Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.32786283A>G | CA3222712 | NPR3 | c.1564A>G (p.Asn522Asp) c.913A>G (p.Asn305Asp) c.1561A>G (p.Asn521Asp) c.916A>G (p.Asn306Asp) c.895A>G (p.Asn299Asp) c.844A>G (p.Asn282Asp) c.787A>G (p.Asn263Asp) c.793A>G (p.Asn265Asp) c.1441A>G (p.Asn481Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.32786283A>T | CA116857589 | NPR3 | c.1564A>T (p.Asn522Tyr) c.913A>T (p.Asn305Tyr) c.1561A>T (p.Asn521Tyr) c.916A>T (p.Asn306Tyr) c.895A>T (p.Asn299Tyr) c.844A>T (p.Asn282Tyr) c.787A>T (p.Asn263Tyr) c.793A>T (p.Asn265Tyr) c.1441A>T (p.Asn481Tyr) | dbSNP gnomAD v4 |
5 | g.32786283A>C | CA116857588 | NPR3 | c.1564A>C (p.Asn522His) c.913A>C (p.Asn305His) c.1561A>C (p.Asn521His) c.916A>C (p.Asn306His) c.895A>C (p.Asn299His) c.844A>C (p.Asn282His) c.787A>C (p.Asn263His) c.793A>C (p.Asn265His) c.1441A>C (p.Asn481His) | dbSNP |