| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 119851 | BAA10g11580 | A10 | 13181290 | C | T | upstream_gene_variant | MODIFIER | c.-4666C>T| |
S193 |
| 119852 | BAA10g11580 | A10 | 13181855 | C | T | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S143 |
| 119853 | BAA10g11580 | A10 | 13182194 | C | T | upstream_gene_variant | MODIFIER | c.-3762C>T| |
S208 S93 |
| 119854 | BAA10g11580 | A10 | 13185304 | C | T | upstream_gene_variant | MODIFIER | c.-652C>T| |
S46 |
| 119855 | BAA10g11580 | A10 | 13186041 | C | T | missense_variant | MODERATE | c.86C>T|p.Ala29Val |
S144 |
| 119856 | BAA10g11580 | A10 | 13186455 | G | A | intron_variant | MODIFIER | c.288+120G>A| |
S148 S30 S31 |
| 119857 | BAA10g11580 | A10 | 13186502 | G | A | intron_variant | MODIFIER | c.288+167G>A| |
S287 |
| 119858 | BAA10g11580 | A10 | 13186507 | C | T | intron_variant | MODIFIER | c.288+172C>T| |
S47 |
| 119859 | BAA10g11580 | A10 | 13187202 | G | A | downstream_gene_variant | MODIFIER | c.*1G>A| |
S13 |
| 119860 | BAA10g11580 | A10 | 13188004 | C | T | downstream_gene_variant | MODIFIER | c.*803C>T| |
S244 |
| 119861 | BAA10g11580 | A10 | 13188122 | G | A | downstream_gene_variant | MODIFIER | c.*921G>A| |
S198 |
| 119862 | BAA10g11590 | A10 | 13189842 | C | T | upstream_gene_variant | MODIFIER | c.-3733C>T| |
S42 |
| 119863 | BAA10g11590 | A10 | 13190913 | C | T | upstream_gene_variant | MODIFIER | c.-2662C>T| |
S274 |
| 119864 | BAA10g11590 | A10 | 13193450 | G | A | upstream_gene_variant | MODIFIER | c.-125G>A| |
S1 S90 |
| 119865 | BAA10g11590 | A10 | 13193656 | G | A | missense_variant | MODERATE | c.82G>A|p.Glu28Lys |
S65 |
| 119866 | BAA10g11590 | A10 | 13194547 | C | T | missense_variant | MODERATE | c.496C>T|p.Leu166Phe |
S79 S91 |
| 119867 | BAA10g11590 | A10 | 13195008 | C | T | synonymous_variant | LOW | c.873C>T|p.Val291Val |
S6 |
| 119868 | BAA10g11590 | A10 | 13195225 | G | A | missense_variant | MODERATE | c.1090G>A|p.Ala364Thr |
S295 |
| 119869 | BAA10g11590 | A10 | 13195259 | C | T | missense_variant | MODERATE | c.1124C>T|p.Ser375Phe |
S143 |
| 119870 | BAA10g11590 | A10 | 13196359 | G | A | missense_variant | MODERATE | c.1772G>A|p.Gly591Glu |
S221 |
| 119871 | BAA10g11590 | A10 | 13196588 | C | T | synonymous_variant | LOW | c.2001C>T|p.His667His |
S282 |
| 119872 | BAA10g11590 | A10 | 13197166 | C | T | downstream_gene_variant | MODIFIER | c.*353C>T| |
S238 |
| 119873 | BAA10g11590 | A10 | 13197176 | C | T | downstream_gene_variant | MODIFIER | c.*363C>T| |
S247 |
| 119874 | BAA10g11590 | A10 | 13197348 | C | T | downstream_gene_variant | MODIFIER | c.*535C>T| |
S277 |
| 119875 | BAA10g11590 | A10 | 13197615 | C | T | downstream_gene_variant | MODIFIER | c.*802C>T| |
S23 |