Related gene-specific medical variations for Gene (Select 91661) - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198182	NM_001040185.3(ZNF765):c.934T>C (p.Ser312Pro)	ZNF765, ZNF765-ZNF761 (S312P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198181	NM_001040185.3(ZNF765):c.915C>G (p.Asp305Glu)	ZNF765, ZNF765-ZNF761 (D305E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198180	NM_001040185.3(ZNF765):c.869G>A (p.Arg290His)	ZNF765, ZNF765-ZNF761 (R237H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198179	NM_001040185.3(ZNF765):c.745G>C (p.Gly249Arg)	ZNF765, ZNF765-ZNF761 (G196R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198178	NM_001040185.3(ZNF765):c.575A>G (p.Tyr192Cys)	ZNF765, ZNF765-ZNF761 (Y139C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198177	NM_001040185.3(ZNF765):c.418C>G (p.Leu140Val)	ZNF765, ZNF765-ZNF761 (L87V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198176	NM_001040185.3(ZNF765):c.290T>C (p.Ile97Thr)	ZNF765, ZNF765-ZNF761 (I44T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198175	NM_001040185.3(ZNF765):c.1491A>C (p.Glu497Asp)	ZNF765, ZNF765-ZNF761 (E497D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198174	NM_001040185.3(ZNF765):c.1421C>A (p.Thr474Asn)	ZNF765, ZNF765-ZNF761 (T421N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198173	NM_001040185.3(ZNF765):c.1237T>G (p.Cys413Gly)	ZNF765, ZNF765-ZNF761 (C413G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198172	NM_001040185.3(ZNF765):c.1213C>A (p.His405Asn)	ZNF765, ZNF765-ZNF761 (H352N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198171	NM_001040185.3(ZNF765):c.106G>T (p.Val36Leu)	ZNF765, ZNF765-ZNF761 (V36L)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2622097	NM_001040185.3(ZNF765):c.103G>C (p.Asp35His)	ZNF765, ZNF765-ZNF761 (D35H)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2593480	NM_001040185.3(ZNF765):c.772G>A (p.Val258Ile)	ZNF765, ZNF765-ZNF761 (V258I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569084	NM_001040185.3(ZNF765):c.1204C>T (p.Arg402Cys)	ZNF765, ZNF765-ZNF761 (R349C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555932	NM_001040185.3(ZNF765):c.589C>G (p.Leu197Val)	ZNF765, ZNF765-ZNF761 (L197V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548829	NM_001040185.3(ZNF765):c.164T>C (p.Met55Thr)	ZNF765, ZNF765-ZNF761 (M2T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536852	NM_001040185.3(ZNF765):c.323G>T (p.Gly108Val)	ZNF765, ZNF765-ZNF761 (G108V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517065	NM_001040185.3(ZNF765):c.950A>G (p.His317Arg)	ZNF765, ZNF765-ZNF761 (H264R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492114	NM_001040185.3(ZNF765):c.397A>T (p.Asn133Tyr)	ZNF765, ZNF765-ZNF761 (N80Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480752	NM_001040185.3(ZNF765):c.959T>C (p.Ile320Thr)	ZNF765, ZNF765-ZNF761 (I320T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458114	NM_001040185.3(ZNF765):c.209A>G (p.His70Arg)	ZNF765, ZNF765-ZNF761 (H70R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411051	NM_001040185.3(ZNF765):c.1037G>A (p.Arg346His)	ZNF765, ZNF765-ZNF761 (R293H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394277	NM_001040185.3(ZNF765):c.578G>T (p.Gly193Val)	ZNF765, ZNF765-ZNF761 (G193V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368430	NM_001040185.3(ZNF765):c.1210C>T (p.Leu404Phe)	ZNF765, ZNF765-ZNF761 (L351F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345868	NM_001040185.3(ZNF765):c.868C>T (p.Arg290Cys)	ZNF765, ZNF765-ZNF761 (R237C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313579	NM_001040185.3(ZNF765):c.283C>A (p.His95Asn)	ZNF765-ZNF761, ZNF765 (H42N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298891	NM_001040185.3(ZNF765):c.694A>G (p.Lys232Glu)	ZNF765, ZNF765-ZNF761 (K232E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294839	NM_001040185.3(ZNF765):c.1498G>A (p.Asp500Asn)	ZNF765, ZNF765-ZNF761 (D447N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266268	NM_001040185.3(ZNF765):c.1567G>A (p.Val523Met)	ZNF765, ZNF765-ZNF761 (V523M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248930	NM_001040185.3(ZNF765):c.374G>A (p.Arg125Gln)	ZNF765, ZNF765-ZNF761 (R125Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235640	NM_001040185.3(ZNF765):c.1126G>C (p.Val376Leu)	ZNF765, ZNF765-ZNF761 (V376L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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Links from Gene

Items: 32