Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g07090 | A04 | 4728938 | G | A | missense_variant | MODERATE | c.2176C>T|p.Leu726Phe |
S104 S52 |
2 | BAA04g07090 | A04 | 4729022 | C | T | missense_variant | MODERATE | c.2092G>A|p.Gly698Arg |
S178 |
3 | BAA04g07090 | A04 | 4730044 | C | T | missense_variant | MODERATE | c.1465G>A|p.Gly489Arg |
S118 |
4 | BAA04g07090 | A04 | 4730380 | C | T | missense_variant | MODERATE | c.1215G>A|p.Met405Ile |
S295 |
5 | BAA04g07090 | A04 | 4730400 | C | T | missense_variant | MODERATE | c.1195G>A|p.Asp399Asn |
S246 |
6 | BAA04g07090 | A04 | 4730407 | G | A | synonymous_variant | LOW | c.1188C>T|p.Phe396Phe |
S269 |
7 | BAA04g07090 | A04 | 4731008 | C | T | synonymous_variant | LOW | c.759G>A|p.Lys253Lys |
S53 |
8 | BAA04g07090 | A04 | 4731302 | G | A | synonymous_variant | LOW | c.541C>T|p.Leu181Leu |
S58 |
9 | BAA04g07090 | A04 | 4731316 | C | T | missense_variant | MODERATE | c.527G>A|p.Gly176Glu |
S237 |
10 | BAA04g07090 | A04 | 4732421 | C | T | missense_variant | MODERATE | c.118G>A|p.Gly40Arg |
S240 |
11 | BAA04g07090 | A04 | 4732462 | G | A | missense_variant | MODERATE | c.77C>T|p.Ser26Phe |
S65 |
12 | BAA04g07090 | A04 | 4732592 | G | A | upstream_gene_variant | MODIFIER | c.-54C>T| |
S17 |
13 | BAA04g07090 | A04 | 4733604 | C | T | upstream_gene_variant | MODIFIER | c.-1066G>A| |
S270 |
14 | BAA04g07090 | A04 | 4735083 | C | T | upstream_gene_variant | MODIFIER | c.-2545G>A| |
S207 |
15 | BAA04g07090 | A04 | 4735443 | G | A | upstream_gene_variant | MODIFIER | c.-2905C>T| |
S142 |