Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13430 | A09 | 7705547 | G | A | upstream_gene_variant | MODIFIER | c.-3694G>A| |
S32 |
2 | BAA09g13430 | A09 | 7705630 | A | G | upstream_gene_variant | MODIFIER | c.-3611A>G| |
S87 |
3 | BAA09g13430 | A09 | 7706510 | C | T | upstream_gene_variant | MODIFIER | c.-2731C>T| |
S293 |
4 | BAA09g13430 | A09 | 7706855 | C | T | upstream_gene_variant | MODIFIER | c.-2386C>T| |
S282 |
5 | BAA09g13430 | A09 | 7707540 | G | A | upstream_gene_variant | MODIFIER | c.-1701G>A| |
S293 |
6 | BAA09g13430 | A09 | 7707673 | C | T | upstream_gene_variant | MODIFIER | c.-1568C>T| |
S120 |
7 | BAA09g13430 | A09 | 7707723 | G | A | upstream_gene_variant | MODIFIER | c.-1518G>A| |
S166 |
8 | BAA09g13430 | A09 | 7708162 | C | T | upstream_gene_variant | MODIFIER | c.-1079C>T| |
S80 |
9 | BAA09g13430 | A09 | 7708303 | C | T | upstream_gene_variant | MODIFIER | c.-938C>T| |
S183 |
10 | BAA09g13430 | A09 | 7708817 | C | T | upstream_gene_variant | MODIFIER | c.-424C>T| |
S12 |
11 | BAA09g13430 | A09 | 7711713 | G | A | missense_variant | MODERATE | c.926G>A|p.Gly309Glu |
S237 |
12 | BAA09g13430 | A09 | 7712800 | C | T | missense_variant | MODERATE | c.1691C>T|p.Ala564Val |
S148 S210 |
13 | BAA09g13430 | A09 | 7713899 | C | T | downstream_gene_variant | MODIFIER | c.*993C>T| |
S107 S68 |
14 | BAA09g13430 | A09 | 7714325 | G | A | downstream_gene_variant | MODIFIER | c.*1419G>A| |
S301 S304 |
15 | BAA09g13430 | A09 | 7714410 | C | T | downstream_gene_variant | MODIFIER | c.*1504C>T| |
S140 |