Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43930 | A09 | 49857503 | G | A | upstream_gene_variant | MODIFIER | c.-4419G>A| |
S128 |
2 | BAA09g43930 | A09 | 49857512 | G | A | upstream_gene_variant | MODIFIER | c.-4410G>A| |
S308 |
3 | BAA09g43930 | A09 | 49857640 | C | T | upstream_gene_variant | MODIFIER | c.-4282C>T| |
S251 |
4 | BAA09g43930 | A09 | 49860320 | C | T | upstream_gene_variant | MODIFIER | c.-1602C>T| |
S232 |
5 | BAA09g43930 | A09 | 49861310 | G | T | upstream_gene_variant | MODIFIER | c.-612G>T| |
S148 S210 |
6 | BAA09g43930 | A09 | 49862212 | C | T | synonymous_variant | LOW | c.291C>T|p.Leu97Leu |
S66 |
7 | BAA09g43930 | A09 | 49862315 | G | A | missense_variant | MODERATE | c.394G>A|p.Val132Ile |
S289 S290 |
8 | BAA09g43930 | A09 | 49862327 | C | T | missense_variant | MODERATE | c.406C>T|p.His136Tyr |
S278 S57 |
9 | BAA09g43930 | A09 | 49862780 | G | A | missense_variant | MODERATE | c.859G>A|p.Asp287Asn |
S167 |
10 | BAA09g43930 | A09 | 49863014 | G | A | missense_variant | MODERATE | c.919G>A|p.Glu307Lys |
S291 |
11 | BAA09g43930 | A09 | 49863134 | C | T | missense_variant | MODERATE | c.1039C>T|p.Leu347Phe |
S186 |