Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00670 | A10 | 326027 | G | A | missense_variant | MODERATE | c.1394C>T|p.Ala465Val |
S140 |
2 | BAA10g00670 | A10 | 326255 | C | T | missense_variant | MODERATE | c.1166G>A|p.Gly389Glu |
S37 |
3 | BAA10g00670 | A10 | 326579 | C | T | missense_variant | MODERATE | c.842G>A|p.Gly281Asp |
S196 |
4 | BAA10g00670 | A10 | 327012 | C | T | missense_variant | MODERATE | c.409G>A|p.Asp137Asn |
S10 |
5 | BAA10g00670 | A10 | 330395 | C | T | upstream_gene_variant | MODIFIER | c.-2975G>A| |
S170 |
6 | BAA10g00670 | A10 | 331712 | G | A | upstream_gene_variant | MODIFIER | c.-4292C>T| |
S76 |
7 | BAA10g00670 | A10 | 331741 | G | A | upstream_gene_variant | MODIFIER | c.-4321C>T| |
S252 |