Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14060 | A09 | 8098570 | G | A | upstream_gene_variant | MODIFIER | c.-2789G>A| |
S193 |
2 | BAA09g14060 | A09 | 8098933 | G | A | upstream_gene_variant | MODIFIER | c.-2426G>A| |
S46 |
3 | BAA09g14060 | A09 | 8099264 | C | T | upstream_gene_variant | MODIFIER | c.-2095C>T| |
S135 |
4 | BAA09g14060 | A09 | 8099733 | C | T | upstream_gene_variant | MODIFIER | c.-1626C>T| |
S217 S248 |
5 | BAA09g14060 | A09 | 8100014 | G | A | upstream_gene_variant | MODIFIER | c.-1345G>A| |
S207 |
6 | BAA09g14060 | A09 | 8100178 | G | A | upstream_gene_variant | MODIFIER | c.-1181G>A| |
S293 |
7 | BAA09g14060 | A09 | 8101943 | C | T | splice_region_variant&intron_variant | LOW | c.392+7C>T| |
S28 |
8 | BAA09g14060 | A09 | 8103132 | G | A | missense_variant | MODERATE | c.661G>A|p.Glu221Lys |
S192 |
9 | BAA09g14060 | A09 | 8103361 | G | A | missense_variant | MODERATE | c.890G>A|p.Gly297Glu |
S122 |
10 | BAA09g14060 | A09 | 8103524 | C | T | synonymous_variant | LOW | c.1053C>T|p.Asn351Asn |
S282 |
11 | BAA09g14060 | A09 | 8103635 | G | A | synonymous_variant | LOW | c.1164G>A|p.Arg388Arg |
S201 |
12 | BAA09g14060 | A09 | 8103759 | A | T | missense_variant | MODERATE | c.1288A>T|p.Met430Leu |
S308 |
13 | BAA09g14060 | A09 | 8103766 | C | T | missense_variant | MODERATE | c.1295C>T|p.Pro432Leu |
S264 |
14 | BAA09g14060 | A09 | 8104514 | C | T | downstream_gene_variant | MODIFIER | c.*57C>T| |
S10 |
15 | BAA09g14060 | A09 | 8104826 | G | A | downstream_gene_variant | MODIFIER | c.*369G>A| |
S205 |
16 | BAA09g14060 | A09 | 8105247 | T | G | downstream_gene_variant | MODIFIER | c.*790T>G| |
S187 S224 S279 |
17 | BAA09g14060 | A09 | 8105386 | G | A | downstream_gene_variant | MODIFIER | c.*929G>A| |
S45 |
18 | BAA09g14060 | A09 | 8107359 | G | A | downstream_gene_variant | MODIFIER | c.*2902G>A| |
S144 |
19 | BAA09g14060 | A09 | 8108098 | C | T | downstream_gene_variant | MODIFIER | c.*3641C>T| |
S171 |
20 | BAA09g14060 | A09 | 8108153 | C | T | downstream_gene_variant | MODIFIER | c.*3696C>T| |
S217 |
21 | BAA09g14060 | A09 | 8108183 | C | T | downstream_gene_variant | MODIFIER | c.*3726C>T| |
S36 |