Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27530 | A10 | 21434869 | C | T | missense_variant | MODERATE | c.1019G>A|p.Arg340Lys |
S176 |
2 | BAA10g27530 | A10 | 21435159 | G | A | synonymous_variant | LOW | c.828C>T|p.Asn276Asn |
S212 |
3 | BAA10g27530 | A10 | 21437433 | C | T | missense_variant | MODERATE | c.76G>A|p.Asp26Asn |
S211 |
4 | BAA10g27530 | A10 | 21437439 | C | T | missense_variant | MODERATE | c.70G>A|p.Val24Ile |
S133 |
5 | BAA10g27530 | A10 | 21437832 | G | A | upstream_gene_variant | MODIFIER | c.-324C>T| |
S263 |
6 | BAA10g27530 | A10 | 21439755 | G | A | upstream_gene_variant | MODIFIER | c.-2247C>T| |
S279 |
7 | BAA10g27530 | A10 | 21439823 | G | A | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S88 |
8 | BAA10g27530 | A10 | 21439864 | G | A | upstream_gene_variant | MODIFIER | c.-2356C>T| |
S172 S217 |
9 | BAA10g27530 | A10 | 21441529 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S153 S213 |