Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02120 | A06 | 1339778 | C | T | upstream_gene_variant | MODIFIER | c.-3275C>T| |
S209 |
2 | BAA06g02120 | A06 | 1341000 | C | T | upstream_gene_variant | MODIFIER | c.-2053C>T| |
S225 S73 |
3 | BAA06g02120 | A06 | 1341341 | C | T | upstream_gene_variant | MODIFIER | c.-1712C>T| |
S164 |
4 | BAA06g02120 | A06 | 1343744 | C | T | missense_variant | MODERATE | c.419C>T|p.Ser140Phe |
S223 |
5 | BAA06g02120 | A06 | 1344109 | G | A | missense_variant | MODERATE | c.563G>A|p.Arg188Gln |
S59 |
6 | BAA06g02120 | A06 | 1344402 | G | A | missense_variant | MODERATE | c.706G>A|p.Asp236Asn |
S118 |
7 | BAA06g02120 | A06 | 1345739 | G | A | synonymous_variant | LOW | c.1308G>A|p.Lys436Lys |
S140 |
8 | BAA06g02120 | A06 | 1347356 | G | A | splice_region_variant&intron_variant | LOW | c.2033+5G>A| |
S1 S90 |
9 | BAA06g02120 | A06 | 1347686 | C | T | missense_variant | MODERATE | c.2219C>T|p.Pro740Leu |
S188 |
10 | BAA06g02120 | A06 | 1347990 | G | A | downstream_gene_variant | MODIFIER | c.*25G>A| |
S54 |
11 | BAA06g02120 | A06 | 1348183 | C | T | downstream_gene_variant | MODIFIER | c.*218C>T| |
S18 |
12 | BAA06g02120 | A06 | 1350325 | C | T | downstream_gene_variant | MODIFIER | c.*2360C>T| |
S236 |