Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16800 | A08 | 13805205 | T | C | upstream_gene_variant | MODIFIER | c.-4913T>C| |
S5 |
2 | BAA08g16800 | A08 | 13805582 | G | A | upstream_gene_variant | MODIFIER | c.-4536G>A| |
S267 |
3 | BAA08g16800 | A08 | 13805955 | T | A | upstream_gene_variant | MODIFIER | c.-4163T>A| |
S26 |
4 | BAA08g16800 | A08 | 13806539 | C | T | upstream_gene_variant | MODIFIER | c.-3579C>T| |
S88 |
5 | BAA08g16800 | A08 | 13806798 | C | T | upstream_gene_variant | MODIFIER | c.-3320C>T| |
S168 |
6 | BAA08g16800 | A08 | 13806965 | C | T | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S60 |
7 | BAA08g16800 | A08 | 13806999 | C | T | upstream_gene_variant | MODIFIER | c.-3119C>T| |
S301 S304 |
8 | BAA08g16800 | A08 | 13808184 | C | T | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S126 |
9 | BAA08g16800 | A08 | 13810739 | G | A | missense_variant | MODERATE | c.335G>A|p.Gly112Glu |
S16 |
10 | BAA08g16800 | A08 | 13810963 | G | A | missense_variant | MODERATE | c.458G>A|p.Gly153Glu |
S155 S211 |
11 | BAA08g16800 | A08 | 13811127 | G | A | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S5 |
12 | BAA08g16800 | A08 | 13811133 | C | T | missense_variant | MODERATE | c.538C>T|p.Pro180Ser |
S177 |
13 | BAA08g16800 | A08 | 13812625 | G | A | missense_variant | MODERATE | c.1276G>A|p.Asp426Asn |
S107 |
14 | BAA08g16800 | A08 | 13813221 | C | T | missense_variant | MODERATE | c.1781C>T|p.Thr594Ile |
S38 |
15 | BAA08g16800 | A08 | 13814111 | C | T | downstream_gene_variant | MODIFIER | c.*826C>T| |
S236 S260 |
16 | BAA08g16800 | A08 | 13814329 | C | T | downstream_gene_variant | MODIFIER | c.*1044C>T| |
S259 |
17 | BAA08g16800 | A08 | 13814383 | G | A | downstream_gene_variant | MODIFIER | c.*1098G>A| |
S14 |