Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23040 | A08 | 17144225 | C | T | splice_region_variant&synonymous_variant | LOW | c.2226G>A|p.Gln742Gln |
S186 |
2 | BAA08g23040 | A08 | 17144332 | C | T | missense_variant | MODERATE | c.2119G>A|p.Glu707Lys |
S177 |
3 | BAA08g23040 | A08 | 17144674 | C | T | synonymous_variant | LOW | c.2013G>A|p.Lys671Lys |
S46 |
4 | BAA08g23040 | A08 | 17145411 | C | T | missense_variant | MODERATE | c.1627G>A|p.Ala543Thr |
S6 |
5 | BAA08g23040 | A08 | 17147299 | G | A | splice_region_variant&intron_variant | LOW | c.879+7C>T| |
S109 |
6 | BAA08g23040 | A08 | 17148194 | C | T | splice_region_variant&intron_variant | LOW | c.618+8G>A| |
S159 |
7 | BAA08g23040 | A08 | 17150229 | C | T | upstream_gene_variant | MODIFIER | c.-904G>A| |
S6 |
8 | BAA08g23040 | A08 | 17154019 | C | T | upstream_gene_variant | MODIFIER | c.-4694G>A| |
S174 S216 S241 |