Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08670 | A10 | 10624970 | G | A | upstream_gene_variant | MODIFIER | c.-4290G>A| |
S71 |
2 | BAA10g08670 | A10 | 10625273 | G | T | upstream_gene_variant | MODIFIER | c.-3987G>T| |
S279 |
3 | BAA10g08670 | A10 | 10625342 | C | T | upstream_gene_variant | MODIFIER | c.-3918C>T| |
S37 |
4 | BAA10g08670 | A10 | 10625863 | G | A | upstream_gene_variant | MODIFIER | c.-3397G>A| |
S13 |
5 | BAA10g08670 | A10 | 10626017 | C | T | upstream_gene_variant | MODIFIER | c.-3243C>T| |
S183 |
6 | BAA10g08670 | A10 | 10627357 | C | T | upstream_gene_variant | MODIFIER | c.-1903C>T| |
S249 |
7 | BAA10g08670 | A10 | 10628060 | C | T | upstream_gene_variant | MODIFIER | c.-1200C>T| |
S114 |
8 | BAA10g08670 | A10 | 10628091 | G | A | upstream_gene_variant | MODIFIER | c.-1169G>A| |
S13 |
9 | BAA10g08670 | A10 | 10628141 | C | A | upstream_gene_variant | MODIFIER | c.-1119C>A| |
S278 |
10 | BAA10g08670 | A10 | 10628286 | C | T | upstream_gene_variant | MODIFIER | c.-974C>T| |
S10 S17 |
11 | BAA10g08670 | A10 | 10628292 | C | T | upstream_gene_variant | MODIFIER | c.-968C>T| |
S48 |
12 | BAA10g08670 | A10 | 10628352 | C | T | upstream_gene_variant | MODIFIER | c.-908C>T| |
S297 |
13 | BAA10g08670 | A10 | 10628450 | C | T | upstream_gene_variant | MODIFIER | c.-810C>T| |
S188 |
14 | BAA10g08670 | A10 | 10629612 | C | T | missense_variant | MODERATE | c.353C>T|p.Ser118Phe |
S86 |
15 | BAA10g08670 | A10 | 10629844 | G | A | synonymous_variant | LOW | c.585G>A|p.Ser195Ser |
S109 |
16 | BAA10g08670 | A10 | 10629883 | G | A | synonymous_variant | LOW | c.624G>A|p.Gln208Gln |
S53 |
17 | BAA10g08670 | A10 | 10630010 | C | T | splice_region_variant&intron_variant | LOW | c.744+7C>T| |
S42 |
18 | BAA10g08670 | A10 | 10631158 | C | T | synonymous_variant | LOW | c.1452C>T|p.His484His |
S200 |