Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g39400 | A07 | 35349931 | G | A | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S6 |
2 | BAA07g39400 | A07 | 35351490 | G | A | upstream_gene_variant | MODIFIER | c.-3403G>A| |
S6 |
3 | BAA07g39400 | A07 | 35353435 | G | A | upstream_gene_variant | MODIFIER | c.-1458G>A| |
S187 |
4 | BAA07g39400 | A07 | 35353755 | C | T | upstream_gene_variant | MODIFIER | c.-1138C>T| |
S124 |
5 | BAA07g39400 | A07 | 35354915 | G | A | missense_variant | MODERATE | c.23G>A|p.Arg8Lys |
S70 |
6 | BAA07g39400 | A07 | 35355051 | G | A | synonymous_variant | LOW | c.159G>A|p.Arg53Arg |
S44 |
7 | BAA07g39400 | A07 | 35355527 | T | G | missense_variant | MODERATE | c.635T>G|p.Val212Gly |
S109 S137 S205 S241 S244 |
8 | BAA07g39400 | A07 | 35355629 | C | T | missense_variant | MODERATE | c.737C>T|p.Ala246Val |
S279 |
9 | BAA07g39400 | A07 | 35355635 | T | G | missense_variant | MODERATE | c.743T>G|p.Val248Gly |
S217 S230 S26 S280 S53 S71 |
10 | BAA07g39400 | A07 | 35355867 | C | T | synonymous_variant | LOW | c.975C>T|p.Asp325Asp |
S67 |
11 | BAA07g39400 | A07 | 35357767 | C | T | downstream_gene_variant | MODIFIER | c.*1765C>T| |
S270 |
12 | BAA07g39400 | A07 | 35357969 | G | A | downstream_gene_variant | MODIFIER | c.*1967G>A| |
S302 S54 |
13 | BAA07g39400 | A07 | 35359389 | C | T | downstream_gene_variant | MODIFIER | c.*3387C>T| |
S58 |
14 | BAA07g39400 | A07 | 35359875 | G | A | downstream_gene_variant | MODIFIER | c.*3873G>A| |
S105 |
15 | BAA07g39400 | A07 | 35360317 | C | T | downstream_gene_variant | MODIFIER | c.*4315C>T| |
S174 |