Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19220 | A10 | 17701429 | C | T | upstream_gene_variant | MODIFIER | c.-2081C>T| |
S224 |
2 | BAA10g19220 | A10 | 17701700 | G | A | upstream_gene_variant | MODIFIER | c.-1810G>A| |
S63 |
3 | BAA10g19220 | A10 | 17701933 | C | T | upstream_gene_variant | MODIFIER | c.-1577C>T| |
S187 |
4 | BAA10g19220 | A10 | 17702062 | G | A | upstream_gene_variant | MODIFIER | c.-1448G>A| |
S111 S117 |
5 | BAA10g19220 | A10 | 17702328 | G | A | upstream_gene_variant | MODIFIER | c.-1182G>A| |
S198 |
6 | BAA10g19220 | A10 | 17702560 | G | A | upstream_gene_variant | MODIFIER | c.-950G>A| |
S212 |
7 | BAA10g19220 | A10 | 17703341 | C | T | upstream_gene_variant | MODIFIER | c.-169C>T| |
S262 |
8 | BAA10g19220 | A10 | 17704394 | G | A | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S50 |
9 | BAA10g19220 | A10 | 17704453 | C | T | splice_region_variant&synonymous_variant | LOW | c.582C>T|p.Ala194Ala |
S242 |
10 | BAA10g19220 | A10 | 17705004 | G | A | missense_variant | MODERATE | c.707G>A|p.Gly236Glu |
S28 |
11 | BAA10g19220 | A10 | 17705418 | G | A | missense_variant | MODERATE | c.1121G>A|p.Gly374Asp |
S112 S97 |
12 | BAA10g19220 | A10 | 17705712 | G | A | missense_variant | MODERATE | c.1415G>A|p.Arg472Lys |
S38 |
13 | BAA10g19220 | A10 | 17706216 | G | A | missense_variant | MODERATE | c.1919G>A|p.Gly640Asp |
S219 S72 |