Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g31680 | A08 | 21004840 | G | A | stop_gained | HIGH | c.2893C>T|p.Gln965* |
S116 |
2 | BAA08g31680 | A08 | 21004893 | C | T | missense_variant | MODERATE | c.2840G>A|p.Gly947Glu |
S168 |
3 | BAA08g31680 | A08 | 21005130 | G | A | synonymous_variant | LOW | c.2692C>T|p.Leu898Leu |
S11 |
4 | BAA08g31680 | A08 | 21005736 | C | T | missense_variant | MODERATE | c.2380G>A|p.Asp794Asn |
S173 |
5 | BAA08g31680 | A08 | 21006471 | G | A | missense_variant | MODERATE | c.1954C>T|p.Leu652Phe |
S242 |
6 | BAA08g31680 | A08 | 21006904 | C | T | missense_variant | MODERATE | c.1787G>A|p.Arg596Lys |
S47 |
7 | BAA08g31680 | A08 | 21008823 | C | T | missense_variant | MODERATE | c.1019G>A|p.Ser340Asn |
S44 |
8 | BAA08g31680 | A08 | 21009067 | G | A | missense_variant | MODERATE | c.895C>T|p.His299Tyr |
S187 |
9 | BAA08g31680 | A08 | 21009308 | C | T | missense_variant | MODERATE | c.770G>A|p.Gly257Glu |
S234 |
10 | BAA08g31680 | A08 | 21009404 | G | A | splice_region_variant&intron_variant | LOW | c.681-7C>T| |
S35 |