Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g32660 | A09 | 41294912 | G | A | downstream_gene_variant | MODIFIER | c.*4828C>T| |
S132 S137 S215 |
2 | BAA09g32660 | A09 | 41295772 | C | T | downstream_gene_variant | MODIFIER | c.*3968G>A| |
S138 |
3 | BAA09g32660 | A09 | 41296143 | G | A | downstream_gene_variant | MODIFIER | c.*3597C>T| |
S67 |
4 | BAA09g32660 | A09 | 41297089 | C | T | downstream_gene_variant | MODIFIER | c.*2651G>A| |
S60 |
5 | BAA09g32660 | A09 | 41297681 | G | A | downstream_gene_variant | MODIFIER | c.*2059C>T| |
S12 |
6 | BAA09g32660 | A09 | 41298670 | A | C | downstream_gene_variant | MODIFIER | c.*1070T>G| |
S114 |
7 | BAA09g32660 | A09 | 41298970 | C | A | downstream_gene_variant | MODIFIER | c.*770G>T| |
S274 |
8 | BAA09g32660 | A09 | 41299763 | G | A | stop_gained | HIGH | c.1417C>T|p.Gln473* |
S205 |
9 | BAA09g32660 | A09 | 41301218 | G | A | intron_variant | MODIFIER | c.627+9C>T| |
S65 |
10 | BAA09g32660 | A09 | 41301402 | G | A | intron_variant | MODIFIER | c.528+23C>T| |
S218 |
11 | BAA09g32660 | A09 | 41301572 | G | A | intron_variant | MODIFIER | c.448+20C>T| |
S177 |
12 | BAA09g32660 | A09 | 41302010 | C | T | intron_variant | MODIFIER | c.147-43G>A| |
S69 |
13 | BAA09g32660 | A09 | 41302644 | G | A | upstream_gene_variant | MODIFIER | c.-433C>T| |
S69 |
14 | BAA09g32660 | A09 | 41302727 | C | T | upstream_gene_variant | MODIFIER | c.-516G>A| |
S296 |
15 | BAA09g32660 | A09 | 41302867 | C | T | upstream_gene_variant | MODIFIER | c.-656G>A| |
S183 S198 |
16 | BAA09g32660 | A09 | 41302886 | C | T | upstream_gene_variant | MODIFIER | c.-675G>A| |
S219 S72 |