Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g13590 | A04 | 18958947 | C | T | missense_variant | MODERATE | c.2014G>A|p.Asp672Asn |
S200 |
2 | BAA04g13590 | A04 | 18959834 | G | A | missense_variant | MODERATE | c.1343C>T|p.Pro448Leu |
S62 |
3 | BAA04g13590 | A04 | 18959837 | G | A | missense_variant | MODERATE | c.1340C>T|p.Ser447Phe |
S169 |
4 | BAA04g13590 | A04 | 18960593 | G | A | splice_region_variant&synonymous_variant | LOW | c.1183C>T|p.Leu395Leu |
S281 |
5 | BAA04g13590 | A04 | 18961026 | G | A | missense_variant | MODERATE | c.829C>T|p.Pro277Ser |
S130 |
6 | BAA04g13590 | A04 | 18961309 | C | T | missense_variant | MODERATE | c.661G>A|p.Glu221Lys |
S180 |
7 | BAA04g13590 | A04 | 18961424 | C | T | missense_variant&splice_region_variant | MODERATE | c.643G>A|p.Glu215Lys |
S255 |
8 | BAA04g13590 | A04 | 18961443 | G | A | synonymous_variant | LOW | c.624C>T|p.Phe208Phe |
S87 |
9 | BAA04g13590 | A04 | 18961448 | C | T | missense_variant | MODERATE | c.619G>A|p.Glu207Lys |
S279 |
10 | BAA04g13590 | A04 | 18961466 | C | T | missense_variant | MODERATE | c.601G>A|p.Ala201Thr |
S159 S243 |
11 | BAA04g13590 | A04 | 18962052 | G | A | stop_gained | HIGH | c.268C>T|p.Arg90* |
S125 |
12 | BAA04g13590 | A04 | 18962108 | G | A | splice_region_variant&intron_variant | LOW | c.217-5C>T| |
S125 |
13 | BAA04g13590 | A04 | 18962554 | G | A | upstream_gene_variant | MODIFIER | c.-163C>T| |
S265 |
14 | BAA04g13590 | A04 | 18963019 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S230 |
15 | BAA04g13590 | A04 | 18964868 | C | T | upstream_gene_variant | MODIFIER | c.-2477G>A| |
S48 |
16 | BAA04g13590 | A04 | 18965045 | G | A | upstream_gene_variant | MODIFIER | c.-2654C>T| |
S282 |