Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g15460 | A08 | 13034385 | G | A | missense_variant | MODERATE | c.2723C>T|p.Pro908Leu |
S94 |
2 | BAA08g15460 | A08 | 13034508 | G | A | missense_variant | MODERATE | c.2600C>T|p.Pro867Leu |
S172 |
3 | BAA08g15460 | A08 | 13034785 | C | T | missense_variant | MODERATE | c.2323G>A|p.Asp775Asn |
S123 |
4 | BAA08g15460 | A08 | 13036261 | C | A | splice_region_variant&synonymous_variant | LOW | c.1608G>T|p.Val536Val |
S183 S198 |
5 | BAA08g15460 | A08 | 13039388 | C | T | missense_variant | MODERATE | c.53G>A|p.Gly18Glu |
S44 |
6 | BAA08g15460 | A08 | 13039689 | C | T | upstream_gene_variant | MODIFIER | c.-249G>A| |
S219 S72 |
7 | BAA08g15460 | A08 | 13039989 | G | A | upstream_gene_variant | MODIFIER | c.-549C>T| |
S62 |
8 | BAA08g15460 | A08 | 13040450 | G | A | upstream_gene_variant | MODIFIER | c.-1010C>T| |
S245 |
9 | BAA08g15460 | A08 | 13040871 | G | A | upstream_gene_variant | MODIFIER | c.-1431C>T| |
S35 |
10 | BAA08g15460 | A08 | 13040920 | C | T | upstream_gene_variant | MODIFIER | c.-1480G>A| |
S139 |
11 | BAA08g15460 | A08 | 13041776 | C | T | upstream_gene_variant | MODIFIER | c.-2336G>A| |
S173 |
12 | BAA08g15460 | A08 | 13043829 | G | A | upstream_gene_variant | MODIFIER | c.-4389C>T| |
S119 |