Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15600 | A05 | 8322236 | C | T | missense_variant | MODERATE | c.2443G>A|p.Asp815Asn |
S73 S91 |
2 | BAA05g15600 | A05 | 8322536 | C | T | missense_variant | MODERATE | c.2143G>A|p.Asp715Asn |
S255 |
3 | BAA05g15600 | A05 | 8322582 | C | T | synonymous_variant | LOW | c.2097G>A|p.Lys699Lys |
S103 |
4 | BAA05g15600 | A05 | 8322826 | G | A | missense_variant | MODERATE | c.1940C>T|p.Thr647Met |
S278 |
5 | BAA05g15600 | A05 | 8323086 | C | T | missense_variant | MODERATE | c.1775G>A|p.Arg592Lys |
S232 |
6 | BAA05g15600 | A05 | 8323248 | G | A | missense_variant | MODERATE | c.1613C>T|p.Pro538Leu |
S80 |
7 | BAA05g15600 | A05 | 8323579 | G | A | missense_variant | MODERATE | c.1282C>T|p.Arg428Cys |
S23 |
8 | BAA05g15600 | A05 | 8323815 | G | A | missense_variant | MODERATE | c.1046C>T|p.Ala349Val |
S75 S81 |
9 | BAA05g15600 | A05 | 8323911 | G | A | missense_variant | MODERATE | c.950C>T|p.Pro317Leu |
S55 |
10 | BAA05g15600 | A05 | 8323935 | G | A | missense_variant | MODERATE | c.926C>T|p.Ser309Leu |
S64 |
11 | BAA05g15600 | A05 | 8324124 | C | T | missense_variant | MODERATE | c.737G>A|p.Arg246Lys |
S281 |
12 | BAA05g15600 | A05 | 8325242 | G | A | splice_region_variant&intron_variant | LOW | c.112-3C>T| |
S282 |
13 | BAA05g15600 | A05 | 8325627 | G | A | upstream_gene_variant | MODIFIER | c.-125C>T| |
S161 |
14 | BAA05g15600 | A05 | 8325946 | G | A | upstream_gene_variant | MODIFIER | c.-444C>T| |
S3 |
15 | BAA05g15600 | A05 | 8325950 | G | A | upstream_gene_variant | MODIFIER | c.-448C>T| |
S296 |
16 | BAA05g15600 | A05 | 8326175 | C | T | upstream_gene_variant | MODIFIER | c.-673G>A| |
S98 |
17 | BAA05g15600 | A05 | 8326266 | C | T | upstream_gene_variant | MODIFIER | c.-764G>A| |
S175 |
18 | BAA05g15600 | A05 | 8327925 | C | T | upstream_gene_variant | MODIFIER | c.-2423G>A| |
S139 |