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

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2540072	NM_003381.4(VIP):c.60C>G (p.Phe20Leu)	VIP (F20L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209362	NM_003381.4(VIP):c.73G>C (p.Ala25Pro)	VIP (A25P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278222	NM_003381.4(VIP):c.182T>C (p.Leu61Ser)	VIP (L61S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188563	NM_003381.4(VIP):c.203A>G (p.Asn68Ser)	VIP (N68S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188564	NM_003381.4(VIP):c.254T>A (p.Val85Asp)	LINC02840, VIP (V85D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3332067	NM_003381.4(VIP):c.271A>G (p.Ser91Gly)	LINC02840, VIP (S91G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2229018	NM_003381.4(VIP):c.311A>G (p.Glu104Gly)	LINC02840, VIP (E104G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553809	NM_003381.4(VIP):c.331G>A (p.Val111Ile)	LINC02840, VIP (V111I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2282814	NM_003381.4(VIP):c.337A>T (p.Ser113Cys)	LINC02840, VIP (S113C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3188565	NM_003381.4(VIP):c.398A>G (p.Asn133Ser)	LINC02840, VIP (N132S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3332066	NM_003381.4(VIP):c.441G>C (p.Leu147Phe)	LINC02840, VIP (L146F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3188567	NM_003381.4(VIP):c.448A>T (p.Ile150Phe)	LINC02840, VIP (I149F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2527381	NM_003381.4(VIP):c.457G>A (p.Gly153Arg)	LINC02840, VIP (G153R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2224416	NM_003381.4(VIP):c.469A>C (p.Ser157Arg)	LINC02840, VIP (S156R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365518	NM_003381.4(VIP):c.485C>T (p.Pro162Leu)	LINC02840, VIP (P161L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance