Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g29150 | A07 | 29981850 | G | A | synonymous_variant | LOW | c.2794C>T|p.Leu932Leu |
S199 |
2 | BAA07g29150 | A07 | 29982933 | C | T | missense_variant | MODERATE | c.1849G>A|p.Val617Ile |
S27 |
3 | BAA07g29150 | A07 | 29982983 | G | A | missense_variant | MODERATE | c.1799C>T|p.Ser600Phe |
S20 |
4 | BAA07g29150 | A07 | 29982987 | C | T | missense_variant | MODERATE | c.1795G>A|p.Glu599Lys |
S159 S243 |
5 | BAA07g29150 | A07 | 29983451 | C | T | missense_variant | MODERATE | c.1331G>A|p.Arg444Lys |
S41 |
6 | BAA07g29150 | A07 | 29983816 | C | T | synonymous_variant | LOW | c.966G>A|p.Arg322Arg |
S62 |
7 | BAA07g29150 | A07 | 29984075 | G | A | missense_variant | MODERATE | c.707C>T|p.Ser236Leu |
S6 |
8 | BAA07g29150 | A07 | 29984621 | C | T | stop_gained | HIGH | c.161G>A|p.Trp54* |
S213 |
9 | BAA07g29150 | A07 | 29984671 | C | T | synonymous_variant | LOW | c.111G>A|p.Leu37Leu |
S213 |
10 | BAA07g29150 | A07 | 29984705 | G | A | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S195 |
11 | BAA07g29150 | A07 | 29988895 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S33 |