| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144451 | BAA10g29140 | A10 | 22042945 | G | A | missense_variant | MODERATE | c.964G>A|p.Asp322Asn |
S62 |
| 144452 | BAA10g29140 | A10 | 22043148 | G | A | missense_variant | MODERATE | c.1087G>A|p.Glu363Lys |
S296 |
| 144453 | BAA10g29130 | A10 | 22045571 | G | A | downstream_gene_variant | MODIFIER | c.*4994G>A| |
S256 |
| 144454 | BAA10g29140 | A10 | 22045939 | C | T | downstream_gene_variant | MODIFIER | c.*1167C>T| |
S166 |
| 144455 | BAA10g29140 | A10 | 22046353 | C | G | downstream_gene_variant | MODIFIER | c.*1581C>G| |
S120 |
| 144456 | BAA10g29140 | A10 | 22047244 | G | A | downstream_gene_variant | MODIFIER | c.*2472G>A| |
S173 |
| 144457 | BAA10g29140 | A10 | 22048640 | G | A | downstream_gene_variant | MODIFIER | c.*3868G>A| |
S127 |
| 144458 | BAA10g29160 | A10 | 22049941 | C | T | upstream_gene_variant | MODIFIER | c.-4981C>T| |
S23 |
| 144459 | BAA10g29150 | A10 | 22052374 | C | T | missense_variant | MODERATE | c.1346G>A|p.Gly449Asp |
S11 |
| 144460 | BAA10g29150 | A10 | 22054309 | G | A | missense_variant | MODERATE | c.184C>T|p.Pro62Ser |
S122 |
| 144461 | BAA10g29150 | A10 | 22054420 | G | A | missense_variant | MODERATE | c.73C>T|p.Arg25Cys |
S230 |
| 144462 | BAA10g29150 | A10 | 22054485 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S79 S84 |
| 144463 | BAA10g29150 | A10 | 22054702 | G | A | upstream_gene_variant | MODIFIER | c.-210C>T| |
S228 |
| 144464 | BAA10g29160 | A10 | 22054989 | G | A | missense_variant | MODERATE | c.68G>A|p.Gly23Glu |
S150 |
| 144465 | BAA10g29160 | A10 | 22055050 | C | T | synonymous_variant | LOW | c.129C>T|p.Asp43Asp |
S33 |
| 144466 | BAA10g29160 | A10 | 22056323 | C | T | missense_variant | MODERATE | c.901C>T|p.Pro301Ser |
S46 |
| 144467 | BAA10g29160 | A10 | 22056362 | G | A | missense_variant | MODERATE | c.940G>A|p.Val314Ile |
S62 |
| 144468 | BAA10g29170 | A10 | 22058974 | G | A | missense_variant | MODERATE | c.1082C>T|p.Pro361Leu |
S173 |
| 144469 | BAA10g29170 | A10 | 22060451 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S112 |
| 144470 | BAA10g29170 | A10 | 22061109 | G | A | upstream_gene_variant | MODIFIER | c.-427C>T| |
S267 |
| 144471 | BAA10g29170 | A10 | 22061559 | C | T | upstream_gene_variant | MODIFIER | c.-877G>A| |
S251 |
| 144472 | BAA10g29170 | A10 | 22063416 | C | T | upstream_gene_variant | MODIFIER | c.-2734G>A| |
S28 |
| 144473 | BAA10g29170 | A10 | 22063954 | C | T | upstream_gene_variant | MODIFIER | c.-3272G>A| |
S229 |
| 144474 | BAA10g29180 | A10 | 22064794 | C | T | missense_variant | MODERATE | c.269G>A|p.Arg90Lys |
S157 S163 |
| 144475 | BAA10g29180 | A10 | 22065918 | C | T | upstream_gene_variant | MODIFIER | c.-856G>A| |
S292 |