List of variants in gene RET reported by Human Genomics Unit, Institute for molecular medicine Finland (FIMM)

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.2437C>T (p.Arg813Trp)	rs779996040	0.00001
NM_020975.6(RET):c.111G>A (p.Trp37Ter)	rs1564489315
NM_020975.6(RET):c.1825T>C (p.Cys609Arg)	rs77558292
NM_020975.6(RET):c.1831T>C (p.Cys611Arg)	rs377767391
NM_020975.6(RET):c.1858T>C (p.Cys620Arg)	rs77316810
NM_020975.6(RET):c.2865dup (p.Pro956fs)	rs1564500612
NM_020975.6(RET):c.3143del (p.Leu1048fs)	rs1564501934
NM_020975.6(RET):c.440T>C (p.Phe147Ser)	rs1564490097
NM_020975.6(RET):c.604G>C (p.Val202Leu)	rs751572082

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