Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05380 | A08 | 4006517 | G | A | upstream_gene_variant | MODIFIER | c.-4709G>A| |
S192 |
2 | BAA08g05380 | A08 | 4006852 | C | T | upstream_gene_variant | MODIFIER | c.-4374C>T| |
S80 |
3 | BAA08g05380 | A08 | 4007330 | G | A | upstream_gene_variant | MODIFIER | c.-3896G>A| |
S298 |
4 | BAA08g05380 | A08 | 4008247 | C | T | upstream_gene_variant | MODIFIER | c.-2979C>T| |
S149 |
5 | BAA08g05380 | A08 | 4009137 | C | T | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S157 S163 |
6 | BAA08g05380 | A08 | 4009292 | G | A | upstream_gene_variant | MODIFIER | c.-1934G>A| |
S109 |
7 | BAA08g05380 | A08 | 4009319 | G | A | upstream_gene_variant | MODIFIER | c.-1907G>A| |
S181 |
8 | BAA08g05380 | A08 | 4011335 | C | T | missense_variant | MODERATE | c.110C>T|p.Ser37Phe |
S155 S211 |
9 | BAA08g05380 | A08 | 4011354 | C | T | synonymous_variant | LOW | c.129C>T|p.Asp43Asp |
S55 |
10 | BAA08g05380 | A08 | 4012926 | C | T | missense_variant | MODERATE | c.1070C>T|p.Ser357Phe |
S161 |