Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08900 | A10 | 10904221 | A | G | upstream_gene_variant | MODIFIER | c.-4667A>G| |
S39 |
2 | BAA10g08900 | A10 | 10904413 | C | T | upstream_gene_variant | MODIFIER | c.-4475C>T| |
S235 |
3 | BAA10g08900 | A10 | 10904628 | C | T | upstream_gene_variant | MODIFIER | c.-4260C>T| |
S143 |
4 | BAA10g08900 | A10 | 10905398 | C | T | upstream_gene_variant | MODIFIER | c.-3490C>T| |
S28 |
5 | BAA10g08900 | A10 | 10905454 | G | A | upstream_gene_variant | MODIFIER | c.-3434G>A| |
S240 |
6 | BAA10g08900 | A10 | 10905460 | G | A | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S291 |
7 | BAA10g08900 | A10 | 10905619 | G | A | upstream_gene_variant | MODIFIER | c.-3269G>A| |
S18 |
8 | BAA10g08900 | A10 | 10906402 | A | G | upstream_gene_variant | MODIFIER | c.-2486A>G| |
S13 |
9 | BAA10g08900 | A10 | 10907442 | G | A | upstream_gene_variant | MODIFIER | c.-1446G>A| |
S192 |
10 | BAA10g08900 | A10 | 10907766 | G | A | upstream_gene_variant | MODIFIER | c.-1122G>A| |
S109 |
11 | BAA10g08900 | A10 | 10908530 | C | T | upstream_gene_variant | MODIFIER | c.-358C>T| |
S8 |
12 | BAA10g08900 | A10 | 10909102 | C | T | missense_variant | MODERATE | c.215C>T|p.Thr72Ile |
S44 |
13 | BAA10g08900 | A10 | 10909381 | C | T | intron_variant | MODIFIER | c.284-95C>T| |
S122 |
14 | BAA10g08900 | A10 | 10909685 | G | A | missense_variant | MODERATE | c.397G>A|p.Val133Ile |
S178 |
15 | BAA10g08900 | A10 | 10909706 | G | A | missense_variant | MODERATE | c.418G>A|p.Ala140Thr |
S45 |
16 | BAA10g08900 | A10 | 10909743 | G | A | missense_variant | MODERATE | c.455G>A|p.Gly152Asp |
S50 |