List of variants in gene NCAM1 studied for not specified

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_181351.5(NCAM1):c.322G>A (p.Ala108Thr)	rs188950571	0.00001
NM_181351.5(NCAM1):c.1056A>T (p.Glu352Asp)	rs2548439337
NM_181351.5(NCAM1):c.1090-386C>T	rs2548516223
NM_181351.5(NCAM1):c.1090-429G>T	rs2548515967
NM_181351.5(NCAM1):c.1246C>T (p.Pro416Ser)	rs2548521704
NM_181351.5(NCAM1):c.1405C>T (p.Pro469Ser)
NM_181351.5(NCAM1):c.1762G>A (p.Ala588Thr)	rs2548534517
NM_181351.5(NCAM1):c.1798G>A (p.Ala600Thr)	rs2548534674
NM_181351.5(NCAM1):c.1831G>A (p.Glu611Lys)
NM_181351.5(NCAM1):c.2002C>T (p.His668Tyr)	rs2548639592
NM_181351.5(NCAM1):c.2083G>A (p.Ala695Thr)
NM_181351.5(NCAM1):c.2086G>A (p.Ala696Thr)	rs1945952650
NM_181351.5(NCAM1):c.2110G>A (p.Ala704Thr)	rs1555123080
NM_181351.5(NCAM1):c.2165G>A (p.Gly722Glu)	rs2548681573
NM_181351.5(NCAM1):c.2167G>C (p.Ala723Pro)	rs1242652487
NM_181351.5(NCAM1):c.2218G>T (p.Asp740Tyr)	rs2548681772
NM_181351.5(NCAM1):c.2269G>A (p.Val757Ile)	rs2548681949
NM_181351.5(NCAM1):c.2380G>A (p.Glu794Lys)	rs2548687029

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