Related gene-specific medical variations for Gene (Select 7432) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 2365518	NM_003381.4(VIP):c.485C>T (p.Pro162Leu)	LINC02840, VIP (P161L +1 more)	Single nucleotide variant (missense variant)	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 2229018	NM_003381.4(VIP):c.311A>G (p.Glu104Gly)	LINC02840, VIP (E104G)	Single nucleotide variant (missense variant)	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 1098679	NM_003381.4(VIP):c.49A>T (p.Ser17Cys)	VIP (S17C)	Single nucleotide variant (missense variant)	See cases	GUncertain significance
Select item 796601	NM_003381.4(VIP):c.396C>T (p.Asp132=)	LINC02840, VIP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 776175	NM_003381.4(VIP):c.384A>C (p.Ala128=)	LINC02840, VIP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 774186	NM_003381.4(VIP):c.399C>T (p.Asn133=)	LINC02840, VIP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 722061	NM_003381.4(VIP):c.342C>T (p.Asn114=)	LINC02840, VIP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 710847	NM_003381.4(VIP):c.231-7G>A	LINC02840, VIP	Single nucleotide variant (intron variant)	not provided	GLikely benign