Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20290 | A06 | 10698647 | G | A | upstream_gene_variant | MODIFIER | c.-4141G>A| |
S50 |
2 | BAA06g20290 | A06 | 10698910 | C | T | upstream_gene_variant | MODIFIER | c.-3878C>T| |
S160 |
3 | BAA06g20290 | A06 | 10700076 | G | A | upstream_gene_variant | MODIFIER | c.-2712G>A| |
S134 S179 |
4 | BAA06g20290 | A06 | 10700847 | C | T | upstream_gene_variant | MODIFIER | c.-1941C>T| |
S231 |
5 | BAA06g20290 | A06 | 10701118 | C | T | upstream_gene_variant | MODIFIER | c.-1670C>T| |
S263 |
6 | BAA06g20290 | A06 | 10702186 | G | A | upstream_gene_variant | MODIFIER | c.-602G>A| |
S173 |
7 | BAA06g20290 | A06 | 10702780 | C | T | upstream_gene_variant | MODIFIER | c.-8C>T| |
S211 S227 |
8 | BAA06g20290 | A06 | 10702795 | C | T | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S79 S91 |
9 | BAA06g20290 | A06 | 10703363 | G | A | missense_variant | MODERATE | c.262G>A|p.Asp88Asn |
S182 |
10 | BAA06g20290 | A06 | 10704379 | G | A | synonymous_variant | LOW | c.1056G>A|p.Lys352Lys |
S1 S90 |
11 | BAA06g20290 | A06 | 10704447 | C | T | missense_variant | MODERATE | c.1124C>T|p.Ala375Val |
S259 |