Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g46190 | A03 | 22139438 | G | A | synonymous_variant | LOW | c.2691C>T|p.Ile897Ile |
S88 |
2 | BAA03g46190 | A03 | 22140394 | G | A | missense_variant | MODERATE | c.1943C>T|p.Ala648Val |
S259 |
3 | BAA03g46190 | A03 | 22140886 | G | A | missense_variant | MODERATE | c.1451C>T|p.Pro484Leu |
S289 S290 |
4 | BAA03g46190 | A03 | 22140948 | C | T | synonymous_variant | LOW | c.1389G>A|p.Gln463Gln |
S143 |
5 | BAA03g46190 | A03 | 22141256 | C | T | missense_variant | MODERATE | c.1081G>A|p.Gly361Arg |
S241 S39 |
6 | BAA03g46190 | A03 | 22141601 | G | A | missense_variant | MODERATE | c.736C>T|p.Leu246Phe |
S170 |
7 | BAA03g46190 | A03 | 22141671 | G | A | synonymous_variant | LOW | c.666C>T|p.Leu222Leu |
S177 |
8 | BAA03g46190 | A03 | 22141893 | C | T | synonymous_variant | LOW | c.444G>A|p.Lys148Lys |
S90 |
9 | BAA03g46190 | A03 | 22141988 | G | A | missense_variant | MODERATE | c.349C>T|p.Pro117Ser |
S175 |
10 | BAA03g46190 | A03 | 22142486 | G | A | upstream_gene_variant | MODIFIER | c.-150C>T| |
S249 |
11 | BAA03g46190 | A03 | 22142940 | G | A | upstream_gene_variant | MODIFIER | c.-604C>T| |
S284 |
12 | BAA03g46190 | A03 | 22143012 | G | A | upstream_gene_variant | MODIFIER | c.-676C>T| |
S68 |
13 | BAA03g46190 | A03 | 22144258 | G | A | upstream_gene_variant | MODIFIER | c.-1922C>T| |
S289 S290 |
14 | BAA03g46190 | A03 | 22144505 | C | T | upstream_gene_variant | MODIFIER | c.-2169G>A| |
S33 |