Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20200 | A10 | 18265765 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S3 |
2 | BAA10g20200 | A10 | 18265996 | C | T | upstream_gene_variant | MODIFIER | c.-149G>A| |
S301 S304 |
3 | BAA10g20200 | A10 | 18267525 | C | T | upstream_gene_variant | MODIFIER | c.-1678G>A| |
S244 |
4 | BAA10g20200 | A10 | 18267962 | G | A | upstream_gene_variant | MODIFIER | c.-2115C>T| |
S112 |
5 | BAA10g20200 | A10 | 18267975 | C | T | upstream_gene_variant | MODIFIER | c.-2128G>A| |
S283 |
6 | BAA10g20200 | A10 | 18268175 | C | T | upstream_gene_variant | MODIFIER | c.-2328G>A| |
S26 |
7 | BAA10g20200 | A10 | 18268213 | C | T | upstream_gene_variant | MODIFIER | c.-2366G>A| |
S302 |
8 | BAA10g20200 | A10 | 18268256 | C | T | upstream_gene_variant | MODIFIER | c.-2409G>A| |
S34 |
9 | BAA10g20200 | A10 | 18269036 | C | T | upstream_gene_variant | MODIFIER | c.-3189G>A| |
S140 |
10 | BAA10g20200 | A10 | 18269800 | G | A | upstream_gene_variant | MODIFIER | c.-3953C>T| |
S150 |
11 | BAA10g20200 | A10 | 18270089 | G | A | upstream_gene_variant | MODIFIER | c.-4242C>T| |
S134 |