List of variants in gene F5 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.5290A>G (p.Met1764Val)	rs6030	0.29437
NM_000130.5(F5):c.2573A>G (p.Lys858Arg)	rs4524	0.24159
NM_000130.5(F5):c.5265A>G (p.Ile1755Met)	rs41272455	0.00113
NM_000130.5(F5):c.1106C>T (p.Ala369Val)	rs200934105	0.00006
NM_000130.5(F5):c.910G>A (p.Gly304Arg)	rs747353298	0.00001
NM_000130.5(F5):c.1265T>C (p.Ile422Thr)	rs2101827179
NM_000130.5(F5):c.1322G>A (p.Arg441His)
NM_000130.5(F5):c.2539A>G (p.Ile847Val)
NM_000130.5(F5):c.2563G>A (p.Gly855Arg)
NM_000130.5(F5):c.3065A>C (p.Lys1022Thr)
NM_000130.5(F5):c.3220A>G (p.Asn1074Asp)
NM_000130.5(F5):c.3335G>C (p.Ser1112Thr)
NM_000130.5(F5):c.6230T>C (p.Ile2077Thr)	rs2101803535
NM_000130.5(F5):c.6404C>T (p.Ala2135Val)
NM_000130.5(F5):c.6530T>A (p.Ile2177Asn)	rs2101801070

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