Related gene-specific medical variations for Gene (Select 58491) - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259318	NM_001370215.1(ZNF71):c.874C>T (p.His292Tyr)	ZNF71, ZNF71-SMIM17 (H232Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259316	NM_001370215.1(ZNF71):c.511T>A (p.Phe171Ile)	ZNF71, ZNF71-SMIM17 (F171I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259315	NM_001370215.1(ZNF71):c.724G>A (p.Gly242Ser)	ZNF71, ZNF71-SMIM17 (G242S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259314	NM_001370215.1(ZNF71):c.1516T>A (p.Ser506Thr)	ZNF71, ZNF71-SMIM17 (S446T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259313	NM_001370215.1(ZNF71):c.257C>T (p.Thr86Met)	ZNF71, ZNF71-SMIM17 (T86M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197923	NM_001370215.1(ZNF71):c.1129C>G (p.Gln377Glu)	ZNF71, ZNF71-SMIM17 (Q317E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197922	NM_001370215.1(ZNF71):c.1128C>G (p.His376Gln)	ZNF71, ZNF71-SMIM17 (H376Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197921	NM_001370215.1(ZNF71):c.268G>A (p.Ala90Thr)	ZNF71, ZNF71-SMIM17 (A30T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197920	NM_001370215.1(ZNF71):c.838G>A (p.Gly280Ser)	ZNF71, ZNF71-SMIM17 (G220S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197919	NM_001370215.1(ZNF71):c.535A>G (p.Lys179Glu)	ZNF71, ZNF71-SMIM17 (K119E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197918	NM_001370215.1(ZNF71):c.500G>A (p.Arg167His)	ZNF71, ZNF71-SMIM17 (R107H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197917	NM_001370215.1(ZNF71):c.481G>T (p.Ala161Ser)	ZNF71, ZNF71-SMIM17 (A101S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197916	NM_001370215.1(ZNF71):c.325C>T (p.Arg109Trp)	ZNF71, ZNF71-SMIM17 (R109W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197915	NM_001370215.1(ZNF71):c.1480G>A (p.Gly494Ser)	ZNF71, ZNF71-SMIM17 (G494S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197913	NM_001370215.1(ZNF71):c.1191G>C (p.Gln397His)	ZNF71, ZNF71-SMIM17 (Q337H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613970	NM_001370215.1(ZNF71):c.307A>C (p.Ser103Arg)	ZNF71, ZNF71-SMIM17 (S103R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613186	NM_001370215.1(ZNF71):c.913G>C (p.Gly305Arg)	ZNF71, ZNF71-SMIM17 (G245R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597711	NM_001370215.1(ZNF71):c.241G>A (p.Ala81Thr)	ZNF71, ZNF71-SMIM17 (A21T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594215	NM_001370215.1(ZNF71):c.467C>T (p.Pro156Leu)	ZNF71, ZNF71-SMIM17 (P156L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588244	NM_001370215.1(ZNF71):c.434G>A (p.Gly145Asp)	ZNF71, ZNF71-SMIM17 (G145D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547490	NM_001370215.1(ZNF71):c.877G>C (p.Glu293Gln)	ZNF71, ZNF71-SMIM17 (E293Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533516	NM_001370215.1(ZNF71):c.997C>T (p.Pro333Ser)	ZNF71, ZNF71-SMIM17 (P333S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522652	NM_001370215.1(ZNF71):c.553G>A (p.Glu185Lys)	ZNF71, ZNF71-SMIM17 (E185K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522095	NM_001370215.1(ZNF71):c.950T>C (p.Leu317Pro)	ZNF71, ZNF71-SMIM17 (L257P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514452	NM_001370215.1(ZNF71):c.1231G>T (p.Val411Leu)	ZNF71, ZNF71-SMIM17 (V411L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510838	NM_001370215.1(ZNF71):c.275G>T (p.Gly92Val)	ZNF71, ZNF71-SMIM17 (G32V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480618	NM_001370215.1(ZNF71):c.1215G>T (p.Gln405His)	ZNF71, ZNF71-SMIM17 (Q345H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458503	NM_001370215.1(ZNF71):c.916G>T (p.Asp306Tyr)	ZNF71, ZNF71-SMIM17 (D306Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370932	NM_001370215.1(ZNF71):c.1283C>T (p.Ser428Leu)	ZNF71, ZNF71-SMIM17 (S368L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338722	NM_001370215.1(ZNF71):c.389G>A (p.Gly130Asp)	ZNF71, ZNF71-SMIM17 (G130D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299357	NM_001370215.1(ZNF71):c.206A>T (p.Asp69Val)	ZNF71, ZNF71-SMIM17 (D9V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299056	NM_001370215.1(ZNF71):c.323C>T (p.Pro108Leu)	ZNF71, ZNF71-SMIM17 (P48L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274308	NM_001370215.1(ZNF71):c.1565G>T (p.Gly522Val)	ZNF71, ZNF71-SMIM17 (G462V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235823	NM_001370215.1(ZNF71):c.1415G>A (p.Cys472Tyr)	ZNF71, ZNF71-SMIM17 (C412Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223667	NM_001370215.1(ZNF71):c.899A>G (p.Lys300Arg)	ZNF71, ZNF71-SMIM17 (K300R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214066	NM_001370215.1(ZNF71):c.952A>G (p.Ile318Val)	ZNF71, ZNF71-SMIM17 (I318V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209851	NM_001370215.1(ZNF71):c.326G>A (p.Arg109Gln)	ZNF71, ZNF71-SMIM17 (R49Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206214	NM_001370215.1(ZNF71):c.313C>T (p.Pro105Ser)	ZNF71, ZNF71-SMIM17 (P105S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777547	NM_001370215.1(ZNF71):c.212C>T (p.Ser71Leu)	ZNF71, ZNF71-SMIM17 (S11L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 39