Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20110 | A10 | 18232752 | C | T | missense_variant | MODERATE | c.1909G>A|p.Glu637Lys |
S180 |
2 | BAA10g20110 | A10 | 18233075 | G | A | missense_variant | MODERATE | c.1586C>T|p.Ser529Phe |
S158 |
3 | BAA10g20110 | A10 | 18233572 | C | T | synonymous_variant | LOW | c.1089G>A|p.Glu363Glu |
S130 |
4 | BAA10g20110 | A10 | 18233850 | C | T | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S187 S243 |
5 | BAA10g20110 | A10 | 18234108 | C | T | missense_variant | MODERATE | c.553G>A|p.Glu185Lys |
S169 |
6 | BAA10g20110 | A10 | 18234248 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S294 |
7 | BAA10g20110 | A10 | 18234465 | G | A | missense_variant | MODERATE | c.196C>T|p.Leu66Phe |
S125 |
8 | BAA10g20110 | A10 | 18234901 | C | T | upstream_gene_variant | MODIFIER | c.-241G>A| |
S2 |
9 | BAA10g20110 | A10 | 18234966 | C | T | upstream_gene_variant | MODIFIER | c.-306G>A| |
S226 |
10 | BAA10g20110 | A10 | 18235295 | G | A | upstream_gene_variant | MODIFIER | c.-635C>T| |
S28 |
11 | BAA10g20110 | A10 | 18236054 | C | T | upstream_gene_variant | MODIFIER | c.-1394G>A| |
S99 |
12 | BAA10g20110 | A10 | 18238671 | G | A | upstream_gene_variant | MODIFIER | c.-4011C>T| |
S295 |