Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g39600 | A07 | 35489283 | A | T | missense_variant | MODERATE | c.425A>T|p.Glu142Val |
S100 S193 S218 S262 S289 S3 |
2 | BAA07g39600 | A07 | 35489431 | C | T | synonymous_variant | LOW | c.573C>T|p.Ile191Ile |
S159 S243 |
3 | BAA07g39600 | A07 | 35489533 | G | A | missense_variant | MODERATE | c.604G>A|p.Gly202Ser |
S40 S49 |
4 | BAA07g39600 | A07 | 35491047 | C | T | missense_variant | MODERATE | c.1540C>T|p.Arg514Cys |
S42 |
5 | BAA07g39600 | A07 | 35491572 | G | A | missense_variant | MODERATE | c.1831G>A|p.Gly611Arg |
S65 |
6 | BAA07g39600 | A07 | 35492076 | G | A | missense_variant | MODERATE | c.2059G>A|p.Val687Met |
S195 |
7 | BAA07g39600 | A07 | 35492495 | C | T | missense_variant | MODERATE | c.2299C>T|p.Pro767Ser |
S197 |
8 | BAA07g39600 | A07 | 35493170 | C | T | synonymous_variant | LOW | c.2688C>T|p.Pro896Pro |
S32 |
9 | BAA07g39600 | A07 | 35494870 | C | T | downstream_gene_variant | MODIFIER | c.*1343C>T| |
S261 |
10 | BAA07g39600 | A07 | 35494897 | G | A | downstream_gene_variant | MODIFIER | c.*1370G>A| |
S112 |