Related gene-specific medical variations for Gene (Select 84812) - ClinVar

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Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3307347	NM_032726.4(PLCD4):c.2195T>G (p.Ile732Ser)	PLCD4, ZNF142 (I732S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3307344	NM_032726.4(PLCD4):c.2276G>C (p.Gly759Ala)	PLCD4, ZNF142 (G759A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3307340	NM_032726.4(PLCD4):c.1516C>T (p.Arg506Cys)	PLCD4, ZNF142 (R506C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3307339	NM_032726.4(PLCD4):c.2269C>G (p.Leu757Val)	PLCD4, ZNF142 (L757V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3307337	NM_032726.4(PLCD4):c.1589G>A (p.Arg530His)	PLCD4, ZNF142 (R530H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3214459	NM_032726.4(PLCD4):c.2063G>A (p.Cys688Tyr)	PLCD4, ZNF142 (C688Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3214458	NM_032726.4(PLCD4):c.1780C>T (p.Arg594Cys)	PLCD4, ZNF142 (R594C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2651884	NM_032726.4(PLCD4):c.2007G>A (p.Gln669=)	PLCD4, ZNF142	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2617298	NM_032726.4(PLCD4):c.2132G>A (p.Arg711Gln)	PLCD4, ZNF142 (R711Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2609557	NM_032726.4(PLCD4):c.2174T>C (p.Met725Thr)	PLCD4, ZNF142 (M725T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2546906	NM_032726.4(PLCD4):c.2156C>T (p.Thr719Ile)	PLCD4, ZNF142 (T719I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2383776	NM_032726.4(PLCD4):c.1646G>A (p.Arg549His)	PLCD4, ZNF142 (R549H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2374351	NM_032726.4(PLCD4):c.1561T>C (p.Ser521Pro)	PLCD4, ZNF142 (S521P)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2346245	NM_032726.4(PLCD4):c.2119G>A (p.Asp707Asn)	PLCD4, ZNF142 (D707N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2338933	NM_032726.4(PLCD4):c.2029A>G (p.Asn677Asp)	PLCD4, ZNF142 (N677D)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2334900	NM_032726.4(PLCD4):c.1645C>T (p.Arg549Cys)	PLCD4, ZNF142 (R549C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2298004	NM_032726.4(PLCD4):c.1988G>A (p.Arg663His)	PLCD4, ZNF142 (R663H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2226382	NM_032726.4(PLCD4):c.1792G>A (p.Gly598Ser)	PLCD4, ZNF142 (G598S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2207102	NM_032726.4(PLCD4):c.2189G>A (p.Arg730His)	PLCD4, ZNF142 (R730H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2206234	NM_032726.4(PLCD4):c.1722G>A (p.Met574Ile)	PLCD4, ZNF142 (M574I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2205385	NM_032726.4(PLCD4):c.1925T>C (p.Val642Ala)	PLCD4, ZNF142 (V642A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 21