Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26500 | A10 | 20989537 | C | T | missense_variant&splice_region_variant | MODERATE | c.1349G>A|p.Gly450Glu |
S46 |
2 | BAA10g26500 | A10 | 20989825 | C | T | synonymous_variant | LOW | c.1152G>A|p.Thr384Thr |
S272 |
3 | BAA10g26500 | A10 | 20990952 | G | A | synonymous_variant | LOW | c.627C>T|p.His209His |
S139 |
4 | BAA10g26500 | A10 | 20994435 | C | T | upstream_gene_variant | MODIFIER | c.-2411G>A| |
S242 |
5 | BAA10g26500 | A10 | 20994901 | C | T | upstream_gene_variant | MODIFIER | c.-2877G>A| |
S269 |
6 | BAA10g26500 | A10 | 20995088 | C | T | upstream_gene_variant | MODIFIER | c.-3064G>A| |
S221 |
7 | BAA10g26500 | A10 | 20995243 | C | T | upstream_gene_variant | MODIFIER | c.-3219G>A| |
S166 |
8 | BAA10g26500 | A10 | 20995686 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S277 |
9 | BAA10g26500 | A10 | 20996451 | C | T | upstream_gene_variant | MODIFIER | c.-4427G>A| |
S247 |
10 | BAA10g26500 | A10 | 20996630 | C | T | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S177 |