"Ambry Genetics"[submitter] AND "NFIC"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2220032	NM_001245002.2(NFIC):c.110G>A (p.Arg37Gln)	NFIC (R37Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621601	NM_001245002.2(NFIC):c.163C>T (p.Arg55Cys)	NFIC (R46C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285261	NM_001245002.2(NFIC):c.283A>G (p.Ser95Gly)	NFIC (S95G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461865	NM_001245002.2(NFIC):c.289A>G (p.Thr97Ala)	NFIC (T97A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299528	NM_001245002.2(NFIC):c.307G>T (p.Gly103Cys)	NFIC (G103C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507625	NM_001245002.2(NFIC):c.550G>C (p.Val184Leu)	NFIC (V175L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361476	NM_001245002.2(NFIC):c.554G>A (p.Arg185His)	NFIC (R176H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383412	NM_001245002.2(NFIC):c.560G>A (p.Arg187Gln)	NFIC (R178Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342757	NM_001245002.2(NFIC):c.566C>A (p.Ala189Glu)	NFIC (A180E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592651	NM_001245002.2(NFIC):c.638C>T (p.Thr213Met)	NFIC (T204M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304811	NM_001245002.2(NFIC):c.643G>T (p.Asp215Tyr)	NFIC (D206Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463259	NM_001245002.2(NFIC):c.670G>A (p.Gly224Ser)	NFIC (G215S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231716	NM_001245002.2(NFIC):c.682G>A (p.Val228Ile)	NFIC (V219I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396918	NM_001245002.2(NFIC):c.715G>A (p.Val239Met)	NFIC (V239M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373244	NM_001245002.2(NFIC):c.794C>G (p.Thr265Ser)	NFIC (T256S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197654	NM_001245002.2(NFIC):c.840G>C (p.Lys280Asn)	NFIC (K280N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197656	NM_001245002.2(NFIC):c.853G>C (p.Gly285Arg)	NFIC (G276R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507582	NM_001245002.2(NFIC):c.890G>A (p.Gly297Asp)	NFIC (G297D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313811	NM_001245002.2(NFIC):c.946G>A (p.Asp316Asn)	NFIC (D316N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313290	NM_001245002.2(NFIC):c.949A>G (p.Met317Val)	NFIC (M308V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390330	NM_001245002.2(NFIC):c.1013C>T (p.Pro338Leu)	NFIC (P329L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540328	NM_001245002.2(NFIC):c.1034G>A (p.Arg345His)	NFIC (R336H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299529	NM_001245002.2(NFIC):c.1061G>A (p.Arg354Gln)	NFIC (R345Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299526	NM_001245002.2(NFIC):c.1066G>A (p.Val356Ile)	NFIC (V347I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299525	NM_001245002.2(NFIC):c.1117C>A (p.Leu373Met)	NFIC (L364M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336318	NM_001245002.2(NFIC):c.1243G>C (p.Asp415His)	NFIC (D406H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197594	NM_001245002.2(NFIC):c.1277G>A (p.Gly426Glu)	NFIC (G417E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285766	NM_001245002.2(NFIC):c.1334C>T (p.Pro445Leu)	NFIC (P436L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356197	NM_001245002.2(NFIC):c.1340C>T (p.Pro447Leu)	NFIC (P447L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241641	NM_001245002.2(NFIC):c.1352G>A (p.Arg451Gln)	NFIC (R451Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508067	NM_001245002.2(NFIC):c.1412C>T (p.Pro471Leu)	NFIC (P471L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538912	NM_001245002.2(NFIC):c.1424C>G (p.Ser475Cys)	NFIC (S466C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197616	NM_001245002.2(NFIC):c.1433C>T (p.Pro478Leu)	NFIC (R427C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409699	NM_001245002.2(NFIC):c.1433C>G (p.Pro478Arg)	NFIC (P469R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411768	NM_001245002.2(NFIC):c.1456C>G (p.Arg486Gly)	NFIC (R477G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2513287	NM_001245002.2(NFIC):c.1499A>G (p.Tyr500Cys)	NFIC (Y491C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 36