Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11750 | A10 | 13321906 | G | A | downstream_gene_variant | MODIFIER | c.*4967C>T| |
S161 |
2 | BAA10g11750 | A10 | 13323082 | C | T | downstream_gene_variant | MODIFIER | c.*3791G>A| |
S266 |
3 | BAA10g11750 | A10 | 13323526 | C | T | downstream_gene_variant | MODIFIER | c.*3347G>A| |
S206 S26 |
4 | BAA10g11750 | A10 | 13324914 | G | A | downstream_gene_variant | MODIFIER | c.*1959C>T| |
S159 S188 S276 |
5 | BAA10g11750 | A10 | 13326754 | G | A | downstream_gene_variant | MODIFIER | c.*119C>T| |
S1 S90 |
6 | BAA10g11750 | A10 | 13327028 | C | T | missense_variant | MODERATE | c.1654G>A|p.Asp552Asn |
S164 |
7 | BAA10g11750 | A10 | 13327080 | C | T | synonymous_variant | LOW | c.1602G>A|p.Glu534Glu |
S260 |
8 | BAA10g11750 | A10 | 13327218 | G | A | intron_variant | MODIFIER | c.1542+38C>T| |
S36 |
9 | BAA10g11750 | A10 | 13327597 | G | A | intron_variant | MODIFIER | c.1357-80C>T| |
S302 |
10 | BAA10g11750 | A10 | 13329320 | C | T | intron_variant | MODIFIER | c.813+28G>A| |
S140 |
11 | BAA10g11750 | A10 | 13329538 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.624-1G>A| |
S131 |
12 | BAA10g11750 | A10 | 13330070 | G | A | missense_variant | MODERATE | c.253C>T|p.Leu85Phe |
S45 |
13 | BAA10g11750 | A10 | 13330222 | G | A | missense_variant | MODERATE | c.101C>T|p.Ser34Phe |
S18 |
14 | BAA10g11750 | A10 | 13330272 | G | A | synonymous_variant | LOW | c.51C>T|p.Arg17Arg |
S35 |
15 | BAA10g11750 | A10 | 13331417 | C | T | upstream_gene_variant | MODIFIER | c.-1095G>A| |
S23 |
16 | BAA10g11750 | A10 | 13332227 | G | A | upstream_gene_variant | MODIFIER | c.-1905C>T| |
S161 |
17 | BAA10g11750 | A10 | 13333128 | G | A | upstream_gene_variant | MODIFIER | c.-2806C>T| |
S296 |
18 | BAA10g11750 | A10 | 13333259 | G | A | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S263 |