List of variants studied for parathyroid gland disorder by Database of Curated Mutations (DoCM)

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Total variants: 16

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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.1826G>A (p.Cys609Tyr)	rs77939446	0.00001
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_001904.4(CTNNB1):c.109T>G (p.Ser37Ala)	rs121913228
NM_001904.4(CTNNB1):c.98C>G (p.Ser33Cys)	rs121913400
NM_020975.6(RET):c.1852T>C (p.Cys618Arg)	rs76262710
NM_020975.6(RET):c.1853G>A (p.Cys618Tyr)	rs79781594
NM_020975.6(RET):c.1859G>A (p.Cys620Tyr)	rs77503355
NM_020975.6(RET):c.1888T>C (p.Cys630Arg)	rs377767404
NM_020975.6(RET):c.1901G>A (p.Cys634Tyr)	rs75996173
NM_020975.6(RET):c.1902C>G (p.Cys634Trp)	rs77709286
NM_020975.6(RET):c.2304G>C (p.Glu768Asp)	rs78014899
NM_020975.6(RET):c.2410G>C (p.Val804Leu)	rs79658334
NM_020975.6(RET):c.2647_2648delinsTT (p.Ala883Phe)	rs377767429
NM_020975.6(RET):c.2753T>C (p.Met918Thr)	rs74799832

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