Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00570 | A05 | 311353 | G | A | upstream_gene_variant | MODIFIER | c.-2743G>A| |
S136 S275 |
2 | BAA05g00570 | A05 | 314848 | C | T | missense_variant | MODERATE | c.530C>T|p.Thr177Ile |
S164 |
3 | BAA05g00570 | A05 | 315095 | G | A | synonymous_variant | LOW | c.777G>A|p.Leu259Leu |
S6 |
4 | BAA05g00570 | A05 | 315713 | G | A | synonymous_variant | LOW | c.1296G>A|p.Pro432Pro |
S144 |
5 | BAA05g00570 | A05 | 315795 | G | A | missense_variant&splice_region_variant | MODERATE | c.1378G>A|p.Gly460Arg |
S142 |
6 | BAA05g00570 | A05 | 315993 | C | T | synonymous_variant | LOW | c.1476C>T|p.Asn492Asn |
S13 S279 |
7 | BAA05g00570 | A05 | 316033 | G | A | missense_variant | MODERATE | c.1516G>A|p.Asp506Asn |
S283 |
8 | BAA05g00570 | A05 | 316350 | G | A | stop_gained | HIGH | c.1706G>A|p.Trp569* |
S142 |
9 | BAA05g00570 | A05 | 317622 | C | T | missense_variant | MODERATE | c.2444C>T|p.Thr815Ile |
S161 |
10 | BAA05g00570 | A05 | 317929 | C | T | synonymous_variant | LOW | c.2658C>T|p.His886His |
S2 |