Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14270 | A09 | 8190173 | G | A | upstream_gene_variant | MODIFIER | c.-1362G>A| |
S78 |
2 | BAA09g14270 | A09 | 8190783 | C | T | upstream_gene_variant | MODIFIER | c.-752C>T| |
S296 |
3 | BAA09g14270 | A09 | 8191884 | G | A | missense_variant | MODERATE | c.191G>A|p.Gly64Glu |
S13 |
4 | BAA09g14270 | A09 | 8192355 | C | T | splice_region_variant&intron_variant | LOW | c.426+7C>T| |
S168 |
5 | BAA09g14270 | A09 | 8192709 | G | A | missense_variant | MODERATE | c.563G>A|p.Gly188Asp |
S11 |
6 | BAA09g14270 | A09 | 8193112 | G | A | missense_variant | MODERATE | c.733G>A|p.Glu245Lys |
S240 |
7 | BAA09g14270 | A09 | 8193314 | C | T | splice_region_variant&synonymous_variant | LOW | c.825C>T|p.Gly275Gly |
S94 |
8 | BAA09g14270 | A09 | 8194581 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1354-1G>A| |
S274 |