S134 |
10 | BAA10g29350 | A10 | 22131303 | G | A | upstream_gene_variant | MODIFIER | c.-4954C>T| |
S32 |