Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14260 | A08 | 12179834 | G | A | upstream_gene_variant | MODIFIER | c.-3926G>A| |
S257 |
2 | BAA08g14260 | A08 | 12180898 | C | G | upstream_gene_variant | MODIFIER | c.-2862C>G| |
S135 S152 S185 S203 S273 S68 |
3 | BAA08g14260 | A08 | 12181173 | G | A | upstream_gene_variant | MODIFIER | c.-2587G>A| |
S109 |
4 | BAA08g14260 | A08 | 12181467 | C | T | upstream_gene_variant | MODIFIER | c.-2293C>T| |
S293 |
5 | BAA08g14260 | A08 | 12183082 | G | A | upstream_gene_variant | MODIFIER | c.-678G>A| |
S221 |
6 | BAA08g14260 | A08 | 12183158 | C | T | upstream_gene_variant | MODIFIER | c.-602C>T| |
S226 |
7 | BAA08g14260 | A08 | 12183261 | G | A | upstream_gene_variant | MODIFIER | c.-499G>A| |
S265 |
8 | BAA08g14260 | A08 | 12183794 | G | A | missense_variant | MODERATE | c.35G>A|p.Cys12Tyr |
S30 |
9 | BAA08g14260 | A08 | 12185309 | G | A | missense_variant | MODERATE | c.802G>A|p.Val268Ile |
S116 |
10 | BAA08g14260 | A08 | 12185703 | C | T | missense_variant | MODERATE | c.1196C>T|p.Thr399Met |
S240 |
11 | BAA08g14260 | A08 | 12186606 | G | A | downstream_gene_variant | MODIFIER | c.*758G>A| |
S5 |
12 | BAA08g14260 | A08 | 12188969 | C | T | downstream_gene_variant | MODIFIER | c.*3121C>T| |
S126 |
13 | BAA08g14260 | A08 | 12189420 | C | T | downstream_gene_variant | MODIFIER | c.*3572C>T| |
S99 |
14 | BAA08g14260 | A08 | 12190227 | G | A | downstream_gene_variant | MODIFIER | c.*4379G>A| |
S116 |
15 | BAA08g14260 | A08 | 12190338 | C | A | downstream_gene_variant | MODIFIER | c.*4490C>A| |
S15 S3 |
16 | BAA08g14260 | A08 | 12190354 | C | T | downstream_gene_variant | MODIFIER | c.*4506C>T| |
S23 |
17 | BAA08g14260 | A08 | 12190612 | C | T | downstream_gene_variant | MODIFIER | c.*4764C>T| |
S162 |
18 | BAA08g14260 | A08 | 12190782 | G | A | downstream_gene_variant | MODIFIER | c.*4934G>A| |
S37 |