Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09230 | A10 | 11248423 | G | A | upstream_gene_variant | MODIFIER | c.-4993G>A| |
S274 |
2 | BAA10g09230 | A10 | 11248497 | C | T | upstream_gene_variant | MODIFIER | c.-4919C>T| |
S165 S44 |
3 | BAA10g09230 | A10 | 11248643 | G | A | upstream_gene_variant | MODIFIER | c.-4773G>A| |
S112 |
4 | BAA10g09230 | A10 | 11249450 | C | T | upstream_gene_variant | MODIFIER | c.-3966C>T| |
S5 |
5 | BAA10g09230 | A10 | 11249857 | C | T | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S113 |
6 | BAA10g09230 | A10 | 11250722 | G | A | upstream_gene_variant | MODIFIER | c.-2694G>A| |
S295 |
7 | BAA10g09230 | A10 | 11251137 | C | T | upstream_gene_variant | MODIFIER | c.-2279C>T| |
S281 |
8 | BAA10g09230 | A10 | 11251478 | C | T | upstream_gene_variant | MODIFIER | c.-1938C>T| |
S249 |
9 | BAA10g09230 | A10 | 11251949 | C | T | upstream_gene_variant | MODIFIER | c.-1467C>T| |
S274 S303 |
10 | BAA10g09230 | A10 | 11253486 | C | T | missense_variant | MODERATE | c.71C>T|p.Ser24Phe |
S123 |
11 | BAA10g09230 | A10 | 11253686 | C | T | splice_region_variant&intron_variant | LOW | c.181+8C>T| |
S6 |
12 | BAA10g09230 | A10 | 11254064 | G | A | missense_variant | MODERATE | c.395G>A|p.Cys132Tyr |
S226 |