Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10620 | A10 | 12361274 | G | A | upstream_gene_variant | MODIFIER | c.-4916G>A| |
S53 |
2 | BAA10g10620 | A10 | 12362114 | C | T | upstream_gene_variant | MODIFIER | c.-4076C>T| |
S162 |
3 | BAA10g10620 | A10 | 12363254 | T | A | upstream_gene_variant | MODIFIER | c.-2936T>A| |
|
4 | BAA10g10620 | A10 | 12363820 | G | A | upstream_gene_variant | MODIFIER | c.-2370G>A| |
S37 |
5 | BAA10g10620 | A10 | 12364917 | G | A | upstream_gene_variant | MODIFIER | c.-1273G>A| |
S57 |
6 | BAA10g10620 | A10 | 12364949 | G | A | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S198 |
7 | BAA10g10620 | A10 | 12365638 | C | T | upstream_gene_variant | MODIFIER | c.-552C>T| |
S122 |
8 | BAA10g10620 | A10 | 12365984 | G | A | upstream_gene_variant | MODIFIER | c.-206G>A| |
S163 |
9 | BAA10g10620 | A10 | 12366549 | G | A | missense_variant | MODERATE | c.281G>A|p.Gly94Asp |
S65 |
10 | BAA10g10620 | A10 | 12366973 | G | A | synonymous_variant | LOW | c.705G>A|p.Lys235Lys |
S113 S115 S117 S23 S297 S65 |
11 | BAA10g10620 | A10 | 12367101 | G | A | missense_variant | MODERATE | c.833G>A|p.Ser278Asn |
S100 |
12 | BAA10g10620 | A10 | 12367291 | C | T | synonymous_variant | LOW | c.1023C>T|p.Tyr341Tyr |
S28 |
13 | BAA10g10620 | A10 | 12367517 | G | A | intron_variant | MODIFIER | c.1226+23G>A| |
S237 |
14 | BAA10g10620 | A10 | 12367896 | G | A | synonymous_variant | LOW | c.1482G>A|p.Arg494Arg |
S284 |
15 | BAA10g10620 | A10 | 12368306 | G | A | missense_variant | MODERATE | c.1892G>A|p.Arg631Lys |
S226 |
16 | BAA10g10620 | A10 | 12369424 | C | G | downstream_gene_variant | MODIFIER | c.*892C>G| |
S1 S90 |
17 | BAA10g10620 | A10 | 12369709 | G | A | downstream_gene_variant | MODIFIER | c.*1177G>A| |
S217 |
18 | BAA10g10620 | A10 | 12370754 | C | T | downstream_gene_variant | MODIFIER | c.*2222C>T| |
S23 |
19 | BAA10g10620 | A10 | 12372025 | C | T | downstream_gene_variant | MODIFIER | c.*3493C>T| |
S114 |
20 | BAA10g10620 | A10 | 12372876 | G | A | downstream_gene_variant | MODIFIER | c.*4344G>A| |
S207 |