Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20890 | A10 | 18582502 | G | A | upstream_gene_variant | MODIFIER | c.-2277G>A| |
S223 |
2 | BAA10g20890 | A10 | 18582558 | C | T | upstream_gene_variant | MODIFIER | c.-2221C>T| |
S92 |
3 | BAA10g20890 | A10 | 18582684 | G | A | upstream_gene_variant | MODIFIER | c.-2095G>A| |
S132 S137 S215 S89 |
4 | BAA10g20890 | A10 | 18582936 | C | T | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S221 |
5 | BAA10g20890 | A10 | 18583844 | G | A | upstream_gene_variant | MODIFIER | c.-935G>A| |
S64 |
6 | BAA10g20890 | A10 | 18584795 | G | A | missense_variant | MODERATE | c.17G>A|p.Arg6Lys |
S42 |
7 | BAA10g20890 | A10 | 18585018 | G | A | synonymous_variant | LOW | c.240G>A|p.Leu80Leu |
S273 |
8 | BAA10g20890 | A10 | 18586145 | G | A | synonymous_variant | LOW | c.1050G>A|p.Gln350Gln |
S166 |
9 | BAA10g20890 | A10 | 18586222 | G | A | missense_variant | MODERATE | c.1127G>A|p.Ser376Asn |
S4 |
10 | BAA10g20890 | A10 | 18586305 | G | A | missense_variant | MODERATE | c.1210G>A|p.Asp404Asn |
S174 |
11 | BAA10g20890 | A10 | 18586595 | C | T | synonymous_variant | LOW | c.1500C>T|p.Asn500Asn |
S10 |
12 | BAA10g20890 | A10 | 18586812 | C | T | missense_variant | MODERATE | c.1717C>T|p.Leu573Phe |
S183 |
13 | BAA10g20890 | A10 | 18588519 | G | A | downstream_gene_variant | MODIFIER | c.*1651G>A| |
S16 |
14 | BAA10g20890 | A10 | 18588990 | G | A | downstream_gene_variant | MODIFIER | c.*2122G>A| |
S57 |
15 | BAA10g20890 | A10 | 18589780 | C | T | downstream_gene_variant | MODIFIER | c.*2912C>T| |
S84 S93 |
16 | BAA10g20890 | A10 | 18589866 | G | A | downstream_gene_variant | MODIFIER | c.*2998G>A| |
S255 |
17 | BAA10g20890 | A10 | 18589870 | C | T | downstream_gene_variant | MODIFIER | c.*3002C>T| |
S294 |