| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 127301 | BAA10g15750 | A10 | 15989380 | C | T | splice_donor_variant&intron_variant | HIGH | c.1632+1G>A| |
S269 |
| 127302 | BAA10g15750 | A10 | 15989696 | C | T | synonymous_variant | LOW | c.1317G>A|p.Arg439Arg |
S294 |
| 127303 | BAA10g15750 | A10 | 15989819 | G | A | synonymous_variant | LOW | c.1194C>T|p.Asn398Asn |
S43 |
| 127304 | BAA10g15750 | A10 | 15989844 | G | A | missense_variant | MODERATE | c.1169C>T|p.Ser390Leu |
S205 |
| 127305 | BAA10g15750 | A10 | 15989914 | C | T | missense_variant | MODERATE | c.1099G>A|p.Asp367Asn |
S282 |
| 127306 | BAA10g15750 | A10 | 15990273 | C | T | stop_gained | HIGH | c.740G>A|p.Trp247* |
S232 |
| 127307 | BAA10g15750 | A10 | 15990798 | C | T | missense_variant | MODERATE | c.215G>A|p.Ser72Asn |
S232 |
| 127308 | BAA10g15760 | A10 | 15992572 | C | T | missense_variant | MODERATE | c.527C>T|p.Ser176Leu |
S10 |
| 127309 | BAA10g15770 | A10 | 15992884 | T | A | synonymous_variant | LOW | c.45T>A|p.Ser15Ser |
S296 |
| 127310 | BAA10g15770 | A10 | 15993337 | G | A | missense_variant | MODERATE | c.260G>A|p.Gly87Glu |
S184 |
| 127311 | BAA10g15770 | A10 | 15993580 | G | A | missense_variant | MODERATE | c.394G>A|p.Glu132Lys |
S9 |
| 127312 | BAA10g15770 | A10 | 15994117 | G | A | stop_gained | HIGH | c.704G>A|p.Trp235* |
S65 |
| 127313 | BAA10g15750 | A10 | 15995404 | C | T | upstream_gene_variant | MODIFIER | c.-4300G>A| |
S202 |
| 127314 | BAA10g15780 | A10 | 15996044 | G | A | missense_variant | MODERATE | c.64G>A|p.Glu22Lys |
S234 |
| 127315 | BAA10g15780 | A10 | 15997210 | C | T | missense_variant | MODERATE | c.487C>T|p.Pro163Ser |
S174 S27 S39 |
| 127316 | BAA10g15780 | A10 | 15997628 | G | A | missense_variant | MODERATE | c.766G>A|p.Asp256Asn |
S303 |
| 127317 | BAA10g15780 | A10 | 15997652 | G | A | missense_variant | MODERATE | c.790G>A|p.Ala264Thr |
S80 |
| 127318 | BAA10g15780 | A10 | 15997950 | G | A | missense_variant | MODERATE | c.992G>A|p.Ser331Asn |
S1 S90 |
| 127319 | BAA10g15770 | A10 | 15998759 | G | A | downstream_gene_variant | MODIFIER | c.*4356G>A| |
S155 S211 |
| 127320 | BAA10g15780 | A10 | 15999734 | C | T | downstream_gene_variant | MODIFIER | c.*1329C>T| |
S260 |
| 127321 | BAA10g15780 | A10 | 16000067 | C | T | downstream_gene_variant | MODIFIER | c.*1662C>T| |
S186 |
| 127322 | BAA10g15780 | A10 | 16001613 | C | T | downstream_gene_variant | MODIFIER | c.*3208C>T| |
S133 |
| 127323 | BAA10g15780 | A10 | 16002375 | C | T | downstream_gene_variant | MODIFIER | c.*3970C>T| |
S301 S304 |
| 127324 | BAA10g15780 | A10 | 16002782 | C | T | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S282 |
| 127325 | BAA10g15780 | A10 | 16002934 | C | T | downstream_gene_variant | MODIFIER | c.*4529C>T| |
S176 |