Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21890 | A08 | 16518531 | C | T | upstream_gene_variant | MODIFIER | c.-4926C>T| |
S237 |
2 | BAA08g21890 | A08 | 16518765 | C | T | upstream_gene_variant | MODIFIER | c.-4692C>T| |
S33 |
3 | BAA08g21890 | A08 | 16519385 | G | A | upstream_gene_variant | MODIFIER | c.-4072G>A| |
S259 |
4 | BAA08g21890 | A08 | 16520258 | C | T | upstream_gene_variant | MODIFIER | c.-3199C>T| |
S166 |
5 | BAA08g21890 | A08 | 16520619 | G | A | upstream_gene_variant | MODIFIER | c.-2838G>A| |
S32 |
6 | BAA08g21890 | A08 | 16521759 | C | T | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S36 |
7 | BAA08g21890 | A08 | 16523877 | C | T | missense_variant | MODERATE | c.421C>T|p.Leu141Phe |
S161 |
8 | BAA08g21890 | A08 | 16524675 | G | A | intron_variant | MODIFIER | c.870+349G>A| |
S259 |
9 | BAA08g21890 | A08 | 16525060 | C | T | synonymous_variant | LOW | c.885C>T|p.Ala295Ala |
S70 |
10 | BAA08g21890 | A08 | 16525427 | G | A | missense_variant | MODERATE | c.1252G>A|p.Asp418Asn |
S65 |
11 | BAA08g21890 | A08 | 16525757 | C | T | downstream_gene_variant | MODIFIER | c.*91C>T| |
S134 |
12 | BAA08g21890 | A08 | 16526791 | G | A | downstream_gene_variant | MODIFIER | c.*1125G>A| |
S150 |
13 | BAA08g21890 | A08 | 16528295 | C | T | downstream_gene_variant | MODIFIER | c.*2629C>T| |
S121 |
14 | BAA08g21890 | A08 | 16528587 | G | A | downstream_gene_variant | MODIFIER | c.*2921G>A| |
S241 |
15 | BAA08g21890 | A08 | 16529523 | C | T | downstream_gene_variant | MODIFIER | c.*3857C>T| |
S247 |
16 | BAA08g21890 | A08 | 16529839 | C | T | downstream_gene_variant | MODIFIER | c.*4173C>T| |
S249 |