List of variants in gene FLVCR1 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met)	rs149834738	0.00032
NM_014053.4(FLVCR1):c.1019C>T (p.Thr340Ile)	rs754655924	0.00001
NM_014053.4(FLVCR1):c.1307+5G>T	rs777846238	0.00001
NM_014053.4(FLVCR1):c.1120G>A (p.Gly374Arg)
NM_014053.4(FLVCR1):c.1319C>G (p.Thr440Ser)
NM_014053.4(FLVCR1):c.30G>A (p.Ala10=)	rs1572001189

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