Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g31900 | A10 | 23135326 | C | T | synonymous_variant | LOW | c.3231G>A|p.Lys1077Lys |
S219 S225 |
2 | BAA10g31900 | A10 | 23135726 | G | A | missense_variant | MODERATE | c.3026C>T|p.Ala1009Val |
S113 |
3 | BAA10g31900 | A10 | 23135890 | G | A | synonymous_variant | LOW | c.2952C>T|p.Thr984Thr |
S181 |
4 | BAA10g31900 | A10 | 23136302 | C | T | missense_variant | MODERATE | c.2686G>A|p.Ala896Thr |
S78 |
5 | BAA10g31900 | A10 | 23136304 | G | A | missense_variant | MODERATE | c.2684C>T|p.Ala895Val |
S225 S73 |
6 | BAA10g31900 | A10 | 23136980 | G | A | synonymous_variant | LOW | c.2400C>T|p.Thr800Thr |
S216 |
7 | BAA10g31900 | A10 | 23137289 | C | T | synonymous_variant | LOW | c.2178G>A|p.Glu726Glu |
S247 |
8 | BAA10g31900 | A10 | 23138478 | C | T | missense_variant | MODERATE | c.1433G>A|p.Gly478Asp |
S292 |
9 | BAA10g31900 | A10 | 23139237 | C | T | synonymous_variant | LOW | c.966G>A|p.Lys322Lys |
S40 S49 |
10 | BAA10g31900 | A10 | 23139554 | C | T | missense_variant | MODERATE | c.649G>A|p.Glu217Lys |
S279 |
11 | BAA10g31900 | A10 | 23146057 | A | G | upstream_gene_variant | MODIFIER | c.-4556T>C| |
S281 |
12 | BAA10g31900 | A10 | 23146267 | C | T | upstream_gene_variant | MODIFIER | c.-4766G>A| |
S206 S26 |