Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00760 | A07 | 524690 | G | A | downstream_gene_variant | MODIFIER | c.*4358C>T| |
S296 |
2 | BAA07g00760 | A07 | 529139 | C | T | missense_variant | MODERATE | c.1076G>A|p.Arg359Lys |
S86 |
3 | BAA07g00760 | A07 | 529186 | G | A | synonymous_variant | LOW | c.1029C>T|p.Ala343Ala |
S223 |
4 | BAA07g00760 | A07 | 529280 | G | A | missense_variant | MODERATE | c.935C>T|p.Ser312Leu |
S146 |
5 | BAA07g00760 | A07 | 529578 | C | T | missense_variant | MODERATE | c.637G>A|p.Asp213Asn |
S174 |
6 | BAA07g00760 | A07 | 530709 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S173 |
7 | BAA07g00760 | A07 | 530716 | A | C | upstream_gene_variant | MODIFIER | c.-502T>G| |
S110 S134 S150 S179 S208 S215 S221 S226 S269 S280 S290 S3 |
8 | BAA07g00760 | A07 | 530804 | G | A | upstream_gene_variant | MODIFIER | c.-590C>T| |
S251 |
9 | BAA07g00760 | A07 | 531388 | G | A | upstream_gene_variant | MODIFIER | c.-1174C>T| |
S119 |
10 | BAA07g00760 | A07 | 531587 | G | A | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S51 |
11 | BAA07g00760 | A07 | 531617 | A | C | upstream_gene_variant | MODIFIER | c.-1403T>G| |
S275 |
12 | BAA07g00760 | A07 | 532335 | G | A | upstream_gene_variant | MODIFIER | c.-2121C>T| |
S188 |
13 | BAA07g00760 | A07 | 532634 | G | A | upstream_gene_variant | MODIFIER | c.-2420C>T| |
S129 |
14 | BAA07g00760 | A07 | 532881 | G | A | upstream_gene_variant | MODIFIER | c.-2667C>T| |
S245 |
15 | BAA07g00760 | A07 | 534135 | C | T | upstream_gene_variant | MODIFIER | c.-3921G>A| |
S95 |
16 | BAA07g00760 | A07 | 534204 | C | T | upstream_gene_variant | MODIFIER | c.-3990G>A| |
S247 |
17 | BAA07g00760 | A07 | 534236 | G | A | upstream_gene_variant | MODIFIER | c.-4022C>T| |
S295 |