Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40450 | A01 | 26804287 | C | T | missense_variant | MODERATE | c.3707G>A|p.Ser1236Asn |
S7 |
2 | BAA01g40450 | A01 | 26805053 | G | A | missense_variant | MODERATE | c.2941C>T|p.Leu981Phe |
S135 |
3 | BAA01g40450 | A01 | 26805210 | C | T | synonymous_variant | LOW | c.2784G>A|p.Gln928Gln |
S302 |
4 | BAA01g40450 | A01 | 26805751 | C | T | missense_variant | MODERATE | c.2243G>A|p.Arg748Lys |
S153 |
5 | BAA01g40450 | A01 | 26805872 | G | T | missense_variant | MODERATE | c.2122C>A|p.Gln708Lys |
S82 S92 |
6 | BAA01g40450 | A01 | 26807005 | G | A | stop_gained | HIGH | c.1393C>T|p.Gln465* |
S177 |
7 | BAA01g40450 | A01 | 26807579 | C | T | stop_gained | HIGH | c.819G>A|p.Trp273* |
S75 S81 |
8 | BAA01g40450 | A01 | 26807924 | C | T | synonymous_variant | LOW | c.474G>A|p.Gln158Gln |
S104 S52 |
9 | BAA01g40450 | A01 | 26808097 | G | A | stop_gained | HIGH | c.301C>T|p.Gln101* |
S255 |
10 | BAA01g40450 | A01 | 26808273 | G | A | missense_variant | MODERATE | c.125C>T|p.Pro42Leu |
S262 |
11 | BAA01g40450 | A01 | 26809588 | G | A | upstream_gene_variant | MODIFIER | c.-1191C>T| |
S202 |
12 | BAA01g40450 | A01 | 26811538 | C | T | upstream_gene_variant | MODIFIER | c.-3141G>A| |
S164 |
13 | BAA01g40450 | A01 | 26811695 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S87 |