Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16870 | A09 | 9995107 | G | A | upstream_gene_variant | MODIFIER | c.-1718G>A| |
S198 |
2 | BAA09g16870 | A09 | 9996271 | C | T | upstream_gene_variant | MODIFIER | c.-554C>T| |
S284 |
3 | BAA09g16870 | A09 | 9997180 | C | A | intron_variant | MODIFIER | c.225-23C>A| |
S85 |
4 | BAA09g16870 | A09 | 9999216 | C | T | synonymous_variant | LOW | c.1155C>T|p.Cys385Cys |
S87 |
5 | BAA09g16870 | A09 | 9999306 | C | T | synonymous_variant | LOW | c.1245C>T|p.Arg415Arg |
S206 S26 |
6 | BAA09g16870 | A09 | 9999465 | G | A | synonymous_variant | LOW | c.1404G>A|p.Glu468Glu |
S249 |
7 | BAA09g16870 | A09 | 9999985 | C | T | missense_variant | MODERATE | c.1762C>T|p.Pro588Ser |
S104 S52 |
8 | BAA09g16870 | A09 | 10000222 | C | T | stop_gained | HIGH | c.1915C>T|p.Gln639* |
S116 |
9 | BAA09g16870 | A09 | 10000284 | C | T | synonymous_variant | LOW | c.1977C>T|p.Val659Val |
S297 |
10 | BAA09g16870 | A09 | 10000534 | G | A | missense_variant | MODERATE | c.2164G>A|p.Glu722Lys |
S301 S304 |
11 | BAA09g16870 | A09 | 10001153 | C | T | synonymous_variant | LOW | c.2484C>T|p.Asn828Asn |
S50 |
12 | BAA09g16870 | A09 | 10006119 | C | T | downstream_gene_variant | MODIFIER | c.*4711C>T| |
S261 |