Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24380 | A10 | 20100462 | G | A | missense_variant | MODERATE | c.1807C>T|p.Arg603Cys |
S192 |
2 | BAA10g24380 | A10 | 20100629 | G | A | missense_variant | MODERATE | c.1640C>T|p.Ser547Phe |
S190 |
3 | BAA10g24380 | A10 | 20100765 | C | T | missense_variant | MODERATE | c.1504G>A|p.Gly502Arg |
S197 |
4 | BAA10g24380 | A10 | 20103379 | G | A | missense_variant | MODERATE | c.706C>T|p.Pro236Ser |
S271 |
5 | BAA10g24380 | A10 | 20103562 | C | T | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S224 |
6 | BAA10g24380 | A10 | 20103693 | C | T | missense_variant | MODERATE | c.392G>A|p.Gly131Asp |
S247 |
7 | BAA10g24380 | A10 | 20103825 | C | T | missense_variant | MODERATE | c.260G>A|p.Cys87Tyr |
S152 |
8 | BAA10g24380 | A10 | 20104795 | G | A | upstream_gene_variant | MODIFIER | c.-633C>T| |
S112 |
9 | BAA10g24380 | A10 | 20105834 | C | T | upstream_gene_variant | MODIFIER | c.-1672G>A| |
S259 |
10 | BAA10g24380 | A10 | 20105988 | C | T | upstream_gene_variant | MODIFIER | c.-1826G>A| |
S12 |
11 | BAA10g24380 | A10 | 20106846 | C | T | upstream_gene_variant | MODIFIER | c.-2684G>A| |
S265 S39 |
12 | BAA10g24380 | A10 | 20107063 | G | A | upstream_gene_variant | MODIFIER | c.-2901C>T| |
S136 |
13 | BAA10g24380 | A10 | 20108162 | C | T | upstream_gene_variant | MODIFIER | c.-4000G>A| |
S169 |
14 | BAA10g24380 | A10 | 20108592 | G | A | upstream_gene_variant | MODIFIER | c.-4430C>T| |
S202 |