Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45120 | A01 | 30068025 | C | T | missense_variant | MODERATE | c.1889G>A|p.Cys630Tyr |
S130 |
2 | BAA01g45120 | A01 | 30068081 | C | T | synonymous_variant | LOW | c.1833G>A|p.Lys611Lys |
S239 |
3 | BAA01g45120 | A01 | 30068297 | C | T | missense_variant&splice_region_variant | MODERATE | c.1700G>A|p.Arg567Lys |
S216 |
4 | BAA01g45120 | A01 | 30068618 | C | T | missense_variant | MODERATE | c.1379G>A|p.Arg460Lys |
S237 |
5 | BAA01g45120 | A01 | 30069384 | C | T | missense_variant | MODERATE | c.945G>A|p.Met315Ile |
S88 |
6 | BAA01g45120 | A01 | 30069516 | G | A | synonymous_variant | LOW | c.813C>T|p.Phe271Phe |
S158 |
7 | BAA01g45120 | A01 | 30069783 | C | T | synonymous_variant | LOW | c.546G>A|p.Ala182Ala |
S263 |
8 | BAA01g45120 | A01 | 30069905 | C | T | missense_variant | MODERATE | c.508G>A|p.Asp170Asn |
S132 S215 |
9 | BAA01g45120 | A01 | 30070159 | G | A | missense_variant | MODERATE | c.343C>T|p.Pro115Ser |
S122 |
10 | BAA01g45120 | A01 | 30072563 | C | T | upstream_gene_variant | MODIFIER | c.-1928G>A| |
S165 |
11 | BAA01g45120 | A01 | 30075390 | C | T | upstream_gene_variant | MODIFIER | c.-4755G>A| |
S133 |