Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11890 | A10 | 13435197 | G | A | missense_variant | MODERATE | c.764C>T|p.Thr255Ile |
S202 |
2 | BAA10g11890 | A10 | 13435450 | G | A | missense_variant | MODERATE | c.511C>T|p.Pro171Ser |
S192 |
3 | BAA10g11890 | A10 | 13435759 | C | T | missense_variant | MODERATE | c.202G>A|p.Gly68Arg |
S23 |
4 | BAA10g11890 | A10 | 13437545 | G | A | upstream_gene_variant | MODIFIER | c.-1505C>T| |
S55 |
5 | BAA10g11890 | A10 | 13437877 | C | T | upstream_gene_variant | MODIFIER | c.-1837G>A| |
S249 |
6 | BAA10g11890 | A10 | 13438538 | G | A | upstream_gene_variant | MODIFIER | c.-2498C>T| |
S234 |
7 | BAA10g11890 | A10 | 13439691 | G | A | upstream_gene_variant | MODIFIER | c.-3651C>T| |
S15 S3 |
8 | BAA10g11890 | A10 | 13440715 | C | T | upstream_gene_variant | MODIFIER | c.-4675G>A| |
S286 |
9 | BAA10g11890 | A10 | 13440802 | G | A | upstream_gene_variant | MODIFIER | c.-4762C>T| |
S34 |