Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32830 | A10 | 23472719 | G | A | missense_variant | MODERATE | c.335G>A|p.Gly112Glu |
S223 |
2 | BAA10g32830 | A10 | 23472722 | G | A | missense_variant | MODERATE | c.338G>A|p.Gly113Glu |
S226 |
3 | BAA10g32830 | A10 | 23474439 | G | A | missense_variant | MODERATE | c.848G>A|p.Ser283Asn |
S180 |
4 | BAA10g32830 | A10 | 23475490 | G | A | intron_variant | MODIFIER | c.1423-15G>A| |
S202 |
5 | BAA10g32830 | A10 | 23475634 | C | T | missense_variant | MODERATE | c.1552C>T|p.Leu518Phe |
S73 S91 |
6 | BAA10g32830 | A10 | 23476130 | G | A | missense_variant | MODERATE | c.1930G>A|p.Glu644Lys |
S249 |
7 | BAA10g32830 | A10 | 23476332 | G | A | missense_variant | MODERATE | c.2132G>A|p.Ser711Asn |
S219 S72 |
8 | BAA10g32830 | A10 | 23482601 | C | T | downstream_gene_variant | MODIFIER | c.*4635C>T| |
S28 |
9 | BAA10g32830 | A10 | 23482946 | G | T | downstream_gene_variant | MODIFIER | c.*4980G>T| |
S5 |