Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09660 | A01 | 4310857 | C | T | splice_region_variant&synonymous_variant | LOW | c.3312G>A|p.Glu1104Glu |
S135 |
2 | BAA01g09660 | A01 | 4312495 | G | A | synonymous_variant | LOW | c.2533C>T|p.Leu845Leu |
S146 |
3 | BAA01g09660 | A01 | 4313200 | G | A | splice_region_variant&intron_variant | LOW | c.2130+4C>T| |
S287 |
4 | BAA01g09660 | A01 | 4313265 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2070-1G>A| |
S286 |
5 | BAA01g09660 | A01 | 4313558 | C | T | missense_variant | MODERATE | c.1936G>A|p.Val646Ile |
S153 S213 |
6 | BAA01g09660 | A01 | 4314164 | G | A | intron_variant | MODIFIER | c.1530-17C>T| |
S201 |
7 | BAA01g09660 | A01 | 4314601 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1332-1G>A| |
S100 |
8 | BAA01g09660 | A01 | 4315458 | C | T | missense_variant | MODERATE | c.1036G>A|p.Asp346Asn |
S71 |
9 | BAA01g09660 | A01 | 4318185 | G | A | upstream_gene_variant | MODIFIER | c.-419C>T| |
S289 S290 |
10 | BAA01g09660 | A01 | 4318698 | C | T | upstream_gene_variant | MODIFIER | c.-932G>A| |
S168 |
11 | BAA01g09660 | A01 | 4318894 | C | T | upstream_gene_variant | MODIFIER | c.-1128G>A| |
S140 |
12 | BAA01g09660 | A01 | 4319465 | G | A | upstream_gene_variant | MODIFIER | c.-1699C>T| |
S178 |