Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41950 | A05 | 39870940 | G | A | downstream_gene_variant | MODIFIER | c.*1402C>T| |
S298 |
2 | BAA05g41950 | A05 | 39872652 | C | T | splice_region_variant&intron_variant | LOW | c.1925-6G>A| |
S279 |
3 | BAA05g41950 | A05 | 39873307 | C | T | missense_variant | MODERATE | c.1651G>A|p.Asp551Asn |
S221 |
4 | BAA05g41950 | A05 | 39873746 | G | A | missense_variant | MODERATE | c.1382C>T|p.Ala461Val |
S94 |
5 | BAA05g41950 | A05 | 39873784 | C | T | synonymous_variant | LOW | c.1344G>A|p.Arg448Arg |
S259 |
6 | BAA05g41950 | A05 | 39874129 | G | A | missense_variant | MODERATE | c.1226C>T|p.Thr409Ile |
S301 |
7 | BAA05g41950 | A05 | 39874785 | C | T | missense_variant&splice_region_variant | MODERATE | c.880G>A|p.Glu294Lys |
S195 |
8 | BAA05g41950 | A05 | 39875697 | G | A | missense_variant | MODERATE | c.203C>T|p.Ser68Phe |
S223 |
9 | BAA05g41950 | A05 | 39875925 | C | T | upstream_gene_variant | MODIFIER | c.-26G>A| |
S28 |
10 | BAA05g41950 | A05 | 39877357 | C | T | upstream_gene_variant | MODIFIER | c.-1458G>A| |
S1 S228 S244 S289 S290 S90 |
11 | BAA05g41950 | A05 | 39877438 | G | A | upstream_gene_variant | MODIFIER | c.-1539C>T| |
S130 |