Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g09160 | A07 | 18071468 | C | T | missense_variant | MODERATE | c.2584G>A|p.Gly862Arg |
S70 |
2 | BAA07g09160 | A07 | 18072654 | C | T | missense_variant | MODERATE | c.1909G>A|p.Glu637Lys |
S232 |
3 | BAA07g09160 | A07 | 18073720 | G | A | splice_region_variant&intron_variant | LOW | c.1377-8C>T| |
S123 |
4 | BAA07g09160 | A07 | 18074181 | G | A | missense_variant | MODERATE | c.1082C>T|p.Thr361Ile |
S74 |
5 | BAA07g09160 | A07 | 18074545 | C | T | missense_variant&splice_region_variant | MODERATE | c.893G>A|p.Ser298Asn |
S86 |
6 | BAA07g09160 | A07 | 18075239 | C | T | missense_variant | MODERATE | c.449G>A|p.Gly150Glu |
S126 |
7 | BAA07g09160 | A07 | 18075383 | G | A | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S295 |
8 | BAA07g09160 | A07 | 18077959 | A | G | upstream_gene_variant | MODIFIER | c.-800T>C| |
S268 |
9 | BAA07g09160 | A07 | 18078831 | G | A | upstream_gene_variant | MODIFIER | c.-1672C>T| |
S219 S72 |
10 | BAA07g09160 | A07 | 18078855 | G | A | upstream_gene_variant | MODIFIER | c.-1696C>T| |
S295 |
11 | BAA07g09160 | A07 | 18078937 | G | A | upstream_gene_variant | MODIFIER | c.-1778C>T| |
S264 |
12 | BAA07g09160 | A07 | 18079221 | G | A | upstream_gene_variant | MODIFIER | c.-2062C>T| |
S10 |
13 | BAA07g09160 | A07 | 18079888 | C | T | upstream_gene_variant | MODIFIER | c.-2729G>A| |
S130 |
14 | BAA07g09160 | A07 | 18079948 | G | A | upstream_gene_variant | MODIFIER | c.-2789C>T| |
S223 |
15 | BAA07g09160 | A07 | 18081646 | C | T | upstream_gene_variant | MODIFIER | c.-4487G>A| |
S302 |
16 | BAA07g09160 | A07 | 18081711 | G | A | upstream_gene_variant | MODIFIER | c.-4552C>T| |
S142 |