Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21090 | A01 | 10399647 | C | T | missense_variant | MODERATE | c.857G>A|p.Gly286Glu |
S20 S89 |
2 | BAA01g21090 | A01 | 10400324 | T | A | missense_variant | MODERATE | c.470A>T|p.Asn157Ile |
S38 |
3 | BAA01g21090 | A01 | 10400373 | C | T | missense_variant | MODERATE | c.421G>A|p.Gly141Arg |
S242 |
4 | BAA01g21090 | A01 | 10400380 | G | A | synonymous_variant | LOW | c.414C>T|p.Ala138Ala |
S302 |
5 | BAA01g21090 | A01 | 10400627 | G | A | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S2 |
6 | BAA01g21090 | A01 | 10402157 | C | T | upstream_gene_variant | MODIFIER | c.-1289G>A| |
S150 S201 |
7 | BAA01g21090 | A01 | 10402495 | G | A | upstream_gene_variant | MODIFIER | c.-1627C>T| |
S224 |
8 | BAA01g21090 | A01 | 10402649 | C | T | upstream_gene_variant | MODIFIER | c.-1781G>A| |
S134 |
9 | BAA01g21090 | A01 | 10403445 | C | T | upstream_gene_variant | MODIFIER | c.-2577G>A| |
S139 |
10 | BAA01g21090 | A01 | 10404132 | T | C | upstream_gene_variant | MODIFIER | c.-3264A>G| |
S37 |
11 | BAA01g21090 | A01 | 10404746 | C | T | upstream_gene_variant | MODIFIER | c.-3878G>A| |
S19 |
12 | BAA01g21090 | A01 | 10405562 | C | T | upstream_gene_variant | MODIFIER | c.-4694G>A| |
S65 |
13 | BAA01g21090 | A01 | 10405581 | G | A | upstream_gene_variant | MODIFIER | c.-4713C>T| |
S280 |