Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21080 | A01 | 10386721 | C | T | upstream_gene_variant | MODIFIER | c.-4756C>T| |
S133 |
2 | BAA01g21080 | A01 | 10387387 | G | A | upstream_gene_variant | MODIFIER | c.-4090G>A| |
S288 |
3 | BAA01g21080 | A01 | 10387543 | C | T | upstream_gene_variant | MODIFIER | c.-3934C>T| |
S267 |
4 | BAA01g21080 | A01 | 10387945 | C | T | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S177 |
5 | BAA01g21080 | A01 | 10387969 | C | T | upstream_gene_variant | MODIFIER | c.-3508C>T| |
S69 |
6 | BAA01g21080 | A01 | 10388325 | G | A | upstream_gene_variant | MODIFIER | c.-3152G>A| |
S32 |
7 | BAA01g21080 | A01 | 10388628 | C | T | upstream_gene_variant | MODIFIER | c.-2849C>T| |
S104 |
8 | BAA01g21080 | A01 | 10388988 | C | T | upstream_gene_variant | MODIFIER | c.-2489C>T| |
S202 |
9 | BAA01g21080 | A01 | 10392939 | G | A | missense_variant | MODERATE | c.644G>A|p.Gly215Asp |
S268 |
10 | BAA01g21080 | A01 | 10394086 | G | A | missense_variant | MODERATE | c.1102G>A|p.Asp368Asn |
S245 |
11 | BAA01g21080 | A01 | 10394212 | G | A | missense_variant | MODERATE | c.1228G>A|p.Asp410Asn |
S204 |
12 | BAA01g21080 | A01 | 10395634 | G | A | downstream_gene_variant | MODIFIER | c.*1222G>A| |
S302 |
13 | BAA01g21080 | A01 | 10396010 | C | T | downstream_gene_variant | MODIFIER | c.*1598C>T| |
S239 |
14 | BAA01g21080 | A01 | 10398840 | G | A | downstream_gene_variant | MODIFIER | c.*4428G>A| |
S209 |