Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26830 | A10 | 21114464 | G | A | missense_variant | MODERATE | c.1096G>A|p.Val366Met |
S191 |
2 | BAA10g26830 | A10 | 21114570 | C | T | missense_variant | MODERATE | c.1202C>T|p.Ser401Phe |
S104 S52 |
3 | BAA10g26830 | A10 | 21115119 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1332-1G>A| |
S207 |
4 | BAA10g26830 | A10 | 21116016 | C | T | missense_variant | MODERATE | c.1969C>T|p.Pro657Ser |
S266 |
5 | BAA10g26830 | A10 | 21116178 | G | A | missense_variant | MODERATE | c.2131G>A|p.Glu711Lys |
S125 |
6 | BAA10g26830 | A10 | 21116480 | C | T | downstream_gene_variant | MODIFIER | c.*234C>T| |
S68 |
7 | BAA10g26830 | A10 | 21116801 | G | A | downstream_gene_variant | MODIFIER | c.*555G>A| |
S80 |
8 | BAA10g26830 | A10 | 21118275 | G | A | downstream_gene_variant | MODIFIER | c.*2029G>A| |
S43 |
9 | BAA10g26830 | A10 | 21118524 | C | T | downstream_gene_variant | MODIFIER | c.*2278C>T| |
S19 |