List of variants in gene CDKN2A reported as not provided

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr)	rs3731249	0.02007
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser)	rs6413464	0.00527
NM_000077.5(CDKN2A):c.174A>C (p.Arg58=)	rs201208890	0.00273
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)	rs116150891	0.00248
NM_000077.5(CDKN2A):c.458-491C>T	rs181044510	0.00229
NM_000077.5(CDKN2A):c.150+37G>C	rs45456595	0.00212
NM_000077.5(CDKN2A):c.273G>A (p.Leu91=)	rs4987127	0.00045
NM_000077.5(CDKN2A):c.458-492G>C	rs527814073	0.00021
NM_000077.5(CDKN2A):c.325G>C (p.Ala109Pro)	rs372481694	0.00009
NM_000077.5(CDKN2A):c.146T>C (p.Ile49Thr)	rs199907548	0.00006
NM_000077.5(CDKN2A):c.150+20C>T	rs550846229	0.00002
NM_000077.5(CDKN2A):c.149A>T (p.Gln50Leu)	rs587778189
NM_000077.5(CDKN2A):c.150+1G>T	rs2131111833
NM_000077.5(CDKN2A):c.151-1G>A	rs730881677
NM_000077.5(CDKN2A):c.151-1G>T	rs730881677
NM_000077.5(CDKN2A):c.151-2A>C	rs1554654224
NM_000077.5(CDKN2A):c.151-2A>G	rs1554654224
NM_000077.5(CDKN2A):c.151-2A>T	rs1554654224
NM_000077.5(CDKN2A):c.16G>A (p.Gly6Arg)	rs587778190
NM_000077.5(CDKN2A):c.203C>T (p.Ala68Val)	rs1060501260
NM_000077.5(CDKN2A):c.250G>A (p.Asp84Asn)	rs11552822
NM_000077.5(CDKN2A):c.297G>T (p.Arg99=)	rs587778191
NM_000077.5(CDKN2A):c.322G>A (p.Asp108Asn)	rs121913381
NM_000077.5(CDKN2A):c.457+1G>A	rs1587330312
NM_000077.5(CDKN2A):c.457+1G>T	rs1587330312
NM_000077.5(CDKN2A):c.457+2T>C	rs1587330309
NM_000077.5(CDKN2A):c.458-1G>A	rs2131079543

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