Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g14130 | A04 | 19333304 | G | A | upstream_gene_variant | MODIFIER | c.-3783G>A| |
S43 |
2 | BAA04g14130 | A04 | 19334390 | G | A | upstream_gene_variant | MODIFIER | c.-2697G>A| |
S244 |
3 | BAA04g14130 | A04 | 19335304 | G | A | upstream_gene_variant | MODIFIER | c.-1783G>A| |
S233 S86 |
4 | BAA04g14130 | A04 | 19335429 | G | A | upstream_gene_variant | MODIFIER | c.-1658G>A| |
S206 S26 |
5 | BAA04g14130 | A04 | 19336257 | G | A | upstream_gene_variant | MODIFIER | c.-830G>A| |
S13 |
6 | BAA04g14130 | A04 | 19336474 | G | A | upstream_gene_variant | MODIFIER | c.-613G>A| |
S99 |
7 | BAA04g14130 | A04 | 19336948 | G | A | upstream_gene_variant | MODIFIER | c.-139G>A| |
S170 |
8 | BAA04g14130 | A04 | 19338990 | C | T | missense_variant | MODERATE | c.317C>T|p.Ser106Phe |
S146 |
9 | BAA04g14130 | A04 | 19339190 | T | A | intron_variant | MODIFIER | c.404+113T>A| |
S168 S279 S33 S64 |
10 | BAA04g14130 | A04 | 19339604 | C | T | intron_variant | MODIFIER | c.501+31C>T| |
S294 |
11 | BAA04g14130 | A04 | 19339871 | C | T | intron_variant | MODIFIER | c.574-50C>T| |
S159 S243 |
12 | BAA04g14130 | A04 | 19340297 | G | A | missense_variant | MODERATE | c.950G>A|p.Gly317Glu |
S144 |
13 | BAA04g14130 | A04 | 19340347 | G | A | missense_variant | MODERATE | c.1000G>A|p.Gly334Arg |
S165 |
14 | BAA04g14130 | A04 | 19341040 | G | A | missense_variant | MODERATE | c.1615G>A|p.Glu539Lys |
S176 |
15 | BAA04g14130 | A04 | 19341704 | G | A | downstream_gene_variant | MODIFIER | c.*317G>A| |
S185 |
16 | BAA04g14130 | A04 | 19344702 | C | T | downstream_gene_variant | MODIFIER | c.*3315C>T| |
S270 |
17 | BAA04g14130 | A04 | 19344960 | G | A | downstream_gene_variant | MODIFIER | c.*3573G>A| |
S205 |