List of variants in gene CDKN1B reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.426G>A (p.Thr142=)	rs149775942	0.00366
NM_004064.5(CDKN1B):c.577C>T (p.Leu193Phe)	rs73281150	0.00338
NM_004064.5(CDKN1B):c.543C>G (p.Ala181=)	rs140177202	0.00064
NM_004064.5(CDKN1B):c.356T>C (p.Ile119Thr)	rs142833529	0.00057
NM_004064.5(CDKN1B):c.407A>G (p.Asp136Gly)	rs546234840	0.00020
NM_004064.5(CDKN1B):c.482C>G (p.Ser161Cys)	rs373917399	0.00014
NM_004064.5(CDKN1B):c.75G>A (p.Lys25=)	rs367611328	0.00009
NM_004064.5(CDKN1B):c.471C>A (p.Thr157=)	rs777875072	0.00004
NM_004064.5(CDKN1B):c.420C>T (p.Ser140=)	rs965015279	0.00001
NM_004064.5(CDKN1B):c.-31AG[1]	rs774454456
NM_004064.5(CDKN1B):c.219G>A (p.Lys73=)	rs573353679
NM_004064.5(CDKN1B):c.55A>C (p.Arg19=)

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