| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 143751 | BAA10g28510 | A10 | 21823628 | G | A | missense_variant&splice_region_variant | MODERATE | c.170G>A|p.Ser57Asn |
S207 |
| 143752 | BAA10g28510 | A10 | 21824077 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.379-1G>A| |
S216 |
| 143753 | BAA10g28510 | A10 | 21826332 | G | A | downstream_gene_variant | MODIFIER | c.*1308G>A| |
S245 |
| 143754 | BAA10g28510 | A10 | 21826488 | C | T | downstream_gene_variant | MODIFIER | c.*1464C>T| |
S287 |
| 143755 | BAA10g28510 | A10 | 21827377 | G | A | downstream_gene_variant | MODIFIER | c.*2353G>A| |
S183 S198 |
| 143756 | BAA10g28510 | A10 | 21827826 | C | T | downstream_gene_variant | MODIFIER | c.*2802C>T| |
S230 |
| 143757 | BAA10g28520 | A10 | 21828454 | C | T | missense_variant | MODERATE | c.2893G>A|p.Val965Met |
S5 |
| 143758 | BAA10g28520 | A10 | 21828483 | G | A | missense_variant | MODERATE | c.2864C>T|p.Thr955Met |
S249 |
| 143759 | BAA10g28520 | A10 | 21829290 | G | A | missense_variant | MODERATE | c.2132C>T|p.Pro711Leu |
S280 |
| 143760 | BAA10g28520 | A10 | 21829555 | G | A | missense_variant | MODERATE | c.1867C>T|p.Leu623Phe |
S252 |
| 143761 | BAA10g28520 | A10 | 21829881 | C | T | missense_variant | MODERATE | c.1541G>A|p.Ser514Asn |
S67 |
| 143762 | BAA10g28520 | A10 | 21830214 | C | T | missense_variant | MODERATE | c.1208G>A|p.Gly403Asp |
S251 |
| 143763 | BAA10g28520 | A10 | 21830787 | C | T | missense_variant | MODERATE | c.713G>A|p.Gly238Glu |
S72 S78 |
| 143764 | BAA10g28520 | A10 | 21830796 | G | A | missense_variant | MODERATE | c.704C>T|p.Ala235Val |
S150 |
| 143765 | BAA10g28520 | A10 | 21830909 | C | T | synonymous_variant | LOW | c.591G>A|p.Lys197Lys |
S40 S49 |
| 143766 | BAA10g28520 | A10 | 21831240 | C | T | missense_variant | MODERATE | c.260G>A|p.Gly87Asp |
S129 |
| 143767 | BAA10g28530 | A10 | 21833394 | C | T | splice_region_variant&intron_variant | LOW | c.1248+5G>A| |
S115 |
| 143768 | BAA10g28530 | A10 | 21833444 | G | A | synonymous_variant | LOW | c.1203C>T|p.Phe401Phe |
S17 |
| 143769 | BAA10g28530 | A10 | 21834305 | G | A | synonymous_variant | LOW | c.882C>T|p.Tyr294Tyr |
S223 |
| 143770 | BAA10g28530 | A10 | 21836274 | G | A | missense_variant | MODERATE | c.32C>T|p.Ser11Leu |
S298 |
| 143771 | BAA10g28540 | A10 | 21837511 | G | A | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S173 |
| 143772 | BAA10g28540 | A10 | 21837742 | G | A | missense_variant | MODERATE | c.74C>T|p.Thr25Met |
S113 |
| 143773 | BAA10g28530 | A10 | 21838131 | G | A | upstream_gene_variant | MODIFIER | c.-1826C>T| |
S249 |
| 143774 | BAA10g28550 | A10 | 21838337 | G | A | synonymous_variant | LOW | c.156G>A|p.Ala52Ala |
S88 |
| 143775 | BAA10g28550 | A10 | 21838403 | C | T | synonymous_variant | LOW | c.222C>T|p.Leu74Leu |
S296 |