Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06900 | A07 | 16223593 | G | A | upstream_gene_variant | MODIFIER | c.-2286G>A| |
S62 |
2 | BAA07g06900 | A07 | 16223793 | G | A | upstream_gene_variant | MODIFIER | c.-2086G>A| |
S112 |
3 | BAA07g06900 | A07 | 16224160 | C | T | upstream_gene_variant | MODIFIER | c.-1719C>T| |
S224 |
4 | BAA07g06900 | A07 | 16225038 | C | T | upstream_gene_variant | MODIFIER | c.-841C>T| |
S242 |
5 | BAA07g06900 | A07 | 16225156 | C | T | upstream_gene_variant | MODIFIER | c.-723C>T| |
S86 |
6 | BAA07g06900 | A07 | 16225255 | C | T | upstream_gene_variant | MODIFIER | c.-624C>T| |
S20 |
7 | BAA07g06900 | A07 | 16225682 | G | A | upstream_gene_variant | MODIFIER | c.-197G>A| |
S57 |
8 | BAA07g06900 | A07 | 16225859 | C | T | upstream_gene_variant | MODIFIER | c.-20C>T| |
S142 |
9 | BAA07g06900 | A07 | 16226139 | G | A | missense_variant | MODERATE | c.184G>A|p.Asp62Asn |
S139 |
10 | BAA07g06900 | A07 | 16226341 | C | T | synonymous_variant | LOW | c.297C>T|p.Asn99Asn |
S136 |
11 | BAA07g06900 | A07 | 16226361 | G | A | missense_variant&splice_region_variant | MODERATE | c.317G>A|p.Gly106Glu |
S40 S49 |
12 | BAA07g06900 | A07 | 16227996 | G | A | downstream_gene_variant | MODIFIER | c.*1009G>A| |
S291 |