Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53980 | A09 | 54903387 | G | A | missense_variant | MODERATE | c.956C>T|p.Ser319Phe |
S39 |
2 | BAA09g53980 | A09 | 54903411 | T | G | missense_variant | MODERATE | c.932A>C|p.Asn311Thr |
S103 S215 S286 S33 |
3 | BAA09g53980 | A09 | 54903444 | G | A | missense_variant | MODERATE | c.899C>T|p.Ala300Val |
S265 |
4 | BAA09g53980 | A09 | 54904032 | G | A | missense_variant | MODERATE | c.311C>T|p.Ser104Phe |
S151 S263 |
5 | BAA09g53980 | A09 | 54904076 | C | T | synonymous_variant | LOW | c.267G>A|p.Arg89Arg |
S122 |
6 | BAA09g53980 | A09 | 54904499 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S231 |
7 | BAA09g53980 | A09 | 54904656 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S251 |
8 | BAA09g53980 | A09 | 54904660 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| |
S259 |
9 | BAA09g53980 | A09 | 54906184 | C | T | upstream_gene_variant | MODIFIER | c.-1842G>A| |
S262 |
10 | BAA09g53980 | A09 | 54907171 | G | A | upstream_gene_variant | MODIFIER | c.-2829C>T| |
S308 |
11 | BAA09g53980 | A09 | 54908267 | C | T | upstream_gene_variant | MODIFIER | c.-3925G>A| |
S37 |
12 | BAA09g53980 | A09 | 54908368 | G | A | upstream_gene_variant | MODIFIER | c.-4026C>T| |
S284 |