List of variants in gene combination FBXO11, LOC100506235 studied for Inborn genetic diseases

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.149A>C (p.Gln50Pro)	rs781277953	0.00370
NM_001190274.2(FBXO11):c.105GCCCCAGCAGCAGCC[1] (p.37QQQPP[1])	rs747252806
NM_001190274.2(FBXO11):c.105GCCCCAGCAGCAGCC[3] (p.37QQQPP[3])	rs747252806
NM_001190274.2(FBXO11):c.149AGC[8] (p.Gln56dup)	rs746953076
NM_001190274.2(FBXO11):c.53G>T (p.Arg18Leu)
NM_001190274.2(FBXO11):c.66_71del (p.Gln25_Gln26del)
NM_001190274.2(FBXO11):c.68AGC[5] (p.Gln26dup)	rs771605473
NM_001190274.2(FBXO11):c.86A>G (p.Gln29Arg)
NM_001190274.2(FBXO11):c.96_107del (p.Pro33_Pro36del)	rs770886918

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