Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02280 | A08 | 1598241 | G | A | missense_variant | MODERATE | c.349C>T|p.Leu117Phe |
S181 |
2 | BAA08g02280 | A08 | 1598373 | G | A | synonymous_variant | LOW | c.288C>T|p.His96His |
S33 |
3 | BAA08g02280 | A08 | 1599789 | G | A | upstream_gene_variant | MODIFIER | c.-18C>T| |
S249 |
4 | BAA08g02280 | A08 | 1600496 | C | T | upstream_gene_variant | MODIFIER | c.-725G>A| |
S261 |
5 | BAA08g02280 | A08 | 1601008 | C | T | upstream_gene_variant | MODIFIER | c.-1237G>A| |
S237 |
6 | BAA08g02280 | A08 | 1601434 | C | T | upstream_gene_variant | MODIFIER | c.-1663G>A| |
S36 |
7 | BAA08g02280 | A08 | 1602142 | G | A | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S165 |
8 | BAA08g02280 | A08 | 1602411 | G | A | upstream_gene_variant | MODIFIER | c.-2640C>T| |
S51 |
9 | BAA08g02280 | A08 | 1602528 | A | G | upstream_gene_variant | MODIFIER | c.-2757T>C| |
S192 |
10 | BAA08g02280 | A08 | 1603080 | G | A | upstream_gene_variant | MODIFIER | c.-3309C>T| |
S206 |