Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g07550 | A06 | 3988625 | C | T | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S46 |
2 | BAA06g07550 | A06 | 3989548 | G | A | upstream_gene_variant | MODIFIER | c.-180G>A| |
S275 |
3 | BAA06g07550 | A06 | 3989601 | C | T | upstream_gene_variant | MODIFIER | c.-127C>T| |
S256 |
4 | BAA06g07550 | A06 | 3990159 | C | T | intron_variant | MODIFIER | c.142-31C>T| |
S175 |
5 | BAA06g07550 | A06 | 3990768 | C | T | intron_variant | MODIFIER | c.406+142C>T| |
S48 |
6 | BAA06g07550 | A06 | 3991576 | C | T | stop_gained | HIGH | c.748C>T|p.Gln250* |
S32 |
7 | BAA06g07550 | A06 | 3991763 | C | T | intron_variant | MODIFIER | c.923+12C>T| |
S225 |
8 | BAA06g07550 | A06 | 3993811 | G | A | synonymous_variant | LOW | c.1557G>A|p.Lys519Lys |
S146 |
9 | BAA06g07550 | A06 | 3996225 | C | T | missense_variant | MODERATE | c.2630C>T|p.Pro877Leu |
S76 |
10 | BAA06g07550 | A06 | 3996258 | C | T | missense_variant | MODERATE | c.2663C>T|p.Ser888Phe |
S80 |
11 | BAA06g07550 | A06 | 3996267 | G | A | missense_variant | MODERATE | c.2672G>A|p.Ser891Asn |
S149 |