Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05560 | A08 | 4217981 | C | T | upstream_gene_variant | MODIFIER | c.-646C>T| |
S66 |
2 | BAA08g05560 | A08 | 4218027 | G | A | upstream_gene_variant | MODIFIER | c.-600G>A| |
S202 |
3 | BAA08g05560 | A08 | 4218051 | C | T | upstream_gene_variant | MODIFIER | c.-576C>T| |
S156 |
4 | BAA08g05560 | A08 | 4218053 | G | A | upstream_gene_variant | MODIFIER | c.-574G>A| |
S265 |
5 | BAA08g05560 | A08 | 4218296 | G | A | upstream_gene_variant | MODIFIER | c.-331G>A| |
S40 S49 |
6 | BAA08g05560 | A08 | 4218684 | G | A | missense_variant | MODERATE | c.58G>A|p.Asp20Asn |
S181 |
7 | BAA08g05560 | A08 | 4218819 | C | T | splice_region_variant&synonymous_variant | LOW | c.193C>T|p.Leu65Leu |
S167 |
8 | BAA08g05560 | A08 | 4219498 | G | A | missense_variant | MODERATE | c.445G>A|p.Asp149Asn |
S262 |
9 | BAA08g05560 | A08 | 4219589 | G | A | missense_variant | MODERATE | c.536G>A|p.Ser179Asn |
S217 |
10 | BAA08g05560 | A08 | 4223345 | C | T | downstream_gene_variant | MODIFIER | c.*2263C>T| |
S14 |
11 | BAA08g05560 | A08 | 4223866 | G | A | downstream_gene_variant | MODIFIER | c.*2784G>A| |
S18 |
12 | BAA08g05560 | A08 | 4224116 | C | T | downstream_gene_variant | MODIFIER | c.*3034C>T| |
S125 |
13 | BAA08g05560 | A08 | 4225107 | C | T | downstream_gene_variant | MODIFIER | c.*4025C>T| |
S170 |
14 | BAA08g05560 | A08 | 4225499 | C | T | downstream_gene_variant | MODIFIER | c.*4417C>T| |
S156 |
15 | BAA08g05560 | A08 | 4225836 | G | A | downstream_gene_variant | MODIFIER | c.*4754G>A| |
S18 |
16 | BAA08g05560 | A08 | 4225987 | G | A | downstream_gene_variant | MODIFIER | c.*4905G>A| |
S18 |
17 | BAA08g05560 | A08 | 4225992 | C | T | downstream_gene_variant | MODIFIER | c.*4910C>T| |
S161 |