Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g31590 | A09 | 39571269 | C | T | upstream_gene_variant | MODIFIER | c.-3658C>T| |
S287 |
2 | BAA09g31590 | A09 | 39571290 | C | T | upstream_gene_variant | MODIFIER | c.-3637C>T| |
S135 |
3 | BAA09g31590 | A09 | 39571374 | G | A | upstream_gene_variant | MODIFIER | c.-3553G>A| |
S20 |
4 | BAA09g31590 | A09 | 39571552 | C | T | upstream_gene_variant | MODIFIER | c.-3375C>T| |
S211 S227 |
5 | BAA09g31590 | A09 | 39571709 | G | A | upstream_gene_variant | MODIFIER | c.-3218G>A| |
S47 |
6 | BAA09g31590 | A09 | 39573739 | C | T | upstream_gene_variant | MODIFIER | c.-1188C>T| |
S6 |
7 | BAA09g31590 | A09 | 39573977 | G | A | upstream_gene_variant | MODIFIER | c.-950G>A| |
S197 |
8 | BAA09g31590 | A09 | 39574004 | C | T | upstream_gene_variant | MODIFIER | c.-923C>T| |
S180 |
9 | BAA09g31590 | A09 | 39574308 | C | T | upstream_gene_variant | MODIFIER | c.-619C>T| |
S36 |
10 | BAA09g31590 | A09 | 39575134 | G | A | missense_variant | MODERATE | c.208G>A|p.Asp70Asn |
S45 |
11 | BAA09g31590 | A09 | 39575775 | G | A | synonymous_variant | LOW | c.849G>A|p.Lys283Lys |
S63 |
12 | BAA09g31590 | A09 | 39575908 | G | A | missense_variant | MODERATE | c.982G>A|p.Ala328Thr |
S233 |
13 | BAA09g31590 | A09 | 39576203 | C | T | missense_variant | MODERATE | c.1277C>T|p.Thr426Ile |
S83 S88 |
14 | BAA09g31590 | A09 | 39576205 | C | T | missense_variant | MODERATE | c.1279C>T|p.His427Tyr |
S234 |
15 | BAA09g31590 | A09 | 39576324 | C | T | synonymous_variant | LOW | c.1398C>T|p.Asn466Asn |
S28 |
16 | BAA09g31590 | A09 | 39580220 | C | T | downstream_gene_variant | MODIFIER | c.*369C>T| |
S83 S88 |