Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20320 | A05 | 12456718 | G | A | downstream_gene_variant | MODIFIER | c.*3695C>T| |
S297 |
2 | BAA05g20320 | A05 | 12456953 | C | T | downstream_gene_variant | MODIFIER | c.*3460G>A| |
S237 |
3 | BAA05g20320 | A05 | 12457221 | G | A | downstream_gene_variant | MODIFIER | c.*3192C>T| |
S298 |
4 | BAA05g20320 | A05 | 12458233 | C | T | downstream_gene_variant | MODIFIER | c.*2180G>A| |
S146 |
5 | BAA05g20320 | A05 | 12459348 | G | A | downstream_gene_variant | MODIFIER | c.*1065C>T| |
S282 |
6 | BAA05g20320 | A05 | 12459617 | C | T | downstream_gene_variant | MODIFIER | c.*796G>A| |
S278 |
7 | BAA05g20320 | A05 | 12459627 | C | T | downstream_gene_variant | MODIFIER | c.*786G>A| |
S189 |
8 | BAA05g20320 | A05 | 12459634 | C | T | downstream_gene_variant | MODIFIER | c.*779G>A| |
S47 |
9 | BAA05g20320 | A05 | 12459689 | C | T | downstream_gene_variant | MODIFIER | c.*724G>A| |
S292 |
10 | BAA05g20320 | A05 | 12459880 | C | T | downstream_gene_variant | MODIFIER | c.*533G>A| |
S87 |
11 | BAA05g20320 | A05 | 12460175 | C | T | downstream_gene_variant | MODIFIER | c.*238G>A| |
S105 S106 |
12 | BAA05g20320 | A05 | 12460770 | C | T | missense_variant | MODERATE | c.1895G>A|p.Arg632Lys |
S57 |
13 | BAA05g20320 | A05 | 12460804 | C | T | missense_variant | MODERATE | c.1861G>A|p.Val621Ile |
S233 |
14 | BAA05g20320 | A05 | 12460922 | G | A | stop_gained | HIGH | c.1825C>T|p.Gln609* |
S278 |
15 | BAA05g20320 | A05 | 12461009 | G | A | stop_gained | HIGH | c.1738C>T|p.Gln580* |
S225 S73 |
16 | BAA05g20320 | A05 | 12463046 | C | T | splice_region_variant&synonymous_variant | LOW | c.795G>A|p.Ser265Ser |
S142 |
17 | BAA05g20320 | A05 | 12463345 | C | T | missense_variant | MODERATE | c.574G>A|p.Glu192Lys |
S271 |
18 | BAA05g20320 | A05 | 12464228 | G | A | missense_variant | MODERATE | c.226C>T|p.Pro76Ser |
S12 |
19 | BAA05g20320 | A05 | 12464394 | C | T | synonymous_variant | LOW | c.183G>A|p.Glu61Glu |
S229 |
20 | BAA05g20320 | A05 | 12464984 | G | A | missense_variant | MODERATE | c.11C>T|p.Ala4Val |
S48 |
21 | BAA05g20320 | A05 | 12468863 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S252 |