Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12670 | A02 | 5685984 | C | T | missense_variant | MODERATE | c.2671G>A|p.Asp891Asn |
S219 |
2 | BAA02g12670 | A02 | 5686857 | G | A | synonymous_variant | LOW | c.2163C>T|p.Phe721Phe |
S72 S78 |
3 | BAA02g12670 | A02 | 5687190 | C | T | splice_region_variant&intron_variant | LOW | c.2027+8G>A| |
S33 |
4 | BAA02g12670 | A02 | 5688435 | C | T | synonymous_variant | LOW | c.1383G>A|p.Lys461Lys |
S245 |
5 | BAA02g12670 | A02 | 5688516 | C | T | splice_donor_variant&intron_variant | HIGH | c.1375+1G>A| |
S103 |
6 | BAA02g12670 | A02 | 5688770 | C | T | missense_variant | MODERATE | c.1241G>A|p.Arg414His |
S100 |
7 | BAA02g12670 | A02 | 5688801 | C | T | missense_variant | MODERATE | c.1210G>A|p.Asp404Asn |
S158 |
8 | BAA02g12670 | A02 | 5692581 | C | T | upstream_gene_variant | MODIFIER | c.-2055G>A| |
S241 |
9 | BAA02g12670 | A02 | 5692823 | C | T | upstream_gene_variant | MODIFIER | c.-2297G>A| |
S234 |
10 | BAA02g12670 | A02 | 5693007 | C | T | upstream_gene_variant | MODIFIER | c.-2481G>A| |
S18 |
11 | BAA02g12670 | A02 | 5694659 | G | A | upstream_gene_variant | MODIFIER | c.-4133C>T| |
S19 |
12 | BAA02g12670 | A02 | 5695162 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S247 |