Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12300 | A10 | 13743321 | G | A | missense_variant | MODERATE | c.3229C>T|p.Pro1077Ser |
S57 |
2 | BAA10g12300 | A10 | 13744974 | C | T | missense_variant | MODERATE | c.2339G>A|p.Gly780Glu |
S63 |
3 | BAA10g12300 | A10 | 13745479 | G | A | missense_variant | MODERATE | c.1927C>T|p.Leu643Phe |
S280 |
4 | BAA10g12300 | A10 | 13747971 | G | A | intron_variant | MODIFIER | c.754+24C>T| |
S216 |
5 | BAA10g12300 | A10 | 13748285 | G | A | intron_variant | MODIFIER | c.663+54C>T| |
S192 |
6 | BAA10g12300 | A10 | 13748438 | G | A | synonymous_variant | LOW | c.564C>T|p.Thr188Thr |
S295 |
7 | BAA10g12300 | A10 | 13748994 | C | T | missense_variant&splice_region_variant | MODERATE | c.298G>A|p.Asp100Asn |
S40 S49 |
8 | BAA10g12300 | A10 | 13749253 | C | T | synonymous_variant | LOW | c.126G>A|p.Leu42Leu |
S187 |
9 | BAA10g12300 | A10 | 13749373 | C | T | intron_variant | MODIFIER | c.65-59G>A| |
S174 |
10 | BAA10g12300 | A10 | 13749667 | C | T | upstream_gene_variant | MODIFIER | c.-144G>A| |
S268 S273 |
11 | BAA10g12300 | A10 | 13752008 | C | T | upstream_gene_variant | MODIFIER | c.-2485G>A| |
S117 |
12 | BAA10g12300 | A10 | 13752976 | C | T | upstream_gene_variant | MODIFIER | c.-3453G>A| |
S46 |
13 | BAA10g12300 | A10 | 13754187 | C | T | upstream_gene_variant | MODIFIER | c.-4664G>A| |
S73 S91 |