| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 34951 | BAA01g23420 | A01 | 12063147 | G | A | upstream_gene_variant | MODIFIER | c.-3757G>A| |
S180 |
| 34952 | BAA01g23420 | A01 | 12063978 | C | T | upstream_gene_variant | MODIFIER | c.-2926C>T| |
S18 |
| 34953 | BAA01g23420 | A01 | 12064215 | G | A | upstream_gene_variant | MODIFIER | c.-2689G>A| |
S238 S252 |
| 34954 | BAA01g23420 | A01 | 12064667 | C | T | upstream_gene_variant | MODIFIER | c.-2237C>T| |
S115 S117 S23 S266 S297 S55 S9 |
| 34955 | BAA01g23420 | A01 | 12066910 | C | T | stop_gained | HIGH | c.7C>T|p.Gln3* |
S275 |
| 34956 | BAA01g23420 | A01 | 12067345 | G | A | missense_variant | MODERATE | c.442G>A|p.Gly148Ser |
S169 |
| 34957 | BAA01g23420 | A01 | 12067724 | G | A | missense_variant | MODERATE | c.821G>A|p.Gly274Glu |
S46 |
| 34958 | BAA01g23420 | A01 | 12067909 | G | A | missense_variant | MODERATE | c.1006G>A|p.Gly336Ser |
S60 |
| 34959 | BAA01g23420 | A01 | 12067928 | G | A | missense_variant | MODERATE | c.1025G>A|p.Ser342Asn |
S262 |
| 34960 | BAA01g23420 | A01 | 12068259 | G | A | synonymous_variant | LOW | c.1356G>A|p.Glu452Glu |
S308 |
| 34961 | BAA01g23420 | A01 | 12069253 | G | A | downstream_gene_variant | MODIFIER | c.*685G>A| |
S84 S93 |
| 34962 | BAA01g23420 | A01 | 12070670 | C | T | downstream_gene_variant | MODIFIER | c.*2102C>T| |
S184 |
| 34963 | BAA01g23420 | A01 | 12072169 | G | A | downstream_gene_variant | MODIFIER | c.*3601G>A| |
S56 |
| 34964 | BAA01g23420 | A01 | 12072704 | C | T | downstream_gene_variant | MODIFIER | c.*4136C>T| |
S10 |
| 34965 | BAA01g23430 | A01 | 12075366 | C | T | upstream_gene_variant | MODIFIER | c.-2625C>T| |
S48 |
| 34966 | BAA01g23430 | A01 | 12075835 | C | T | upstream_gene_variant | MODIFIER | c.-2156C>T| |
S107 |
| 34967 | BAA01g23430 | A01 | 12078327 | G | A | intron_variant | MODIFIER | c.291+46G>A| |
S105 S106 |
| 34968 | BAA01g23430 | A01 | 12079475 | C | T | missense_variant | MODERATE | c.593C>T|p.Ser198Phe |
S130 |
| 34969 | BAA01g23440 | A01 | 12080549 | C | T | downstream_gene_variant | MODIFIER | c.*3985G>A| |
S200 |
| 34970 | BAA01g23440 | A01 | 12080908 | G | A | downstream_gene_variant | MODIFIER | c.*3626C>T| |
S67 |
| 34971 | BAA01g23430 | A01 | 12081427 | G | A | missense_variant | MODERATE | c.1404G>A|p.Met468Ile |
S60 |
| 34972 | BAA01g23430 | A01 | 12083050 | C | T | downstream_gene_variant | MODIFIER | c.*1620C>T| |
S261 |
| 34973 | BAA01g23440 | A01 | 12084901 | C | T | missense_variant | MODERATE | c.451G>A|p.Asp151Asn |
S125 |
| 34974 | BAA01g23440 | A01 | 12085514 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S250 |
| 34975 | BAA01g23440 | A01 | 12085604 | G | A | missense_variant | MODERATE | c.55C>T|p.Pro19Ser |
S100 |