Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10930 | A10 | 12653416 | G | A | missense_variant | MODERATE | c.865C>T|p.Pro289Ser |
S66 |
2 | BAA10g10930 | A10 | 12656425 | G | A | upstream_gene_variant | MODIFIER | c.-802C>T| |
S288 |
3 | BAA10g10930 | A10 | 12656975 | G | A | upstream_gene_variant | MODIFIER | c.-1352C>T| |
S184 |
4 | BAA10g10930 | A10 | 12657658 | C | T | upstream_gene_variant | MODIFIER | c.-2035G>A| |
S89 |
5 | BAA10g10930 | A10 | 12658283 | G | A | upstream_gene_variant | MODIFIER | c.-2660C>T| |
S257 S262 S263 |
6 | BAA10g10930 | A10 | 12659658 | C | T | upstream_gene_variant | MODIFIER | c.-4035G>A| |
S121 |
7 | BAA10g10930 | A10 | 12659953 | C | T | upstream_gene_variant | MODIFIER | c.-4330G>A| |
S181 |