Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16740 | A10 | 16397912 | C | T | upstream_gene_variant | MODIFIER | c.-4612C>T| |
S235 |
2 | BAA10g16740 | A10 | 16398155 | G | A | upstream_gene_variant | MODIFIER | c.-4369G>A| |
S290 |
3 | BAA10g16740 | A10 | 16398631 | C | T | upstream_gene_variant | MODIFIER | c.-3893C>T| |
S175 |
4 | BAA10g16740 | A10 | 16398889 | C | T | upstream_gene_variant | MODIFIER | c.-3635C>T| |
S189 |
5 | BAA10g16740 | A10 | 16399767 | G | A | upstream_gene_variant | MODIFIER | c.-2757G>A| |
S128 |
6 | BAA10g16740 | A10 | 16402461 | C | T | upstream_gene_variant | MODIFIER | c.-63C>T| |
S48 |
7 | BAA10g16740 | A10 | 16403760 | C | T | synonymous_variant | LOW | c.321C>T|p.Asn107Asn |
S277 |
8 | BAA10g16740 | A10 | 16403989 | G | A | missense_variant | MODERATE | c.550G>A|p.Asp184Asn |
S160 |
9 | BAA10g16740 | A10 | 16404275 | G | A | missense_variant | MODERATE | c.836G>A|p.Arg279Gln |
S174 S216 S241 S265 |
10 | BAA10g16740 | A10 | 16404397 | G | A | missense_variant | MODERATE | c.958G>A|p.Ala320Thr |
S138 |
11 | BAA10g16740 | A10 | 16404516 | G | A | synonymous_variant | LOW | c.1077G>A|p.Ala359Ala |
S198 |
12 | BAA10g16740 | A10 | 16404652 | G | A | missense_variant | MODERATE | c.1213G>A|p.Asp405Asn |
S148 S30 S31 |
13 | BAA10g16740 | A10 | 16404676 | G | A | missense_variant | MODERATE | c.1237G>A|p.Glu413Lys |
S129 |
14 | BAA10g16740 | A10 | 16404717 | C | T | synonymous_variant | LOW | c.1278C>T|p.Phe426Phe |
S119 |
15 | BAA10g16740 | A10 | 16404858 | G | A | synonymous_variant | LOW | c.1419G>A|p.Ala473Ala |
S125 |
16 | BAA10g16740 | A10 | 16406165 | C | T | downstream_gene_variant | MODIFIER | c.*1073C>T| |
S259 |