Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g56090 | A09 | 55917680 | C | T | missense_variant | MODERATE | c.395C>T|p.Thr132Ile |
S223 |
2 | BAA09g56090 | A09 | 55918093 | T | C | splice_region_variant&intron_variant | LOW | c.804+4T>C| |
S16 |
3 | BAA09g56090 | A09 | 55919781 | G | A | missense_variant | MODERATE | c.1846G>A|p.Glu616Lys |
S275 |
4 | BAA09g56090 | A09 | 55919802 | G | A | missense_variant | MODERATE | c.1867G>A|p.Glu623Lys |
S209 |
5 | BAA09g56090 | A09 | 55919877 | G | A | missense_variant | MODERATE | c.1942G>A|p.Asp648Asn |
S2 |
6 | BAA09g56090 | A09 | 55920465 | G | A | synonymous_variant | LOW | c.2229G>A|p.Lys743Lys |
S298 |
7 | BAA09g56090 | A09 | 55920766 | G | A | intron_variant | MODIFIER | c.2398-20G>A| |
S42 |
8 | BAA09g56090 | A09 | 55920996 | C | T | missense_variant | MODERATE | c.2515C>T|p.Leu839Phe |
S237 |
9 | BAA09g56090 | A09 | 55921126 | G | A | intron_variant | MODIFIER | c.2562+83G>A| |
S88 |
10 | BAA09g56090 | A09 | 55921242 | C | T | intron_variant | MODIFIER | c.2562+199C>T| |
S117 |
11 | BAA09g56090 | A09 | 55931229 | G | A | downstream_gene_variant | MODIFIER | c.*1730G>A| |
S127 |