List of variants in gene CDKN1B reported 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
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004064.5(CDKN1B):c.-266C>G	rs3093728	0.00372
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.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.154A>C (p.Met52Leu)	rs760647541	0.00003
NM_004064.5(CDKN1B):c.349C>T (p.Pro117Ser)	rs754936421	0.00002
NM_004064.5(CDKN1B):c.420C>T (p.Ser140=)	rs965015279	0.00001
NM_004064.5(CDKN1B):c.51C>A (p.Asp17Glu)	rs552533838	0.00001
NM_004064.5(CDKN1B):c.-31AG[1]	rs774454456
NM_004064.5(CDKN1B):c.215dup (p.Lys73fs)	rs1555085549
NM_004064.5(CDKN1B):c.219G>A (p.Lys73=)	rs573353679
NM_004064.5(CDKN1B):c.220T>C (p.Tyr74His)	rs1555085554
NM_004064.5(CDKN1B):c.320del (p.Gln107fs)	rs755301027
NM_004064.5(CDKN1B):c.370A>G (p.Asn124Asp)	rs1946496907
NM_004064.5(CDKN1B):c.55A>C (p.Arg19=)

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