Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08760 | A10 | 10742715 | G | A | upstream_gene_variant | MODIFIER | c.-2962G>A| |
S296 |
2 | BAA10g08760 | A10 | 10743154 | G | A | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S45 |
3 | BAA10g08760 | A10 | 10744431 | C | T | upstream_gene_variant | MODIFIER | c.-1246C>T| |
S269 |
4 | BAA10g08760 | A10 | 10744560 | G | A | upstream_gene_variant | MODIFIER | c.-1117G>A| |
S120 |
5 | BAA10g08760 | A10 | 10744967 | C | T | upstream_gene_variant | MODIFIER | c.-710C>T| |
S199 |
6 | BAA10g08760 | A10 | 10745343 | C | T | upstream_gene_variant | MODIFIER | c.-334C>T| |
S282 |
7 | BAA10g08760 | A10 | 10745498 | G | A | upstream_gene_variant | MODIFIER | c.-179G>A| |
S234 |
8 | BAA10g08760 | A10 | 10745559 | C | T | upstream_gene_variant | MODIFIER | c.-118C>T| |
S270 |
9 | BAA10g08760 | A10 | 10745617 | G | A | upstream_gene_variant | MODIFIER | c.-60G>A| |
S55 |
10 | BAA10g08760 | A10 | 10745651 | C | T | upstream_gene_variant | MODIFIER | c.-26C>T| |
S247 |
11 | BAA10g08760 | A10 | 10745888 | C | T | missense_variant | MODERATE | c.212C>T|p.Ser71Phe |
S133 |
12 | BAA10g08760 | A10 | 10746508 | G | A | downstream_gene_variant | MODIFIER | c.*607G>A| |
S159 S187 S188 S243 S276 |
13 | BAA10g08760 | A10 | 10746725 | C | T | downstream_gene_variant | MODIFIER | c.*824C>T| |
S44 |
14 | BAA10g08760 | A10 | 10747281 | C | T | downstream_gene_variant | MODIFIER | c.*1380C>T| |
S132 S137 S215 S89 |
15 | BAA10g08760 | A10 | 10747315 | C | T | downstream_gene_variant | MODIFIER | c.*1414C>T| |
S17 |
16 | BAA10g08760 | A10 | 10748269 | C | T | downstream_gene_variant | MODIFIER | c.*2368C>T| |
S208 S93 |
17 | BAA10g08760 | A10 | 10749147 | G | A | downstream_gene_variant | MODIFIER | c.*3246G>A| |
S13 |
18 | BAA10g08760 | A10 | 10749510 | C | T | downstream_gene_variant | MODIFIER | c.*3609C>T| |
S70 |
19 | BAA10g08760 | A10 | 10750152 | C | T | downstream_gene_variant | MODIFIER | c.*4251C>T| |
S132 S137 S89 |