Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11890 | A08 | 10469315 | C | T | intron_variant | MODIFIER | c.1157-507G>A| |
S294 |
2 | BAA08g11890 | A08 | 10469372 | G | A | intron_variant | MODIFIER | c.1157-564C>T| |
S136 |
3 | BAA08g11890 | A08 | 10470045 | G | A | intron_variant | MODIFIER | c.1156+302C>T| |
S298 |
4 | BAA08g11890 | A08 | 10472325 | C | T | missense_variant | MODERATE | c.415G>A|p.Asp139Asn |
S9 |
5 | BAA08g11890 | A08 | 10472371 | G | A | synonymous_variant | LOW | c.369C>T|p.Phe123Phe |
S301 S304 |
6 | BAA08g11890 | A08 | 10472603 | C | T | intron_variant | MODIFIER | c.217-80G>A| |
S1 S136 S90 |
7 | BAA08g11890 | A08 | 10472748 | C | T | missense_variant | MODERATE | c.202G>A|p.Asp68Asn |
S73 |
8 | BAA08g11890 | A08 | 10473916 | G | A | upstream_gene_variant | MODIFIER | c.-797C>T| |
S281 |
9 | BAA08g11890 | A08 | 10473922 | G | A | upstream_gene_variant | MODIFIER | c.-803C>T| |
S5 |
10 | BAA08g11890 | A08 | 10474230 | G | A | upstream_gene_variant | MODIFIER | c.-1111C>T| |
S20 |
11 | BAA08g11890 | A08 | 10475795 | C | T | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S7 |
12 | BAA08g11890 | A08 | 10476304 | C | T | upstream_gene_variant | MODIFIER | c.-3185G>A| |
S171 |
13 | BAA08g11890 | A08 | 10477831 | G | A | upstream_gene_variant | MODIFIER | c.-4712C>T| |
S119 |