NFATC2IP[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2326294	NM_032815.4(NFATC2IP):c.11C>T (p.Pro4Leu)	NFATC2IP (P4L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312681	NM_032815.4(NFATC2IP):c.80G>C (p.Gly27Ala)	NFATC2IP (G27A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315974	NM_032815.4(NFATC2IP):c.116C>T (p.Ser39Phe)	NFATC2IP (S39F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196647	NM_032815.4(NFATC2IP):c.142G>A (p.Val48Met)	NFATC2IP (V48M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618793	NM_032815.4(NFATC2IP):c.173T>G (p.Ile58Ser)	NFATC2IP (I58S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196653	NM_032815.4(NFATC2IP):c.224C>G (p.Pro75Arg)	NFATC2IP (P75R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243461	NM_032815.4(NFATC2IP):c.242C>T (p.Pro81Leu)	NFATC2IP (P81L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387149	NM_032815.4(NFATC2IP):c.329G>T (p.Arg110Leu)	NFATC2IP (R110L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238866	NM_032815.4(NFATC2IP):c.383G>A (p.Gly128Glu)	NFATC2IP (G128E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2512004	NM_032815.4(NFATC2IP):c.455A>C (p.Glu152Ala)	NFATC2IP (E152A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388277	NM_032815.4(NFATC2IP):c.632C>T (p.Thr211Met)	NFATC2IP (T211M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513826	NM_032815.4(NFATC2IP):c.640C>T (p.Arg214Trp)	NFATC2IP (R214W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341303	NM_032815.4(NFATC2IP):c.784C>T (p.Pro262Ser)	NFATC2IP (P262S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196677	NM_032815.4(NFATC2IP):c.808C>T (p.Arg270Cys)	NFATC2IP (R270C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223747	NM_032815.4(NFATC2IP):c.815G>A (p.Arg272Gln)	NFATC2IP (R245Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340183	NM_032815.4(NFATC2IP):c.973G>A (p.Gly325Arg)	NFATC2IP (G298R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2340814	NM_032815.4(NFATC2IP):c.1124T>G (p.Met375Arg)	NFATC2IP (M290R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance