Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g08590 | A07 | 17623904 | C | T | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S128 |
2 | BAA07g08590 | A07 | 17624148 | C | T | upstream_gene_variant | MODIFIER | c.-4607C>T| |
S181 |
3 | BAA07g08590 | A07 | 17624989 | C | T | upstream_gene_variant | MODIFIER | c.-3766C>T| |
S247 |
4 | BAA07g08590 | A07 | 17625915 | G | A | upstream_gene_variant | MODIFIER | c.-2840G>A| |
S219 |
5 | BAA07g08590 | A07 | 17625938 | G | A | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S280 |
6 | BAA07g08590 | A07 | 17628035 | A | T | upstream_gene_variant | MODIFIER | c.-720A>T| |
S175 |
7 | BAA07g08590 | A07 | 17628671 | C | T | upstream_gene_variant | MODIFIER | c.-84C>T| |
S139 |
8 | BAA07g08590 | A07 | 17628767 | C | T | missense_variant | MODERATE | c.13C>T|p.Pro5Ser |
S218 |
9 | BAA07g08590 | A07 | 17628926 | T | A | intron_variant | MODIFIER | c.105+67T>A| |
S303 |
10 | BAA07g08590 | A07 | 17629255 | C | T | missense_variant | MODERATE | c.272C>T|p.Ser91Phe |
S120 S18 |
11 | BAA07g08590 | A07 | 17632101 | G | A | synonymous_variant | LOW | c.1626G>A|p.Leu542Leu |
S2 |
12 | BAA07g08590 | A07 | 17632167 | G | A | synonymous_variant | LOW | c.1692G>A|p.Lys564Lys |
S129 |