Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18700 | A05 | 10807369 | C | T | upstream_gene_variant | MODIFIER | c.-2671C>T| |
S128 |
2 | BAA05g18700 | A05 | 10807777 | G | A | upstream_gene_variant | MODIFIER | c.-2263G>A| |
S90 |
3 | BAA05g18700 | A05 | 10808768 | C | T | upstream_gene_variant | MODIFIER | c.-1272C>T| |
S12 |
4 | BAA05g18700 | A05 | 10809614 | C | T | upstream_gene_variant | MODIFIER | c.-426C>T| |
S184 |
5 | BAA05g18700 | A05 | 10810008 | C | T | upstream_gene_variant | MODIFIER | c.-32C>T| |
S1 S161 S228 S90 |
6 | BAA05g18700 | A05 | 10810664 | C | T | missense_variant | MODERATE | c.535C>T|p.Pro179Ser |
S140 |
7 | BAA05g18700 | A05 | 10810948 | C | T | intron_variant | MODIFIER | c.626+193C>T| |
S180 |
8 | BAA05g18700 | A05 | 10811155 | G | A | intron_variant | MODIFIER | c.626+400G>A| |
S152 |
9 | BAA05g18700 | A05 | 10811194 | G | A | intron_variant | MODIFIER | c.626+439G>A| |
S206 S26 |
10 | BAA05g18700 | A05 | 10812751 | G | A | missense_variant | MODERATE | c.1093G>A|p.Asp365Asn |
S46 |
11 | BAA05g18700 | A05 | 10813645 | G | A | missense_variant | MODERATE | c.1514G>A|p.Gly505Glu |
S150 |
12 | BAA05g18700 | A05 | 10814286 | C | T | missense_variant | MODERATE | c.1979C>T|p.Ala660Val |
S188 |
13 | BAA05g18700 | A05 | 10814965 | G | A | missense_variant | MODERATE | c.2372G>A|p.Arg791Lys |
S174 S241 S27 S39 |
14 | BAA05g18700 | A05 | 10815609 | C | T | downstream_gene_variant | MODIFIER | c.*343C>T| |
S259 |
15 | BAA05g18700 | A05 | 10816446 | G | A | downstream_gene_variant | MODIFIER | c.*1180G>A| |
S156 |
16 | BAA05g18700 | A05 | 10817211 | C | T | downstream_gene_variant | MODIFIER | c.*1945C>T| |
S108 |
17 | BAA05g18700 | A05 | 10817258 | G | A | downstream_gene_variant | MODIFIER | c.*1992G>A| |
S172 |
18 | BAA05g18700 | A05 | 10817945 | C | T | downstream_gene_variant | MODIFIER | c.*2679C>T| |
S36 |