Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01500 | A10 | 752606 | C | T | missense_variant | MODERATE | c.2675G>A|p.Arg892Lys |
S182 |
2 | BAA10g01500 | A10 | 753071 | G | A | missense_variant | MODERATE | c.2210C>T|p.Ala737Val |
S178 |
3 | BAA10g01500 | A10 | 754229 | G | A | missense_variant | MODERATE | c.1132C>T|p.Leu378Phe |
S274 |
4 | BAA10g01500 | A10 | 754583 | C | T | missense_variant | MODERATE | c.877G>A|p.Gly293Arg |
S151 S166 S262 S263 |
5 | BAA10g01500 | A10 | 754686 | G | A | synonymous_variant | LOW | c.774C>T|p.Arg258Arg |
S171 |
6 | BAA10g01500 | A10 | 755058 | C | T | synonymous_variant | LOW | c.402G>A|p.Gly134Gly |
S123 |
7 | BAA10g01500 | A10 | 755693 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S230 |
8 | BAA10g01500 | A10 | 756081 | G | A | upstream_gene_variant | MODIFIER | c.-622C>T| |
S192 |
9 | BAA10g01500 | A10 | 758114 | C | T | upstream_gene_variant | MODIFIER | c.-2655G>A| |
S104 S52 |