Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46810 | A01 | 31172606 | C | T | missense_variant | MODERATE | c.1723G>A|p.Asp575Asn |
S69 |
2 | BAA01g46810 | A01 | 31172811 | C | T | synonymous_variant | LOW | c.1518G>A|p.Arg506Arg |
S8 |
3 | BAA01g46810 | A01 | 31172826 | C | T | synonymous_variant | LOW | c.1503G>A|p.Ala501Ala |
S292 |
4 | BAA01g46810 | A01 | 31173170 | G | A | missense_variant | MODERATE | c.1337C>T|p.Thr446Ile |
S34 |
5 | BAA01g46810 | A01 | 31173592 | G | A | missense_variant | MODERATE | c.1006C>T|p.Pro336Ser |
S298 |
6 | BAA01g46810 | A01 | 31173853 | G | A | missense_variant | MODERATE | c.935C>T|p.Ser312Phe |
S135 S273 S68 |
7 | BAA01g46810 | A01 | 31174105 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.778-1G>A| |
S184 |
8 | BAA01g46810 | A01 | 31177731 | C | T | upstream_gene_variant | MODIFIER | c.-2242G>A| |
S166 |
9 | BAA01g46810 | A01 | 31178078 | G | A | upstream_gene_variant | MODIFIER | c.-2589C>T| |
S107 |
10 | BAA01g46810 | A01 | 31178755 | C | T | upstream_gene_variant | MODIFIER | c.-3266G>A| |
S15 S156 S3 S34 S4 S6 |
11 | BAA01g46810 | A01 | 31178956 | G | A | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S279 |
12 | BAA01g46810 | A01 | 31179248 | T | C | upstream_gene_variant | MODIFIER | c.-3759A>G| |
S115 S117 S121 S122 S23 S266 S297 S55 S65 S8 |
13 | BAA01g46810 | A01 | 31179853 | G | A | upstream_gene_variant | MODIFIER | c.-4364C>T| |
S87 |