Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g03990 | A08 | 2773619 | G | A | downstream_gene_variant | MODIFIER | c.*4138C>T| |
S16 |
2 | BAA08g03990 | A08 | 2775907 | G | A | downstream_gene_variant | MODIFIER | c.*1850C>T| |
S242 |
3 | BAA08g03990 | A08 | 2776626 | C | T | downstream_gene_variant | MODIFIER | c.*1131G>A| |
S104 S52 |
4 | BAA08g03990 | A08 | 2777667 | C | G | downstream_gene_variant | MODIFIER | c.*90G>C| |
S56 |
5 | BAA08g03990 | A08 | 2777851 | C | T | missense_variant | MODERATE | c.1256G>A|p.Ser419Asn |
S213 |
6 | BAA08g03990 | A08 | 2777910 | C | T | synonymous_variant | LOW | c.1197G>A|p.Gln399Gln |
S183 S198 |
7 | BAA08g03990 | A08 | 2778413 | G | A | intron_variant | MODIFIER | c.827-39C>T| |
S18 |
8 | BAA08g03990 | A08 | 2778562 | C | T | synonymous_variant | LOW | c.729G>A|p.Lys243Lys |
S110 |
9 | BAA08g03990 | A08 | 2778829 | C | T | missense_variant | MODERATE | c.462G>A|p.Met154Ile |
S28 |
10 | BAA08g03990 | A08 | 2779022 | G | A | intron_variant | MODIFIER | c.331+37C>T| |
S33 |
11 | BAA08g03990 | A08 | 2779416 | G | A | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S94 |
12 | BAA08g03990 | A08 | 2780688 | G | A | upstream_gene_variant | MODIFIER | c.-1196C>T| |
S288 |
13 | BAA08g03990 | A08 | 2780690 | G | A | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S297 |
14 | BAA08g03990 | A08 | 2780837 | G | A | upstream_gene_variant | MODIFIER | c.-1345C>T| |
S193 |
15 | BAA08g03990 | A08 | 2781809 | C | T | upstream_gene_variant | MODIFIER | c.-2317G>A| |
S216 |
16 | BAA08g03990 | A08 | 2781865 | G | A | upstream_gene_variant | MODIFIER | c.-2373C>T| |
S62 |
17 | BAA08g03990 | A08 | 2782018 | G | A | upstream_gene_variant | MODIFIER | c.-2526C>T| |
S223 |