| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 95151 | BAA10g03930 | A10 | 1925263 | C | T | synonymous_variant | LOW | c.423G>A|p.Gln141Gln |
S143 |
| 95152 | BAA10g03930 | A10 | 1925352 | C | T | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S51 |
| 95153 | BAA10g03940 | A10 | 1926862 | C | T | synonymous_variant | LOW | c.2262G>A|p.Lys754Lys |
S35 |
| 95154 | BAA10g03940 | A10 | 1926955 | G | A | synonymous_variant | LOW | c.2169C>T|p.Ser723Ser |
S263 |
| 95155 | BAA10g03940 | A10 | 1927185 | C | T | missense_variant | MODERATE | c.1939G>A|p.Ala647Thr |
S173 |
| 95156 | BAA10g03940 | A10 | 1927217 | C | T | missense_variant | MODERATE | c.1907G>A|p.Cys636Tyr |
S135 |
| 95157 | BAA10g03940 | A10 | 1927240 | G | A | synonymous_variant | LOW | c.1884C>T|p.Phe628Phe |
S64 |
| 95158 | BAA10g03940 | A10 | 1927343 | G | A | missense_variant | MODERATE | c.1781C>T|p.Ser594Phe |
S32 |
| 95159 | BAA10g03940 | A10 | 1927471 | G | A | synonymous_variant | LOW | c.1653C>T|p.Cys551Cys |
S17 S290 |
| 95160 | BAA10g03940 | A10 | 1928731 | C | T | synonymous_variant | LOW | c.393G>A|p.Ala131Ala |
S265 |
| 95161 | BAA10g03950 | A10 | 1930691 | C | T | synonymous_variant | LOW | c.1026G>A|p.Lys342Lys |
S202 |
| 95162 | BAA10g03950 | A10 | 1931477 | C | T | missense_variant | MODERATE | c.353G>A|p.Gly118Asp |
S204 |
| 95163 | BAA10g03950 | A10 | 1932061 | G | A | synonymous_variant | LOW | c.225C>T|p.Arg75Arg |
S133 |
| 95164 | BAA10g03940 | A10 | 1932675 | C | T | upstream_gene_variant | MODIFIER | c.-3552G>A| |
S247 |
| 95165 | BAA10g03940 | A10 | 1932789 | G | A | upstream_gene_variant | MODIFIER | c.-3666C>T| |
S223 |
| 95166 | BAA10g03940 | A10 | 1933795 | G | A | upstream_gene_variant | MODIFIER | c.-4672C>T| |
S64 |
| 95167 | BAA10g03940 | A10 | 1934062 | G | A | upstream_gene_variant | MODIFIER | c.-4939C>T| |
S301 S304 |
| 95168 | BAA10g03960 | A10 | 1934104 | C | T | stop_gained | HIGH | c.1215G>A|p.Trp405* |
S202 |
| 95169 | BAA10g03960 | A10 | 1934217 | C | T | missense_variant | MODERATE | c.1102G>A|p.Ala368Thr |
S200 |
| 95170 | BAA10g03950 | A10 | 1934600 | G | A | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S17 |
| 95171 | BAA10g03960 | A10 | 1935059 | C | T | missense_variant | MODERATE | c.800G>A|p.Arg267Gln |
S247 |
| 95172 | BAA10g03950 | A10 | 1936099 | G | A | upstream_gene_variant | MODIFIER | c.-3814C>T| |
S62 |
| 95173 | BAA10g03960 | A10 | 1936427 | C | T | synonymous_variant | LOW | c.75G>A|p.Thr25Thr |
S125 |
| 95174 | BAA10g03970 | A10 | 1944974 | G | A | intron_variant | MODIFIER | c.1569-715C>T| |
S95 |
| 95175 | BAA10g03980 | A10 | 1945642 | G | A | downstream_gene_variant | MODIFIER | c.*4335C>T| |
S120 |