Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19200 | A03 | 8514499 | C | T | synonymous_variant | LOW | c.1713G>A|p.Lys571Lys |
S163 |
2 | BAA03g19200 | A03 | 8514600 | C | T | missense_variant | MODERATE | c.1612G>A|p.Asp538Asn |
S159 S243 S298 S299 |
3 | BAA03g19200 | A03 | 8515269 | G | A | synonymous_variant | LOW | c.1245C>T|p.Tyr415Tyr |
S284 |
4 | BAA03g19200 | A03 | 8515286 | C | T | missense_variant | MODERATE | c.1228G>A|p.Ala410Thr |
S240 |
5 | BAA03g19200 | A03 | 8516119 | G | A | missense_variant&splice_region_variant | MODERATE | c.790C>T|p.Leu264Phe |
S184 |
6 | BAA03g19200 | A03 | 8516562 | C | T | missense_variant | MODERATE | c.580G>A|p.Asp194Asn |
S58 |
7 | BAA03g19200 | A03 | 8517177 | G | A | splice_region_variant&intron_variant | LOW | c.204+3C>T| |
S261 |
8 | BAA03g19200 | A03 | 8517197 | G | A | missense_variant | MODERATE | c.187C>T|p.Leu63Phe |
S192 |
9 | BAA03g19200 | A03 | 8517401 | G | A | missense_variant | MODERATE | c.82C>T|p.Leu28Phe |
S176 |
10 | BAA03g19200 | A03 | 8517662 | C | T | upstream_gene_variant | MODIFIER | c.-180G>A| |
S213 S4 S6 |
11 | BAA03g19200 | A03 | 8517957 | C | T | upstream_gene_variant | MODIFIER | c.-475G>A| |
S260 |
12 | BAA03g19200 | A03 | 8520526 | G | A | upstream_gene_variant | MODIFIER | c.-3044C>T| |
S128 |
13 | BAA03g19200 | A03 | 8521341 | C | T | upstream_gene_variant | MODIFIER | c.-3859G>A| |
S18 |
14 | BAA03g19200 | A03 | 8522282 | C | T | upstream_gene_variant | MODIFIER | c.-4800G>A| |
S156 |