Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31630 | A02 | 19063331 | C | T | upstream_gene_variant | MODIFIER | c.-2498C>T| |
S164 |
2 | BAA02g31630 | A02 | 19063868 | G | A | upstream_gene_variant | MODIFIER | c.-1961G>A| |
S197 |
3 | BAA02g31630 | A02 | 19063905 | G | A | upstream_gene_variant | MODIFIER | c.-1924G>A| |
S279 |
4 | BAA02g31630 | A02 | 19064193 | C | T | upstream_gene_variant | MODIFIER | c.-1636C>T| |
S255 |
5 | BAA02g31630 | A02 | 19064510 | C | T | upstream_gene_variant | MODIFIER | c.-1319C>T| |
S212 |
6 | BAA02g31630 | A02 | 19065868 | C | T | missense_variant | MODERATE | c.40C>T|p.Pro14Ser |
S15 S153 S156 S213 S3 S34 S38 |
7 | BAA02g31630 | A02 | 19066005 | C | T | synonymous_variant | LOW | c.177C>T|p.Asn59Asn |
S73 |
8 | BAA02g31630 | A02 | 19066103 | C | T | missense_variant | MODERATE | c.275C>T|p.Ser92Phe |
S167 |
9 | BAA02g31630 | A02 | 19066142 | C | T | missense_variant | MODERATE | c.314C>T|p.Ser105Phe |
S167 |
10 | BAA02g31630 | A02 | 19066182 | C | T | synonymous_variant | LOW | c.354C>T|p.Gly118Gly |
S162 |
11 | BAA02g31630 | A02 | 19066228 | C | T | missense_variant | MODERATE | c.400C>T|p.Arg134Cys |
S182 |
12 | BAA02g31630 | A02 | 19067343 | C | T | downstream_gene_variant | MODIFIER | c.*981C>T| |
S61 |
13 | BAA02g31630 | A02 | 19067381 | C | T | downstream_gene_variant | MODIFIER | c.*1019C>T| |
S107 |
14 | BAA02g31630 | A02 | 19067655 | C | T | downstream_gene_variant | MODIFIER | c.*1293C>T| |
S242 |