| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140301 | BAA10g25440 | A10 | 20565880 | G | A | missense_variant | MODERATE | c.622C>T|p.Leu208Phe |
S181 |
| 140302 | BAA10g25440 | A10 | 20566067 | C | T | synonymous_variant | LOW | c.435G>A|p.Glu145Glu |
S79 S91 |
| 140303 | BAA10g25440 | A10 | 20566104 | C | T | missense_variant | MODERATE | c.398G>A|p.Arg133Lys |
S36 |
| 140304 | BAA10g25440 | A10 | 20566408 | C | T | missense_variant | MODERATE | c.94G>A|p.Glu32Lys |
S68 |
| 140305 | BAA10g25430 | A10 | 20566564 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S296 |
| 140306 | BAA10g25450 | A10 | 20567700 | G | A | stop_gained | HIGH | c.365G>A|p.Trp122* |
S272 |
| 140307 | BAA10g25440 | A10 | 20569207 | C | T | upstream_gene_variant | MODIFIER | c.-2706G>A| |
S250 |
| 140308 | BAA10g25460 | A10 | 20570152 | G | A | missense_variant | MODERATE | c.451C>T|p.Leu151Phe |
S192 |
| 140309 | BAA10g25460 | A10 | 20573665 | G | A | upstream_gene_variant | MODIFIER | c.-2569C>T| |
S182 |
| 140310 | BAA10g25460 | A10 | 20575204 | C | T | upstream_gene_variant | MODIFIER | c.-4108G>A| |
S161 |
| 140311 | BAA10g25480 | A10 | 20577272 | G | A | upstream_gene_variant | MODIFIER | c.-625C>T| |
S207 |
| 140312 | BAA10g25480 | A10 | 20577716 | C | T | upstream_gene_variant | MODIFIER | c.-1069G>A| |
S294 |
| 140313 | BAA10g25480 | A10 | 20578901 | C | T | upstream_gene_variant | MODIFIER | c.-2254G>A| |
S204 |
| 140314 | BAA10g25490 | A10 | 20580141 | G | A | synonymous_variant | LOW | c.117C>T|p.Ile39Ile |
S1 S90 |
| 140315 | BAA10g25480 | A10 | 20580952 | C | T | upstream_gene_variant | MODIFIER | c.-4305G>A| |
S155 S211 |
| 140316 | BAA10g25500 | A10 | 20582169 | G | A | missense_variant | MODERATE | c.616G>A|p.Asp206Asn |
S32 |
| 140317 | BAA10g25490 | A10 | 20584551 | G | A | upstream_gene_variant | MODIFIER | c.-4294C>T| |
S106 |
| 140318 | BAA10g25490 | A10 | 20584602 | C | T | upstream_gene_variant | MODIFIER | c.-4345G>A| |
S153 S213 |
| 140319 | BAA10g25490 | A10 | 20584724 | T | A | upstream_gene_variant | MODIFIER | c.-4467A>T| |
S74 |
| 140320 | BAA10g25510 | A10 | 20585758 | C | T | missense_variant | MODERATE | c.734C>T|p.Ser245Phe |
S107 |
| 140321 | BAA10g25510 | A10 | 20585780 | C | T | synonymous_variant | LOW | c.756C>T|p.Pro252Pro |
S68 |
| 140322 | BAA10g25520 | A10 | 20586877 | G | A | upstream_gene_variant | MODIFIER | c.-534G>A| |
S134 |
| 140323 | BAA10g25520 | A10 | 20587196 | G | A | upstream_gene_variant | MODIFIER | c.-215G>A| |
S67 |
| 140324 | BAA10g25520 | A10 | 20589345 | C | T | missense_variant | MODERATE | c.1297C>T|p.Pro433Ser |
S8 |
| 140325 | BAA10g25520 | A10 | 20589452 | C | T | synonymous_variant | LOW | c.1404C>T|p.Asp468Asp |
S36 |