List of variants in gene IL1RAPL1 reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014271.4(IL1RAPL1):c.1205A>G (p.Asn402Ser)	rs1427250835	0.00001
NM_014271.4(IL1RAPL1):c.1204A>G (p.Asn402Asp)
NM_014271.4(IL1RAPL1):c.1275A>T (p.Glu425Asp)
NM_014271.4(IL1RAPL1):c.1452A>G (p.Arg484=)	rs1601899898
NM_014271.4(IL1RAPL1):c.2038G>A (p.Ala680Thr)	rs1601900327
NM_014271.4(IL1RAPL1):c.349G>A (p.Ala117Thr)	rs778199033
NM_014271.4(IL1RAPL1):c.61G>T (p.Val21Phe)	rs1936510432
NM_014271.4(IL1RAPL1):c.87T>C (p.Asp29=)

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