Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20950 | A10 | 18616829 | C | T | missense_variant | MODERATE | c.1954G>A|p.Gly652Arg |
S78 |
2 | BAA10g20950 | A10 | 18616895 | C | T | missense_variant | MODERATE | c.1888G>A|p.Val630Met |
S187 |
3 | BAA10g20950 | A10 | 18617058 | C | T | missense_variant | MODERATE | c.1810G>A|p.Val604Ile |
S199 |
4 | BAA10g20950 | A10 | 18617218 | G | A | synonymous_variant | LOW | c.1650C>T|p.Ile550Ile |
S293 |
5 | BAA10g20950 | A10 | 18617262 | C | T | missense_variant | MODERATE | c.1606G>A|p.Asp536Asn |
S177 |
6 | BAA10g20950 | A10 | 18617266 | C | T | synonymous_variant | LOW | c.1602G>A|p.Gln534Gln |
S153 S213 |
7 | BAA10g20950 | A10 | 18618278 | C | T | missense_variant | MODERATE | c.1099G>A|p.Glu367Lys |
S200 |
8 | BAA10g20950 | A10 | 18618714 | G | A | synonymous_variant | LOW | c.663C>T|p.Arg221Arg |
S57 |
9 | BAA10g20950 | A10 | 18619273 | G | A | missense_variant | MODERATE | c.104C>T|p.Ala35Val |
S82 S92 |
10 | BAA10g20950 | A10 | 18619431 | G | A | upstream_gene_variant | MODIFIER | c.-55C>T| |
S295 |
11 | BAA10g20950 | A10 | 18620099 | C | T | upstream_gene_variant | MODIFIER | c.-723G>A| |
S73 |
12 | BAA10g20950 | A10 | 18622160 | C | T | upstream_gene_variant | MODIFIER | c.-2784G>A| |
S183 |
13 | BAA10g20950 | A10 | 18622729 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S132 S137 S215 |
14 | BAA10g20950 | A10 | 18622806 | C | T | upstream_gene_variant | MODIFIER | c.-3430G>A| |
S135 |
15 | BAA10g20950 | A10 | 18623603 | G | A | upstream_gene_variant | MODIFIER | c.-4227C>T| |
S112 |