Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00890 | A10 | 412211 | C | T | upstream_gene_variant | MODIFIER | c.-3783C>T| |
S132 S137 S89 |
2 | BAA10g00890 | A10 | 412859 | C | T | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S270 |
3 | BAA10g00890 | A10 | 413054 | G | A | upstream_gene_variant | MODIFIER | c.-2940G>A| |
S136 |
4 | BAA10g00890 | A10 | 415009 | G | A | upstream_gene_variant | MODIFIER | c.-985G>A| |
S242 |
5 | BAA10g00890 | A10 | 415837 | C | T | upstream_gene_variant | MODIFIER | c.-157C>T| |
S52 |
6 | BAA10g00890 | A10 | 416324 | G | A | splice_region_variant&intron_variant | LOW | c.152-4G>A| |
S1 S293 |
7 | BAA10g00890 | A10 | 417466 | C | T | missense_variant | MODERATE | c.580C>T|p.Pro194Ser |
S8 |
8 | BAA10g00890 | A10 | 421000 | C | T | downstream_gene_variant | MODIFIER | c.*2214C>T| |
S225 S73 |
9 | BAA10g00890 | A10 | 421052 | G | A | downstream_gene_variant | MODIFIER | c.*2266G>A| |
S148 S30 |
10 | BAA10g00890 | A10 | 421335 | C | T | downstream_gene_variant | MODIFIER | c.*2549C>T| |
S287 |
11 | BAA10g00890 | A10 | 421397 | G | A | downstream_gene_variant | MODIFIER | c.*2611G>A| |
S46 |