Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21330 | A02 | 11433424 | G | A | upstream_gene_variant | MODIFIER | c.-4199G>A| |
S48 |
2 | BAA02g21330 | A02 | 11433888 | C | T | upstream_gene_variant | MODIFIER | c.-3735C>T| |
S1 S90 |
3 | BAA02g21330 | A02 | 11434217 | C | T | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S15 S156 S3 S34 |
4 | BAA02g21330 | A02 | 11436915 | C | T | upstream_gene_variant | MODIFIER | c.-708C>T| |
S170 |
5 | BAA02g21330 | A02 | 11436921 | C | T | upstream_gene_variant | MODIFIER | c.-702C>T| |
S293 |
6 | BAA02g21330 | A02 | 11437010 | C | T | upstream_gene_variant | MODIFIER | c.-613C>T| |
S234 |
7 | BAA02g21330 | A02 | 11437669 | C | T | missense_variant | MODERATE | c.47C>T|p.Ser16Phe |
S38 |
8 | BAA02g21330 | A02 | 11438820 | G | A | missense_variant | MODERATE | c.1040G>A|p.Gly347Glu |
S10 |
9 | BAA02g21330 | A02 | 11439281 | G | A | missense_variant | MODERATE | c.1333G>A|p.Asp445Asn |
S293 |
10 | BAA02g21330 | A02 | 11439393 | G | A | missense_variant&splice_region_variant | MODERATE | c.1375G>A|p.Val459Ile |
S23 |