| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144401 | BAA10g29090 | A10 | 22029512 | G | A | missense_variant | MODERATE | c.89G>A|p.Gly30Glu |
S50 |
| 144402 | BAA10g29090 | A10 | 22029643 | G | A | missense_variant | MODERATE | c.220G>A|p.Glu74Lys |
S262 |
| 144403 | BAA10g29090 | A10 | 22029905 | G | A | missense_variant | MODERATE | c.482G>A|p.Arg161Lys |
S50 |
| 144404 | BAA10g29080 | A10 | 22030590 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S48 |
| 144405 | BAA10g29080 | A10 | 22032155 | C | T | upstream_gene_variant | MODIFIER | c.-3161G>A| |
S208 |
| 144406 | BAA10g29080 | A10 | 22032800 | C | T | upstream_gene_variant | MODIFIER | c.-3806G>A| |
S67 |
| 144407 | BAA10g29110 | A10 | 22033119 | G | A | missense_variant | MODERATE | c.605C>T|p.Thr202Met |
S143 |
| 144408 | BAA10g29110 | A10 | 22033595 | G | A | synonymous_variant | LOW | c.129C>T|p.Gly43Gly |
S257 |
| 144409 | BAA10g29110 | A10 | 22033707 | G | A | missense_variant | MODERATE | c.17C>T|p.Pro6Leu |
S106 |
| 144410 | BAA10g29110 | A10 | 22033712 | C | T | synonymous_variant | LOW | c.12G>A|p.Glu4Glu |
S79 S91 |
| 144411 | BAA10g29100 | A10 | 22034473 | C | T | upstream_gene_variant | MODIFIER | c.-2980G>A| |
S255 |
| 144412 | BAA10g29100 | A10 | 22034656 | G | A | upstream_gene_variant | MODIFIER | c.-3163C>T| |
S150 |
| 144413 | BAA10g29100 | A10 | 22034849 | G | A | upstream_gene_variant | MODIFIER | c.-3356C>T| |
S4 |
| 144414 | BAA10g29100 | A10 | 22035477 | C | T | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S100 |
| 144415 | BAA10g29120 | A10 | 22036386 | G | A | splice_donor_variant&intron_variant | HIGH | c.587+1G>A| |
S65 |
| 144416 | BAA10g29120 | A10 | 22036749 | G | A | missense_variant | MODERATE | c.775G>A|p.Val259Ile |
S118 |
| 144417 | BAA10g29120 | A10 | 22036775 | G | A | synonymous_variant | LOW | c.801G>A|p.Glu267Glu |
S223 |
| 144418 | BAA10g29120 | A10 | 22036954 | G | A | missense_variant | MODERATE | c.980G>A|p.Gly327Glu |
S62 |
| 144419 | BAA10g29130 | A10 | 22038639 | C | T | missense_variant | MODERATE | c.152C>T|p.Ser51Leu |
S2 |
| 144420 | BAA10g29130 | A10 | 22039234 | C | T | synonymous_variant | LOW | c.747C>T|p.Val249Val |
S262 |
| 144421 | BAA10g29140 | A10 | 22040696 | C | T | upstream_gene_variant | MODIFIER | c.-311C>T| |
S187 |
| 144422 | BAA10g29140 | A10 | 22040743 | G | A | upstream_gene_variant | MODIFIER | c.-264G>A| |
S35 |
| 144423 | BAA10g29140 | A10 | 22041012 | C | T | synonymous_variant | LOW | c.6C>T|p.Ser2Ser |
S44 |
| 144424 | BAA10g29140 | A10 | 22041147 | C | T | synonymous_variant | LOW | c.141C>T|p.Thr47Thr |
S282 |
| 144425 | BAA10g29140 | A10 | 22041334 | G | A | missense_variant | MODERATE | c.328G>A|p.Asp110Asn |
S298 |