"Ambry Genetics"[submitter] AND "IQCF6"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2316574	NM_001368369.1(IQCF6):c.424G>A (p.Glu142Lys)	IQCF6 (E103K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254097	NM_001368369.1(IQCF6):c.406C>T (p.Arg136Trp)	IQCF6 (R117W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286360	NM_001368369.1(IQCF6):c.391G>C (p.Glu131Gln)	IQCF6 (E92Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335444	NM_001368369.1(IQCF6):c.379C>G (p.Arg127Gly)	IQCF6 (R108G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483989	NM_001368369.1(IQCF6):c.349T>C (p.Trp117Arg)	IQCF6 (W117R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407543	NM_001368369.1(IQCF6):c.314G>A (p.Arg105His)	IQCF6 (R86H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592721	NM_001368369.1(IQCF6):c.313C>T (p.Arg105Cys)	IQCF6 (R86C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607925	NM_001368369.1(IQCF6):c.245A>G (p.Glu82Gly)	IQCF6 (E63G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110457	NM_001368369.1(IQCF6):c.236C>A (p.Thr79Asn)	IQCF6 (T40N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389370	NM_001368369.1(IQCF6):c.211C>T (p.Arg71Trp)	IQCF6 (R52W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318516	NM_001368369.1(IQCF6):c.151A>G (p.Arg51Gly)	IQCF6 (R12G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance