Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g13760 | A06 | 6813301 | C | T | missense_variant | MODERATE | c.2267G>A|p.Ser756Asn |
S170 |
2 | BAA06g13760 | A06 | 6813454 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2115-1G>A| |
S162 |
3 | BAA06g13760 | A06 | 6814163 | G | A | missense_variant | MODERATE | c.1684C>T|p.Leu562Phe |
S1 S90 |
4 | BAA06g13760 | A06 | 6814199 | C | T | missense_variant | MODERATE | c.1648G>A|p.Asp550Asn |
S7 |
5 | BAA06g13760 | A06 | 6814834 | G | A | synonymous_variant | LOW | c.1281C>T|p.Tyr427Tyr |
S262 |
6 | BAA06g13760 | A06 | 6815224 | G | A | synonymous_variant | LOW | c.1050C>T|p.Asn350Asn |
S100 |
7 | BAA06g13760 | A06 | 6815842 | C | T | missense_variant | MODERATE | c.676G>A|p.Gly226Arg |
S43 |
8 | BAA06g13760 | A06 | 6815976 | G | A | missense_variant | MODERATE | c.542C>T|p.Ser181Phe |
S32 |
9 | BAA06g13760 | A06 | 6816786 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S177 |
10 | BAA06g13760 | A06 | 6817173 | C | T | upstream_gene_variant | MODIFIER | c.-544G>A| |
S242 |
11 | BAA06g13760 | A06 | 6817429 | C | T | upstream_gene_variant | MODIFIER | c.-800G>A| |
S87 |
12 | BAA06g13760 | A06 | 6818075 | G | A | upstream_gene_variant | MODIFIER | c.-1446C>T| |
S273 |
13 | BAA06g13760 | A06 | 6818168 | C | T | upstream_gene_variant | MODIFIER | c.-1539G>A| |
S282 |
14 | BAA06g13760 | A06 | 6819520 | C | T | upstream_gene_variant | MODIFIER | c.-2891G>A| |
S125 |