Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00320 | A07 | 159543 | G | A | missense_variant&splice_region_variant | MODERATE | c.149C>T|p.Ser50Phe |
S71 |
2 | BAA07g00320 | A07 | 163642 | C | T | intron_variant | MODIFIER | c.81+2533G>A| |
S124 |
3 | BAA07g00320 | A07 | 164444 | C | T | intron_variant | MODIFIER | c.81+1731G>A| |
S79 S91 |
4 | BAA07g00320 | A07 | 164512 | C | T | intron_variant | MODIFIER | c.81+1663G>A| |
S103 |
5 | BAA07g00320 | A07 | 166625 | C | T | upstream_gene_variant | MODIFIER | c.-370G>A| |
S32 |
6 | BAA07g00320 | A07 | 167270 | G | A | upstream_gene_variant | MODIFIER | c.-1015C>T| |
S262 |
7 | BAA07g00320 | A07 | 167373 | G | A | upstream_gene_variant | MODIFIER | c.-1118C>T| |
S112 |
8 | BAA07g00320 | A07 | 167791 | C | T | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S79 S91 |
9 | BAA07g00320 | A07 | 167942 | C | T | upstream_gene_variant | MODIFIER | c.-1687G>A| |
S212 |