List of variants reported as uncertain significance for Peutz-Jeghers syndrome; Melanoma, cutaneous malignant, susceptibility to, 1; Familial pancreatic carcinoma; Germ cell tumor of testis by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.1069G>A (p.Glu357Lys)	rs759473833	0.00006
NM_000455.5(STK11):c.1254C>G (p.Cys418Trp)	rs587780715	0.00005
NM_000455.5(STK11):c.588C>T (p.Gly196=)	rs769309428	0.00003
NM_000455.5(STK11):c.911G>A (p.Arg304Gln)	rs376280361	0.00003
NM_000455.5(STK11):c.608C>T (p.Pro203Leu)	rs587782379	0.00002
NM_000455.5(STK11):c.1208A>G (p.Lys403Arg)	rs587781633	0.00001
NM_000455.5(STK11):c.448G>A (p.Val150Met)	rs1225872771	0.00001
NM_000455.5(STK11):c.61G>A (p.Gly21Ser)	rs1064793751	0.00001
NM_000455.5(STK11):c.833G>A (p.Cys278Tyr)	rs2080782575	0.00001
NM_000455.5(STK11):c.947C>G (p.Ala316Gly)	rs751709130	0.00001
NM_000455.5(STK11):c.1123G>A (p.Glu375Lys)	rs2080821619
NM_000455.5(STK11):c.1274G>T (p.Arg425Leu)	rs730881992
NM_000455.5(STK11):c.14A>G (p.Asp5Gly)	rs1178249537
NM_000455.5(STK11):c.54G>A (p.Met18Ile)	rs755436889
NM_000455.5(STK11):c.712A>G (p.Ile238Val)	rs2080777009
NM_000455.5(STK11):c.749C>T (p.Thr250Met)	rs876661238

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