Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08080 | A01 | 3513080 | G | A | downstream_gene_variant | MODIFIER | c.*941C>T| |
S162 |
2 | BAA01g08080 | A01 | 3513633 | C | G | downstream_gene_variant | MODIFIER | c.*388G>C| |
S257 |
3 | BAA01g08080 | A01 | 3514259 | C | T | missense_variant | MODERATE | c.2471G>A|p.Ser824Asn |
S268 |
4 | BAA01g08080 | A01 | 3514310 | C | T | missense_variant | MODERATE | c.2420G>A|p.Gly807Asp |
S109 |
5 | BAA01g08080 | A01 | 3514359 | G | A | synonymous_variant | LOW | c.2371C>T|p.Leu791Leu |
S202 |
6 | BAA01g08080 | A01 | 3514926 | C | T | missense_variant | MODERATE | c.1804G>A|p.Gly602Arg |
S2 |
7 | BAA01g08080 | A01 | 3515123 | C | T | missense_variant | MODERATE | c.1607G>A|p.Ser536Asn |
S242 |
8 | BAA01g08080 | A01 | 3515196 | G | A | missense_variant | MODERATE | c.1534C>T|p.Pro512Ser |
S142 |
9 | BAA01g08080 | A01 | 3515809 | C | T | missense_variant | MODERATE | c.1087G>A|p.Glu363Lys |
S132 S137 S215 S89 |
10 | BAA01g08080 | A01 | 3515967 | C | T | missense_variant | MODERATE | c.929G>A|p.Gly310Glu |
S16 |
11 | BAA01g08080 | A01 | 3516285 | G | A | missense_variant | MODERATE | c.611C>T|p.Pro204Leu |
S209 |
12 | BAA01g08080 | A01 | 3516982 | G | A | upstream_gene_variant | MODIFIER | c.-87C>T| |
S23 |
13 | BAA01g08080 | A01 | 3517332 | A | T | upstream_gene_variant | MODIFIER | c.-437T>A| |
|
14 | BAA01g08080 | A01 | 3517557 | G | A | upstream_gene_variant | MODIFIER | c.-662C>T| |
S8 |
15 | BAA01g08080 | A01 | 3518018 | C | T | upstream_gene_variant | MODIFIER | c.-1123G>A| |
S148 S210 S30 S31 |
16 | BAA01g08080 | A01 | 3518064 | G | A | upstream_gene_variant | MODIFIER | c.-1169C>T| |
S187 |
17 | BAA01g08080 | A01 | 3519324 | C | T | upstream_gene_variant | MODIFIER | c.-2429G>A| |
S182 |
18 | BAA01g08080 | A01 | 3520758 | C | T | upstream_gene_variant | MODIFIER | c.-3863G>A| |
S252 |
19 | BAA01g08080 | A01 | 3521378 | C | T | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S266 |
20 | BAA01g08080 | A01 | 3521455 | C | T | upstream_gene_variant | MODIFIER | c.-4560G>A| |
S211 S227 |