Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02480 | A04 | 1478046 | C | T | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S46 |
2 | BAA04g02480 | A04 | 1478235 | C | T | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S293 |
3 | BAA04g02480 | A04 | 1479734 | G | A | upstream_gene_variant | MODIFIER | c.-1636G>A| |
S224 |
4 | BAA04g02480 | A04 | 1480653 | G | A | upstream_gene_variant | MODIFIER | c.-717G>A| |
S167 |
5 | BAA04g02480 | A04 | 1480793 | C | T | upstream_gene_variant | MODIFIER | c.-577C>T| |
S180 |
6 | BAA04g02480 | A04 | 1481488 | C | T | missense_variant | MODERATE | c.119C>T|p.Ser40Phe |
S233 |
7 | BAA04g02480 | A04 | 1482343 | C | T | intron_variant | MODIFIER | c.219+755C>T| |
S295 |
8 | BAA04g02480 | A04 | 1484185 | G | A | intron_variant | MODIFIER | c.486+38G>A| |
S60 |
9 | BAA04g02480 | A04 | 1484311 | C | T | intron_variant | MODIFIER | c.486+164C>T| |
S18 |
10 | BAA04g02480 | A04 | 1484383 | C | T | intron_variant | MODIFIER | c.487-145C>T| |
S173 |
11 | BAA04g02480 | A04 | 1485402 | C | T | intron_variant | MODIFIER | c.885-116C>T| |
S96 |
12 | BAA04g02480 | A04 | 1486003 | C | T | missense_variant | MODERATE | c.1213C>T|p.Leu405Phe |
S296 |
13 | BAA04g02480 | A04 | 1486386 | G | A | splice_region_variant&stop_retained_variant | LOW | c.1412G>A|p.Ter471Ter |
S66 |
14 | BAA04g02480 | A04 | 1486931 | G | A | downstream_gene_variant | MODIFIER | c.*544G>A| |
S11 |
15 | BAA04g02480 | A04 | 1487040 | C | T | downstream_gene_variant | MODIFIER | c.*653C>T| |
S260 |