Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16010 | A01 | 7806917 | C | T | missense_variant | MODERATE | c.983G>A|p.Gly328Glu |
S221 |
2 | BAA01g16010 | A01 | 7807066 | G | A | missense_variant&splice_region_variant | MODERATE | c.959C>T|p.Pro320Leu |
S149 |
3 | BAA01g16010 | A01 | 7807305 | C | T | synonymous_variant | LOW | c.720G>A|p.Ser240Ser |
S135 |
4 | BAA01g16010 | A01 | 7807488 | G | A | intron_variant | MODIFIER | c.632-95C>T| |
S116 |
5 | BAA01g16010 | A01 | 7807673 | C | T | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S294 |
6 | BAA01g16010 | A01 | 7807779 | C | T | synonymous_variant | LOW | c.489G>A|p.Glu163Glu |
S16 S182 |
7 | BAA01g16010 | A01 | 7808017 | C | T | intron_variant | MODIFIER | c.264-13G>A| |
S113 |
8 | BAA01g16010 | A01 | 7808764 | A | G | upstream_gene_variant | MODIFIER | c.-29T>C| |
S168 |
9 | BAA01g16010 | A01 | 7809222 | C | T | upstream_gene_variant | MODIFIER | c.-487G>A| |
S295 |
10 | BAA01g16010 | A01 | 7809824 | C | T | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S179 |
11 | BAA01g16010 | A01 | 7810429 | G | A | upstream_gene_variant | MODIFIER | c.-1694C>T| |
S45 |
12 | BAA01g16010 | A01 | 7810876 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S260 |
13 | BAA01g16010 | A01 | 7811469 | G | A | upstream_gene_variant | MODIFIER | c.-2734C>T| |
S152 |
14 | BAA01g16010 | A01 | 7812924 | G | A | upstream_gene_variant | MODIFIER | c.-4189C>T| |
S244 |
15 | BAA01g16010 | A01 | 7812968 | C | T | upstream_gene_variant | MODIFIER | c.-4233G>A| |
S16 |
16 | BAA01g16010 | A01 | 7813418 | G | A | upstream_gene_variant | MODIFIER | c.-4683C>T| |
S60 |
17 | BAA01g16010 | A01 | 7813466 | G | A | upstream_gene_variant | MODIFIER | c.-4731C>T| |
S172 S217 |
18 | BAA01g16010 | A01 | 7813603 | G | A | upstream_gene_variant | MODIFIER | c.-4868C>T| |
S268 |