Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g46040 | A06 | 29299940 | G | A | synonymous_variant | LOW | c.3657C>T|p.Val1219Val |
S50 |
2 | BAA06g46040 | A06 | 29300704 | G | A | stop_gained | HIGH | c.2893C>T|p.Gln965* |
S284 |
3 | BAA06g46040 | A06 | 29300840 | G | A | synonymous_variant | LOW | c.2757C>T|p.Ser919Ser |
S50 |
4 | BAA06g46040 | A06 | 29301039 | C | T | missense_variant | MODERATE | c.2558G>A|p.Gly853Glu |
S144 |
5 | BAA06g46040 | A06 | 29301837 | C | T | missense_variant | MODERATE | c.1760G>A|p.Gly587Glu |
S34 |
6 | BAA06g46040 | A06 | 29302549 | C | T | missense_variant | MODERATE | c.1048G>A|p.Asp350Asn |
S149 |
7 | BAA06g46040 | A06 | 29302588 | C | T | missense_variant | MODERATE | c.1009G>A|p.Asp337Asn |
S43 |
8 | BAA06g46040 | A06 | 29302773 | C | T | stop_gained | HIGH | c.824G>A|p.Trp275* |
S10 |
9 | BAA06g46040 | A06 | 29303220 | G | A | missense_variant | MODERATE | c.497C>T|p.Ser166Phe |
S152 |
10 | BAA06g46040 | A06 | 29303396 | C | T | stop_gained | HIGH | c.321G>A|p.Trp107* |
S127 |
11 | BAA06g46040 | A06 | 29303967 | C | T | missense_variant | MODERATE | c.133G>A|p.Asp45Asn |
S78 S83 |
12 | BAA06g46040 | A06 | 29304108 | C | T | upstream_gene_variant | MODIFIER | c.-9G>A| |
S282 |
13 | BAA06g46040 | A06 | 29304541 | G | A | upstream_gene_variant | MODIFIER | c.-442C>T| |
S162 |
14 | BAA06g46040 | A06 | 29307354 | G | A | upstream_gene_variant | MODIFIER | c.-3255C>T| |
S166 |