Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41920 | A03 | 19764719 | C | T | upstream_gene_variant | MODIFIER | c.-4964C>T| |
S142 |
2 | BAA03g41920 | A03 | 19765002 | C | T | upstream_gene_variant | MODIFIER | c.-4681C>T| |
S2 |
3 | BAA03g41920 | A03 | 19765144 | G | A | upstream_gene_variant | MODIFIER | c.-4539G>A| |
S249 |
4 | BAA03g41920 | A03 | 19765184 | G | A | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S257 |
5 | BAA03g41920 | A03 | 19767170 | C | T | upstream_gene_variant | MODIFIER | c.-2513C>T| |
S279 |
6 | BAA03g41920 | A03 | 19767722 | C | T | upstream_gene_variant | MODIFIER | c.-1961C>T| |
S37 |
7 | BAA03g41920 | A03 | 19768171 | C | T | upstream_gene_variant | MODIFIER | c.-1512C>T| |
S115 |
8 | BAA03g41920 | A03 | 19768686 | C | T | upstream_gene_variant | MODIFIER | c.-997C>T| |
S67 |
9 | BAA03g41920 | A03 | 19769112 | T | C | upstream_gene_variant | MODIFIER | c.-571T>C| |
S43 |
10 | BAA03g41920 | A03 | 19769927 | G | A | missense_variant | MODERATE | c.170G>A|p.Arg57Gln |
S213 |
11 | BAA03g41920 | A03 | 19770148 | C | T | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S125 |
12 | BAA03g41920 | A03 | 19771881 | C | T | intron_variant | MODIFIER | c.1429+45C>T| |
S264 |
13 | BAA03g41920 | A03 | 19771946 | G | A | synonymous_variant | LOW | c.1446G>A|p.Leu482Leu |
S164 |
14 | BAA03g41920 | A03 | 19773127 | C | T | missense_variant | MODERATE | c.2342C>T|p.Ser781Phe |
S8 |
15 | BAA03g41920 | A03 | 19773307 | C | T | missense_variant | MODERATE | c.2522C>T|p.Ala841Val |
S105 S106 |
16 | BAA03g41920 | A03 | 19774364 | G | A | synonymous_variant | LOW | c.3579G>A|p.Gln1193Gln |
S9 |
17 | BAA03g41920 | A03 | 19774727 | G | A | synonymous_variant | LOW | c.3942G>A|p.Leu1314Leu |
S257 |
18 | BAA03g41920 | A03 | 19778516 | G | A | downstream_gene_variant | MODIFIER | c.*3444G>A| |
S236 |