Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02120 | A10 | 995065 | G | A | downstream_gene_variant | MODIFIER | c.*968C>T| |
S18 |
2 | BAA10g02120 | A10 | 996767 | G | A | missense_variant | MODERATE | c.658C>T|p.Pro220Ser |
S126 |
3 | BAA10g02120 | A10 | 996852 | C | T | synonymous_variant | LOW | c.573G>A|p.Gln191Gln |
S297 |
4 | BAA10g02120 | A10 | 997074 | C | T | synonymous_variant | LOW | c.351G>A|p.Leu117Leu |
S35 |
5 | BAA10g02120 | A10 | 997781 | G | A | upstream_gene_variant | MODIFIER | c.-357C>T| |
S176 S303 |
6 | BAA10g02120 | A10 | 999409 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S176 |
7 | BAA10g02120 | A10 | 999640 | C | T | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S270 |
8 | BAA10g02120 | A10 | 1000857 | C | T | upstream_gene_variant | MODIFIER | c.-3433G>A| |
S11 |
9 | BAA10g02120 | A10 | 1001161 | G | A | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S20 |
10 | BAA10g02120 | A10 | 1001980 | G | A | upstream_gene_variant | MODIFIER | c.-4556C>T| |
S216 |