Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02490 | A06 | 1507826 | C | T | upstream_gene_variant | MODIFIER | c.-1984C>T| |
S133 |
2 | BAA06g02490 | A06 | 1509895 | C | T | splice_region_variant&intron_variant | LOW | c.82+4C>T| |
S10 |
3 | BAA06g02490 | A06 | 1512676 | G | A | missense_variant | MODERATE | c.1196G>A|p.Ser399Asn |
S77 S82 |
4 | BAA06g02490 | A06 | 1513269 | G | A | synonymous_variant | LOW | c.1491G>A|p.Lys497Lys |
S294 |
5 | BAA06g02490 | A06 | 1513420 | G | A | missense_variant | MODERATE | c.1538G>A|p.Arg513Lys |
S166 |
6 | BAA06g02490 | A06 | 1513647 | G | A | synonymous_variant | LOW | c.1671G>A|p.Thr557Thr |
S38 |
7 | BAA06g02490 | A06 | 1513982 | G | A | missense_variant | MODERATE | c.1931G>A|p.Cys644Tyr |
S265 |
8 | BAA06g02490 | A06 | 1514279 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2069-1G>A| |
S203 |
9 | BAA06g02490 | A06 | 1515109 | G | A | missense_variant | MODERATE | c.2295G>A|p.Met765Ile |
S61 |
10 | BAA06g02490 | A06 | 1515191 | G | A | missense_variant | MODERATE | c.2377G>A|p.Asp793Asn |
S138 |