Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09340 | A10 | 11327717 | C | T | downstream_gene_variant | MODIFIER | c.*204G>A| |
S294 |
2 | BAA10g09340 | A10 | 11328859 | G | A | intron_variant | MODIFIER | c.621+32C>T| |
S263 |
3 | BAA10g09340 | A10 | 11328958 | G | A | missense_variant | MODERATE | c.554C>T|p.Ala185Val |
S202 |
4 | BAA10g09340 | A10 | 11329261 | G | A | intron_variant | MODIFIER | c.351-100C>T| |
S295 |
5 | BAA10g09340 | A10 | 11329510 | C | T | intron_variant | MODIFIER | c.351-349G>A| |
S185 |
6 | BAA10g09340 | A10 | 11329635 | G | A | intron_variant | MODIFIER | c.351-474C>T| |
S172 S217 |
7 | BAA10g09340 | A10 | 11329966 | G | A | intron_variant | MODIFIER | c.350+151C>T| |
S73 |
8 | BAA10g09340 | A10 | 11330196 | G | A | missense_variant | MODERATE | c.271C>T|p.Pro91Ser |
S48 |
9 | BAA10g09340 | A10 | 11331529 | G | A | upstream_gene_variant | MODIFIER | c.-972C>T| |
S95 |
10 | BAA10g09340 | A10 | 11331845 | C | T | upstream_gene_variant | MODIFIER | c.-1288G>A| |
S297 |
11 | BAA10g09340 | A10 | 11331900 | C | T | upstream_gene_variant | MODIFIER | c.-1343G>A| |
S199 |
12 | BAA10g09340 | A10 | 11332475 | C | T | upstream_gene_variant | MODIFIER | c.-1918G>A| |
S206 S26 |