ClinVar for Gene (Select 284408) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259575	NM_206894.4(ZNF790):c.1114G>A (p.Gly372Arg)	ZNF790, ZNF790-AS1 (G372R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259574	NM_206894.4(ZNF790):c.1385G>A (p.Gly462Asp)	ZNF790, ZNF790-AS1 (G462D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259573	NM_206894.4(ZNF790):c.1774A>G (p.Thr592Ala)	ZNF790, ZNF790-AS1 (T592A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259572	NM_206894.4(ZNF790):c.1852G>A (p.Glu618Lys)	ZNF790, ZNF790-AS1 (E618K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198436	NM_206894.4(ZNF790):c.952G>A (p.Ala318Thr)	ZNF790, ZNF790-AS1 (A318T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198435	NM_206894.4(ZNF790):c.920A>G (p.Glu307Gly)	ZNF790, ZNF790-AS1 (E307G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198434	NM_206894.4(ZNF790):c.55T>G (p.Trp19Gly)	ZNF790, ZNF790-AS1 (W19G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3198433	NM_206894.4(ZNF790):c.466G>A (p.Val156Met)	ZNF790, ZNF790-AS1 (V156M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198432	NM_206894.4(ZNF790):c.32C>G (p.Ala11Gly)	ZNF790, ZNF790-AS1 (A11G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3198431	NM_206894.4(ZNF790):c.307A>T (p.Ile103Leu)	ZNF790, ZNF790-AS1 (I103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198430	NM_206894.4(ZNF790):c.249G>C (p.Gln83His)	ZNF790, ZNF790-AS1 (Q83H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198428	NM_206894.4(ZNF790):c.1829T>G (p.Ile610Ser)	ZNF790, ZNF790-AS1 (I610S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198427	NM_206894.4(ZNF790):c.1523G>A (p.Cys508Tyr)	ZNF790, ZNF790-AS1 (C508Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198425	NM_206894.4(ZNF790):c.1267G>C (p.Glu423Gln)	ZNF790, ZNF790-AS1 (E423Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615416	NM_206894.4(ZNF790):c.401A>C (p.Gln134Pro)	ZNF790, ZNF790-AS1 (Q134P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613792	NM_206894.4(ZNF790):c.989G>T (p.Arg330Ile)	ZNF790, ZNF790-AS1 (R330I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612169	NM_206894.4(ZNF790):c.1421G>C (p.Gly474Ala)	ZNF790, ZNF790-AS1 (G474A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608246	NM_206894.4(ZNF790):c.315A>C (p.Arg105Ser)	ZNF790, ZNF790-AS1 (R105S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569283	NM_206894.4(ZNF790):c.821G>A (p.Arg274Gln)	ZNF790, ZNF790-AS1 (R274Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555768	NM_206894.4(ZNF790):c.1435G>A (p.Glu479Lys)	ZNF790, ZNF790-AS1 (E479K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546019	NM_206894.4(ZNF790):c.925C>T (p.Pro309Ser)	ZNF790, ZNF790-AS1 (P309S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527100	NM_206894.4(ZNF790):c.1838T>C (p.Phe613Ser)	ZNF790, ZNF790-AS1 (F613S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516592	NM_206894.4(ZNF790):c.1488C>G (p.His496Gln)	ZNF790, ZNF790-AS1 (H496Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489303	NM_206894.4(ZNF790):c.931G>C (p.Glu311Gln)	ZNF790, ZNF790-AS1 (E311Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485735	NM_206894.4(ZNF790):c.347G>A (p.Cys116Tyr)	ZNF790, ZNF790-AS1 (C116Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457818	NM_206894.4(ZNF790):c.1391A>G (p.Glu464Gly)	ZNF790, ZNF790-AS1 (E464G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406806	NM_206894.4(ZNF790):c.1885A>G (p.Ser629Gly)	ZNF790, ZNF790-AS1 (S629G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406629	NM_206894.4(ZNF790):c.1299G>C (p.Trp433Cys)	ZNF790, ZNF790-AS1 (W433C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403994	NM_206894.4(ZNF790):c.1603G>A (p.Val535Ile)	ZNF790, ZNF790-AS1 (V535I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378130	NM_206894.4(ZNF790):c.1402C>T (p.His468Tyr)	ZNF790, ZNF790-AS1 (H468Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367764	NM_206894.4(ZNF790):c.1393T>C (p.Phe465Leu)	ZNF790, ZNF790-AS1 (F465L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365034	NM_206894.4(ZNF790):c.1529A>G (p.Glu510Gly)	ZNF790, ZNF790-AS1 (E510G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357682	NM_206894.4(ZNF790):c.373A>G (p.Thr125Ala)	ZNF790, ZNF790-AS1 (T125A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350619	NM_206894.4(ZNF790):c.1130G>A (p.Arg377His)	ZNF790, ZNF790-AS1 (R377H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339799	NM_206894.4(ZNF790):c.1781A>C (p.Tyr594Ser)	ZNF790, ZNF790-AS1 (Y594S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331817	NM_206894.4(ZNF790):c.971A>T (p.His324Leu)	ZNF790, ZNF790-AS1 (H324L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331815	NM_206894.4(ZNF790):c.970C>A (p.His324Asn)	ZNF790, ZNF790-AS1 (H324N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310916	NM_206894.4(ZNF790):c.1324A>G (p.Lys442Glu)	ZNF790, ZNF790-AS1 (K442E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282151	NM_206894.4(ZNF790):c.35T>A (p.Val12Glu)	ZNF790, ZNF790-AS1 (V12E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2276532	NM_206894.4(ZNF790):c.334C>G (p.Leu112Val)	ZNF790, ZNF790-AS1 (L112V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271526	NM_206894.4(ZNF790):c.1552G>C (p.Gly518Arg)	ZNF790, ZNF790-AS1 (G518R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245007	NM_206894.4(ZNF790):c.720T>A (p.Ser240Arg)	ZNF790, ZNF790-AS1 (S240R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 147631	GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	ALKBH6, ANKRD27 +439 more	Copy number loss	See cases	GPathogenic
Select item 146619	GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	ALKBH6, ANKRD27 +459 more	Copy number loss	See cases	GPathogenic
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 45