| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 98051 | BAA10g05770 | A10 | 2958087 | G | A | upstream_gene_variant | MODIFIER | c.-1567G>A| |
S245 |
| 98052 | BAA10g05760 | A10 | 2958520 | G | A | synonymous_variant | LOW | c.252C>T|p.Pro84Pro |
S12 |
| 98053 | BAA10g05760 | A10 | 2959014 | G | A | upstream_gene_variant | MODIFIER | c.-243C>T| |
S153 S213 |
| 98054 | BAA10g05760 | A10 | 2959259 | G | A | upstream_gene_variant | MODIFIER | c.-488C>T| |
S295 |
| 98055 | BAA10g05760 | A10 | 2959315 | C | T | upstream_gene_variant | MODIFIER | c.-544G>A| |
S252 |
| 98056 | BAA10g05760 | A10 | 2959368 | G | A | upstream_gene_variant | MODIFIER | c.-597C>T| |
S293 |
| 98057 | BAA10g05770 | A10 | 2960936 | G | A | synonymous_variant | LOW | c.837G>A|p.Glu279Glu |
S129 |
| 98058 | BAA10g05770 | A10 | 2961247 | C | T | missense_variant | MODERATE | c.1063C>T|p.Pro355Ser |
S92 |
| 98059 | BAA10g05760 | A10 | 2961651 | G | A | upstream_gene_variant | MODIFIER | c.-2880C>T| |
S9 |
| 98060 | BAA10g05760 | A10 | 2962152 | C | T | upstream_gene_variant | MODIFIER | c.-3381G>A| |
S233 |
| 98061 | BAA10g05760 | A10 | 2962357 | G | A | upstream_gene_variant | MODIFIER | c.-3586C>T| |
S100 |
| 98062 | BAA10g05760 | A10 | 2962435 | G | A | upstream_gene_variant | MODIFIER | c.-3664C>T| |
S12 |
| 98063 | BAA10g05760 | A10 | 2963077 | G | A | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S208 S219 |
| 98064 | BAA10g05780 | A10 | 2963950 | C | T | missense_variant | MODERATE | c.460G>A|p.Asp154Asn |
S23 |
| 98065 | BAA10g05780 | A10 | 2963958 | G | A | missense_variant | MODERATE | c.452C>T|p.Thr151Ile |
S167 |
| 98066 | BAA10g05780 | A10 | 2964003 | G | A | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S293 |
| 98067 | BAA10g05780 | A10 | 2964092 | C | T | synonymous_variant | LOW | c.318G>A|p.Pro106Pro |
S305 |
| 98068 | BAA10g05780 | A10 | 2964234 | G | A | missense_variant | MODERATE | c.176C>T|p.Thr59Ile |
S1 S90 |
| 98069 | BAA10g05780 | A10 | 2964340 | C | T | missense_variant | MODERATE | c.70G>A|p.Glu24Lys |
S44 |
| 98070 | BAA10g05780 | A10 | 2965346 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S174 S175 S27 |
| 98071 | BAA10g05780 | A10 | 2965730 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S82 S92 |
| 98072 | BAA10g05780 | A10 | 2965988 | C | T | upstream_gene_variant | MODIFIER | c.-1579G>A| |
S202 |
| 98073 | BAA10g05780 | A10 | 2966425 | C | T | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S42 |
| 98074 | BAA10g05780 | A10 | 2967018 | C | T | upstream_gene_variant | MODIFIER | c.-2609G>A| |
S281 |
| 98075 | BAA10g05780 | A10 | 2967272 | G | A | upstream_gene_variant | MODIFIER | c.-2863C>T| |
S115 |