Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41950 | A09 | 48508395 | G | A | upstream_gene_variant | MODIFIER | c.-4924G>A| |
S204 |
2 | BAA09g41950 | A09 | 48509188 | G | A | upstream_gene_variant | MODIFIER | c.-4131G>A| |
S298 |
3 | BAA09g41950 | A09 | 48509485 | C | T | upstream_gene_variant | MODIFIER | c.-3834C>T| |
S37 |
4 | BAA09g41950 | A09 | 48509673 | G | A | upstream_gene_variant | MODIFIER | c.-3646G>A| |
S151 S263 |
5 | BAA09g41950 | A09 | 48510485 | C | T | upstream_gene_variant | MODIFIER | c.-2834C>T| |
S202 |
6 | BAA09g41950 | A09 | 48510724 | C | T | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S91 |
7 | BAA09g41950 | A09 | 48511992 | G | A | upstream_gene_variant | MODIFIER | c.-1327G>A| |
S62 |
8 | BAA09g41950 | A09 | 48513552 | G | A | synonymous_variant | LOW | c.234G>A|p.Thr78Thr |
S59 |
9 | BAA09g41950 | A09 | 48514155 | G | A | synonymous_variant | LOW | c.837G>A|p.Lys279Lys |
S196 |
10 | BAA09g41950 | A09 | 48514184 | C | T | missense_variant | MODERATE | c.866C>T|p.Thr289Ile |
S247 |
11 | BAA09g41950 | A09 | 48514221 | A | G | synonymous_variant | LOW | c.903A>G|p.Lys301Lys |
S257 |
12 | BAA09g41950 | A09 | 48514636 | C | T | missense_variant | MODERATE | c.1318C>T|p.His440Tyr |
S103 |
13 | BAA09g41950 | A09 | 48514740 | G | A | synonymous_variant | LOW | c.1422G>A|p.Glu474Glu |
S38 |
14 | BAA09g41950 | A09 | 48514973 | G | A | intron_variant | MODIFIER | c.1588-13G>A| |
S289 S290 |
15 | BAA09g41950 | A09 | 48516592 | C | T | synonymous_variant | LOW | c.1863C>T|p.Leu621Leu |
S240 |
16 | BAA09g41950 | A09 | 48518083 | G | A | downstream_gene_variant | MODIFIER | c.*1257G>A| |
S167 |
17 | BAA09g41950 | A09 | 48518120 | G | A | downstream_gene_variant | MODIFIER | c.*1294G>A| |
S250 |