Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21890 | A01 | 10895351 | C | T | synonymous_variant | LOW | c.513G>A|p.Glu171Glu |
S201 |
2 | BAA01g21890 | A01 | 10895568 | C | T | missense_variant&splice_region_variant | MODERATE | c.374G>A|p.Arg125Lys |
S184 |
3 | BAA01g21890 | A01 | 10895701 | G | A | missense_variant | MODERATE | c.322C>T|p.His108Tyr |
S107 |
4 | BAA01g21890 | A01 | 10895912 | G | A | synonymous_variant | LOW | c.111C>T|p.Asn37Asn |
S172 S217 |
5 | BAA01g21890 | A01 | 10895918 | C | T | synonymous_variant | LOW | c.105G>A|p.Lys35Lys |
S210 |
6 | BAA01g21890 | A01 | 10895950 | G | A | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S195 |
7 | BAA01g21890 | A01 | 10896231 | G | A | upstream_gene_variant | MODIFIER | c.-123C>T| |
S132 S137 |
8 | BAA01g21890 | A01 | 10897326 | G | A | upstream_gene_variant | MODIFIER | c.-1218C>T| |
S79 S91 |
9 | BAA01g21890 | A01 | 10897475 | G | A | upstream_gene_variant | MODIFIER | c.-1367C>T| |
S301 S304 |
10 | BAA01g21890 | A01 | 10897689 | C | T | upstream_gene_variant | MODIFIER | c.-1581G>A| |
S41 |
11 | BAA01g21890 | A01 | 10898364 | G | A | upstream_gene_variant | MODIFIER | c.-2256C>T| |
S302 |
12 | BAA01g21890 | A01 | 10898900 | C | T | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S205 |
13 | BAA01g21890 | A01 | 10898912 | G | A | upstream_gene_variant | MODIFIER | c.-2804C>T| |
S149 S157 |
14 | BAA01g21890 | A01 | 10899698 | G | A | upstream_gene_variant | MODIFIER | c.-3590C>T| |
S144 |
15 | BAA01g21890 | A01 | 10899907 | G | A | upstream_gene_variant | MODIFIER | c.-3799C>T| |
S58 |
16 | BAA01g21890 | A01 | 10900810 | G | A | upstream_gene_variant | MODIFIER | c.-4702C>T| |
S58 |
17 | BAA01g21890 | A01 | 10901095 | G | A | upstream_gene_variant | MODIFIER | c.-4987C>T| |
S298 |