Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00830 | A10 | 388322 | G | A | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S69 |
2 | BAA10g00830 | A10 | 388333 | G | A | synonymous_variant | LOW | c.654C>T|p.Asp218Asp |
S83 S88 |
3 | BAA10g00830 | A10 | 388951 | C | T | missense_variant | MODERATE | c.323G>A|p.Arg108Lys |
S54 |
4 | BAA10g00830 | A10 | 389048 | C | T | missense_variant | MODERATE | c.226G>A|p.Asp76Asn |
S10 |
5 | BAA10g00830 | A10 | 389760 | C | T | upstream_gene_variant | MODIFIER | c.-44G>A| |
S175 |
6 | BAA10g00830 | A10 | 390783 | C | T | upstream_gene_variant | MODIFIER | c.-1067G>A| |
S266 |
7 | BAA10g00830 | A10 | 391464 | G | A | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S159 S243 |
8 | BAA10g00830 | A10 | 392016 | C | T | upstream_gene_variant | MODIFIER | c.-2300G>A| |
S108 |
9 | BAA10g00830 | A10 | 392168 | G | A | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S18 |
10 | BAA10g00830 | A10 | 392703 | T | C | upstream_gene_variant | MODIFIER | c.-2987A>G| |
S263 |
11 | BAA10g00830 | A10 | 392801 | G | A | upstream_gene_variant | MODIFIER | c.-3085C>T| |
S64 |