Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05460 | A08 | 4158956 | G | A | upstream_gene_variant | MODIFIER | c.-2521G>A| |
S191 |
2 | BAA08g05460 | A08 | 4159166 | G | A | upstream_gene_variant | MODIFIER | c.-2311G>A| |
S282 |
3 | BAA08g05460 | A08 | 4159261 | G | A | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S192 |
4 | BAA08g05460 | A08 | 4159508 | G | A | upstream_gene_variant | MODIFIER | c.-1969G>A| |
S153 |
5 | BAA08g05460 | A08 | 4159964 | C | T | upstream_gene_variant | MODIFIER | c.-1513C>T| |
S175 S177 |
6 | BAA08g05460 | A08 | 4161818 | G | A | missense_variant | MODERATE | c.165G>A|p.Met55Ile |
S290 |
7 | BAA08g05460 | A08 | 4161897 | G | T | stop_gained | HIGH | c.244G>T|p.Gly82* |
S132 S137 S89 |
8 | BAA08g05460 | A08 | 4162554 | G | A | missense_variant | MODERATE | c.868G>A|p.Gly290Ser |
S263 |
9 | BAA08g05460 | A08 | 4162728 | A | T | missense_variant | MODERATE | c.1042A>T|p.Asn348Tyr |
S64 |
10 | BAA08g05460 | A08 | 4162778 | C | T | synonymous_variant | LOW | c.1092C>T|p.Ser364Ser |
S219 S72 |
11 | BAA08g05460 | A08 | 4162830 | G | A | missense_variant | MODERATE | c.1144G>A|p.Glu382Lys |
S237 |
12 | BAA08g05460 | A08 | 4162873 | G | A | missense_variant | MODERATE | c.1187G>A|p.Cys396Tyr |
S192 |
13 | BAA08g05460 | A08 | 4162909 | G | A | missense_variant | MODERATE | c.1223G>A|p.Gly408Glu |
S65 |
14 | BAA08g05460 | A08 | 4163004 | G | A | missense_variant | MODERATE | c.1318G>A|p.Asp440Asn |
S5 |
15 | BAA08g05460 | A08 | 4164804 | G | A | missense_variant | MODERATE | c.2710G>A|p.Val904Ile |
S35 |