Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00090 | A01 | 34172 | G | A | upstream_gene_variant | MODIFIER | c.-4861G>A| |
S9 |
2 | BAA01g00090 | A01 | 34349 | C | T | upstream_gene_variant | MODIFIER | c.-4684C>T| |
S206 S26 |
3 | BAA01g00090 | A01 | 34748 | C | T | upstream_gene_variant | MODIFIER | c.-4285C>T| |
S8 |
4 | BAA01g00090 | A01 | 35758 | G | A | upstream_gene_variant | MODIFIER | c.-3275G>A| |
S6 |
5 | BAA01g00090 | A01 | 35818 | C | T | upstream_gene_variant | MODIFIER | c.-3215C>T| |
S1 S90 |
6 | BAA01g00090 | A01 | 36003 | G | A | upstream_gene_variant | MODIFIER | c.-3030G>A| |
S122 |
7 | BAA01g00090 | A01 | 36014 | C | T | upstream_gene_variant | MODIFIER | c.-3019C>T| |
S277 |
8 | BAA01g00090 | A01 | 39133 | C | T | missense_variant | MODERATE | c.101C>T|p.Ser34Phe |
S144 |
9 | BAA01g00090 | A01 | 39149 | G | A | synonymous_variant | LOW | c.117G>A|p.Leu39Leu |
S172 |
10 | BAA01g00090 | A01 | 39290 | G | A | missense_variant | MODERATE | c.258G>A|p.Met86Ile |
S131 |
11 | BAA01g00090 | A01 | 39777 | G | A | synonymous_variant | LOW | c.627G>A|p.Gln209Gln |
S23 |
12 | BAA01g00090 | A01 | 39858 | G | A | synonymous_variant | LOW | c.708G>A|p.Gln236Gln |
S242 |
13 | BAA01g00090 | A01 | 40084 | G | A | missense_variant | MODERATE | c.934G>A|p.Asp312Asn |
S217 S248 |