Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39370 | A09 | 47004651 | G | A | missense_variant | MODERATE | c.487C>T|p.Pro163Ser |
S88 |
2 | BAA09g39370 | A09 | 47004678 | C | T | missense_variant | MODERATE | c.460G>A|p.Asp154Asn |
S113 |
3 | BAA09g39370 | A09 | 47004732 | C | T | missense_variant&splice_region_variant | MODERATE | c.406G>A|p.Glu136Lys |
S155 S211 |
4 | BAA09g39370 | A09 | 47005193 | C | T | missense_variant | MODERATE | c.115G>A|p.Asp39Asn |
S211 S227 |
5 | BAA09g39370 | A09 | 47006771 | G | A | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S231 |
6 | BAA09g39370 | A09 | 47007389 | C | T | upstream_gene_variant | MODIFIER | c.-2005G>A| |
S277 |
7 | BAA09g39370 | A09 | 47007420 | C | T | upstream_gene_variant | MODIFIER | c.-2036G>A| |
S66 |
8 | BAA09g39370 | A09 | 47009008 | G | A | upstream_gene_variant | MODIFIER | c.-3624C>T| |
S134 |
9 | BAA09g39370 | A09 | 47009129 | G | A | upstream_gene_variant | MODIFIER | c.-3745C>T| |
S268 |