Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40560 | A09 | 47641291 | C | T | upstream_gene_variant | MODIFIER | c.-3037C>T| |
S18 |
2 | BAA09g40560 | A09 | 47642296 | C | T | upstream_gene_variant | MODIFIER | c.-2032C>T| |
S108 |
3 | BAA09g40560 | A09 | 47642397 | C | T | upstream_gene_variant | MODIFIER | c.-1931C>T| |
S54 |
4 | BAA09g40560 | A09 | 47642716 | C | T | upstream_gene_variant | MODIFIER | c.-1612C>T| |
S245 |
5 | BAA09g40560 | A09 | 47643702 | G | A | upstream_gene_variant | MODIFIER | c.-626G>A| |
S48 |
6 | BAA09g40560 | A09 | 47644137 | T | C | upstream_gene_variant | MODIFIER | c.-191T>C| |
S121 |
7 | BAA09g40560 | A09 | 47644204 | C | T | upstream_gene_variant | MODIFIER | c.-124C>T| |
S292 |
8 | BAA09g40560 | A09 | 47644315 | G | A | upstream_gene_variant | MODIFIER | c.-13G>A| |
S178 |
9 | BAA09g40560 | A09 | 47646257 | G | A | missense_variant&splice_region_variant | MODERATE | c.812G>A|p.Gly271Asp |
S177 |
10 | BAA09g40560 | A09 | 47646311 | C | T | missense_variant | MODERATE | c.866C>T|p.Ser289Phe |
S9 |