Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09770 | A05 | 4967662 | G | A | downstream_gene_variant | MODIFIER | c.*2568C>T| |
S37 |
2 | BAA05g09770 | A05 | 4968245 | G | A | downstream_gene_variant | MODIFIER | c.*1985C>T| |
S284 |
3 | BAA05g09770 | A05 | 4968266 | C | T | downstream_gene_variant | MODIFIER | c.*1964G>A| |
S270 |
4 | BAA05g09770 | A05 | 4968555 | C | T | downstream_gene_variant | MODIFIER | c.*1675G>A| |
S308 |
5 | BAA05g09770 | A05 | 4968627 | C | T | downstream_gene_variant | MODIFIER | c.*1603G>A| |
S35 |
6 | BAA05g09770 | A05 | 4968932 | C | T | downstream_gene_variant | MODIFIER | c.*1298G>A| |
S115 |
7 | BAA05g09770 | A05 | 4969090 | C | T | downstream_gene_variant | MODIFIER | c.*1140G>A| |
S50 |
8 | BAA05g09770 | A05 | 4969213 | C | T | downstream_gene_variant | MODIFIER | c.*1017G>A| |
S81 S85 |
9 | BAA05g09770 | A05 | 4969317 | C | T | downstream_gene_variant | MODIFIER | c.*913G>A| |
S98 |
10 | BAA05g09770 | A05 | 4969373 | C | T | downstream_gene_variant | MODIFIER | c.*857G>A| |
S130 |
11 | BAA05g09770 | A05 | 4969668 | C | T | downstream_gene_variant | MODIFIER | c.*562G>A| |
S207 |
12 | BAA05g09770 | A05 | 4970526 | C | T | missense_variant | MODERATE | c.799G>A|p.Asp267Asn |
S189 |
13 | BAA05g09770 | A05 | 4970911 | C | T | missense_variant | MODERATE | c.646G>A|p.Glu216Lys |
S65 |
14 | BAA05g09770 | A05 | 4973654 | G | A | upstream_gene_variant | MODIFIER | c.-1659C>T| |
S90 |
15 | BAA05g09770 | A05 | 4974359 | G | A | upstream_gene_variant | MODIFIER | c.-2364C>T| |
S200 |
16 | BAA05g09770 | A05 | 4974805 | C | T | upstream_gene_variant | MODIFIER | c.-2810G>A| |
S20 |
17 | BAA05g09770 | A05 | 4976768 | G | A | upstream_gene_variant | MODIFIER | c.-4773C>T| |
S125 |