Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g04060 | A04 | 2497391 | G | A | upstream_gene_variant | MODIFIER | c.-4960G>A| |
S133 |
2 | BAA04g04060 | A04 | 2497612 | G | A | upstream_gene_variant | MODIFIER | c.-4739G>A| |
S47 |
3 | BAA04g04060 | A04 | 2498925 | C | T | upstream_gene_variant | MODIFIER | c.-3426C>T| |
S247 |
4 | BAA04g04060 | A04 | 2499890 | C | T | upstream_gene_variant | MODIFIER | c.-2461C>T| |
S139 |
5 | BAA04g04060 | A04 | 2500207 | G | A | upstream_gene_variant | MODIFIER | c.-2144G>A| |
S256 |
6 | BAA04g04060 | A04 | 2500538 | G | A | upstream_gene_variant | MODIFIER | c.-1813G>A| |
S245 |
7 | BAA04g04060 | A04 | 2500722 | C | T | upstream_gene_variant | MODIFIER | c.-1629C>T| |
S152 S182 |
8 | BAA04g04060 | A04 | 2500809 | T | A | upstream_gene_variant | MODIFIER | c.-1542T>A| |
S20 |
9 | BAA04g04060 | A04 | 2502128 | C | T | upstream_gene_variant | MODIFIER | c.-223C>T| |
S140 |
10 | BAA04g04060 | A04 | 2502211 | G | A | upstream_gene_variant | MODIFIER | c.-140G>A| |
S45 |
11 | BAA04g04060 | A04 | 2502355 | C | T | missense_variant | MODERATE | c.5C>T|p.Ala2Val |
S206 S26 |
12 | BAA04g04060 | A04 | 2502560 | C | T | synonymous_variant | LOW | c.210C>T|p.Gly70Gly |
S136 |
13 | BAA04g04060 | A04 | 2502625 | G | A | missense_variant | MODERATE | c.275G>A|p.Gly92Glu |
S17 |
14 | BAA04g04060 | A04 | 2502648 | G | A | missense_variant | MODERATE | c.298G>A|p.Gly100Arg |
S105 S106 |
15 | BAA04g04060 | A04 | 2502696 | G | A | missense_variant | MODERATE | c.346G>A|p.Gly116Arg |
S232 |
16 | BAA04g04060 | A04 | 2502801 | C | T | missense_variant | MODERATE | c.451C>T|p.Arg151Cys |
S72 S78 |
17 | BAA04g04060 | A04 | 2503559 | G | A | synonymous_variant | LOW | c.1209G>A|p.Glu403Glu |
S161 |
18 | BAA04g04060 | A04 | 2504155 | G | A | missense_variant | MODERATE | c.1729G>A|p.Asp577Asn |
S250 |
19 | BAA04g04060 | A04 | 2504603 | C | T | missense_variant | MODERATE | c.2177C>T|p.Ser726Phe |
S9 |