Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09550 | A10 | 11498940 | C | T | downstream_gene_variant | MODIFIER | c.*43G>A| |
S247 |
2 | BAA10g09550 | A10 | 11499146 | G | A | missense_variant | MODERATE | c.950C>T|p.Ala317Val |
S295 |
3 | BAA10g09550 | A10 | 11500160 | C | T | intron_variant | MODIFIER | c.395-270G>A| |
S121 |
4 | BAA10g09550 | A10 | 11500371 | T | A | intron_variant | MODIFIER | c.395-481A>T| |
S225 S73 |
5 | BAA10g09550 | A10 | 11500786 | G | A | intron_variant | MODIFIER | c.394+270C>T| |
S163 |
6 | BAA10g09550 | A10 | 11501001 | G | A | intron_variant | MODIFIER | c.394+55C>T| |
S221 |
7 | BAA10g09550 | A10 | 11501123 | C | T | synonymous_variant | LOW | c.327G>A|p.Arg109Arg |
S166 |
8 | BAA10g09550 | A10 | 11501798 | C | T | upstream_gene_variant | MODIFIER | c.-67G>A| |
S60 |
9 | BAA10g09550 | A10 | 11502200 | C | T | upstream_gene_variant | MODIFIER | c.-469G>A| |
S143 |
10 | BAA10g09550 | A10 | 11502550 | G | A | upstream_gene_variant | MODIFIER | c.-819C>T| |
S18 |
11 | BAA10g09550 | A10 | 11502842 | C | T | upstream_gene_variant | MODIFIER | c.-1111G>A| |
S166 |
12 | BAA10g09550 | A10 | 11504736 | C | T | upstream_gene_variant | MODIFIER | c.-3005G>A| |
S166 |
13 | BAA10g09550 | A10 | 11505889 | C | T | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S180 |
14 | BAA10g09550 | A10 | 11506174 | C | T | upstream_gene_variant | MODIFIER | c.-4443G>A| |
S185 |