List of variants in gene RET reported by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.884C>G (p.Thr295Arg)	rs758159521	0.00003
NM_020975.6(RET):c.406G>A (p.Glu136Lys)	rs79014735	0.00002
NM_020975.6(RET):c.867+4del	rs398124368	0.00002
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.1852T>G (p.Cys618Gly)	rs76262710
NM_020975.6(RET):c.1859G>A (p.Cys620Tyr)	rs77503355
NM_020975.6(RET):c.2753T>C (p.Met918Thr)	rs74799832
NM_020975.6(RET):c.860G>A (p.Arg287Gln)	rs1564491460
NM_020975.6(RET):c.95C>T (p.Ser32Leu)	rs76764689

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