Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05660 | A08 | 4346960 | G | A | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S240 |
2 | BAA08g05660 | A08 | 4347027 | C | T | upstream_gene_variant | MODIFIER | c.-3235C>T| |
S47 |
3 | BAA08g05660 | A08 | 4347458 | C | T | upstream_gene_variant | MODIFIER | c.-2804C>T| |
S28 |
4 | BAA08g05660 | A08 | 4348412 | C | T | upstream_gene_variant | MODIFIER | c.-1850C>T| |
S59 |
5 | BAA08g05660 | A08 | 4348545 | C | T | upstream_gene_variant | MODIFIER | c.-1717C>T| |
S192 |
6 | BAA08g05660 | A08 | 4348638 | G | A | upstream_gene_variant | MODIFIER | c.-1624G>A| |
S87 |
7 | BAA08g05660 | A08 | 4349418 | C | T | upstream_gene_variant | MODIFIER | c.-844C>T| |
S83 S88 |
8 | BAA08g05660 | A08 | 4349471 | C | T | upstream_gene_variant | MODIFIER | c.-791C>T| |
S157 S163 |
9 | BAA08g05660 | A08 | 4349906 | C | T | upstream_gene_variant | MODIFIER | c.-356C>T| |
S134 |
10 | BAA08g05660 | A08 | 4349973 | G | A | upstream_gene_variant | MODIFIER | c.-289G>A| |
S23 |
11 | BAA08g05660 | A08 | 4350521 | C | T | synonymous_variant | LOW | c.168C>T|p.Phe56Phe |
S186 |
12 | BAA08g05660 | A08 | 4350633 | G | A | missense_variant | MODERATE | c.280G>A|p.Asp94Asn |
S87 |
13 | BAA08g05660 | A08 | 4350645 | G | A | missense_variant | MODERATE | c.292G>A|p.Gly98Arg |
S291 |
14 | BAA08g05660 | A08 | 4352846 | G | A | downstream_gene_variant | MODIFIER | c.*2136G>A| |
S125 |
15 | BAA08g05660 | A08 | 4353751 | C | T | downstream_gene_variant | MODIFIER | c.*3041C>T| |
S183 S198 |
16 | BAA08g05660 | A08 | 4354082 | G | A | downstream_gene_variant | MODIFIER | c.*3372G>A| |
S40 S49 |
17 | BAA08g05660 | A08 | 4354285 | G | A | downstream_gene_variant | MODIFIER | c.*3575G>A| |
S148 |