Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15570 | A10 | 15893826 | G | A | missense_variant | MODERATE | c.389C>T|p.Ser130Phe |
S303 |
2 | BAA10g15570 | A10 | 15893828 | G | A | synonymous_variant | LOW | c.387C>T|p.Pro129Pro |
S105 S106 |
3 | BAA10g15570 | A10 | 15894051 | G | A | missense_variant | MODERATE | c.250C>T|p.Leu84Phe |
S71 |
4 | BAA10g15570 | A10 | 15894271 | G | A | splice_region_variant&intron_variant | LOW | c.96+7C>T| |
S27 |
5 | BAA10g15570 | A10 | 15895061 | G | A | upstream_gene_variant | MODIFIER | c.-538C>T| |
S267 |
6 | BAA10g15570 | A10 | 15895886 | G | A | upstream_gene_variant | MODIFIER | c.-1363C>T| |
S174 S216 S241 S265 |
7 | BAA10g15570 | A10 | 15895937 | G | A | upstream_gene_variant | MODIFIER | c.-1414C>T| |
S155 |
8 | BAA10g15570 | A10 | 15896368 | C | T | upstream_gene_variant | MODIFIER | c.-1845G>A| |
S183 |
9 | BAA10g15570 | A10 | 15897256 | C | T | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S28 |
10 | BAA10g15570 | A10 | 15897820 | C | T | upstream_gene_variant | MODIFIER | c.-3297G>A| |
S259 |
11 | BAA10g15570 | A10 | 15898051 | G | A | upstream_gene_variant | MODIFIER | c.-3528C>T| |
S303 |