Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00660 | A05 | 372443 | C | T | missense_variant | MODERATE | c.1265G>A|p.Gly422Glu |
S195 |
2 | BAA05g00660 | A05 | 372591 | C | T | missense_variant | MODERATE | c.1201G>A|p.Glu401Lys |
S308 |
3 | BAA05g00660 | A05 | 373596 | G | A | missense_variant | MODERATE | c.704C>T|p.Pro235Leu |
S266 |
4 | BAA05g00660 | A05 | 373834 | C | T | intron_variant | MODIFIER | c.618+137G>A| |
S257 |
5 | BAA05g00660 | A05 | 374066 | C | T | missense_variant | MODERATE | c.523G>A|p.Ala175Thr |
S87 |
6 | BAA05g00660 | A05 | 375077 | C | T | missense_variant | MODERATE | c.118G>A|p.Asp40Asn |
S293 |
7 | BAA05g00660 | A05 | 375716 | C | T | upstream_gene_variant | MODIFIER | c.-522G>A| |
S201 |
8 | BAA05g00660 | A05 | 375797 | C | T | upstream_gene_variant | MODIFIER | c.-603G>A| |
S188 |
9 | BAA05g00660 | A05 | 376313 | G | A | upstream_gene_variant | MODIFIER | c.-1119C>T| |
S224 |
10 | BAA05g00660 | A05 | 376415 | G | A | upstream_gene_variant | MODIFIER | c.-1221C>T| |
S165 |
11 | BAA05g00660 | A05 | 376463 | C | T | upstream_gene_variant | MODIFIER | c.-1269G>A| |
S38 |
12 | BAA05g00660 | A05 | 378032 | G | A | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S293 |
13 | BAA05g00660 | A05 | 379065 | G | A | upstream_gene_variant | MODIFIER | c.-3871C>T| |
S138 |
14 | BAA05g00660 | A05 | 379194 | G | A | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S105 S106 |
15 | BAA05g00660 | A05 | 379360 | C | T | upstream_gene_variant | MODIFIER | c.-4166G>A| |
S13 S140 S168 |
16 | BAA05g00660 | A05 | 379679 | C | T | upstream_gene_variant | MODIFIER | c.-4485G>A| |
S61 |