List of variants in gene RET reported by Clinical Genetics and Genomics, Karolinska University 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe)	rs75030001	0.00001
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_020975.6(RET):c.433G>A (p.Val145Ile)	rs1311922451	0.00001
NM_020975.6(RET):c.1098G>C (p.Glu366Asp)	rs1362164894
NM_020975.6(RET):c.1832G>A (p.Cys611Tyr)	rs377767397
NM_020975.6(RET):c.1852T>G (p.Cys618Gly)	rs76262710
NM_020975.6(RET):c.1853G>C (p.Cys618Ser)	rs79781594
NM_020975.6(RET):c.1858T>C (p.Cys620Arg)	rs77316810
NM_020975.6(RET):c.1859G>T (p.Cys620Phe)	rs77503355
NM_020975.6(RET):c.1900T>G (p.Cys634Gly)	rs75076352
NM_020975.6(RET):c.2753T>C (p.Met918Thr)	rs74799832
NM_020975.6(RET):c.440_442del (p.Phe147del)	rs1837660523

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