Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55490 | A09 | 55610948 | C | T | upstream_gene_variant | MODIFIER | c.-2396C>T| |
S19 |
2 | BAA09g55490 | A09 | 55611441 | C | T | upstream_gene_variant | MODIFIER | c.-1903C>T| |
S278 |
3 | BAA09g55490 | A09 | 55612002 | C | T | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S301 S304 |
4 | BAA09g55490 | A09 | 55612200 | G | A | upstream_gene_variant | MODIFIER | c.-1144G>A| |
S210 S225 |
5 | BAA09g55490 | A09 | 55612878 | A | G | upstream_gene_variant | MODIFIER | c.-466A>G| |
S125 S139 S147 S162 S178 S210 S225 S234 S28 |
6 | BAA09g55490 | A09 | 55613449 | G | A | missense_variant | MODERATE | c.106G>A|p.Asp36Asn |
S249 |
7 | BAA09g55490 | A09 | 55613675 | G | A | missense_variant | MODERATE | c.332G>A|p.Gly111Glu |
S243 |
8 | BAA09g55490 | A09 | 55613743 | C | T | missense_variant | MODERATE | c.400C>T|p.Leu134Phe |
S260 |
9 | BAA09g55490 | A09 | 55614033 | G | A | synonymous_variant | LOW | c.690G>A|p.Thr230Thr |
S82 S92 |