Related gene-specific medical variations for Gene (Select 285989) - ClinVar

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Links from Gene

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198406	NM_213603.3(ZNF789):c.781G>A (p.Asp261Asn)	ZNF394, ZNF789 (D166N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198405	NM_213603.3(ZNF789):c.456G>C (p.Arg152Ser)	ZNF394, ZNF789 (R152S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198404	NM_213603.3(ZNF789):c.359A>C (p.Glu120Ala)	ZNF394, ZNF789 (E103A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198402	NM_213603.3(ZNF789):c.1012C>T (p.Pro338Ser)	ZNF394, ZNF789 (P243S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621408	NM_213603.3(ZNF789):c.388C>G (p.His130Asp)	ZNF394, ZNF789 (H113D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615485	NM_213603.3(ZNF789):c.1205G>A (p.Cys402Tyr)	ZNF394, ZNF789 (C364Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613791	NM_213603.3(ZNF789):c.538A>G (p.Lys180Glu)	ZNF394, ZNF789 (K180E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529120	NM_213603.3(ZNF789):c.824A>G (p.His275Arg)	ZNF394, ZNF789 (H180R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486752	NM_213603.3(ZNF789):c.1130C>T (p.Thr377Met)	ZNF394, ZNF789 (T360M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485805	NM_213603.3(ZNF789):c.961G>T (p.Ala321Ser)	ZNF394, ZNF789 (A304S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485606	NM_213603.3(ZNF789):c.1222T>C (p.Trp408Arg)	ZNF394, ZNF789 (W313R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2465782	NM_213603.3(ZNF789):c.662G>T (p.Arg221Ile)	ZNF394, ZNF789 (R126I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393803	NM_213603.3(ZNF789):c.389A>G (p.His130Arg)	ZNF394, ZNF789 (H113R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391051	NM_213603.3(ZNF789):c.670T>C (p.Phe224Leu)	ZNF394, ZNF789 (F129L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360083	NM_213603.3(ZNF789):c.970C>T (p.Arg324Trp)	ZNF394, ZNF789 (R229W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337113	NM_213603.3(ZNF789):c.437G>C (p.Ser146Thr)	ZNF394, ZNF789 (S129T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310366	NM_213603.3(ZNF789):c.703G>A (p.Gly235Arg)	ZNF394, ZNF789 (G235R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286758	NM_213603.3(ZNF789):c.1238T>C (p.Ile413Thr)	ZNF394, ZNF789 (I396T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238393	NM_213603.3(ZNF789):c.808G>A (p.Ala270Thr)	ZNF394, ZNF789 (A270T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232895	NM_213603.3(ZNF789):c.911A>C (p.Gln304Pro)	ZNF394, ZNF789 (Q304P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 20