| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 89851 | BAA10g00050 | A10 | 15080 | C | T | splice_region_variant&intron_variant | LOW | c.1313+5G>A| |
S132 S137 S237 |
| 89852 | BAA10g00030 | A10 | 15176 | C | T | upstream_gene_variant | MODIFIER | c.-2576G>A| |
S283 |
| 89853 | BAA10g00030 | A10 | 15413 | G | A | upstream_gene_variant | MODIFIER | c.-2813C>T| |
S71 |
| 89854 | BAA10g00050 | A10 | 15723 | G | A | missense_variant | MODERATE | c.1037C>T|p.Thr346Met |
S293 |
| 89855 | BAA10g00050 | A10 | 15863 | C | T | missense_variant | MODERATE | c.989G>A|p.Ser330Asn |
S266 |
| 89856 | BAA10g00030 | A10 | 16162 | G | A | upstream_gene_variant | MODIFIER | c.-3562C>T| |
S219 S72 |
| 89857 | BAA10g00050 | A10 | 16822 | C | T | missense_variant | MODERATE | c.583G>A|p.Gly195Ser |
S116 |
| 89858 | BAA10g00040 | A10 | 17765 | G | A | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S80 |
| 89859 | BAA10g00060 | A10 | 18577 | C | T | missense_variant | MODERATE | c.167C>T|p.Pro56Leu |
S62 |
| 89860 | BAA10g00060 | A10 | 19183 | C | T | missense_variant | MODERATE | c.400C>T|p.Leu134Phe |
S122 |
| 89861 | BAA10g00040 | A10 | 19426 | G | A | upstream_gene_variant | MODIFIER | c.-4985C>T| |
S301 S304 |
| 89862 | BAA10g00070 | A10 | 20802 | C | T | missense_variant | MODERATE | c.1288G>A|p.Ala430Thr |
S68 |
| 89863 | BAA10g00050 | A10 | 21278 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S135 |
| 89864 | BAA10g00050 | A10 | 21448 | C | T | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S265 |
| 89865 | BAA10g00070 | A10 | 21714 | G | A | missense_variant | MODERATE | c.887C>T|p.Ala296Val |
S156 |
| 89866 | BAA10g00050 | A10 | 22885 | G | A | upstream_gene_variant | MODIFIER | c.-4739C>T| |
S76 |
| 89867 | BAA10g00070 | A10 | 22934 | G | A | synonymous_variant | LOW | c.537C>T|p.Ser179Ser |
S45 |
| 89868 | BAA10g00070 | A10 | 23018 | G | A | splice_region_variant&synonymous_variant | LOW | c.453C>T|p.Tyr151Tyr |
S289 |
| 89869 | BAA10g00070 | A10 | 24333 | C | T | upstream_gene_variant | MODIFIER | c.-497G>A| |
S23 |
| 89870 | BAA10g00070 | A10 | 25440 | G | A | upstream_gene_variant | MODIFIER | c.-1604C>T| |
S48 |
| 89871 | BAA10g00090 | A10 | 25561 | C | T | missense_variant | MODERATE | c.947G>A|p.Cys316Tyr |
S165 |
| 89872 | BAA10g00090 | A10 | 25724 | C | T | missense_variant | MODERATE | c.868G>A|p.Glu290Lys |
S88 |
| 89873 | BAA10g00070 | A10 | 28161 | C | T | upstream_gene_variant | MODIFIER | c.-4325G>A| |
S271 |
| 89874 | BAA10g00100 | A10 | 28515 | C | T | synonymous_variant | LOW | c.543G>A|p.Lys181Lys |
S263 |
| 89875 | BAA10g00100 | A10 | 28737 | G | A | synonymous_variant | LOW | c.321C>T|p.Ser107Ser |
S223 |