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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2329257	NM_001321142.2(CIDEC):c.680C>T (p.Ser227Leu)	CIDEC (S240L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271837	NM_001321142.2(CIDEC):c.676G>C (p.Ala226Pro)	CIDEC (A239P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412194	NM_001321142.2(CIDEC):c.585G>A (p.Met195Ile)	CIDEC (M205I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 434768	NM_001321142.2(CIDEC):c.467T>C (p.Ile156Thr)	CIDEC (I156T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475855	NM_001321142.2(CIDEC):c.424C>T (p.Arg142Cys)	CIDEC (R142C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290009	NM_001321142.2(CIDEC):c.389T>C (p.Leu130Pro)	CIDEC (L140P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144988	NM_001321142.2(CIDEC):c.380C>T (p.Pro127Leu)	CIDEC (P127L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252784	NM_001321142.2(CIDEC):c.356C>T (p.Pro119Leu)	CIDEC (P119L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144987	NM_001321142.2(CIDEC):c.340C>G (p.Gln114Glu)	CIDEC (Q40E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617664	NM_001321142.2(CIDEC):c.329T>C (p.Leu110Pro)	CIDEC (L123P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612947	NM_001321142.2(CIDEC):c.292T>C (p.Phe98Leu)	CIDEC (F108L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144986	NM_001321142.2(CIDEC):c.160G>C (p.Val54Leu)	CIDEC (V67L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208593	NM_001321142.2(CIDEC):c.155G>A (p.Arg52Gln)	CIDEC (R65Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393147	NM_001321142.2(CIDEC):c.127C>T (p.Arg43Trp)	CIDEC (R56W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3144991	NM_001321142.2(CIDEC):c.97T>C (p.Ser33Pro)	CIDEC (S33P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215540	NM_001321142.2(CIDEC):c.88C>G (p.Gln30Glu)	CIDEC (Q30E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance