Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24470 | A10 | 20149194 | C | T | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S305 |
2 | BAA10g24470 | A10 | 20150142 | C | T | upstream_gene_variant | MODIFIER | c.-3214C>T| |
S148 S210 S30 S31 |
3 | BAA10g24470 | A10 | 20150492 | G | A | upstream_gene_variant | MODIFIER | c.-2864G>A| |
S71 |
4 | BAA10g24470 | A10 | 20150638 | G | A | upstream_gene_variant | MODIFIER | c.-2718G>A| |
S208 |
5 | BAA10g24470 | A10 | 20151985 | G | A | upstream_gene_variant | MODIFIER | c.-1371G>A| |
S264 |
6 | BAA10g24470 | A10 | 20152019 | C | T | upstream_gene_variant | MODIFIER | c.-1337C>T| |
S221 |
7 | BAA10g24470 | A10 | 20152026 | G | A | upstream_gene_variant | MODIFIER | c.-1330G>A| |
S63 |
8 | BAA10g24470 | A10 | 20152056 | G | A | upstream_gene_variant | MODIFIER | c.-1300G>A| |
S15 S3 |
9 | BAA10g24470 | A10 | 20152072 | C | T | upstream_gene_variant | MODIFIER | c.-1284C>T| |
S20 |
10 | BAA10g24470 | A10 | 20152195 | G | A | upstream_gene_variant | MODIFIER | c.-1161G>A| |
S62 |
11 | BAA10g24470 | A10 | 20152213 | G | A | upstream_gene_variant | MODIFIER | c.-1143G>A| |
S65 |
12 | BAA10g24470 | A10 | 20152659 | C | T | upstream_gene_variant | MODIFIER | c.-697C>T| |
S125 |
13 | BAA10g24470 | A10 | 20153436 | C | T | synonymous_variant | LOW | c.81C>T|p.Ser27Ser |
S123 |
14 | BAA10g24470 | A10 | 20153708 | G | A | missense_variant | MODERATE | c.271G>A|p.Val91Ile |
S95 |
15 | BAA10g24470 | A10 | 20154167 | G | A | intron_variant | MODIFIER | c.686-25G>A| |
S182 |
16 | BAA10g24470 | A10 | 20155988 | C | T | synonymous_variant | LOW | c.2178C>T|p.Leu726Leu |
S210 S225 |
17 | BAA10g24470 | A10 | 20156082 | G | A | missense_variant | MODERATE | c.2272G>A|p.Glu758Lys |
S80 |
18 | BAA10g24470 | A10 | 20156776 | G | A | missense_variant | MODERATE | c.2656G>A|p.Asp886Asn |
S64 |
19 | BAA10g24470 | A10 | 20156803 | C | T | missense_variant | MODERATE | c.2683C>T|p.Pro895Ser |
S189 |
20 | BAA10g24470 | A10 | 20157058 | G | A | missense_variant | MODERATE | c.2938G>A|p.Glu980Lys |
S158 |