Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15690 | A05 | 8392790 | G | A | downstream_gene_variant | MODIFIER | c.*1504C>T| |
S134 |
2 | BAA05g15690 | A05 | 8394353 | C | T | missense_variant | MODERATE | c.1399G>A|p.Ala467Thr |
S276 |
3 | BAA05g15690 | A05 | 8394721 | C | T | missense_variant | MODERATE | c.1175G>A|p.Arg392Lys |
S100 |
4 | BAA05g15690 | A05 | 8394951 | C | T | synonymous_variant | LOW | c.1044G>A|p.Leu348Leu |
S112 |
5 | BAA05g15690 | A05 | 8395027 | C | T | missense_variant | MODERATE | c.968G>A|p.Gly323Glu |
S136 |
6 | BAA05g15690 | A05 | 8395052 | C | T | missense_variant&splice_region_variant | MODERATE | c.943G>A|p.Asp315Asn |
S57 |
7 | BAA05g15690 | A05 | 8399029 | G | A | upstream_gene_variant | MODIFIER | c.-232C>T| |
S23 |
8 | BAA05g15690 | A05 | 8399045 | C | G | upstream_gene_variant | MODIFIER | c.-248G>C| |
S288 |
9 | BAA05g15690 | A05 | 8400025 | G | A | upstream_gene_variant | MODIFIER | c.-1228C>T| |
S129 |
10 | BAA05g15690 | A05 | 8400228 | G | A | upstream_gene_variant | MODIFIER | c.-1431C>T| |
S86 |
11 | BAA05g15690 | A05 | 8401639 | C | T | upstream_gene_variant | MODIFIER | c.-2842G>A| |
S100 |
12 | BAA05g15690 | A05 | 8401880 | G | A | upstream_gene_variant | MODIFIER | c.-3083C>T| |
S297 |
13 | BAA05g15690 | A05 | 8402080 | G | A | upstream_gene_variant | MODIFIER | c.-3283C>T| |
|