Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14020 | A09 | 8073318 | G | A | upstream_gene_variant | MODIFIER | c.-1447G>A| |
S241 |
2 | BAA09g14020 | A09 | 8073852 | G | A | upstream_gene_variant | MODIFIER | c.-913G>A| |
S247 |
3 | BAA09g14020 | A09 | 8073997 | C | T | upstream_gene_variant | MODIFIER | c.-768C>T| |
S270 |
4 | BAA09g14020 | A09 | 8074800 | T | C | synonymous_variant | LOW | c.36T>C|p.Gly12Gly |
S160 |
5 | BAA09g14020 | A09 | 8074921 | C | T | missense_variant | MODERATE | c.157C>T|p.Leu53Phe |
S66 |
6 | BAA09g14020 | A09 | 8075061 | C | T | synonymous_variant | LOW | c.297C>T|p.Ser99Ser |
S306 S308 |
7 | BAA09g14020 | A09 | 8075156 | C | T | missense_variant | MODERATE | c.392C>T|p.Ser131Phe |
S35 |
8 | BAA09g14020 | A09 | 8075164 | G | A | missense_variant | MODERATE | c.400G>A|p.Glu134Lys |
S189 |
9 | BAA09g14020 | A09 | 8075356 | G | A | missense_variant | MODERATE | c.592G>A|p.Gly198Arg |
S123 |
10 | BAA09g14020 | A09 | 8075459 | C | T | missense_variant | MODERATE | c.695C>T|p.Ser232Phe |
S6 |
11 | BAA09g14020 | A09 | 8076528 | G | A | missense_variant | MODERATE | c.1666G>A|p.Ala556Thr |
S280 |
12 | BAA09g14020 | A09 | 8079100 | C | T | downstream_gene_variant | MODIFIER | c.*2318C>T| |
S117 |
13 | BAA09g14020 | A09 | 8079126 | C | T | downstream_gene_variant | MODIFIER | c.*2344C>T| |
S18 |
14 | BAA09g14020 | A09 | 8079895 | C | T | downstream_gene_variant | MODIFIER | c.*3113C>T| |
S158 |
15 | BAA09g14020 | A09 | 8080090 | G | A | downstream_gene_variant | MODIFIER | c.*3308G>A| |
S180 |
16 | BAA09g14020 | A09 | 8080832 | G | A | downstream_gene_variant | MODIFIER | c.*4050G>A| |
S210 S225 |