Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19970 | A01 | 9824219 | G | A | upstream_gene_variant | MODIFIER | c.-3106G>A| |
S276 |
2 | BAA01g19970 | A01 | 9825250 | C | T | upstream_gene_variant | MODIFIER | c.-2075C>T| |
S40 S49 |
3 | BAA01g19970 | A01 | 9826029 | G | A | upstream_gene_variant | MODIFIER | c.-1296G>A| |
S131 |
4 | BAA01g19970 | A01 | 9826928 | G | A | upstream_gene_variant | MODIFIER | c.-397G>A| |
S110 |
5 | BAA01g19970 | A01 | 9827821 | G | A | synonymous_variant | LOW | c.363G>A|p.Lys121Lys |
S119 |
6 | BAA01g19970 | A01 | 9828671 | C | T | synonymous_variant | LOW | c.1002C>T|p.Asn334Asn |
S207 |
7 | BAA01g19970 | A01 | 9828705 | C | T | missense_variant | MODERATE | c.1036C>T|p.Pro346Ser |
S261 |
8 | BAA01g19970 | A01 | 9829502 | C | T | synonymous_variant | LOW | c.1666C>T|p.Leu556Leu |
S155 S211 |
9 | BAA01g19970 | A01 | 9829616 | C | T | missense_variant | MODERATE | c.1780C>T|p.Pro594Ser |
S231 |
10 | BAA01g19970 | A01 | 9829626 | G | A | splice_region_variant&stop_retained_variant | LOW | c.1790G>A|p.Ter597Ter |
S204 |