Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g28500 | A05 | 32383294 | C | T | missense_variant | MODERATE | c.2239G>A|p.Asp747Asn |
S271 |
2 | BAA05g28500 | A05 | 32384122 | C | T | missense_variant | MODERATE | c.1787G>A|p.Gly596Asp |
S57 |
3 | BAA05g28500 | A05 | 32384641 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1351-1G>A| |
S232 |
4 | BAA05g28500 | A05 | 32385119 | G | A | missense_variant | MODERATE | c.1297C>T|p.Arg433Cys |
S161 |
5 | BAA05g28500 | A05 | 32385172 | G | A | missense_variant | MODERATE | c.1244C>T|p.Ala415Val |
S6 |
6 | BAA05g28500 | A05 | 32387080 | C | T | splice_region_variant&synonymous_variant | LOW | c.288G>A|p.Gln96Gln |
S259 |
7 | BAA05g28500 | A05 | 32388119 | C | T | upstream_gene_variant | MODIFIER | c.-752G>A| |
S61 |
8 | BAA05g28500 | A05 | 32388183 | G | A | upstream_gene_variant | MODIFIER | c.-816C>T| |
S296 |
9 | BAA05g28500 | A05 | 32388263 | G | A | upstream_gene_variant | MODIFIER | c.-896C>T| |
S301 S304 |
10 | BAA05g28500 | A05 | 32388773 | G | A | upstream_gene_variant | MODIFIER | c.-1406C>T| |
S197 |
11 | BAA05g28500 | A05 | 32388854 | T | A | upstream_gene_variant | MODIFIER | c.-1487A>T| |
S94 |
12 | BAA05g28500 | A05 | 32389412 | C | T | upstream_gene_variant | MODIFIER | c.-2045G>A| |
S140 |
13 | BAA05g28500 | A05 | 32389637 | G | A | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S20 |
14 | BAA05g28500 | A05 | 32389684 | A | T | upstream_gene_variant | MODIFIER | c.-2317T>A| |
S242 |
15 | BAA05g28500 | A05 | 32390148 | C | T | upstream_gene_variant | MODIFIER | c.-2781G>A| |
S202 |