Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19490 | A10 | 17849402 | G | A | missense_variant | MODERATE | c.2072C>T|p.Ser691Phe |
S57 |
2 | BAA10g19490 | A10 | 17849469 | G | A | missense_variant | MODERATE | c.2005C>T|p.Arg669Trp |
S155 |
3 | BAA10g19490 | A10 | 17852833 | G | T | missense_variant | MODERATE | c.715C>A|p.Leu239Met |
S304 |
4 | BAA10g19490 | A10 | 17853611 | C | T | synonymous_variant | LOW | c.462G>A|p.Gly154Gly |
S76 |
5 | BAA10g19490 | A10 | 17853969 | C | T | missense_variant | MODERATE | c.104G>A|p.Arg35Lys |
S260 |
6 | BAA10g19490 | A10 | 17857545 | C | T | upstream_gene_variant | MODIFIER | c.-3473G>A| |
S117 |
7 | BAA10g19490 | A10 | 17857893 | G | A | upstream_gene_variant | MODIFIER | c.-3821C>T| |
S42 |
8 | BAA10g19490 | A10 | 17858259 | C | T | upstream_gene_variant | MODIFIER | c.-4187G>A| |
S26 |
9 | BAA10g19490 | A10 | 17858302 | G | A | upstream_gene_variant | MODIFIER | c.-4230C>T| |
S262 |
10 | BAA10g19490 | A10 | 17858521 | G | A | upstream_gene_variant | MODIFIER | c.-4449C>T| |
S74 |
11 | BAA10g19490 | A10 | 17858608 | G | T | upstream_gene_variant | MODIFIER | c.-4536C>A| |
S116 |
12 | BAA10g19490 | A10 | 17858830 | G | A | upstream_gene_variant | MODIFIER | c.-4758C>T| |
S88 |