Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00370 | A09 | 440075 | C | T | upstream_gene_variant | MODIFIER | c.-688C>T| |
S202 |
2 | BAA09g00370 | A09 | 440218 | C | T | upstream_gene_variant | MODIFIER | c.-545C>T| |
S125 |
3 | BAA09g00370 | A09 | 440472 | G | A | upstream_gene_variant | MODIFIER | c.-291G>A| |
S107 |
4 | BAA09g00370 | A09 | 440809 | G | A | missense_variant | MODERATE | c.47G>A|p.Gly16Asp |
S170 |
5 | BAA09g00370 | A09 | 440991 | G | A | missense_variant | MODERATE | c.154G>A|p.Asp52Asn |
S202 |
6 | BAA09g00370 | A09 | 441436 | G | A | missense_variant | MODERATE | c.599G>A|p.Arg200Lys |
S205 |
7 | BAA09g00370 | A09 | 442359 | C | T | missense_variant | MODERATE | c.1522C>T|p.Pro508Ser |
S132 S137 S89 |
8 | BAA09g00370 | A09 | 442814 | G | A | missense_variant | MODERATE | c.1808G>A|p.Ser603Asn |
S289 S290 |
9 | BAA09g00370 | A09 | 442849 | G | A | missense_variant | MODERATE | c.1843G>A|p.Asp615Asn |
S281 |
10 | BAA09g00370 | A09 | 447181 | C | T | downstream_gene_variant | MODIFIER | c.*3566C>T| |
S268 |