Related gene-specific medical variations for Gene (Select 11244) - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3193522	NM_007222.5(ZHX1):c.511G>A (p.Val171Ile)	ZHX1, ZHX1-C8orf76 (V171I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193521	NM_007222.5(ZHX1):c.272C>T (p.Ser91Leu)	ZHX1, ZHX1-C8orf76 (S91L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193520	NM_007222.5(ZHX1):c.26C>T (p.Thr9Ile)	ZHX1, ZHX1-C8orf76 (T9I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193519	NM_007222.5(ZHX1):c.226A>C (p.Thr76Pro)	ZHX1, ZHX1-C8orf76 (T76P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193518	NM_007222.5(ZHX1):c.2237G>A (p.Gly746Glu)	ZHX1, ZHX1-C8orf76 (G746E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193517	NM_007222.5(ZHX1):c.1963G>T (p.Ala655Ser)	ZHX1, ZHX1-C8orf76 (A655S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193516	NM_007222.5(ZHX1):c.1952A>G (p.Asp651Gly)	ZHX1, ZHX1-C8orf76 (D651G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193515	NM_007222.5(ZHX1):c.1765A>T (p.Asn589Tyr)	ZHX1, ZHX1-C8orf76 (N589Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193514	NM_007222.5(ZHX1):c.164C>T (p.Ser55Phe)	ZHX1, ZHX1-C8orf76 (S55F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193513	NM_007222.5(ZHX1):c.1511C>T (p.Thr504Met)	ZHX1, ZHX1-C8orf76 (T504M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193512	NM_007222.5(ZHX1):c.1475C>T (p.Ser492Leu)	ZHX1, ZHX1-C8orf76 (S492L)	Single nucleotide variant (intron variant +2 more)	not specified	GUncertain significance
Select item 2681654	NM_007222.5(ZHX1):c.1140T>C (p.Gly380=)	ZHX1, ZHX1-C8orf76	Single nucleotide variant (synonymous variant +2 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2611383	NM_007222.5(ZHX1):c.2596C>T (p.Arg866Trp)	ZHX1, ZHX1-C8orf76 (R866W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2605285	NM_007222.5(ZHX1):c.730C>A (p.Pro244Thr)	ZHX1, ZHX1-C8orf76 (P244T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2550428	NM_007222.5(ZHX1):c.1967C>G (p.Pro656Arg)	ZHX1, ZHX1-C8orf76 (P656R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2538085	NM_007222.5(ZHX1):c.647C>G (p.Pro216Arg)	ZHX1, ZHX1-C8orf76 (P216R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2526439	NM_007222.5(ZHX1):c.2282G>C (p.Arg761Thr)	ZHX1, ZHX1-C8orf76 (R761T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2493436	NM_007222.5(ZHX1):c.1775T>C (p.Val592Ala)	ZHX1-C8orf76, ZHX1 (V592A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2479609	NM_007222.5(ZHX1):c.110C>T (p.Pro37Leu)	ZHX1, ZHX1-C8orf76 (P37L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2466120	NM_007222.5(ZHX1):c.2251C>T (p.Arg751Trp)	ZHX1-C8orf76, ZHX1 (R751W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459696	NM_007222.5(ZHX1):c.1493T>C (p.Met498Thr)	ZHX1, ZHX1-C8orf76 (M498T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2395150	NM_007222.5(ZHX1):c.1325C>T (p.Pro442Leu)	ZHX1, ZHX1-C8orf76 (P442L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2358523	NM_007222.5(ZHX1):c.1300G>A (p.Ala434Thr)	ZHX1, ZHX1-C8orf76 (A434T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2319787	NM_007222.5(ZHX1):c.442A>G (p.Ile148Val)	ZHX1, ZHX1-C8orf76 (I148V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2313353	NM_007222.5(ZHX1):c.712A>G (p.Ile238Val)	ZHX1, ZHX1-C8orf76 (I238V)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2302551	NM_007222.5(ZHX1):c.158A>G (p.His53Arg)	ZHX1, ZHX1-C8orf76 (H53R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2258343	NM_007222.5(ZHX1):c.703A>G (p.Ser235Gly)	ZHX1, ZHX1-C8orf76 (S235G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255677	NM_007222.5(ZHX1):c.484A>T (p.Asn162Tyr)	ZHX1, ZHX1-C8orf76 (N162Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2217869	NM_007222.5(ZHX1):c.931A>G (p.Met311Val)	ZHX1, ZHX1-C8orf76 (M311V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2211772	NM_007222.5(ZHX1):c.1309A>G (p.Thr437Ala)	ZHX1, ZHX1-C8orf76 (T437A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2210144	NM_007222.5(ZHX1):c.851A>G (p.Asn284Ser)	ZHX1, ZHX1-C8orf76 (N284S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Links from Gene

Items: 31