Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g12950 | A09 | 7442994 | C | T | upstream_gene_variant | MODIFIER | c.-1469C>T| |
S213 |
2 | BAA09g12950 | A09 | 7443076 | C | T | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S297 |
3 | BAA09g12950 | A09 | 7443428 | G | A | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S20 |
4 | BAA09g12950 | A09 | 7443555 | C | T | upstream_gene_variant | MODIFIER | c.-908C>T| |
S6 |
5 | BAA09g12950 | A09 | 7443759 | G | A | upstream_gene_variant | MODIFIER | c.-704G>A| |
S277 |
6 | BAA09g12950 | A09 | 7443904 | G | A | upstream_gene_variant | MODIFIER | c.-559G>A| |
S203 |
7 | BAA09g12950 | A09 | 7444093 | G | A | upstream_gene_variant | MODIFIER | c.-370G>A| |
S238 |
8 | BAA09g12950 | A09 | 7444508 | C | T | synonymous_variant | LOW | c.46C>T|p.Leu16Leu |
S94 |
9 | BAA09g12950 | A09 | 7445116 | G | A | missense_variant | MODERATE | c.503G>A|p.Arg168His |
S278 |
10 | BAA09g12950 | A09 | 7446005 | G | A | missense_variant&splice_region_variant | MODERATE | c.958G>A|p.Asp320Asn |
S198 |
11 | BAA09g12950 | A09 | 7446315 | G | A | synonymous_variant | LOW | c.1095G>A|p.Arg365Arg |
S74 |
12 | BAA09g12950 | A09 | 7446485 | G | A | splice_donor_variant&intron_variant | HIGH | c.1186+1G>A| |
S165 |
13 | BAA09g12950 | A09 | 7446700 | C | T | synonymous_variant | LOW | c.1308C>T|p.Ile436Ile |
S2 |
14 | BAA09g12950 | A09 | 7450832 | C | T | downstream_gene_variant | MODIFIER | c.*4120C>T| |
S206 S26 |