Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01850 | A10 | 892145 | G | A | missense_variant | MODERATE | c.3250C>T|p.Leu1084Phe |
S242 |
2 | BAA10g01850 | A10 | 892372 | G | A | missense_variant | MODERATE | c.3023C>T|p.Ser1008Phe |
S140 |
3 | BAA10g01850 | A10 | 893256 | C | T | synonymous_variant | LOW | c.2139G>A|p.Glu713Glu |
S44 |
4 | BAA10g01850 | A10 | 893393 | G | A | synonymous_variant | LOW | c.2002C>T|p.Leu668Leu |
S171 |
5 | BAA10g01850 | A10 | 893737 | G | A | missense_variant | MODERATE | c.1658C>T|p.Ala553Val |
S256 |
6 | BAA10g01850 | A10 | 893781 | G | A | synonymous_variant | LOW | c.1614C>T|p.Ala538Ala |
S47 |
7 | BAA10g01850 | A10 | 895031 | C | T | missense_variant | MODERATE | c.364G>A|p.Glu122Lys |
S263 |
8 | BAA10g01850 | A10 | 895430 | C | T | missense_variant | MODERATE | c.53G>A|p.Ser18Asn |
S116 |
9 | BAA10g01850 | A10 | 895534 | G | A | upstream_gene_variant | MODIFIER | c.-52C>T| |
S1 S90 |
10 | BAA10g01850 | A10 | 895546 | G | A | upstream_gene_variant | MODIFIER | c.-64C>T| |
S79 S84 |
11 | BAA10g01850 | A10 | 896043 | G | A | upstream_gene_variant | MODIFIER | c.-561C>T| |
S64 |
12 | BAA10g01850 | A10 | 897050 | C | T | upstream_gene_variant | MODIFIER | c.-1568G>A| |
S131 |
13 | BAA10g01850 | A10 | 897146 | C | T | upstream_gene_variant | MODIFIER | c.-1664G>A| |
S288 |
14 | BAA10g01850 | A10 | 897700 | C | T | upstream_gene_variant | MODIFIER | c.-2218G>A| |
S225 |
15 | BAA10g01850 | A10 | 898440 | C | T | upstream_gene_variant | MODIFIER | c.-2958G>A| |
S176 |