Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18770 | A06 | 9604141 | C | T | missense_variant | MODERATE | c.2008G>A|p.Glu670Lys |
S264 |
2 | BAA06g18770 | A06 | 9604552 | G | A | missense_variant | MODERATE | c.1597C>T|p.Leu533Phe |
S234 |
3 | BAA06g18770 | A06 | 9604734 | G | A | missense_variant | MODERATE | c.1415C>T|p.Thr472Ile |
S177 |
4 | BAA06g18770 | A06 | 9604770 | G | A | missense_variant | MODERATE | c.1379C>T|p.Ser460Phe |
S71 |
5 | BAA06g18770 | A06 | 9605397 | G | A | missense_variant | MODERATE | c.752C>T|p.Thr251Met |
S158 |
6 | BAA06g18770 | A06 | 9605762 | C | T | synonymous_variant | LOW | c.387G>A|p.Lys129Lys |
S200 |
7 | BAA06g18770 | A06 | 9605867 | C | T | synonymous_variant | LOW | c.282G>A|p.Arg94Arg |
S65 |
8 | BAA06g18770 | A06 | 9607442 | G | A | upstream_gene_variant | MODIFIER | c.-1294C>T| |
S204 |
9 | BAA06g18770 | A06 | 9607455 | C | T | upstream_gene_variant | MODIFIER | c.-1307G>A| |
S293 |
10 | BAA06g18770 | A06 | 9607770 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S113 |
11 | BAA06g18770 | A06 | 9608432 | C | T | upstream_gene_variant | MODIFIER | c.-2284G>A| |
S148 S30 |