Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03000 | A01 | 1374278 | G | A | upstream_gene_variant | MODIFIER | c.-2425G>A| |
S267 |
2 | BAA01g03000 | A01 | 1377837 | G | A | synonymous_variant | LOW | c.891G>A|p.Gln297Gln |
S239 |
3 | BAA01g03000 | A01 | 1378679 | G | A | synonymous_variant | LOW | c.1473G>A|p.Leu491Leu |
S115 |
4 | BAA01g03000 | A01 | 1382295 | C | T | missense_variant | MODERATE | c.4808C>T|p.Ser1603Leu |
S219 |
5 | BAA01g03000 | A01 | 1382640 | C | T | missense_variant | MODERATE | c.5153C>T|p.Pro1718Leu |
S36 |
6 | BAA01g03000 | A01 | 1383197 | C | T | missense_variant | MODERATE | c.5461C>T|p.Pro1821Ser |
S137 |
7 | BAA01g03000 | A01 | 1384337 | C | T | splice_region_variant&intron_variant | LOW | c.5629-6C>T| |
S212 |
8 | BAA01g03000 | A01 | 1384835 | C | T | missense_variant | MODERATE | c.6121C>T|p.Arg2041Trp |
S192 |
9 | BAA01g03000 | A01 | 1385900 | C | T | missense_variant | MODERATE | c.6919C>T|p.His2307Tyr |
S18 |
10 | BAA01g03000 | A01 | 1386638 | C | T | synonymous_variant | LOW | c.7404C>T|p.Ile2468Ile |
S155 S211 |
11 | BAA01g03000 | A01 | 1387199 | C | T | synonymous_variant | LOW | c.7695C>T|p.Asn2565Asn |
S134 |
12 | BAA01g03000 | A01 | 1388835 | C | T | downstream_gene_variant | MODIFIER | c.*789C>T| |
S164 |